Next Article in Journal
Differences in Chemical Constituents between Dalbergia oliveri Heartwood and Sapwood and Their Effect on Wood Color
Next Article in Special Issue
Phenolic Compounds Recovery from Blood Orange Peels Using a Novel Green Infrared Technology Ired-Irrad®, and Their Effect on the Inhibition of Aspergillus flavus Proliferation and Aflatoxin B1 Production
Previous Article in Journal
Structure-Activity Relationship Studies Based on 3D-QSAR CoMFA/CoMSIA for Thieno-Pyrimidine Derivatives as Triple Negative Breast Cancer Inhibitors
Previous Article in Special Issue
Overview of the Polyphenols in Salicornia: From Recovery to Health-Promoting Effect
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Natural Polyphenol Recovery from Apple-, Cereal-, and Tomato-Processing By-Products and Related Health-Promoting Properties

by
Katalin Szabo
1,2,
Laura Mitrea
1,2,
Lavinia Florina Călinoiu
2,
Bernadette-Emőke Teleky
2,
Gheorghe Adrian Martău
2,
Diana Plamada
2,
Mihaela Stefana Pascuta
2,
Silvia-Amalia Nemeş
2,
Rodica-Anita Varvara
2 and
Dan Cristian Vodnar
2,*
1
Institute of Life Sciences, University of Agricultural Sciences and Veterinary Medicine, 400372 Cluj-Napoca, Romania
2
Department of Food Science and Technology, University of Agricultural Sciences and Veterinary Medicine, 400372 Cluj-Napoca, Romania
*
Author to whom correspondence should be addressed.
Molecules 2022, 27(22), 7977; https://doi.org/10.3390/molecules27227977
Submission received: 14 October 2022 / Revised: 9 November 2022 / Accepted: 11 November 2022 / Published: 17 November 2022
(This article belongs to the Special Issue Natural Polyphenols in Human Health)

Abstract

:
Polyphenols of plant origin are a broad family of secondary metabolites that range from basic phenolic acids to more complex compounds such as stilbenes, flavonoids, and tannins, all of which have several phenol units in their structure. Considerable health benefits, such as having prebiotic potential and cardio-protective and weight control effects, have been linked to diets based on polyphenol-enriched foods and plant-based products, indicating the potential role of these substances in the prevention or treatment of numerous pathologies. The most representative phenolic compounds in apple pomace are phloridzin, chlorogenic acid, and epicatechin, with major health implications in diabetes, cancer, and cardiovascular and neurocognitive diseases. The cereal byproducts are rich in flavonoids (cyanidin 3-glucoside) and phenolic acids (ferulic acid), all with significant results in reducing the incidence of noncommunicable diseases. Quercetin, naringenin, and rutin are the predominant phenolic molecules in tomato by-products, having important antioxidant and antimicrobial activities. The present understanding of the functionality of polyphenols in health outcomes, specifically, noncommunicable illnesses, is summarized in this review, focusing on the applicability of this evidence in three extensive agrifood industries (apple, cereal, and tomato processing). Moreover, the reintegration of by-products into the food chain via functional food products and personalized nutrition (e.g., 3D food printing) is detailed, supporting a novel direction to be explored within the circular economy concept.

Graphical Abstract

1. Introduction

By-products of agro-industrial provenance and food waste are severe global concerns, particularly in many developed countries [1]. Food consumption has increased as a consequence of urbanization, population expansion, and economic growth, and it remains a consistent issue worldwide in the long run [2,3]. The most bothersome sectors are the wheat flour production, apple juice production, and tomato-processing industries, which generate massive amounts of residues, as a result of the extensive yearly processed tonnage (Figure 1). On the other hand, the low cost and straightforward availability of this residual biomass shelter the economic prospects of its potentially valuable components [4].
In general, cereal grains are the world’s main food source, contributing up to 300 million tons (Mt) of food products yearly according to FAOSTAT (http://www.fao.org/ accessed on 10 October 2022) [5]. The primary cereals produced are maize, wheat, rice, barley, and oat crops, from which maize is mainly submerged as flour, animal feed, and substrate in ethanol production [6], while wheat is consumed worldwide mostly in the form of flour [7].
Maize (Zea mays L.), cultivated globally, is the prime cereal grown in the world [8]. As presented in Figure 1A, its production increased by more than 50% in the last 20 years and is the most significant starch supply, and subsequently, it is one of the main organic by-product generators in the world [6]. In Europe, cereal production increased more than four times from 2000 to 2020, with the highest production in Western and Eastern Europe (Figure 1B). According to a recent study, in Europe, these cereal by-products, via integration with foodstuffs, could replace as many as 8.8 Mt of edible grains [9].
Wheat (Triticum aestivum L.) is one of the world’s most prominent cereals. According to FAOSTAT, the global output in 2020 was over 760 million tons (Mt), up from 580 Mt in 2000, showing a 30.97% increase in wheat production over the last two decades, and the global output is expected to increase gradually in the future [10]. In agreement with the European Flour Millers’ Report (2016), more than 45 Mt of wheat and oats is processed annually in Europe, creating over 6.5 Mt of by-products, which are predominantly used for animal nutrition [11]. By-products such as bran are a rich source of beneficial phytochemicals such as dietary fibers, minerals, vitamins, polyphenols, and phytosterols, known for their health-promoting properties [7,11,12,13]. Phenolic acids are among these components since they are categorized as bioactive phytochemicals and have a significant impact on human health [14].
Apple (Malus domestica sp.) is one of the most widespread fruits on the global scale. In 2020, the global output was over 86 Mt, up from just over 59 Mt in 2000, indicating an incremental tendency of apple production, with 46.19% in the last two decades [5]. China is the leading contributor to overall production with 46.85%, followed by the USA with 5.38%, and Turkey with 4.97%, and from Europe, the main contributor is Poland with 4.11%, as shown in Figure 1C. Furthermore, the worldwide output is predicted to rise steadily in the future [15,16].
The resulting by-product of apple pressing/processing, which derives from juice, cider, wine, distilled spirits, and vinegar production, as well as the formulation of jellies, is known as apple pomace (AP). Solid pomace makes up to 20–35% of the apple fruit’s fresh weight and is composed of a mixture of pulp, peel, core, seed, and calyx. Approximately 95.5% of the solid waste is produced by epi-mesocarp [17]. Dietary fiber, which makes up around 65% of the dry weight of AP, is the main component from a nutritional point of view, and the majority of dietary fiber in all pomace is insoluble. Apple seeds include significant amounts of proteins and lipids, up to 49.5 and 24%, respectively. Additionally, hemicellulose is the second-most significant fiber in AP (19.9–32.2%), and cellulose accounts for a crucial part, comprising 43% of the pomace [18]. The by-products of the seed and peel are rich in phenolic chemicals, primarily chlorogenic acid and phloridzin [19].
Tomatoes (Solanum lycopersicum L.) are considered one of the world’s most popular vegetables but are classified as a fruit. In Europe, it was first domesticated in Spain [20], and the main producers are represented in Figure 1D. The global output of tomatoes increased to 186 Mt in 2020, up from just over 109 Mt in 2000 [5]. According to FAOSTAT, a substantial increase in tomato production can be observed in the last two decades, precisely above 70%. The major producers are China with 34.67%, followed by India with 11.01%, Turkey with 7.07%, and the USA with 6.54% of global tomato crop production. Additionally, the global output is expected to increase gradually in the future [2]. More than one-third of the tomatoes are processed due to their perishable nature, and considerable amounts of by-products are generated via juice, sauces, ketchup, or puree production, among other meals. The removal of tomato peels, seeds, and tiny amounts of pulp can add between 5 and 30% to the cost of the primary products, and the by-products are a source of environmental discomfort due to their high moisture content, which favors bacterial growth and carbon dioxide emission [21]. The scientific literature confirms the presence of health-promoting compounds such as carotenoids, polyphenols, tocopherols, terpenes, and sterols in industrial tomatoes and their by-products, and endorses their extraction and revalorization in functional food products, as the bioactive substances resist to industrial processes [22,23].
Polyphenols are secondary metabolites that contain one or more hydroxyl groups, being one of the largest classes of valuable bioactive compounds for supporting human health [24,25]. Phenols are essentially made up of a hydroxyl group (-OH) linked directly to an aromatic hydrocarbon group, whereas polyphenols are larger polymers of 12 phenolic hydroxyl groups linked to five-to-seven aromatic rings [26,27]. Based on recent trends regarding healthier lifestyles and an increase in the consumption of foodstuffs derived from natural resources without any environmental drawbacks, the reintegration of by-products generated by the food industry is an important topic [28,29].
Green alternatives to lessen environmental pollution and waste generation include renewable biomaterials, and wheat-, apple-, and tomato-processing by-products can be framed into this category. In recent years, innovative and inventive applications of these by-products have contributed to the steady advancement of bioeconomy and biotechnology through the extraction and/or revalorization of natural phenolic compounds [30].
The use of agro-industrial derivatives might provide an additional source of income, and it could reduce by-product disposal and improve the nutritional profile of functional food items at the same time. Utilizing grain, tomato, and apple by-products from industrial production may provide a generous supply of nutrients, and their repurposing might represent a substantial source of revenue. Therefore, the objective of the current literature review is to highlight the primary phenolic components linked to human health, which can be found in the by-products of these three major agrifood industries (apple, cereal, and tomato processing), and to encourage their recovery and, accordingly, reintegration into the food chain using circular economy principles. Nonetheless, based on the findings of this study, it is projected that the food-processing industries could better manage their by-products and waste (e.g., through the incorporation of by-products into food formulations to boost the nutritional value), therefore avoiding a major environmental concern.

2. Polyphenols in Apple-Processing By-Products

Apples are one of the most consumed fruits worldwide, both in industry and at the individual population level [31]. Approximately 11 million metric tons of apples is produced and used annually in the apple-processing industry and alcoholic beverage production in Europe [32]. Apple pomace is one of the most widely produced agrifood wastes, with an annual production rate of about 4 million tons worldwide [33]. The recovery rate for this by-product, however, is modest. Pomace is frequently discarded and dumped in landfills as waste, which causes environmental issues and presents a potential risk to public health [3,34].
The amount of pomace resulting after apple processing can be reused in biotechnological routs as a substrate for the production of different compounds, such as flavoring compounds, pigments, fuel, and citric acid, or as raw materials for the extraction of fibers and phenolic compounds [35,36,37,38].
From a nutritional point of view, apple pomace is a by-product rich in fibers, vitamins, minerals, phenolic compounds, and pigments [19]. All these macronutrients have a significant role in the human organism through their effects on metabolism. Therefore, apple pomace has attracted researchers’ consideration, as well as stakeholders’ attention, by virtue of its valuable composition and by presenting suitable properties for further sustainable use [39].
The nutritional profile of apple pomace is mainly represented by phenolic compounds, carbohydrates, and fibers, as presented in table Table 1. These constituents can help treat gastrointestinal disorders, decrease serum triglycerides and LDL-cholesterol, and regulate glycemia [40,41]. All these effects in the human organism can be explained through their high concentration of the beneficial compounds mentioned above, primarily exerting anti-inflammatory and antioxidant roles [42].
In addition to the benefits, the consumption of apple pomace may raise questions associated with toxicity when it comes to its applicability in the food industry [44], with seeds representing 4–5% of the apple pomace [45]. Apple seeds contain a plant toxin called cyanogenic glycoside amygdalin, which can interact with digestive enzymes, resulting in the release of hydrogen cyanide. This toxin can cause different symptoms, from mild symptoms such as dizziness to severe symptoms such as paralysis and coma [46]. However, to reach poisoning levels, the ingested quantity must be significantly high; more exactly, between 83–500 apple seeds are needed to reach the poisoning level, or the person must consume more than 800 g of apple pomace [33,47]. Studies on apple seed oil have confirmed the safety of its use, as the limit was found to be below the toxicity level [48].
Phenolic compounds are concentrated mainly in the core, seeds, peel, calyx, and stem, as well as in smaller amounts in the pulp, highlighting how apple pomace can be valorized through its high amount of antioxidant compounds. As shown in Figure 2, the total phenolic content of seeds has a higher value compared with the pulp, followed by the peel, both being part of apple pomace.
The predominant phenolic compound families in apple pomace are dihydrochalcones, procyanidins, flavan-3-ol monomers, flavonols, anthocyanidins, and hydroxycinnamic acids. The most representative compounds are phlorizin from the dihydrochalcones family, chlorogenic acid from the hydroxycinnamic acids family, and epicatechin from the flavan-3-ol monomer family [50].
One of the representative phenolic compounds in apples and, remarkably, apple pomace, is phlorizin (Figure 3A). As the main compound from the dihydrochalcone family, the amount of phlorizin in apple pomace is approximately 1.6 mg/g dry weight, highlighted in a study by Lavelli et al. on the stability of phenolic compounds in apple pomace [51]. Phlorizin is used as a marker of apple varieties and is mainly concentrated in apple seeds. This polyphenol is also used as a reliable marker for spotting the presence of apples, a less expensive alternative compared with the reported fruits [52].
Nevertheless, it also acts as a strong antioxidant, anti-inflammatory, and antimicrobial compound [53,54]. Regarding its benefits, phlorizin exerts several health benefits, mainly in diabetes, due to its ability to alter the glucose absorbed and excreted. A recent study illustrated that the intestine and kidney’s sodium/glucose cotransporters are specifically and competitively inhibited by phlorizin. In addition, postprandial hyperglycemia therapy in diabetes and other associated illnesses, such as obesity, may benefit from this characteristic [55]. A study conducted on streptozotocin-induced diabetic mice showed that a diet containing 0.5% phlorizin significantly improves the exacerbated elevations in blood glucose levels [56,57]. Another health benefit can be seen in colitis, where it acts as a protective compound for the intestinal brush border [58].
Chlorogenic acid (Figure 3B) is representative in the peel and flesh of apples compared with their seeds. Chlorogenic acid is a powerful antioxidant known for counteracting pathologies caused by oxidative processes [59,60]. A study conducted on the improvement of mood and cognition in the elderly showed enhanced results after the administration of enriched decaffeinated coffee with chlorogenic acid, displaying that the consumption of products containing chlorogenic acid can help in the treatment of neuro-cognitive diseases [61]. Besides the benefits mentioned previously, chlorogenic acid can also confer positive effects by lowering blood pressure, confirmed in a randomized trial involving healthy volunteers after the administration of 400 mg chlorogenic acid in 400 mL low-nitrate water. This effect can be explained by the ability of phenolic compounds to increase nitric oxide, which improves cardiovascular health [62].
The third phenolic compound found in apple pomace in smaller amounts is epicatechin (Figure 3C). Besides all its fulfilled roles (e.g., antioxidation, anti-inflammation), epicatechin can exert its role in diabetes, cancer, and cardiovascular disease, acting as a neuroprotective compound, and it improves muscle performance [63]. Cilleros et al. showed, in an in vitro study, the effect of epicatechin in regulating glucose uptake and bolstering the insulin signaling pathway [64]. A study conducted on human monocytic cells (THP1 cells) showed similar results regarding the beneficial effects of epicatechin in diabetes through the attenuation of high-glucose-induced inflammation [65].

3. Polyphenols in Cereal-Processing By-Products

Rice, wheat, barley, and corn are the most prevalent cereals globally, accounting for more than 90% of total cereal consumption [8]. By-products from the grain processing food industry include bran, straw, germ, and spent brewery grain [8,14]. Recent scientific studies confirm that the by-products of grain milling contain a wide range of beneficial components that support human health. These components, illustrated in Figure 4, include dietary fiber, vitamins, minerals, phytosterols, and polyphenols [66].
The most common polyphenols in cereal by-products are flavonoids and phenolic acids, categorized into two large classes: hydroxybenzoic acids and hydroxycinnamic acids [67]. Gallic, vanillic, p-hydroxybenzoic, protocatechuic, syringic, and salicylic acids are all hydroxybenzoic acids with a C6-C1 structure. Hydroxycinnamic acids, on the other hand, have a C6-C3 structure comprising caffeic, ferulic, p-coumaric, chlorogenic, and synaptic acids [68].
Most of the phytochemicals found in cereal grains are identified in the bran fraction and are primarily bound to dietary fiber components, such as cellulose, hemicellulose, and lignin. In cereal by-products, a smaller amount of phenolic acid is present in a free form, and a larger amount is present in a bound form. In corn, for example, the free phenolic fraction ranges between 1 and 5 mg/100 g DW, while the bound fraction ranges between 150 and 300 mg/100 g DW [69]. The common phytochemical composition of cereal bran is presented in Table 2.
Ferulic acid is primarily found in cereal by-products with values over 1000 μg/g DW [69]. Wheat bran contains 90% ferulic acid, while oat bran contains 75% ferulic acid [84]. The metabolism of phenylalanine and tyrosine is responsible for their widespread presence in plant-based sources. Ferulic acid may be found in cereals in several forms, including free ferulic acid, γ-oryzanol, ferulic acid monoesters, and certain triterpene alcohols [84]. Ferulic acid is covalently linked to cell wall molecules, such as lignin, polysaccharides, long-chain fatty acids, and flavonoids via ester, ether, and amide bonds [85,86]. Because of the position of the hydrogen atom in the hydroxyl group of ferulic acid, it reacts with a free radical to produce an antioxidant effect [69,87].
Cereal bran is also rich in vanillic, syringic, salicylic, caffeic, and p-coumaric acids [68]. Vanillic acid (4-hydroxy-3-methoxybenzoic acid) is a hydroxybenzoic acid, a major component of vanilla flavor, which is used in the food industry for flavoring and preserving applications, along with the beverage, pharmaceutical, cosmetic, and tobacco industries [88].
Another predominant phenolic acid found in cereal bran is p-coumaric acid, which is the most available form of cinnamic acid and the most common cinnamic acid isomer in nature [89]. Coumaric acid, like the vast majority of phenolic acids, is found in lower concentrations in the endosperm of grains, with significantly increased concentrations in the peripheral tissues. Barley (230 μg/g), wheat (166 μg/g), oats (165 μg/g), and corn (2555 μg/g) have the highest levels of p-coumaric acid in their pericarp fractions [89].
Generally, phenolic acids have powerful biological effects such as antioxidant activity, antibacterial activity, anticancer properties, and anti-inflammatory effects, along with flavonoids. Flavonoids derived from grain-processing by-products contain antioxidant and anti-inflammatory functional groups. Flavonoid glycosides, such as cyanidin 3-glucoside, have been found to provide antioxidant and anti-inflammatory effects, and their gastrointestinal absorption rate is high. These chemicals’ bioavailability is poor, ranging from 1–100 nmol/L of the total plasma concentration [87]. However, bounded polyphenols can be released in the colon by intestinal bacteria and certain enzymes, resulting in bioavailable phenolic metabolites with possible health advantages.
A study conducted on the effects of phenolic compounds on the large intestine’s modulation showed that chlorogenic acid was converted into caffeic acid during the first stage of microbial biotransformation (dehydroxylation, dehydrogenation, or ester hydrolysis), and the primary metabolites found included di- and mono-hydroxylated phenylpropionic acids, m-coumaric, and hippuric acid [90].
An in vivo study conducted by Nuria Mateo Anson and colleagues [91] investigated how processed bran from whole wheat bread modifies the bioavailability of phenolic acids and exerts antioxidant and anti-inflammatory effects by examining postprandial plasma. The results showed a two- to three-fold increase in the bioavailability of ferulic acid, vanillic acid, sinapic acid, and 3,4-dimethoxybenzoic acid after eating bioprocessed bread. Furthermore, the ratio of pro-anti-inflammatory cytokines was significantly lower [92]. Another study examined the impact of regulated ferulic acid intake on lipid profiles, oxidative stress, and inflammatory activity in hyperlipidemic individuals. The improvement of the lipid profile, oxidation of LDL-cholesterol, decrease in oxidative stress, and reduction in inflammation were noticed after the consumption of 1000 mg of ferulic acid daily [93]. Thus, a diet rich in phenolic compounds can help prevent illnesses caused by oxidative stress and inflammation, as well as relieve symptoms associated with chronic diseases, including cardiovascular disease, obesity, and metabolic syndrome.

4. Polyphenols in Tomato-Processing By-Products

Tomatoes are highly appreciated and consumed for their appetizing taste and various shapes and colors, as well as for their antioxidant properties and chemoprotective and cardioprotective effects. Tomato-based food products such as juices, ketchup, sauces, paste, and puree generate large quantities of wet solid by-products with harmful environmental consequences; however, paradoxically, these solid wastes are a promising source of health-promoting compounds, such as carotenoids and polyphenols [2,22,94,95]. The main tomato-processing by-products are peels and seeds, together with small amounts of pulp. For instance, the seeds account for 10% of the fruit and 60% of the total waste [96].
Tomatoes contain various phytochemicals and bioactive compounds that are able to endure industrial treatments and still remain in the tomato waste [97]. Therefore, the valorization of tomato by-products could be a valuable source of natural bioactive molecules for human health. Their reintegration into the food chain may be achieved by using them as natural additives in food production and/or nutraceuticals [2]. Bioactive compounds found in tomato by-products are carotenoids, polyphenols, vitamins, proteins, and high-quality fatty acids [95,98,99]. Among these active molecules, polyphenols have antioxidant and anti-inflammatory properties that play an essential role in human health [25]. The primary phenolic compounds found in tomato by-products are flavonols and phenolic acids, illustrated in Figure 5, with quercetin, naringenin, and rutin being the predominant molecules [100].
Tomato peels contain a significantly higher level of phenolic compounds in comparison with the seeds and pulp; 83% of the flavonols in tomatoes are present in the peels [101]. As an example, a higher level of polyphenol content in tomato peel by-products (33.5 mg TAE/100 g dried peel) was reported by Sarkar and Kaul (2014) compared with tomato seed by-products (20.11 TAE/100 g meal) [94]. However, the profile of polyphenol contents found in tomato by-products is dependent on several factors, such as the fruit varieties [99], the geographical origin of the fruits [101], and the extraction methods used on the target compound [102]. Some examples regarding the total phenolic content in tomato by-products considering location and extraction method, as well as their antimicrobial and antioxidant activity, are provided in Table 3. Given the fact that tomato-processing by-products are most abundant in carotenoids as primary bioactive molecules, the antioxidant activity and antimicrobial effects might be attributed to the synergistic antioxidative effects of lycopene with other bioactive compounds to enhance their overall antioxidant activity [103].
The antioxidant and antimicrobial capacity of polyphenols has attracted increasing interest. These compounds have the ability to scavenge free radicals and reactive oxygen species, which are known to be involved in the development of cardiovascular diseases and several cancers [106]. For a more thorough study regarding the mechanism of action of polyphenols, Zhang and Tsao (2016) critically reviewed their biological activities, including antioxidative stress activity, anti-inflammatory effects, etc. [107].
The antioxidant capacity of tomato by-products can be divided between the hydrophilic and the lipophilic fractions. The antioxidant activity generated by polyphenols is attributed to the hydrophilic fraction since these molecules are soluble in water. The entrapment of polyphenols in the major insoluble fraction of tomato peels, formed mainly by hemicelluloses, leads to low antioxidant activity. The antioxidant activity of tomato peel fiber was found to be 3.90 µmol TE/g for the hydrophilic extract, lower than expected [105]. The mean value of the antioxidant activity of ten varieties of tomato by-products was found to be about 4.90 µmol TE/g, with the highest value being 5.74 µmol TE/g. Furthermore, little to any correlation has been found between the total phenolic content and antioxidant activity [99]. However, antioxidant activity might not always correlate with the number of phenols; it could be connected to the mutual interactions between all hydrophilic antioxidants and other constituents of the tomato by-products [95].
Even though tomato peels and seeds have relatively modest antioxidant activities, it is necessary to consider other remarkable attributes of these by-products, such as the antimicrobial capacity of polyphenols. Due to their hydrophobicity, phenolic compounds such as flavonols are capable of penetrating the cell phospholipid membranes of bacteria, able to exert their antibacterial activity inside the cell [108]. Gram-negative bacteria have cell walls surrounded by external membranes, which have high lipopolysaccharide contents. This makes Gram-negative bacteria less sensitive to the action of bioactive compounds such as polyphenols. This phenomenon was proved when the phenolic extracts of ten varieties of tomato by-products were tested against seven bacterial strains. The Gram-positive bacteria showed a higher sensitivity to the extract compared with the Gram-negative bacteria. All extracts were effective against Staphylococcus aureus, especially the Tiny Tim tomato variety, with a higher amount of flavonol glycosides and isochlorogenic acid. The Mirsini extract presented moderate antibacterial activity against Gram-negative bacteria (Pseudomonas aeruginosa, Salmonella typhimurium, Klebsiella pneumoniae, and Escherichia coli) [99].
The microbial contamination of soil can also influence the antimicrobial activity of fresh tomato by-products. When the Portuguese national microbiological guidelines for ready-to-eat foods were considered, unwashed and impure tomato by-products showed unsatisfactory Enterobacteriaceae, yeast, and Bacillus cereus spp. microbial counts for these food products. Washed and disinfected tomato by-products maintained these bacteria within satisfactory limits. Thus, tomato by-products have antimicrobial potential and can be used in food formulations or for cooking also considering their carotenoid content as natural food colorants. Furthermore, 6 months of frozen storage causes no substantial variation in microbial counts. Storing dry tomato by-products at room temperature slightly decreases the microbial counts of tested microorganisms [109]. Therefore, tomato by-products may control microbiological growth and may play an important role in the prevention of foodborne diseases.

5. Health-Promoting Properties of Polyphenol-Rich Diets

Since ancient times, the consumption of fresh vegetables, various green leaves, seeds, and fruits has promoted an optimal health state in the human organism without people knowing the exact mechanism of action. Polyphenols have contributed significantly to the enhancement of health status in humans over time, mainly due to their antioxidant properties, prebiotic potential, and, in some cases, their antimicrobial effects [25,110]. Based on their antioxidant effects, the polyphenolic structures are involved in the stimulation of the immune response against the progression of degenerative disorders such as metabolic syndrome, neurological affections, and different types of cancer. In addition, diets rich in polyphenols have been proven to sustain the optimal functioning of the immune system, as they enhance the activation of the NF-κB signaling pathway in macrophages that intervene in the management of inflammation processes [111]. Furthermore, multiple associations have been made between polyphenols and protective effects against chronic diseases based on chronic inflammation, and substantial evidence highlights the precautionary consequences of a polyphenol-rich dietary pattern [112,113,114].
The generous number of scientific reports available in recent years point out the strong antioxidant potential of vegetable-based polyphenols manifested through their antidiabetic, anti-obesity, anti-inflammatory, anticancer, hepatoprotective, cardioprotective, nephroprotective, neuroprotective, and osteoprotective effects, confirmed through various in vitro and in vivo studies [112]. In the same line, Condezo-Hoyos et al. highlighted, through a systematic review, the role of polyphenol-rich diets in clinical trials. The main results of the investigation showed substantial differences considering the consumption of 2564 mg of polyphenols (including hydroxycinnamic acids) per day [115].
Apples are among the most polyphenol-abundant fruits that are broadly consumed worldwide. Both the peels and pulp of apple fruits are rich in polyphenols, such as catechins, quercetin, rutin, phloridzin, phloretin, and chlorogenic acid, which are confirmed to exert positive effects, especially in reducing the evolution of neurodegenerative disorders [31]. At the same time, in vitro studies conducted on mice have proved that polyphenols extracted from apples have a protective effect on damaged gastrointestinal mucosa induced by drugs [31]. In addition, plenty of in vitro studies and clinical trials demonstrate the positive biological effects of polyphenol-rich foods such as apples on human and animal health, especially by stimulating the immune system. Diets consisting of moderate apple consumption maintain the general health state and accelerate the immune system’s response to pathogenic threats [116]. Due to the lower water percentage in apple by-products, the phenolic content increases compared with fresh fruit. Additionally, the exterior layer of the apple contains enzymatic and nonenzymatic antioxidants as a consequence of outer environment exposure, which is valuable for homeostasis maintenance [117].
In addition, cereal bran represents a valuable source of polyphenolic compounds. Bran derived from wheat, corn, rice, barley, sorghum, rye, oat, and millet has been proven to contain high concentrations of phenolics, flavonoids, and anthocyanins, which can inhibit the oxidation of human low-density lipoprotein (LDL) cholesterol. Moreover, the bioactive compounds found in cereal bran have great biological potential in the prevention of chronic disease development, such as cardiovascular disease, diabetes, and cancer [118].
In the same line, tomato-processing by-products contain different concentrations of polyphenolic compounds, mainly phenolic acids and flavonoids, which have been validated to be involved in decreasing triglyceride levels and regulating lipid metabolism. Nonetheless, tomato peel-derived polyphenols have shown anticarcinogenic, anti-inflammatory, anti-aggregation, and vasodilating effects in vitro and in clinical studies [119,120].

5.1. The Prebiotic Potential of Phenolic Compounds

Phenolic compounds may play an important role in the gut microbiota’s health state, acting as a prebiotic substrate for a diversity of probiotic strains [25,121]. In addition, polyphenols are considered prebiotics in the consensus document of the International Scientific Association for Probiotics and Prebiotics (ISAPP) [122]. Polyphenols such as catechin, gallic, vanillic, ferulic, and protocatechuic acids selectively stimulate probiotic strains and inhibit pathogenic ones. A study conducted by Pacheco-Ordaz et al. [123] investigated the effect of the five abovementioned polyphenols on the development of two probiotic strains, Lactobacillus rhamnosus GG ATCC 53103 and Lactobacillus acidophilus NRRLB 4495, and two pathogens, Escherichia coli 0157:H7 ATCC 43890 and Salmonella enterica serovar Typhimurium ATCC 14028. The authors observed that the combination of phenols allows for the selective growth of probiotics and inhibits the development of pathogenic bacteria [123].
Apple pomace, composed especially of seeds and peel, contains the more significant part of phenolic compounds, primarily phloridzin, chlorogenic acid, and soluble/insoluble fibers. These contribute to the diminished glycemic index and amended mineral bioavailability [124]. Besides improving the nutritional quality of food products, their applicability in food fortification promotes the viability and fermentation period of lactic acid bacteria, which can further upgrade sourdough quality [3].

5.2. Cardioprotective Effects of Polyphenols

The imbalance between free radical accumulation and antioxidant activity is one of the critical indicators contributing to the high prevalence of cardiovascular disease. This noncommunicable illness is the primary cause of mortality worldwide [125]. The current pandemic also highlighted the importance of nutrition and a healthy lifestyle regarding the immune system and the prevention of certain chronic diseases, particularly cardiovascular disease [126].
Diets comprising polyphenols extracted from apples, cereals’ bran, tomato peels showed positive activity close-connected to the well-functioning of the cardiovascular system [31]. For instance, in vivo studies on mice with cardiovascular disorders, treated with polyphenolic extracts from apple peels, showed improved results considering blood pressure, endothelial function, lipid homeostasis, and insulin resistance compared with the control group [127].
A double-blind, placebo-controlled investigation on 24 hyperlipidemic adults found that taking 1000 mg of ferulic acid daily for six weeks resulted in a significant reduction in total cholesterol (8.1%), LDL-cholesterol (9.3%), triglyceride (12.1%), and significantly increased HDL-cholesterol (4.3%) compared with placebo subjects [73]. Additionally, studies have demonstrated that regular whole grain consumption lowers the chance of developing particular illnesses, including type 2 diabetes, cardiovascular diseases, metabolic syndrome, and obesity [72,103,104]. Particular attention has been paid to the use of polyphenols in the prevention of cardiovascular-associated diseases, as these represent one of the main causes of increased mortality worldwide [105]. Moreover, ferulic acid, which abounds in wheat and oat brans, has good cardioprotective potential, as it maintains blood pressure, cholesterol, and glycemia at their optimal levels [128]. Furthermore, phenolic compounds found in tomato peels and seeds influence the cardiovascular system, mainly through their antithrombotic activity, imprinting ischemic injury prevention at the same time [129].

5.3. Polyphenols in Weight-Control Diets

Gut homeostasis is perturbed by obesity and overweightness, and it consequently enhances the ratio of Firmicutes/Bacteriodetes, which accelerate adiposity [130]. Studies conducted on polyphenols extracted from apples showed the positive impact of these compounds on weight loss and on the microbial communities of the guts of obese individuals [131]. Moreover, studies conducted on the effect of phenolic acids extracted from grain bran showed their output in reducing obesity risk and attenuating insulin resistance, thus contributing to maintaining a balanced body weight [132]. Polysaccharides, such as arabinoxylans and xylooligosaccharides extracted from cereal by-products, have a prebiotic effect, which also contributes to various metabolic dysfunctions and decreases blood cholesterol and glucose [133,134].
Polyphenols have shown a positive impact on the control of blood glucose levels, thus resulting in their positive attributes in the management of metabolic-related afflictions, such as diabetes [135]. In a systematic review performed by Coe and Ryan, several randomized clinical trials studying the effect of polyphenols in connection with carbohydrates on acute postprandial glycemic and insulin responses were analyzed. The results of the study pointed out that polyphenol-rich sources diminished the peak and early-phase glycemic response and also maintained the glycemic response in the later digestion phases. In addition, the polyphenol intake exhibited the mitigation of the insulin response, in particular, when they were consumed with bread, thus sustaining the beneficial properties in diminishing type 2 diabetes incidence [135].

6. Applicability of Recovered Polyphenols from Apple-, Cereal-, and Tomato-Processing By-Products in Functional Food Products in the Food Chain

The present concept of functional foods is the result of the gradual recognition that healthy diets derive from eating nutritious foods and from the identification of the mechanisms by which foods modulate metabolism and health. Some groups of foods, in addition to their nutritional properties, have supplementary properties for health. These types of foods are called functional foods and may be defined as any food that has a positive impact on an individual’s health, physical performance, or state of mind, in addition to its nutritious value.

6.1. Apple-Processing-Derived By-Products

The by-products of apple processing can be efficiently integrated into various foodstuffs, as specified in Table 4. Due to high fiber content, such as pectin and starch, which increases the viscosity of the products, these by-products can be integrated efficiently into functional food products, such as jellies, jams, or other foodstuffs [30]. In addition, due to several favorable health-related effects, the integration of AP is becoming more and more popular in various forms and applications [3,136].
One of the most efficient methods of preserving and integrating AP is drying and grinding it to obtain a powder, namely, AP flour. As indicated by Martau et al., 2021, the fortification of sourdough with 5 or 10% AP flour improved the microorganism’s viability due to high sugar content and enhanced the flavor of the sourdough [137]. Another study indicated an increased dietary fiber content after the inclusion of AP flour in wheat and rye crispbreads, from 9.39 to 15.89 g/100g and 15.8 to 19.89 g/100, respectively [138]. Besides, no browning reaction could be observed in the final products even if the AP flour contained increased reducing sugar content. The same results could be observed in other studies, as shown in Table 4.
AP can also be applied to snacks or yogurts through extrusion and freeze-drying or even to pork meat to prepare salami products [139,140,141]. The main phenolic compound, phlorizin, has also been efficiently integrated into chewing gums, which can be dissolved after 5 min of chewing, thus contributing to administering bioactive compounds [142].
On another note, from apple by-products, several other important compounds can be obtained, such as pectin, via extraction and various organic chemicals (e.g., butanol, propionic acid, bio-succinic acid) using fermentation processes [143]. In addition, from the extracted pectin, efficient biofilm solutions can be produced, which can be further applied in the production of active packaging that can be additionally enriched with AP-derived antioxidants [144]. Introducing these bioactive compounds results in biodegradable, water-soluble packages that improve the quality and shelf-life of wrapped foodstuffs.

6.2. Cereal-Processing-Derived By-Products

By-products belonging to the cereal industry mainly include rice, corn, wheat, barley, and other cereals used in the production of bakery products and alcoholic beverages. Cereal grains comprise one of the primary assets of human food, and recently, their manufacturing has expanded; the by-products originating from these resources have also increased [28,145]. The direct derivatives of these cereals are bran, germ, husk, hulls, and brewery wastes (brewer’s spect disposal) [133]. These comprise diverse, major compounds with significant health effects [14,134].
The need for gluten-free diets, especially in humans with Celiac disease, has grown steadily, and finding products with enhanced nutritional properties is of foremost importance [146]. The integration of by-products can contribute to the improvement of gluten-free products. A recent study improved the nutritional content of rice muffins through the integration of sweet corncob flour. This increased the fiber and ferulic content of the final product [147]. Another efficient method is the integration of oat proteins, which are usually removed through processing and can be efficiently integrated into various functional food products [148,149].
Several other kinds of cereal, native to their respective countries, contain important functional and nutritional properties. One of these is quinoa, a pseudo-cereal that originates from the Andean region. This cereal can also be efficiently used in the production of gluten-free products, especially after sourdough fermentation [150]. Through fermentation, the overall characteristics of the final foodstuff obtained from cereal by-products are improved, through prolonged shelf life, improved texture, flavor, diminished antinutrients, and growth in phytochemicals [151,152].

6.3. Tomato-Processing-Derived By-Products

Tomatoes are consumed in high quantities worldwide; thus, the by-products originating from this vegetable are consistent. Various studies have handled the reutilization of this by-product, as it contains essential amounts of organic acids, sugars, antioxidants, fibers, vitamins, proteins, and oils that are crucial to the effective functioning of the human body [22,153].
The main compounds recovered from tomato-industry-derived by-products are carotenoids, which can be efficiently integrated into various functional food products. They contribute to the sensory properties and shelf life and increase the bioactive ingredients [97,154,155]. Several studies tackle the troubles that are encountered through their inclusion in food products, such as their hydrophobic nature. A recent study by Szabo et al., 2022, efficiently incorporated these carotenoids in microcapsules that improved bioaccessibility through in vitro digestion model [2]. In a recent study, tomato by-products were integrated with various vegetable oils [154]. These extracts decreased the viscosity in the cases of hempseed and grapeseed oils and increased the viscosity in the case of flaxseed oil. This variation in viscosity can be attributed to the fact that the enrichment increased the thermal motion of the oil molecules and decreased the intermolecular resilience. These oils can be easily integrated with functional foods and are an efficient delivery system for these carotenoid extracts.
A high portion of tomato by-products is composed of seeds (5–10%), from which tomato seed oil can be extracted. These seeds consist of proteins (34%), lipids (30%), and fibers [129], as well as unsaturated fatty acids (palmitic, oleic, and linoleic acid). Generally, the proportion of oil extraction from tomato seeds ranges between 10 and 35% DW, depending on the extraction method [156].
Table 4. Examples of the reintegration of apple-, cereal-, and tomato-processing by-products in functional food products.
Table 4. Examples of the reintegration of apple-, cereal-, and tomato-processing by-products in functional food products.
Food ProductEffect On Food ProductRef.
AppleAP flour (5, 10%)Bakery product—sourdough+ cell viability; ↑ organic acid content (malic, oxalic, and citric acid) [3]
AP flour (5, 10, 15%)Cereal crispbread↑ total dietary fiber; ↑ hardness and crispiness [139]
Apple peel powderMuffin↑ dietary fiber; ↑ bioactive compounds; + color and texture; + organoleptic characteristics (12%) [157]
AP flour (2.5, 5, 7, 10%)Pasta↓ carbohydrate content; ↑ fiber, protein, fat, and ash content; ↑ swelling index, cooking water absorption, and cooking loss; ↓ optimum cooking time; ↓ texture and structure of pasta (10%) [32]
AP (2, 3, 6, 9%)Freeze-dried snacks↑ AP; ↓ lightness coefficient; ↑ cutting force; ↑ organoleptic properties (2%); ↓ water activity [158]
AP 20%GF corn snacks↑x36 chlorogenic acid; ↑x4 cryptochlorogenic acid; ↑x6 catechin; ↑x3 procyanidin; ↑x8 epicatechin; ↑x25 phlorizin; ↑x3 total soluble and insoluble dietary fiber; ↑ organoleptic scores [159]
AP powderYogurt↓ sensory profile; ↑ protein and fat content; ↑ rheological attributes [141]
Freeze-dried AP powder (0.5, 1%)Set-type yogurt↑ gelation pH; ↓ fermentation time (1%); firmer and consistent yogurt (cold storage); stable structure (0.5%); stabilizer and texturizer [43]
Dried AP (7, 14%)Italian salami↓ fat and calories; ↑ fiber and phenol content [140]
Defatted apple seed flourChewing gum↑ phlorizin content (52–67% and 75–83% of the total phenolics) [143]
CerealWB & BFBread↑ dietary fibers content [160]
↑ alveograph profile
↑ volume of bread
SCC (10, 20, and 30%)GF rice muffin↑ dietary fibers and ferulic acid content; ↑ nutritional value; + height, color, and texture (20% SCC) [147]
BRFBuns and muffins↑ dietary fibers, iron, zinc, and calcium; ↑ antioxidant capacity and phytonutrient content; ↓ carbohydrates and sensory acceptability; moderate glycemic index and glycemic load; ↑ shelf life [161]
OPC & OPIYogurt↑ nutritional benefits (OPI); ↑ product quality and sustainability (OPC); ↑ nutritional (OPC) [149]
BMG + PBD (1:1)Cereal composite bar+ essential minerals and fiber; ↑ sensorial evaluation; antifungal properties [162]
BSGYogurt↑ viscosity and shear stress; ↓ fermentation time; maintained flow behavior and stability [163]
BRG+PFPF+WPGF breakfast cerealsAverage acceptance; + total, soluble, and insoluble dietary fiber; ↑ darkness, protein, and carbohydrate content; ↓ expansion and consumer acceptance [164]
PHGel-based foods↑ textural and sensory characteristics; syneresis and fat loss during cooking avoidance; ↑ gelling properties [165]
TomatoCTHemp, flaxseed, grapeseed oil↑ oil quality; ↑ viscosity (flaxseed oil); ↓ viscosity (hemp and grapeseed oil); intense color [154]
TBPPbiofilms↑ aesthetic impact and coloring; ↓ transparency [166]
TBPPbiofilms↑ physical properties (diameter, thickness, density, weight); ↑ antimicrobial effect; ↑ total phenolic content [155]
TPPGF ready to cook snack↑ fiber, mineral, and lycopene content; ↑ antioxidant activity; ↓ oil uptake [167]
TPFSpreadable cheese↑ spreadability; ↑ antioxidant activity and phenolic content; ↑ fibers [168]
TBPPassata↑ total dietary fiber; ↑ lycopene and polyphenols [169]
TPP (5, 10, 15, 20, 25%)cookies↓ lightness values; ↑ redness and yellowness; acceptable by consumers (5%) [170]
TPF (15%)pasta↑ carotenoids and dietary fiber; ↓ sensory scores for elasticity, odor, and firmness [171]
Food manufacturing through 3D-printing technology is an innovative method of delivering personalized food, meeting our nutritional needs and expectations regarding taste, texture, color, and other aspects [172]. In addition, personalized, 3D-printed food products are promising in the prevention of different noncommunicable diseases due to the possibility of enhancing them with bioactive compounds (e.g., polyphenols, dietary fibers, proteins, etc.) [173].
As for future perspectives, bioactive compounds, such as polyphenols, vitamins, and/or proteins found in food processing by-products, could be easily integrated into functional foods by associating 3D-printed food with molecular gastronomy [174]. Alongside a facile integration of recovered polyphenols, the inner biological activities and nutritional profile can be enhanced, obtaining fortified nourishment [175]. In addition, delivering fortified foods via 3D printing is a sustainable approach to food-waste management, according to circular economy principles [174].

7. Conclusions

All things considered, apple-, cereal-, and tomato-processing by-products are a valuable source of phenolic compounds that can be safely reintegrated with the food chain within recommended parameters. Apple pomace possesses a significant number of beneficial effects for the human body, most of them offered by their antioxidant and anti-inflammatory properties. The three main compounds identified in apple pomace—phlorizin, chlorogenic acid, and epicatechin—can act upon metabolic diseases, being important pillars in the prevention and treatment of the ailment.
Studies demonstrate that regular whole grain consumption lowers the chance of developing noncommunicable diseases, the cause for these health effects being the synergy between the polyphenols and dietary fibers found in the outer layers of the grains, which are unfortunately discarded as by-products.
It is necessary to consider the remarkable antimicrobial capacity of polyphenols derived from tomato by-products, with a focus on flavonol glycosides and isochlorogenic acid against Staphylococcus aureus.
In addition to altering the composition of the gut microbiota, which is closely linked with health benefits, gut bacteria also metabolize polyphenols to create bioactive chemicals that have therapeutic effects. Polyphenols such as catechin, gallic, vanillic, ferulic, and protocatechuic acids selectively stimulate probiotic strains and inhibit pathogenic ones.
In light of this, polyphenols seem to be promising candidates for use in both functional food products and personalized nutrition (e.g., 3D-printed food). To fully take advantage of their outstanding qualities, various pharmacokinetic concerns, such as decreased intestinal absorption and bioavailability and quick metabolic alterations, should be considered.

Author Contributions

Conceptualization, K.S.; validation, K.S. and D.C.V.; investigation, R.-A.V., B.-E.T., M.S.P., D.P., S.-A.N., L.M., L.F.C. and G.A.M.; writing—original draft preparation, R.-A.V., B.-E.T., K.S., D.P., S.-A.N., L.M., M.S.P., L.F.C. and G.A.M.; writing—review and editing, K.S.; visualization, K.S.; supervision, D.C.V.; project administration, K.S. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by “Unitatea Executiva pentru Finantarea Invatamantului Superior a Cercetarii Dezvoltarii si Inovarii” (UEFISCDI), Grant No. PN-III-P1-1.1-PD-2021-0672.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

Sample Availability

Samples of the compounds are available from the authors.

References

  1. Gu, B.; Zhang, X.; Bai, X.; Fu, B.; Chen, D. Four steps to food security for swelling cities. Nature 2019, 566, 31–33. [Google Scholar] [CrossRef] [PubMed]
  2. Szabo, K.; Teleky, E.B.; Ranga, F.; Simon, E.; Pop, L.O.; Babalau-Fuss, V.; Kapsalis, N.; Cristian, D. Bioaccessibility of microencapsulated carotenoids, recovered from tomato processing industrial by-products, using in vitro digestion model. LWT 2021, 152, 112285. [Google Scholar] [CrossRef]
  3. Martău, G.A.; Teleky, B.E.; Ranga, F.; Pop, I.D.; Vodnar, D.C. Apple Pomace as a Sustainable Substrate in Sourdough Fermentation. Front. Microbiol. 2021, 12, 3850. [Google Scholar] [CrossRef] [PubMed]
  4. Iriondo-Dehond, M.; Miguel, E.; Del Castillo, M.D. Food byproducts as sustainable ingredients for innovative and healthy dairy foods. Nutrients 2018, 10, 1358. [Google Scholar] [CrossRef] [Green Version]
  5. Food and Agriculture Organization. Available online: https://www.fao.org/home/en (accessed on 10 October 2022).
  6. Zhang, R.; Ma, S.; Li, L.; Zhang, M.; Tian, S.; Wang, D.; Liu, K.; Liu, H.; Zhu, W.; Wang, X. Grain & Oil Science and Technology Comprehensive utilization of corn starch processing by-products: A review. Grain Oil Sci. Technol. 2021, 4, 89–107. [Google Scholar]
  7. Deroover, L.; Tie, Y.; Verspreet, J.; Courtin, C.M.; Verbeke, K. Modifying wheat bran to improve its health benefits. Crit. Rev. Food Sci. Nutr. 2020, 60, 1104–1122. [Google Scholar] [CrossRef]
  8. Fărcaș, A.C.; Socaci, S.A.; Nemeș, S.A.; Pop, O.L.; Coldea, T.E.; Fogarasi, M.; Biriș-Dorhoi, E.S. An Update Regarding the Bioactive Compound of Cereal By-Products: Health Benefits and Potential Applications. Nutrients 2022, 14, 3470. [Google Scholar] [CrossRef]
  9. Sandström, V.; Chrysafi, A.; Lamminen, M.; Troell, M.; Jalava, M.; Piipponen, J.; Siebert, S.; Van Hal, O.; Virkki, V.; Kummu, M. Food system by-products upcycled in livestock and aquaculture feeds can increase global food supply. Nat. Food 2022, 3, 729–740. [Google Scholar] [CrossRef]
  10. Vodnar, D.C.; Calinoiub, L.F.; Mitrea, L.; Precup, G.; Bindea, M.; Pacurar, A.M.; Szabo, K.; Stefanescu, B.E. A New Generation of Probiotic Functional Beverages Using Bioactive Compounds from Agro-Industrial Waste; Academic Press: Cambridge, MA, USA, 2019; ISBN 9780128163979. [Google Scholar]
  11. Călinoiu, L.F.; Vodnar, D.C. Thermal processing for the release of phenolic compounds from wheat and oat bran. Biomolecules 2020, 10, 21. [Google Scholar] [CrossRef] [Green Version]
  12. Călinoiu, L.F.; Vodnar, D.C. Whole Grains and Phenolic Acids: A Review on Bioactivity, Functionality, Health Benefits and Bioavailability. Nutrients 2018, 10, 1615. [Google Scholar] [CrossRef] [Green Version]
  13. Martău, G.A.; Unger, P.; Schneider, R.; Venus, J.; Vodnar, D.C.; López-Gómez, J.P. Integration of solid state and submerged fermentations for the valorization of organic municipal solid waste. J. Fungi 2021, 7, 766. [Google Scholar] [CrossRef] [PubMed]
  14. Florina, L.; Adriana-florinela, C.; Vodnar, D.C. Solid-State Yeast Fermented Wheat and Oat Bran as A Route for Delivery of Antioxidants. Antioxidants 2019, 8, 372. [Google Scholar]
  15. Purić, M.; Rabrenović, B.; Rac, V.; Pezo, L.; Tomašević, I.; Demin, M. Application of defatted apple seed cakes as a by-product for the enrichment of wheat bread. LWT 2020, 130, 109391. [Google Scholar] [CrossRef]
  16. Spengler, R.N. Origins of the apple: The role of megafaunal mutualism in the domestication of Malus and rosaceous trees. Front. Plant Sci. 2019, 10, 617. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  17. Giovanetti Canteri, M.H.; Nogueira, A.; de Oliveira Petkowicz, C.L.; Wosiacki, G. Characterization of Apple Pectin—A Chromatographic Approach. Chromatogr. Most Versatile Method Chem. Anal. 2012. [Google Scholar] [CrossRef] [Green Version]
  18. Rupasinghe, H.P.V.; Wang, L.; Huber, G.M.; Pitts, N.L. Effect of baking on dietary fibre and phenolics of muffins incorporated with apple skin powder. Food Chem. 2008, 107, 1217–1224. [Google Scholar] [CrossRef]
  19. Rabetafika, H.N.; Bchir, B.; Blecker, C.; Richel, A. Fractionation of apple by-products as source of new ingredients: Current situation and perspectives. Trends Food Sci. Technol. 2014, 40, 99–114. [Google Scholar] [CrossRef]
  20. Laranjeira, T.; Costa, A.; Faria-Silva, C.; Ribeiro, D.; Ferreira, M.P.; Sim, S.; Ascenso, A. Sustainable Valorization of Tomato By-Products to Obtain Bioactive Compounds: Their Potential in Inflammation and Cancer Management. Molecules 2022, 27, 1701. [Google Scholar] [CrossRef]
  21. Kumar, R.; Hyun, S.; Keum, Y. An updated review on use of tomato pomace and crustacean processing waste to recover commercially vital carotenoids. Food Res. Int. 2018, 108, 516–529. [Google Scholar]
  22. Szabo, K.; Cătoi, A.-F.; Vodnar, D.C. Bioactive Compounds Extracted from Tomato Processing by-Products as a Source of Valuable Nutrients. Plant Foods Hum. Nutr. 2018, 73, 268–277. [Google Scholar] [CrossRef]
  23. Strati, I.F.; Oreopoulou, V. Recovery of carotenoids from tomato processing by-products—A review. Food Res. Int. 2014, 65, 311–321. [Google Scholar] [CrossRef]
  24. Wang, D.; Wang, T.; Zhang, Z.; Li, Z.; Guo, Y.; Zhao, G.; Wu, L. Recent advances in the effects of dietary polyphenols on inflammation in vivo: Potential molecular mechanisms, receptor targets, safety issues, and uses of nanodelivery system and polyphenol polymers. Curr. Opin. Food Sci. 2022, 48, 100921. [Google Scholar] [CrossRef]
  25. Plamada, D.; Vodnar, D.C. Polyphenols—Gut Microbiota Interrelationship: A Transition to a New Generation of Prebiotics. Nutrients 2022, 14, 137. [Google Scholar] [CrossRef] [PubMed]
  26. Martins, N.; Ferreira, I.C.F.R. Wastes and by-products: Upcoming sources of carotenoids for biotechnological purposes and health-related applications. Trends Food Sci. Technol. 2017, 62, 33–48. [Google Scholar] [CrossRef]
  27. Ding, Y.; Morozova, K.; Scampicchio, M.; Ferrentino, G. Non-Extractable polyphenols from food by-products: Current knowledge on recovery, characterisation, and potential applications. Processes 2020, 8, 925. [Google Scholar] [CrossRef]
  28. Čolović, D.; Rakita, S.; Banjac, V.; Đuragić, O.; Čabarkapa, I. Plant food by-products as feed: Characteristics, possibilities, environmental benefits, and negative sides. Food Rev. Int. 2019, 35, 363–389. [Google Scholar] [CrossRef]
  29. Precup, G.; Mitrea, L.; Călinoiu, L.F.; Martău, A.G.; Nemeş, A.; Emoke Teleky, B.; Coman, V.; Vodnar, D.C. Food processing by-products and molecular gastronomy. Gastron. Food Sci. 2021, 8, 137–163. [Google Scholar]
  30. Coman, V.; Teleky, B.-E.; Mitrea, L.; Martău, G.A.; Szabo, K.; Călinoiu, L.-F.; Vodnar, D.C. Bioactive Potential of Fruit and Vegetable Wastes; Academic Press: Cambridge, MA, USA, 2020; Volume 91, ISBN 9780128204702. [Google Scholar]
  31. Francini, A.; Sebastiani, L. Phenolic compounds in apple (Malus x domestica borkh.): Compounds characterization and stability during postharvest and after processing. Antioxidants 2013, 2, 181–193. [Google Scholar] [CrossRef] [Green Version]
  32. Bchir, B.; Karoui, R.; Danthine, S.; Blecker, C.; Besbes, S.; Attia, H. Date, Apple, and Pear By-Products as Functional Ingredients in Pasta: Cooking Quality Attributes and Physicochemical, Rheological, and Sensorial Properties. Foods 2022, 11, 1393. [Google Scholar] [CrossRef]
  33. Gołębiewska, E.; Kalinowska, M.; Yildiz, G. Sustainable Use of Apple Pomace (AP) in Different Industrial Sectors. Materials 2022, 15, 1788. [Google Scholar] [CrossRef]
  34. Lyu, F.; Luiz, S.F.; Azeredo, D.R.P.; Cruz, A.G.; Ajlouni, S.; Ranadheera, C.S. Apple pomace as a functional and healthy ingredient in food products: A review. Processes 2020, 8, 319. [Google Scholar] [CrossRef] [Green Version]
  35. Ricci, A.; Cirlini, M.; Guido, A.; Liberatore, C.M.; Ganino, T.; Lazzi, C.; Chiancone, B. From byproduct to resource: Fermented apple pomace as beer flavoring. Foods 2019, 8, 309. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  36. Le Deun, E.; Van Der Werf, R.; Le Bail, G.; Le Quéré, J.M.; Guyot, S. HPLC-DAD-MS Profiling of Polyphenols Responsible for the Yellow-Orange Color in Apple Juices of Different French Cider Apple Varieties. J. Agric. Food Chem. 2015, 63, 7675–7684. [Google Scholar] [CrossRef] [PubMed]
  37. Molinuevo-Salces, B.; Riaño, B.; Hijosa-Valsero, M.; González-García, I.; Paniagua-García, A.I.; Hernández, D.; Garita-Cambronero, J.; Díez-Antolínez, R.; García-González, M.C. Valorization of apple pomaces for biofuel production: A biorefinery approach. Biomass Bioenergy 2020, 142, 105785. [Google Scholar] [CrossRef]
  38. Shojaosadati, S.A.; Babaeipour, V. Citric acid production from apple pomace in multi-layer packed bed solid-state bioreactor. Process Biochem. 2002, 37, 909–914. [Google Scholar] [CrossRef]
  39. Sato, M.F.; Vieira, R.G.; Zardo, D.M.; Falcão, L.D.; Nogueira, A.; Wosiacki, G. Apple pomace from eleven cultivars: An approach to identify sources of bioactive compounds. Acta Sci. Agron. 2010, 32, 29–35. [Google Scholar]
  40. Kasprzak-Drozd, K.; Oniszczuk, T.; Stasiak, M.; Oniszczuk, A. Beneficial effects of phenolic compounds on gut microbiota and metabolic syndrome. Int. J. Mol. Sci. 2021, 22, 3715. [Google Scholar] [CrossRef]
  41. Sergent, T.; Piront, N.; Meurice, J.; Toussaint, O.; Schneider, Y.J. Anti-inflammatory effects of dietary phenolic compounds in an in vitro model of inflamed human intestinal epithelium. Chem. Biol. Interact. 2010, 188, 659–667. [Google Scholar] [CrossRef]
  42. Skinner, R.C.; Gigliotti, J.C.; Ku, K.M.; Tou, J.C. A comprehensive analysis of the composition, health benefits, and safety of apple pomace. Nutr. Rev. 2018, 76, 893–909. [Google Scholar] [CrossRef]
  43. Wang, X.; Kristo, E.; LaPointe, G. The effect of apple pomace on the texture, rheology and microstructure of set type yogurt. Food Hydrocoll. 2019, 91, 83–91. [Google Scholar] [CrossRef]
  44. Gumul, D.; Ziobro, R.; Korus, J.; Kruczek, M. Apple pomace as a source of bioactive polyphenol compounds in gluten-free breads. Antioxidants 2021, 10, 807. [Google Scholar] [CrossRef] [PubMed]
  45. Walia, M.; Rawat, K.; Bhushan, S.; Padwad, Y.S.; Singh, B. Fatty acid composition, physicochemical properties, antioxidant and cytotoxic activity of apple seed oil obtained from apple pomace. J. Sci. Food Agric. 2014, 94, 929–934. [Google Scholar] [CrossRef] [PubMed]
  46. Bolarinwa, I.F.; Orfila, C.; Morgan, M.R.A. Determination of amygdalin in apple seeds, fresh apples and processed apple juices. Food Chem. 2015, 170, 437–442. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  47. Opyd, P.M.; Jurgoński, A.; Juśkiewicz, J.; Milala, J.; Zduńczyk, Z.; Król, B. Nutritional and health-related effects of a diet containing apple seed meal in rats: The case of amygdalin. Nutrients 2017, 9, 1091. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  48. Montañés, F.; Catchpole, O.J.; Tallon, S.; Mitchell, K.A.; Scott, D.; Webby, R.F. Extraction of apple seed oil by supercritical carbon dioxide at pressures up to 1300 bar. J. Supercrit. Fluids 2018, 141, 128–136. [Google Scholar] [CrossRef]
  49. Feng, S.; Yi, J.; Li, X.; Wu, X.; Zhao, Y.; Ma, Y.; Bi, J. Systematic Review of Phenolic Compounds in Apple Fruits: Compositions, Distribution, Absorption, Metabolism, and Processing Stability. J. Agric. Food Chem. 2021, 69, 7–27. [Google Scholar] [CrossRef]
  50. Pollini, L.; Cossignani, L.; Juan, C.; Mañes, J. Extraction of phenolic compounds from fresh apple pomace by different non-conventional techniques. Molecules 2021, 26, 4272. [Google Scholar] [CrossRef]
  51. Lavelli, V.; Corti, S. Phloridzin and other phytochemicals in apple pomace: Stability evaluation upon dehydration and storage of dried product. Food Chem. 2011, 129, 1578–1583. [Google Scholar] [CrossRef]
  52. Hrubá, M.; Baxant, J.; Čížková, H.; Smutná, V.; Kovařík, F.; Ševčík, R.; Hanušová, K.; Rajchl, A. Phloridzin as a marker for evaluation of fruit product’s authenticity. Czech J. Food Sci. 2021, 39, 49–57. [Google Scholar] [CrossRef]
  53. Rana, S.; Gupta, S.; Rana, A.; Bhushan, S. Functional properties, phenolic constituents and antioxidant potential of industrial apple pomace for utilization as active food ingredient. Food Sci. Hum. Wellness 2015, 4, 180–187. [Google Scholar] [CrossRef] [Green Version]
  54. Táborský, J.; Sus, J.; Lachman, J.; Šebková, B.; Adamcová, A.; Šatínský, D. Dynamics of phloridzin and related compounds in four cultivars of apple trees during the vegetation period. Molecules 2021, 26, 3816. [Google Scholar] [CrossRef] [PubMed]
  55. Najafian, M.; Jahromi, M.Z.; Nowroznejhad, M.J.; Khajeaian, P.; Kargar, M.M.; Sadeghi, M.; Arasteh, A. Phloridzin reduces blood glucose levels and improves lipids metabolism in streptozotocin-induced diabetic rats. Mol. Biol. Rep. 2012, 39, 5299–5306. [Google Scholar] [CrossRef] [PubMed]
  56. Kamdi, S.P.; Badwaik, H.R.; Raval, A.; Ajazuddin; Nakhate, K.T. Ameliorative potential of phloridzin in type 2 diabetes-induced memory deficits in rats. Eur. J. Pharmacol. 2021, 913, 174645. [Google Scholar] [CrossRef] [PubMed]
  57. Masumoto, S.; Akimoto, Y.; Oike, H.; Kobori, M. Dietary Phloridzin Reduces Blood Glucose Levels and Reverses Sglt1 Expression in the Small Intestine in Streptozotocin-lnduced Diabetic Mice. J. Agric. Food Chem. 2009, 57, 4651–4656. [Google Scholar] [CrossRef]
  58. Lu, Y.Y.; Liang, J.; Chen, S.X.; Wang, B.X.; Yuan, H.; Li, C.T.; Wu, Y.Y.; Wu, Y.F.; Shi, X.G.; Gao, J.; et al. Phloridzin alleviate colitis in mice by protecting the intestinal brush border and improving the expression of sodium glycogen transporter 1. J. Funct. Foods 2018, 45, 348–354. [Google Scholar] [CrossRef]
  59. Fang, Y.Z.; Yang, S.; Wu, G. Free radicals, antioxidants, and nutrition. Nutrition 2002, 18, 872–879. [Google Scholar] [CrossRef]
  60. Upadhyay, R.; Mohan Rao, L.J. An Outlook on Chlorogenic Acids-Occurrence, Chemistry, Technology, and Biological Activities. Crit. Rev. Food Sci. Nutr. 2013, 53, 968–984. [Google Scholar] [CrossRef]
  61. Cropley, V.; Croft, R.; Silber, B.; Neale, C.; Scholey, A.; Stough, C.; Schmitt, J. Does coffee enriched with chlorogenic acids improve mood and cognition after acute administration in healthy elderly? A pilot study. Psychopharmacology 2012, 219, 737–749. [Google Scholar] [CrossRef]
  62. Mubarak, A.; Catherine, P.B.; Liu, A.H.; Considine, M.J.; Rich, L.; Mas, E.; Croft, K.D.; Hodgson, J.M. Acute effects of chlorogenic acid on nitric oxide status, endothelial function and blood pressure in healthy volunteers: A randomised trial. J. Agric. Food Chem. 2012, 60, 9130–9136. [Google Scholar] [CrossRef]
  63. Qu, Z.; Liu, A.; Li, P.; Liu, C.; Xiao, W.; Huang, J.; Liu, Z.; Zhang, S. Advances in physiological functions and mechanisms of (-)-epicatechin. Crit. Rev. Food Sci. Nutr. 2021, 61, 211–233. [Google Scholar] [CrossRef]
  64. Cilleros, D.Á.; Martín, M.Á.; Ramos, S. (−)-Epicatechin and the colonic 2,3-dihydroxybenzoic acid metabolite regulate glucose uptake, glucose production, and improve insulin signalling in renal NRK-52E cells. Mol. Nutr. Food Res. 2018, 62, 1700470. [Google Scholar]
  65. Cordero-Herrera, I.; Chen, X.; Ramos, S.; Devaraj, S. (−)-Epicatechin attenuates high-glucose-induced inflammation by epigenetic modulation in human monocytes. Eur. J. Nutr. 2017, 56, 1369–1373. [Google Scholar] [CrossRef] [PubMed]
  66. Luithui, Y.; Baghya Nisha, R.; Meera, M.S. Cereal by-products as an important functional ingredient: Effect of processing. J. Food Sci. Technol. 2019, 56, 1–11. [Google Scholar] [CrossRef] [PubMed]
  67. Fărcaș, A.; Drețcanu, G.; Pop, T.D.; Enaru, B.; Socaci, S.; Diaconeasa, Z. Cereal processing by-products as rich sources of phenolic compounds and their potential bioactivities. Nutrients 2021, 13, 3934. [Google Scholar] [CrossRef] [PubMed]
  68. Roasa, J.; De Villa, R.; Mine, Y.; Tsao, R. Phenolics of cereal, pulse and oilseed processing by-products and potential effects of solid-state fermentation on their bioaccessibility, bioavailability and health benefits: A review. Trends Food Sci. Technol. 2021, 116, 954–974. [Google Scholar] [CrossRef]
  69. Tylewicz, U.; Nowacka, M.; Martín-García, B.; Wiktor, A.; Gómez Caravaca, A.M. Target Sources of Polyphenols in Different Food Products and Their Processing By-Products; Elsevier: Amsterdam, The Netherlands, 2018; ISBN 9780128135723. [Google Scholar]
  70. Apprich, S.; Tirpanalan, Ö.; Hell, J.; Reisinger, M.; Böhmdorfer, S.; Siebenhandl-Ehn, S.; Novalin, S.; Kneifel, W. Wheat bran-based biorefinery 2: Valorization of products. LWT 2014, 56, 222–231. [Google Scholar] [CrossRef]
  71. Bannikova, A.; Zyainitdinov, D.; Evteev, A.; Drevko, Y.; Evdokimov, I. Microencapsulation of polyphenols and xylooligosaccharides from oat bran in whey protein-maltodextrin complex coacervates: In-vitro evaluation and controlled release. Bioact. Carbohydr. Diet. Fibre 2020, 23, 100236. [Google Scholar] [CrossRef]
  72. Zhuang, X.; Yin, T.; Han, W.; Zhang, X. Nutritional Ingredients and Active Compositions of Defatted Rice Bran; Elsevier Inc.: Amsterdam, The Netherlands, 2019; ISBN 9780128128282. [Google Scholar]
  73. Yadav, M.P.; Moreau, R.A.; Hicks, K.B. Phenolic acids, lipids, and proteins associated with purified corn fiber arabinoxylans. J. Agric. Food Chem. 2007, 55, 943–947. [Google Scholar] [CrossRef]
  74. Moongngarm, A.; Daomukda, N.; Khumpika, S. Chemical Compositions, Phytochemicals, and Antioxidant Capacity of Rice Bran, Rice Bran Layer, and Rice Germ. APCBEE Procedia 2012, 2, 73–79. [Google Scholar] [CrossRef] [Green Version]
  75. Yue, Z.; Sun, L.L.; Sun, S.N.; Cao, X.F.; Wen, J.L.; Zhu, M.Q. Structure of corn bran hemicelluloses isolated with aqueous ethanol solutions and their potential to produce furfural. Carbohydr. Polym. 2022, 288, 119420. [Google Scholar] [CrossRef]
  76. Feng, S.; Wang, L.; Shao, P.; Lu, B.; Chen, Y.; Sun, P. Simultaneous analysis of free phytosterols and phytosterol glycosides in rice bran by SPE/GC–MS. Food Chem. 2022, 387, 132742. [Google Scholar] [CrossRef] [PubMed]
  77. Duţă, D.E.; Culeţu, A.; Mohan, G. Reutilization of Cereal Processing By-Products in Bread Making; Woodhead Publishing Series in Food Science; Woodhead Publishing: Sawston, UK, 2018; ISBN 9780081022146. [Google Scholar]
  78. Moreau, R.A.; Hicks, K.B. The composition of corn oil obtained by the alcohol extraction of ground corn. JAOCS J. Am. Oil Chem. Soc. 2005, 82, 809–815. [Google Scholar] [CrossRef]
  79. Arzami, A.N.; Ho, T.M.; Mikkonen, K.S. Valorization of cereal by-product hemicelluloses: Fractionation and purity considerations. Food Res. Int. 2022, 151, 110818. [Google Scholar] [CrossRef] [PubMed]
  80. Schmitz, E.; Nordberg Karlsson, E.; Adlercreutz, P. Warming weather changes the chemical composition of oat hulls. Plant Biol. 2020, 22, 1086–1091. [Google Scholar] [CrossRef] [PubMed]
  81. Li, S.; Chen, H.; Cheng, W.; Yang, K.; Cai, L.; He, L.; Du, L.; Liu, Y.; Liu, A.; Zeng, Z.; et al. Impact of arabinoxylan on characteristics, stability and lipid oxidation of oil-in-water emulsions: Arabinoxylan from wheat bran, corn bran, rice bran, and rye bran. Food Chem. 2021, 358, 129813. [Google Scholar] [CrossRef]
  82. Ndolo, V.U.; Beta, T. Comparative studies on composition and distribution of phenolic acids in cereal grain botanical fractions. Cereal Chem. 2014, 91, 522–530. [Google Scholar] [CrossRef]
  83. Martín-Diana, A.B.; García-Casas, M.J.; Martínez-Villaluenga, C.; Frías, J.; Peñas, E.; Rico, D. Wheat and oat brans as sources of polyphenol compounds for development of antioxidant nutraceutical ingredients. Foods 2021, 10, 115. [Google Scholar] [CrossRef]
  84. Yin, Z.N.; Wu, W.J.; Sun, C.Z.; Liu, H.F.; Chen, W.B.; Zhan, Q.P.; Lei, Z.G.; Xin, X.; Ma, J.J.; Yao, K.; et al. Antioxidant and Anti-inflammatory Capacity of Ferulic Acid Released from Wheat Bran by Solid-state Fermentation of Aspergillus niger. Biomed. Environ. Sci. 2019, 32, 11–21. [Google Scholar]
  85. Long, L.; Wu, L.; Lin, Q.; Ding, S. Highly Efficient Extraction of Ferulic Acid from Cereal Brans by a New Type A Feruloyl Esterase from Eupenicillium parvum in Combination with Dilute Phosphoric Acid Pretreatment. Appl. Biochem. Biotechnol. 2020, 190, 1561–1578. [Google Scholar] [CrossRef]
  86. Upadhyay, P.; Singh, N.K.; Tupe, R.; Odenath, A.; Lali, A. Biotransformation of corn bran derived ferulic acid to vanillic acid using engineered Pseudomonas putida KT2440. Prep. Biochem. Biotechnol. 2020, 50, 341–348. [Google Scholar] [CrossRef]
  87. Ed Nignpense, B.; Francis, N.; Blanchard, C.; Santhakumar, A.B. Bioaccessibility and bioactivity of cereal polyphenols: A review. Foods 2021, 10, 1595. [Google Scholar] [CrossRef] [PubMed]
  88. Martău, G.A.; Călinoiu, L.F.; Vodnar, D.C. Bio-vanillin: Towards a sustainable industrial production. Trends Food Sci. Technol. 2021, 109, 579–592. [Google Scholar] [CrossRef]
  89. Boz, H. p-Coumaric acid in cereals: Presence, antioxidant and antimicrobial effects. Int. J. Food Sci. Technol. 2015, 50, 2323–2328. [Google Scholar] [CrossRef]
  90. Mosele, J.I.; Macià, A.; Motilva, M.J. Metabolic and microbial modulation of the large intestine ecosystem by non-absorbed diet phenolic compounds: A review. Molecules 2015, 20, 17429–17468. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  91. Anson, N.M.; Aura, A.M.; Selinheimo, E.; Mattila, I.; Poutanen, K.; Van Den Berg, R.; Havenaar, R.; Bast, A.; Haenen, G.R.M.M. Bioprocessing of wheat bran in whole wheat bread increases the bioavailability of phenolic acids in men and exerts antiinflammatory effects ex vivo1-3. J. Nutr. 2011, 141, 137–143. [Google Scholar] [CrossRef] [Green Version]
  92. Hamadou, M.; Martin Alain, M.M.; Obadias, F.V.; Hashmi, M.Z.; Başaran, B.; Jean Paul, B.; Samuel René, M. Consumption of underutilised grain legumes and the prevention of type II diabetes and cardiometabolic diseases: Evidence from field investigation and physicochemical analyses. Environ. Chall. 2022, 9, 100621. [Google Scholar] [CrossRef]
  93. Bumrungpert, A.; Lilitchan, S.; Tuntipopipat, S.; Tirawanchai, N.; Komindr, S. Ferulic acid supplementation improves lipid profiles, oxidative stress, and inflammatory status in hyperlipidemic subjects: A randomized, double-blind, placebo-controlled clinical trial. Nutrients 2018, 10, 713. [Google Scholar] [CrossRef]
  94. Sarkar, A.; Kaul, P. Evaluation of tomato processing by-products: A comparative study in a pilot scale setup. J. Food Process Eng. 2014, 37, 299–307. [Google Scholar] [CrossRef]
  95. Szabo, K.; Diaconeasa, Z.; Cătoi, A.-F.; Vodnar, D.C. Screening of ten tomato varieties processing waste for bioactive components and their related antioxidant and antimicrobial activities. Antioxidants 2019, 8, 292. [Google Scholar] [CrossRef] [Green Version]
  96. Schieber, A. By-Products of Plant Food Processing as a Source of Valuable Compounds. Ref. Modul. Food Sci. 2019, 12, 401–413. [Google Scholar]
  97. Szabo, K.; Dulf, F.V.; Eleni, P.; Boukouvalas, C.; Krokida, M.; Kapsalis, N.; Rusu, A.V.; Socol, C.T.; Vodnar, D.C. Evaluation of the Bioactive Compounds Found in Tomato Seed Oil and Tomato Peels Influenced by Industrial Heat Treatments. Foods 2021, 10, 110. [Google Scholar] [CrossRef] [PubMed]
  98. Popescu, M.; Iancu, P.; Plesu, V.; Todasca, M.C.; Isopencu, G.O.; Bildea, C.S. Valuable Natural Antioxidant Products Recovered from Tomatoes by Green Extraction. Molecules 2022, 27, 4191. [Google Scholar] [CrossRef] [PubMed]
  99. Szabo, K.; Dulf, F.V.; Diaconeasa, Z.; Vodnar, D.C. Antimicrobial and antioxidant properties of tomato processing byproducts and their correlation with the biochemical composition. LWT—Food Sci. Technol. 2019, 116, 108558. [Google Scholar] [CrossRef]
  100. Cruz-Carrión, Á.; Calani, L.; de Azua, M.J.R.; Mena, P.; Del Rio, D.; Suárez, M.; Arola-Arnal, A. (Poly)phenolic composition of tomatoes from different growing locations and their absorption in rats: A comparative study. Food Chem. 2022, 388, 132984. [Google Scholar] [CrossRef] [PubMed]
  101. Shahidi, F.; Varatharajan, V.; Oh, W.Y.; Peng, H. Phenolic compounds in agri-food by-products, their bioavailability and health effects. J. Food Bioact. 2019, 5, 57–119. [Google Scholar] [CrossRef] [Green Version]
  102. Ebrahimi, P.; Lante, A. Environmentally Friendly Techniques for the Recovery of Polyphenols from Food By-Products and Their Impact on Polyphenol Oxidase: A Critical Review. Appl. Sci. 2022, 12, 1923. [Google Scholar] [CrossRef]
  103. Shixian, Q.; Dai, Y.; Kakuda, Y.; Shi, J.; Mittal, G.; Yeung, D.; Jiang, Y. Synergistic anti-oxidative effects of lycopene with other bioactive compounds. Food Rev. Int. 2005, 21, 295–311. [Google Scholar] [CrossRef]
  104. Ara, H.; Santos, D.; Campos, D.A.; Ratinho, M.; Rodrigues, I.M.; Pintado, M.E. Development of Frozen Pulps and Powders from Carrot and Tomato by-Products: Impact of Processing and Storage Time on Bioactive and Biological Properties. Horticulturae 2021, 7, 185. [Google Scholar]
  105. Navarro-González, I.; García-Valverde, V.; García-Alonso, J.; Periago, M.J. Chemical profile, functional and antioxidant properties of tomato peel fiber. Food Res. Int. 2011, 44, 1528–1535. [Google Scholar] [CrossRef]
  106. Venturi, F.; Sanmartin, C.; Taglieri, I.; Andrich, G.; Zinnai, A. A simplified method to estimate Sc-CO2 extraction of bioactive compounds from different matrices: Chili pepper vs. tomato by-products. Appl. Sci. 2017, 7, 361. [Google Scholar] [CrossRef] [Green Version]
  107. Zhang, H.; Tsao, R. Dietary polyphenols, oxidative stress and antioxidant and anti-inflammatory effects. Curr. Opin. Food Sci. 2016, 8, 33–42. [Google Scholar] [CrossRef]
  108. Daglia, M. Polyphenols as antimicrobial agents. Curr. Opin. Biotechnol. 2012, 23, 174–181. [Google Scholar] [CrossRef]
  109. Araújo-Rodrigues, H.; Santos, D.; Campos, D.A.; Guerreiro, S.; Ratinho, M.; Rodrigues, I.M.; Pintado, M.E. Impact of processing approach and storage time on bioactive and biological properties of rocket, spinach and watercress byproducts. Foods 2021, 10, 2301. [Google Scholar] [CrossRef]
  110. Nemes, S.; Mitrea, L.; Adrian, G.; Szabo, K.; Mihai, M.; Vodnar, D.C.; Cris, G. Microencapsulation and Bioaccessibility of Phenolic Compounds of Vaccinium Leaf Extracts. Antioxidants 2022, 11, 674. [Google Scholar]
  111. Petroff, O.A.C. Book Review: GABA and Glutamate in the Human Brain. Neurosci. 2002, 8, 562–573. [Google Scholar] [CrossRef]
  112. Pattern, H.P.D.; Del Bo, C.; Bernardi, S.; Marino, M.; Porrini, M.; Tucci, M.; Guglielmetti, S.; Cherubini, A.; Carrieri, B.; Kirkup, B.; et al. Systematic Review on Polyphenol Intake and Health Outcomes: Is there Su ffi cient Evidence to define a health-promoting polyphenol-rich dietary pattern. Nutrients 2019, 11, 1355. [Google Scholar]
  113. Ganesan, K.; Xu, B. Polyphenol-Rich Dry Common Beans ( Phaseolus vulgaris L.) and Their Health Benefits. Int. J. Mol. Sci. 2017, 18, 2331. [Google Scholar] [CrossRef] [Green Version]
  114. Mitrea, L.; Nemes, S.-A.; Szabo, K.; Teleky, B.-E.; Vodnar, D.-C. Guts Imbalance Imbalances the Brain: A Review of Gut Microbiota Association with Neurological and Psychiatric Disorders. Front. Med. 2022, 9, 813204. [Google Scholar] [CrossRef]
  115. Condezo-hoyos, L.; Gazi, C.; Jara, P. Design of polyphenol-rich diets in clinical trials: A systematic review. Food Res. Int. 2021, 149, 110655. [Google Scholar] [CrossRef]
  116. Bergmann, H.; Triebel, S.; Kahle, K.; Richling, E. The Metabolic Fate of Apple Polyphenols in Humans. Curr. Nutr. Food Sci. 2010, 6, 19–35. [Google Scholar] [CrossRef]
  117. Barreira, J.C.M.; Arraibi, A.A.; Ferreira, I.C.F.R. Bioactive and functional compounds in apple pomace from juice and cider manufacturing: Potential use in dermal formulations. Trends Food Sci. Technol. 2019, 90, 76–87. [Google Scholar] [CrossRef]
  118. Hung, P. Van Critical Reviews in Food Science and Nutrition Phenolic compounds of cereals and their antioxidant capacity. Crit. Rev. Food Sci. Nutr. 2014, 56, 25–35. [Google Scholar] [CrossRef]
  119. Lourenzi, E.; Novelli, B.; Okoshi, K.; Politi, M.; Paulino, B.; Muzio, D.; Guimara, J.F.C. Influence of rutin treatment on biochemical alterations in experimental diabetes. Biomed. Pharmacother. 2010, 64, 214–219. [Google Scholar]
  120. Elbadrawy, E.; Sello, A. Evaluation of nutritional value and antioxidant activity of tomato peel extracts. Arab. J. Chem. 2011, 9, S1010–S1018. [Google Scholar] [CrossRef] [Green Version]
  121. De Souza, E.L.; Mariano, T.; De Albuquerque, R. Potential interactions among phenolic compounds and probiotics for mutual boosting of their health- promoting properties and food functionalities—A review. Crit. Rev. Food Sci. Nutr. 2019, 59, 1645–1659. [Google Scholar] [CrossRef]
  122. Moorthy, M.; Chaiyakunapruk, N.; Anne, S.; Palanisamy, U.D. Trends in Food Science & Technology Prebiotic potential of polyphenols, its effect on gut microbiota and anthropometric / clinical markers: A systematic review of randomised controlled trials. Trends Food Sci. Technol. 2020, 99, 634–649. [Google Scholar]
  123. Pacheco-Ordaz, R.; Wall-Medrano, A.; Goñi, M.G.; Ramos-Clamont-Montfort, G.; Ayala-Zavala, J.F.; González-Aguilar, G.A. Effect of phenolic compounds on the growth of selected probiotic and pathogenic bacteria. Lett. Appl. Microbiol. 2018, 66, 25–31. [Google Scholar] [CrossRef]
  124. Gobbetti, M.; De Angelis, M.; Di Cagno, R.; Polo, A.; Rizzello, C.G. The sourdough fermentation is the powerful process to exploit the potential of legumes, pseudo-cereals and milling by-products in baking industry. Crit. Rev. Food Sci. Nutr. 2020, 60, 2158–2173. [Google Scholar] [CrossRef]
  125. Nishiga, M.; Wang, D.W.; Han, Y.; Lewis, D.B.; Wu, J.C. COVID-19 and cardiovascular disease: From basic mechanisms to clinical perspectives. Nat. Rev. Cardiol. 2020, 17, 543–558. [Google Scholar] [CrossRef]
  126. Vodnar, D.C.; Mitrea, L.; Teleky, B.E.; Szabo, K.; Călinoiu, L.F.; Nemeş, S.A.; Martău, G.A. Coronavirus Disease (COVID-19) Caused by (SARS-CoV-2) Infections: A Real Challenge for Human Gut Microbiota. Front. Cell. Infect. Microbiol. 2020, 10, 575559. [Google Scholar] [CrossRef]
  127. Tian, J.; Wu, X.; Zhang, M.; Zhou, Z.; Liu, Y. Comparative study on the effects of apple peel polyphenols and apple flesh polyphenols on cardiovascular risk factors in mice. Clin. Exp. Hypertens. 2017, 40, 65–72. [Google Scholar] [CrossRef] [PubMed]
  128. Alam, A. Anti-hypertensive Effect of Cereal Antioxidant Ferulic Acid and Its Mechanism of Action. Front. Nutr. 2019, 6, 121. [Google Scholar] [CrossRef]
  129. Kumar, M.; Chandran, D.; Tomar, M.; Bhuyan, D.J.; Grasso, S.; Sá, A.G.A.; Carciofi, B.A.M.; Dhumal, S.; Singh, S.; Senapathy, M.; et al. Valorization Potential of Tomato (Solanum lycopersicum L.) Seed: Nutraceutical Quality, Food Properties, Safety Aspects, and Application as a Health-Promoting Ingredient in Foods. Horticulturae 2022, 8, 265. [Google Scholar] [CrossRef]
  130. Magne, F.; Gotteland, M.; Gauthier, L.; Zazueta, A.; Pesoa, S.; Navarrete, P.; Balamurugan, R. The firmicutes/bacteroidetes ratio: A relevant marker of gut dysbiosis in obese patients? Nutrients 2020, 12, 1474. [Google Scholar] [CrossRef]
  131. Rastmanesh, R. Chemico-Biological Interactions High polyphenol, low probiotic diet for weight loss because of intestinal microbiota interaction. Chem. Biol. Interact. 2011, 189, 1–8. [Google Scholar] [CrossRef]
  132. Patel, S. Cereal bran fortified-functional foods for obesity and diabetes management: Triumphs, hurdles and possibilities. J. Funct. Foods 2015, 14, 255–269. [Google Scholar] [CrossRef]
  133. Dapčević-Hadnadev, T.; Hadnadev, M.; Pojić, M. The Healthy Components of Cereal By-Products and Their Functional Properties; Woodhead Publishing Series in Food Science; Woodhead Publishing: Sawston, UK, 2018; ISBN 9780081022146. [Google Scholar]
  134. Precup, G.; Pocol, C.B. Awareness, Knowledge, and Interest about Prebiotics—A Study among Romanian Consumers. Int. J. Environ. Res. Public Health 2022, 19, 1208. [Google Scholar] [CrossRef]
  135. Coe, S.; Ryan, L. Impact of polyphenol-rich sources on acute postprandial glycaemia: A systematic review. J. Nutr. Sci. 2016, 5, 1–11. [Google Scholar] [CrossRef]
  136. O’Shea, N.; Ktenioudaki, A.; Smyth, T.P.; McLoughlin, P.; Doran, L.; Auty, M.A.E.; Arendt, E.; Gallagher, E. Physicochemical assessment of two fruit by-products as functional ingredients: Apple and orange pomace. J. Food Eng. 2015, 153, 89–95. [Google Scholar] [CrossRef]
  137. Allaqaband, S.; Dar, A.H.; Patel, U.; Kumar, N.; Alabdallah, N.M.; Kumar, P.; Pandey, V.K.; Kovács, B. Utilization of Fruit Seed-Based Bioactive Compounds for Formulating the Nutraceuticals and Functional Food: A Review. Front. Nutr. 2022, 9, 902554. [Google Scholar] [CrossRef]
  138. Muntean, M.V.; Fărcaş, A.C.; Medeleanu, M.; Salanţă, L.C.; Borşa, A. A Sustainable Approach for the Development of Innovative Products from Fruit and Vegetable By-Products. Sustainability 2022, 14, 10862. [Google Scholar] [CrossRef]
  139. Konrade, D.; Klava, D.; Gramatina, I. Cereal Crispbread Improvement with Dietary Fibre from Apple By-Products. CBU Int. Conf. Proc. 2017, 5, 1143–1148. [Google Scholar] [CrossRef] [Green Version]
  140. Grispoldi, L.; Ianni, F.; Blasi, F.; Pollini, L.; Crotti, S.; Cruciani, D.; Cenci-Goga, B.T.; Cossignani, L. Apple Pomace as Valuable Food Ingredient for Enhancing Nutritional and Antioxidant Properties of Italian Salami. Antioxidants 2022, 11, 1221. [Google Scholar] [CrossRef]
  141. Ahmed, M.; Ali, A.; Sarfraz, A.; Hong, Q.; Boran, H. Effect of Freeze-Drying on Apple Pomace and Pomegranate Peel Powders Used as a Source of Bioactive Ingredients for the Development of Functional Yogurt. J. Food Qual. 2022, 2022, 3327401. [Google Scholar] [CrossRef]
  142. Karwacka, M.; Ciurzyńska, A.; Galus, S.; Janowicz, M. Freeze-dried snacks obtained from frozen vegetable by-products and apple pomace—Selected properties, energy consumption and carbon footprint. Innov. Food Sci. Emerg. Technol. 2022, 77, 102949. [Google Scholar] [CrossRef]
  143. Gunes, R.; Palabiyik, I.; Toker, O.S.; Konar, N.; Kurultay, S. Incorporation of defatted apple seeds in chewing gum system and phloridzin dissolution kinetics. J. Food Eng. 2019, 255, 9–14. [Google Scholar] [CrossRef]
  144. Awasthi, M.K.; Ferreira, J.A.; Sirohi, R.; Sarsaiya, S.; Khoshnevisan, B.; Baladi, S.; Sindhu, R.; Binod, P.; Pandey, A.; Juneja, A.; et al. A critical review on the development stage of biorefinery systems towards the management of apple processing-derived waste. Renew. Sustain. Energy Rev. 2021, 143, 110972. [Google Scholar] [CrossRef]
  145. Antioxidants, P.; Mitrea, L.; Plamada, D.; Nemes, S.A.; Lavinia-Florina, C.; Pascuta, M.S.; Varvara, R.; Szabo, K. Development of Pectin and Poly ( vinyl alcohol ) -Based Active Packaging Enriched with Itaconic Acid and Apple. Antioxidants 2022, 11, 1729. [Google Scholar]
  146. Majzoobi, M.; Poor, Z.V.; Jamalian, J.; Farahnaky, A. Improvement of the quality of gluten-free sponge cake using different levels and particle sizes of carrot pomace powder. Int. J. Food Sci. Technol. 2016, 51, 1369–1377. [Google Scholar] [CrossRef]
  147. Lau, T.; Clayton, T.; Harbourne, N.; Rodriguez-Garcia, J.; Oruna-Concha, M.J. Sweet corn cob as a functional ingredient in bakery products. Food Chem. X 2022, 13, 100180. [Google Scholar] [CrossRef]
  148. Kumar, L.; Sehrawat, R.; Kong, Y. Oat proteins: A perspective on functional properties. LWT 2021, 152, 112307. [Google Scholar] [CrossRef]
  149. Brückner-Gühmann, M.; Benthin, A.; Drusch, S. Enrichment of yoghurt with oat protein fractions: Structure formation, textural properties and sensory evaluation. Food Hydrocoll. 2019, 86, 146–153. [Google Scholar] [CrossRef]
  150. Chi, M.S.; Adriana, P.; Man, S.M.; Vodnar, D.C.; Teleky, B.; Pop, C.R.; Stan, L.; Borsai, O.; Kadar, C.B.; Urcan, A.C. Quinoa Sourdough Fermented with Lactobacillus plantarum ATCC 8014 Designed for Gluten-Free Muffins—A Powerful Tool to Enhance Bioactive Compounds. Appl. Sci. 2020, 10, 7140. [Google Scholar] [CrossRef]
  151. Verni, M.; Rizzello, C.G.; Coda, R. Fermentation biotechnology applied to cereal industry by-products: Nutritional and functional insights. Front. Nutr. 2019, 6, 42. [Google Scholar] [CrossRef] [PubMed]
  152. Teleky, B.E.; Martău, G.A.; Ranga, F.; Pop, I.D.; Vodnar, D.C. Biofunctional soy-based sourdough for improved rheological properties during storage. Sci. Rep. 2022, 12, 17535. [Google Scholar] [CrossRef] [PubMed]
  153. Campbell, J.K.; Canene-Adams, K.; Lindshield, B.L.; Boileau, T.W.-M.; Clinton, S.K.; Erdman, J.W.J. Tomato phytochemicals and prostate cancer risk. J. Nutr. 2004, 134, 3486S–3492S. [Google Scholar] [CrossRef] [Green Version]
  154. Szabo, K.; Teleky, B.; Ranga, F.; Roman, I.; Khaoula, H.; Boudaya, E.; Ltaief, A.B.; Aouani, W.; Thiamrat, M.; Vodnar, D.C. Carotenoid Recovery from Tomato Processing By-Products through Green Chemistry. Molecules 2022, 27, 3771. [Google Scholar] [CrossRef]
  155. Szabo, K.; Teleky, B.E.; Mitrea, L.; Călinoiu, L.F.; Martău, G.A.; Simon, E.; Varvara, R.A.; Vodnar, D.C. Active packaging-poly (vinyl alcohol) films enriched with tomato by-products extract. Coatings 2020, 10, 141. [Google Scholar] [CrossRef] [Green Version]
  156. PA Silva, Y.; Borba, B.C.; Pereira, V.A.; Reis, M.G.; Caliari, M.; Brooks, M.S.L.; Ferreira, T.A. Characterization of tomato processing by-product for use as a potential functional food ingredient: Nutritional composition, antioxidant activity and bioactive compounds. Int. J. Food Sci. Nutr. 2019, 70, 150–160. [Google Scholar] [CrossRef]
  157. Kaur, M.; Kaur, M.; Kaur, H. Apple peel as a source of dietary fiber and antioxidants: Effect on batter rheology and nutritional composition, textural and sensory quality attributes of muffins. J. Food Meas. Charact. 2022, 16, 2411–2421. [Google Scholar] [CrossRef]
  158. Ciurzyńska, A.; Popkowicz, P.; Galus, S.; Janowicz, M. Innovative Freeze-Dried Snacks with Sodium Alginate and Fruit Pomace (Only Apple or Only Chokeberry) Obtained within the Framework of Sustainable Production. Molecules 2022, 27, 3095. [Google Scholar] [CrossRef] [PubMed]
  159. Gumul, D.; Ziobro, R.; Kruczek, M.; Rosicka-Kaczmarek, J. Fruit Waste as a Matrix of Health-Promoting Compounds in the Production of Corn Snacks. Int. J. Food Sci. 2022, 2022, 7341118. [Google Scholar] [CrossRef] [PubMed]
  160. Chaari, F.; Zouari-Ellouzi, S.; Belguith-Fendri, L.; Yosra, M.; Ellouz-Chaabouni, S.; Ellouz-Ghorbel, R. Valorization of Cereal by Products Extracted Fibre and Potential use in Breadmaking. Chem. Afr. 2022. [Google Scholar] [CrossRef]
  161. Barbhai, M.D.; Hymavathi, T.V.; Kuna, A.; Mulinti, S.; Voliveru, S.R. Quality assessment of nutri-cereal bran rich fraction enriched buns and muffins. J. Food Sci. Technol. 2022, 59, 2231–2242. [Google Scholar] [CrossRef]
  162. Khojah, E.Y.; Badr, A.N.; Mohamed, D.A.; Abdel-Razek, A.G. Bioactives of Pomegranate By-Products and Barley Malt Grass Engage in Cereal Composite Bar to Achieve Antimycotic and Anti-Aflatoxigenic Attributes. Foods 2022, 11, 119. [Google Scholar] [CrossRef]
  163. Naibaho, J.; Butula, N.; Jonuzi, E.; Korzeniowska, M.; Laaksonen, O.; Föste, M.; Kütt, M.L.; Yang, B. Potential of brewers’ spent grain in yogurt fermentation and evaluation of its impact in rheological behaviour, consistency, microstructural properties and acidity profile during the refrigerated storage. Food Hydrocoll. 2022, 125, 107412. [Google Scholar] [CrossRef]
  164. Alonso dos Santos, P.; Caliari, M.; Soares Soares Júnior, M.; Soares Silva, K.; Fleury Viana, L.; Gonçalves Caixeta Garcia, L.; Siqueira de Lima, M. Use of agricultural by-products in extruded gluten-free breakfast cereals. Food Chem. 2019, 297, 124956. [Google Scholar] [CrossRef]
  165. Noguerol, A.T.; Marta Igual, M.; Pagán, M.J. Developing psyllium fibre gel-based foods: Physicochemical, nutritional, optical and mechanical properties. Food Hydrocoll. 2022, 122, 107108. [Google Scholar] [CrossRef]
  166. Mitrea, L.; Călinoiu, L.-F.F.; Martău, G.-A.; Szabo, K.; Teleky, B.-E.E.; Mureșan, V.; Rusu, A.-V.V.; Socol, C.-T.T.; Vodnar, D.-C.C.; Mărtau, G.A.; et al. Poly(vinyl alcohol)-based biofilms plasticized with polyols and colored with pigments extracted from tomato by-products. Polymers 2020, 12, 532. [Google Scholar] [CrossRef] [Green Version]
  167. Rehal, J.K.; Aggarwal, P.; Dhaliwal, I.; Sharma, M.; Kaushik, P. A Tomato Pomace Enriched Gluten-Free Ready-to-Cook Snack’s Nutritional Profile, Quality, and Shelf Life Evaluation. Horticulturae 2022, 8, 403. [Google Scholar] [CrossRef]
  168. Lucera, A.; Costa, C.; Marinelli, V.; Saccotelli, M.A.; Alessandro, M.; Nobile, D.; Conte, A. Fruit and Vegetable By-Products to Fortify Spreadable Cheese. Antioxidants 2018, 7, 61. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  169. Sandei, L.; Stingone, C.; Vitelli, R.; Cocconi, E.; Zanotti, A.; Zoni, C. Processing tomato by-products re-use, secondary raw material for tomato product with new functionality. Acta Hortic. 2019, 1233, 255–260. [Google Scholar] [CrossRef]
  170. Ahmad Bhat, M.; Ahsan, H. Physico-Chemical Characteristics of Cookies Prepared with Tomato Pomace Powder. J. Food Process. Technol. 2016, 7, 543. [Google Scholar] [CrossRef]
  171. Padalino, L.; Conte, A.; Lecce, L.; Likyova, D.; Sicari, V.; Pellicanò, T.M.; Poiana, M.; Del Nobile, M.A. Functional pasta with tomato by-product as a source of antioxidant compounds and dietary fibre. Czech J. Food Sci. 2017, 35, 48–56. [Google Scholar]
  172. Dankar, I.; Haddarah, A.; Omar, F.E.; Sepulcre, F.; Pujolà, M. 3D printing technology: The new era for food customization and elaboration. Trends Food Sci. Technol. 2018, 75, 231–242. [Google Scholar] [CrossRef]
  173. Sehrawat, N.; Yadav, M.; Singh, M.; Kumar, V.; Ruchi, V. Seminars in Cancer Biology Probiotics in microbiome ecological balance providing a therapeutic window against cancer. Semin. Cancer Biol. 2021, 70, 24–36. [Google Scholar] [CrossRef]
  174. Varvara, R.A.; Szabo, K.; Vodnar, D.C. 3D food printing: Principles of obtaining digitally-designed nourishment. Nutrients 2021, 13, 3617. [Google Scholar] [CrossRef]
  175. Oliveira, S.M.; Gruppi, A.; Vieira, M.V.; Matos, G.S.; Spigno, G.; Pastrana, L.M.; Teixeira, A.C.; Fuci, P. How additive manufacturing can boost the bioactivity of baked functional foods. J. Food Eng. 2021, 294, 110394. [Google Scholar] [CrossRef]
Figure 1. Production of cereal, apples, and tomatoes (tons) in Europe. (A) Evolution of world cereal, apple, and tomato production over the last two decades; (B) production of wheat (tons) in Europe for every country in 2020; (C) production of apples (tons) in Europe for every country in 2020; (D) production of tomatoes (tons) in Europe for every country in 2020 (http://www.fao.org/faostat, accessed on 22 April 2022).
Figure 1. Production of cereal, apples, and tomatoes (tons) in Europe. (A) Evolution of world cereal, apple, and tomato production over the last two decades; (B) production of wheat (tons) in Europe for every country in 2020; (C) production of apples (tons) in Europe for every country in 2020; (D) production of tomatoes (tons) in Europe for every country in 2020 (http://www.fao.org/faostat, accessed on 22 April 2022).
Molecules 27 07977 g001
Figure 2. Distribution of phenolic compounds in apple fruit, according to Feng et al. [49]. TPC—total phenolic content; DW—dry weight.
Figure 2. Distribution of phenolic compounds in apple fruit, according to Feng et al. [49]. TPC—total phenolic content; DW—dry weight.
Molecules 27 07977 g002
Figure 3. The chemical structure of the predominant phenolic compounds identified in apple pomace: chlorogenic acid (A); epicatechin (B); phlorizin (C). Source: ChemDraw Software.
Figure 3. The chemical structure of the predominant phenolic compounds identified in apple pomace: chlorogenic acid (A); epicatechin (B); phlorizin (C). Source: ChemDraw Software.
Molecules 27 07977 g003
Figure 4. The most common cereals and their primary bioactive compounds.
Figure 4. The most common cereals and their primary bioactive compounds.
Molecules 27 07977 g004
Figure 5. The chemical structure of the predominant phenolic compounds identified in tomato-processing by-products: rutin (A); quercetin (B); naringenin (C). Source: ChemDraw Software.
Figure 5. The chemical structure of the predominant phenolic compounds identified in tomato-processing by-products: rutin (A); quercetin (B); naringenin (C). Source: ChemDraw Software.
Molecules 27 07977 g005
Table 1. The nutritional and polyphenolic profile of apple pomace 1 [43].
Table 1. The nutritional and polyphenolic profile of apple pomace 1 [43].
CompositionAmount (% DW)
Total sugar45.1 ± 5.3
Total dietary fiber26.5 ± 0.8
Insoluble fiber18.4 ± 0.4
Soluble fiber8.2 ± 0.5
Total phenolic content (mg EGA/100 g AP)289.1 ± 24.2
Fat3.8 ± 0.2
Protein 23.8 ± 0.0
Polyphenolic profile(mg/100 g dry matter)
Quercetin-3-O-galactoside22.55 ± 0.34
Quercetin-3-O-xyloside13.91 ± 0.03
Quercetin-3-O-rhamnoside19.21 ± 0.00
Chlorogenic acid20.55 ± 0.12
p-coumaroylquinic acid0.16 ± 0.03
Catechin1.44 ± 0.02
Procyanidin B22.61 ± 0.00
Phloretin-2-O-xylosyl-glucoside1.48 ± 0.14
Phlorizin15.52 ± 0.00
1 Values represent mean ± standard deviation, based on [43]; 2 nitrogen to protein conversion factor was 5.7.
Table 2. Chemical composition of cereal bran.
Table 2. Chemical composition of cereal bran.
CompoundAmount (% DW)References
Wheat BranRice BranOat BranCorn Bran
Water12.18.72-29.4–31.24 [70,71,72,73]
Protein13.2–18.410–165.9–6.79.5–10.1 [71,74,75]
Fat3.5–3.915–226.471.92–6.41 [74,76,77,78]
Total carbohydrates 56.834.1–52.366.2278.05–79.7 [74,76,77,78]
Starch13.8–24.918.19–32.452.5–16.327.7–28.2 [70,72]
Cellulose10.5–14.815.83.423–23.1 [72,79]
Hemicellulose35.5–39.231.335%26.1–27 [72,79,80]
Lignin8.3–12.511.611.222.2–6.5 [72,79]
Total arabinoxylans10.9–26.04.8–5.1317.5–17.7 [70,79,81]
Total β-glucan2.1–2.50.04–0.215.4–8.5- [79,81]
Phenolic acids 1.11.570.7–12.2-2.7 [71,74,82]
Ferulic acid 0.02–1.50.0041.761.5–1.9 [70,82,83]
Phytic acid 4.2–5.450.68 *-- [74]
Ash 3.4–8.110.6510.3–10.94 [71,73]
* Phytic acid content of rice bran is expressed as mg/g DW.
Table 3. Total phenolic content and antimicrobial and antioxidant activity considering the localization and extraction methods.
Table 3. Total phenolic content and antimicrobial and antioxidant activity considering the localization and extraction methods.
Geographical OriginTomato By-ProductsExtraction MethodTotal Phenolic ContentAntioxidant ActivityAntimicrobial ActivityReference
IndiaPeelsSolvent extraction33.5 mg TAE/100 g21.0% inhibition/g- [94]
Seeds20.11 mg TAE/100 g meal34.0% inhibition/g-
RomaniaSeeds and peels of 10 varieties of tomato111.9 to 407.7 mg/100 g DWMean value of 489.9 ± 41.5 µmol TE/100 gGram-positive and Gram-negative bacteria [99]
Peels of 10 varieties of tomato35 to 157 mg/ 100 g DWMean value of 201 ± 44 µmol TE/100 g [95]
Portugal Whole tomato408.89 ± 12.11 and 277.24 ± 11.29 mg GAE/100 g DM (fresh and after 6 months of frozen storage); 310.33 ± 10.38 and 283.64 ± 11.84 mg GAE/100 g DW (before and after 6 months of powder storage)ABTS (694.07 ± 45.00 and 558.73 ± 29.06 mg TE/100 g in fresh and after 6 months of frozen storage; 350.15 ± 14.37 and 407.56 ± 25.93 mg TE/100 g before and after 6 months of powder storage) Enterobacteriaceae, Bacillus cereus spp., yeasts, and molds [104]
ORAC (3165.18 ± 77.48 mg TE/100 g, 3285.77 ± 271.25 mg TE/100 g 1771.66 ± 31.25 mg TE/100 g in fresh and after 1 to 6 months of frozen storage; 1581.76 ± 124.90 TE/100 g, 1610.74 ± 46.51 mg TE/100 g and 1229.74 ± 38.52 mg TE/100 g before and after 2 to 6 months of powder storage)
DPPH (418.79 ± 30.92, 648.06 ± 55.38, 388.53 ± 27.18 mg TE/100 g in fresh and after 3 to 6 months of frozen storage; 117.78 ± 4.99 to 130.44 ± 3.51 mg TE/ 100 g before and after 6 months of powder storage)
SpainPeels fiberEnzyme hydrolysis291.14 ± 11.1 to 353.15 ± 19.6 mg GAE/kg3.90 µmol TEAC/g- [105]
Maceration749.84 ± 15.55 mg GAE/kg
Ultrasonic assistance (5 to 15 min)985.78 ± 112.93 to 1056.18 ±67.9 mg GAE/kg
DW—dry weight; GAE—gallic acid equivalents.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Szabo, K.; Mitrea, L.; Călinoiu, L.F.; Teleky, B.-E.; Martău, G.A.; Plamada, D.; Pascuta, M.S.; Nemeş, S.-A.; Varvara, R.-A.; Vodnar, D.C. Natural Polyphenol Recovery from Apple-, Cereal-, and Tomato-Processing By-Products and Related Health-Promoting Properties. Molecules 2022, 27, 7977. https://doi.org/10.3390/molecules27227977

AMA Style

Szabo K, Mitrea L, Călinoiu LF, Teleky B-E, Martău GA, Plamada D, Pascuta MS, Nemeş S-A, Varvara R-A, Vodnar DC. Natural Polyphenol Recovery from Apple-, Cereal-, and Tomato-Processing By-Products and Related Health-Promoting Properties. Molecules. 2022; 27(22):7977. https://doi.org/10.3390/molecules27227977

Chicago/Turabian Style

Szabo, Katalin, Laura Mitrea, Lavinia Florina Călinoiu, Bernadette-Emőke Teleky, Gheorghe Adrian Martău, Diana Plamada, Mihaela Stefana Pascuta, Silvia-Amalia Nemeş, Rodica-Anita Varvara, and Dan Cristian Vodnar. 2022. "Natural Polyphenol Recovery from Apple-, Cereal-, and Tomato-Processing By-Products and Related Health-Promoting Properties" Molecules 27, no. 22: 7977. https://doi.org/10.3390/molecules27227977

Article Metrics

Back to TopTop