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Review

Advancements in the Use of Fermented Fruit Juices by Lactic Acid Bacteria as Functional Foods: Prospects and Challenges of Lactiplantibacillus (Lpb.) plantarum subsp. plantarum Application

Laboratory of Food Processing, Department of Agricultural Development, Democritus University of Thrace, 68200 Orestiada, Greece
Fermentation 2022, 8(1), 6; https://doi.org/10.3390/fermentation8010006
Submission received: 7 December 2021 / Revised: 22 December 2021 / Accepted: 22 December 2021 / Published: 26 December 2021
(This article belongs to the Special Issue Fermented and Functional Food)

Abstract

:
Lactic acid fermentation of fresh fruit juices is a low-cost and sustainable process, that aims to preserve and even enhance the organoleptic and nutritional features of the raw matrices and extend their shelf life. Selected Lactic Acid Bacteria (LAB) were evaluated in the fermentation of various fruit juices, leading in some cases to fruit beverages, with enhanced nutritional and sensorial characteristics. Among LAB, Lactiplantibacillus (Lpb.) plantarum subsp. plantarum strains are quite interesting, regarding their application in the fermentation of a broad range of plant-derived substrates, such as vegetables and fruit juices, since they have genome plasticity and high versatility and flexibility. L. plantarum exhibits a remarkable portfolio of enzymes that make it very important and multi-functional in fruit juice fermentations. Therefore, L. plantarum has the potential for the production of various bioactive compounds, which enhance the nutritional value and the shelf life of the final product. In addition, L. plantarum can positively modify the flavor of fruit juices, leading to higher content of desirable volatile compounds. All these features are sought in the frame of this review, aiming at the potential and challenges of L. plantarum applications in the fermentation of fruit juices.

1. Introduction

The focus of innovations in the food industry has turned to new functions of food, which are prevention from various lifestyle diseases, mainly through the development of dietary supplements, that can affect the intestinal microbial composition. In addition, the preference of many consumers to foods free of additives has also boosted the facilitation and promotion of various novel products by the food industry called functional foods. Functional foods are foods that can positively affect specific human body functions beyond adequate nutritional effects, leading to the delivery of various health benefits to humans [1]. Functional foods mainly include probiotics, prebiotics, and more recently symbiotics [2,3]. Dairy products such as cheese, sour milk, yogurt and others are considered as the main representatives of probiotic foods. However, other alternative food products are being developed as probiotic substrates in the last few years [4,5]. The main reason for this shift is that dairy products display some drawbacks, affecting consumers’ attitudes, such as milk cholesterol content, lactose intolerance and dairy allergies [6,7]. Thus, alternative food substrates were proposed as ideal carriers or mediums for probiotics, in order to tackle these disadvantages, such as cereals, vegetables and fruits in fermented and unfermented forms [7]. Particularly, fruit juices are presumed as attractive good substrates for probiotic delivery. The advantages of fruit juices, as probiotic “vehicles” include: (i) high nutritional value, (ii) positive health effects, and (iii) wide acceptance and consumption by consumers worldwide [8,9,10]. Many fruit juices were inspected, explored and evaluated, regarding their suitability, as viable and shelf-stable probiotic carriers, through lactic acid fermentation. Nevertheless, fermentation is a complex process, which needs control and selection of appropriate conditions in order to achieve desirable food characteristics and preserve probiotic cell functionality and viability. Likewise, the proper selection of the starter culture for the fermentation of fruit juices and possible modifications of fruit juices (before fermentation) are considered critical parameters. Lactic acid bacteria (LAB) are the most common microorganisms applied for the fermentation of fruit juice. Particularly, Lactobacillus plantarum or, as it has lately been denoted, Lactiplantibacillus (Lpb.) plantarum subsp. plantarum [11] is an interesting and well-studied strain in the fermentation of fruit juices. The scope of this review is to provide an overview of recent findings, regarding the challenges and the opportunities of L. plantarum application in fruit juices fermentations.

2. Lactic Acid Fermentation of Fruit Juices

The preference of consumers to fruit juices, nectars and ready-to-drink juice drinks was boosted in the last decade worldwide [12]. This is mainly, due to the shift of consumers’ preference to more natural foods containing less or no chemical preservatives and the better awareness of consumers, regarding the nutritional values of foods [13]. In particular, fruit juices contain appreciable amounts of dietary fibers, antioxidants, polyphenols, minerals and vitamins and meet the consumer’s claims for healthy, tasty, and practical foods.
On the other hand, fresh fruit juices are susceptible to spoilage by different microorganisms [14]. The shelf life of fresh fruit juices is very short and varies between 5 to 7 days at 4 °C [15]. Therefore, the preservation of fruit juices should be controlled by the addition of various synthetic preservatives, such as potassium sorbate and sodium benzoate [16]. Nevertheless, fresh juices extracted from fruits are commercialized as refrigerated products, without preservatives and with a very short shelf-life [17]. However, currently, consumers prefer fruit juices free of chemical additives and safe for consumption. Lactic acid fermentation of fruit juices seems a good alternative and could satisfy consumers’ demands and preferences. Several studies were reported in the literature, verifying a clear positive impact in the extension of self-life of fruit juices, through fermentation by LAB. This impact depends on the kind of fruit juice and its chemical composition, the strain applied and the conditions of fermentation and storage (time, temperature, etc.). Lactic acid fermentation of fruit juices can keep or ameliorate: (i) the self-life [18], (ii) the nutritional, and (iii) the sensorial properties of the final product [19,20]. It is also considered as a mild processing method for preservation, which meets the standards regarding the consumption of fresh-like minimal processed beverages [21]. The most common microbiocidal group applied for lactic acid fermentation of fruit juices is LAB. Several studies were conducted and published in the literature and some examples are presented in Table 1, with the respective advantages.
Likewise, fermented pomegranate juice by LAB, was preserved for 45 days (approximately 38 days more than the unfermented juice), under cold storage (4 °C), without any additive addition [37]. Addition of fermented cantaloupe juice by LAB, to fresh cantaloupe juice stored at 8 °C, extended the self-life of the final product for 6 months [38]. No microbiological spoilage of fermented pomegranate juice by L. plantarum ATCC 14917 was observed after 28 days of cold storage (4 °C), whereas fresh pomegranate juice is usually spoiled 5 to 7 days, under cold storage at 4 °C [25].
Nevertheless, functionality and physiological status of LAB during lactic acid fermentation and cold storage of fermented juices, can be affected by exposure to certain types of stress, such as acid and cold. Specifically, some fruit juices are very acidic, such as cranberry (pH 2.7), pomegranate (pH 3.0-3.5), lemon and lime juices (pH 2.8) [39], exhibiting severe impact on the viability of LAB, [40] during the production process and storage [41]. Especially, in the case of probiotic LAB strains, survival in harsh conditions is an essential prerequisite for probiotic delivery [42]. These obstacles could be tackled, with mainly 5 ways: (i) pre-adaptation or adaptive evolution, (ii) encapsulation, (iii) physical treatments (iv) mixing with a second juice and (v) proper selection of a probiotic LAB.
The most commonly way for stress adaptation is the modification of the growth medium and/or incubation conditions. Pre-adaptation or adaptive evolution [43] involves the treatment of a microorganism to a sublethal stress (pH, cold, osmotic press etc,) for a limited time; this treatment would act on strain resistance, when exposed to a higher level of stress or to another stress. This method has been applied in lactic acid fermentation of fruit juices by probiotics, with very promising results [44,45].
Microencapsulation is considered as a promising method for the improvement of probiotics’ viability in functional beverages. Microencapsulation of probiotics leads to high preservation of the probiotic load and strengthen cells, versus various physicochemical changes, such as pH, temperature, bile salts, etc. [46,47,48]. Another target of probiotic microencapsulation, is the improvement of the resistance of the probiotic cells in the gastro-intestinal tract, besides enhancing the viability of the bacterial strains in the food products. Various methods have been proposed for probiotic cell microencapsulation, such as emulsification, spay freeze drying and extrusion, with numerous encapsulating agents [49]. The most commonly employed encapsulating agents are natural biopolymer, such as alginate and κ-carrageenan, as well as prebiotics, such as resistant starch, inulin, fructooligosaccharide and fiber [50]. Application of prebiotics as encapsulating agents seems more attractive, because it is a cost-effective technology for the industrial scale and offers encouraging results [47,49]. The functionality of LAB could be significantly ameliorated employing physical treatments. The most common applied technology is ultrasound (US). Probiotic L. casei NRRL B442 manage to survive for at least 21 days at 4 °C in a sonicated pineapple juice [51]. In another report, L. reuteri, L. plantarum, L. casei, bifidobacteria, and propionibacteria were treated with US, before the inoculation in an organic rice beverage and maintained the pH and sensory scores for at least 7 days [52,53]. Addition of a second juice (fresh or fermented) to the main one is a quite interesting perspective. The main reason for this treatment, is the slight increase of the low pH value of the main juice, in order the survival of the probiotic strain to be ameliorated. Likewise, carrot juice has been proposed for this purpose, since it has approximately a pH value of 6 [24]. Furthermore, addition of 5% acerola juice to orange juice, prevented the production of carbon dioxide gas for three weeks and has no impact on the probiotic content during four weeks of storage at 8 °C [54].
In addition, the type of LAB strains applied for lactic acid fermentation is also critical, in order cells to endure the harsh conditions of fruit juice matrix (especially low pH values). Probiotic LAB strains have gained attention lately, since they are considered as acid tolerance strains. However, there are examples that viability of certain probiotics could also be decreased, during lactic acid fermentation and storage, especially at low temperatures for more than 14 days. In general, fruity food matrix can influence the viability of probiotics in positive, none and negative way. However, the decrease of probiotic viability is inevitable, during cold storage of fermented fruit juices in more than 3 weeks. The question is the level of the decrease, especially in the case of probiotic strains. A final viability of a probiotic LAB above 6 log cfu/mL in the fermented juice, after 28 days of cold storage (4 °C) is welcomed, since the product contain the desirable probiotic features [24]. For instance, probiotic L. reuteri was strongly affected by the kind of juice. It survived in pineapple, orange and apple juices, while it experienced a strong reduction in red fruit [55]. In another study, viability of probiotic L. plantarum ATCC 14917 cells in Cornelian cherry juice decreased about 4 folds after 28 days of cold storage [26], while acai pulp ameliorated the viability of L. acidophilus, B. animalis ssp. lactis and B. longum throughout 4 weeks of cold storage [56]. Nevertheless, most of the probiotic strains applied for lactic acid fermentation of fruit juice seem at least to preserve their viability to the least limit (6 log cfu/mL) and they can deliver probiotic properties to the final product [57,58]. Thus, the selection of a proper LAB, with the ability to overcome the harsh environmental conditions in the fruit juice matrix and furthermore to enhance the functional characteristics of the juice, seems to be an interesting perspective. In this manner, probiotic L. plantarum strains seems to be very interesting strain and has gained attention lately.

3. Main Advantages of L. plantarum Application in Food Fermentations

L. plantarum is a safe microorganism (Generally Regard as Safe — GRAS) and has been widely used in food-fermentation technologies [59,60]. It has also been employed in probiotic food production, such as L. plantarum 299v strain, which is widely marketed [61]. It is a facultative heterofermentative LAB, that can tolerate the combination of high acidity and ethanol concentration and survive under conditions, that are usually fatal to LAB [62]. The adaptability of L. plantarum to a fermentation process and its metabolic flexibility and versatility are some of the critical attributes, that makes it unique among the other LAB [63]. L. plantarum has been isolated through numerous food sources, such as cereals, meats, dairy products, vegetables, fruits and drinks [64,65,66,67,68], as well as human and mammals niches [69]. L. plantarum can adapt to various niches, probably due to its genome size (average 3.3 Mb), which is one of the largest detected within Lactobacillus genus [70].
In addition, L. plantarum can be involved in several biochemical reactions, usually ended in desirable metabolites, due to its specific enzymatic composition. L. plantarum contains a variety of extracellular enzymes, that contribute to the secretion and modification of proteins and to the modification and degradation of extracellular compounds, allowing for the use of such molecules as a source of nutrients [71,72]. Specifically, L. plantarum possesses enzymes, such as tannase, β-glucosidase, α-glucosidase and β-galactosidase p-coumaric acid decarboxylase and general decarboxylase, that catalyze the production of high added-value compounds, such as phenolic compounds leading to the production of compounds, that influence positively food aroma and increase the antioxidant activity [73]. The production of aryl β-glucosidases, by L. plantarum initiates an increase in the functionally (antioxidant activity and bioavailability) of glycosylated phenolic compounds. Besides, employment of L. plantarum to various plant-based products, such as fruit juices, with high content of tannins, attenuated the phenolic astringency, which is responsible of the unpalatability of many fruit juices [74].
Recently, probiotic strains of L. plantarum has been successfully applied in medical fields, with encouraging outcome. Specifically, the efficacy of L plantarum strains in the cure or treatment of gastrointestinal disorders, cholesterol lowering and reduction in the irritable bowel syndrome (IBS) symptoms has been highlighted in human trials [75].
Several strains of L. plantarum have been exhibited antimicrobial and antagonistic activity, against some adverse microorganisms, antifungal activities and antiviral effects [76]. In addition, it should be highlighted the wide range of bacteriocins and exopolysaccharides (EPS), that L. plantarum is able to produce [77]. Bacteriocins show a broad antimicrobial activity spectrum against Gram-positive and Gram-negative bacteria, while EPS provide potential health-promoting properties in the advances of functional foods [78].

Application of L. plantarum Strains in Various Fruit Juices Fermentations

A great variety of fruit juices has been successfully fermented by L. plantarum strains leading to final products with potentially functional properties. Most of these reported positive effects are presented in Table 1 and are recapitulated to: (i) enhanced antioxidant activity, (ii) increased total phenolic and total anthocyanin content, (iii) extension of the shelf-life of fruit juices and (iv) better sensorial features. It has been reported, that L. plantarum ATCC14917 modified the phenolic composition of apple juice after fermentation and enhanced its overall antioxidant capacity, as well as the bioavailability of polyphenols of apples [30]. The absorption of food phenolics in humans, is necessary for the exhibition of their beneficial effects. It is mainly evaluated by their chemical structure, which depends on factors such as the degree of glycosylation and conjugation with other phenolics [79].
On the other hand, food industry is seeking ways to produce novel products with increased nutritional value. Moreover, there are many reports, that application of a probiotic bacteria in the fermentation of fruit juices may lead to a final product, with functional properties and specific health benefits [80,81,82].
Even though, L. plantarum can grow generally at temperatures between 15–30 °C and at pH values near to 4 [83], there are specific probiotic strains of L. plantarum with respectable tolerance at low pH values (approximately 3.2) and at low temperatures in the matrix of fruit juices (4–8 °C) [84]. For instance, viability of probiotic L. plantarum NCIMB 8826 decreased during cold storage (4 °C) of cranberry, pomegranate and lemon & lime juices with initial pH values approximately 3. However, only in the case of lemon & lime juice cells were viable until the 35th day [39]. This could be explained by: (i) the high levels of phenolic compounds in cranberry juice [39] and pomegranate juice [85], which are known to have strong antimicrobial properties [86] and (ii) the fact that cells were pre-adapted to citric acid, which is the main antimicrobial compound in the lemon & lime juice, leading to higher viabilities to this juice compared to the others [39]. In another recent study, cell viability of probiotic L. plantarum ATCC14917 was remained at high levels throughout the 21 days of cold storage (4 °C) of fermented pomegranate juice (initially 11.43 log cfu/mL) and decreased to 8.83 log cfu/mL at the 4th week of storage, above the limit for the exhibition of probiotic properties. The same observations were made, during cold storage (4 °C) of fermented Cornelian cherry [87] and pomegranate juice [24], with L. plantarum ATCC 14917 and fermented sweet lemon juice (Citrus limetta) with L. plantarum LS5 [88].
Furthermore, L. plantarum has a positive effect on the flavor of fruit juices, leading to higher content of desirable volatile compounds during fermentation. Lactic acid fermentation of jujube juice by L. plantarum significantly enhanced the composition and production of desirable volatile compounds, leading to aroma complexity and better sensorial characteristics [31]. L. plantarum 285 exhibited interesting features, in terms of total aromatic potential, as well as in the type of volatiles compounds produced through lactic acid fermentation of elderberry juice [20]. Fermentation of blueberry juices with L. plantarum enhanced the acceptability of the final product [89].
Besides, Food Industry has selected probiotic L. plantarum strains in single or mixed culture, in order to produce a variety of probiotic fruit beverages, through fermentation (Table 2). The commercialization of the whole fermentation system, which includes L. plantarum verifies the eligibility of this important LAB. A proposed route for the scale up of the whole procedure could be feasible and it is presented in Figure 1. However, research is continuing and it is possible, that through in vivo tests and human trials, more interesting outcomes may be recorded. The main reason for this assumption is the biological activities, that this microorganism has exhibited so far.

4. Biological Activities

Various strains of L. plantarum have been studied thorough using in vivo and in vitro models, regarding health-promoting properties such as antitumor, antioxidation, immunomodulation and biocompatibility. Likewise, L. plantarum is a very well-studied strain with very good perspectives in medical biotechnology. Most of these biological activities are attributed to exopolysaccharides and bacteriocins, that L. plantarum can potentially produce.
L. plantarum is considered as distinguished microorganism for its potential EPS-producing properties and have received considerable attention (Table 3). The EPS-producing L. plantarum strains have been isolated from different fermented foods, besides human gut [91]. These polysaccharides can be either homopolysaccharides, consisted mainly of glucans and fructans, or heteropolysaccharides with oligosaccharide repeating units containing different monosaccharides [92]. The physiological functions of the EPSs were related to their molecular characteristics. For example, α-1,3-linkages in EPS molecules seems to improve the texture of the dairy products. Modification of the EPSs, e.g., by acetylation, phosphorylation and carboxymethylation, could improve their bioactivities. The EPSs containing acetyl, phosphoryl groups or amino acid residues might possess specific physiological functions such as antitumor, antioxidation or immunoenhancement [93]. L. plantarum C88 isolated from fermented dairy, produced a high molecular mass polysaccharide (1.1×106 Da) with antioxidant activities [94]. L. plantarum YW11 isolated from a traditional beverage Tibet kefir produced EPS with very promising health potential [95]. L. plantarum CIDCA 8327 isolated from kefir was able to produce an EPS, with health promoting properties [96]. EPS with antioxidant properties was produced for L. plantarum K041 isolated from traditional Chinese pickle juice [97]. There is huge research revealing the potential of some EPS produced by L. plantarum to be applied as bioactive natural products in medical applications, with various effects, such as immunomodulatory, antitumor and antioxidant effects [97,98].
Furthermore, L. plantarum strains produce a broad range of bacteriocins. Most of the produced bacteriocins display a broad range of inhibition against Gram-positive and Gram-negative bacteria including food-borne pathogens, such as Listeria monocytogenes, Escherichia coli, Staphylococcus aureus, Clostridium perfringens, Pseudomonas spp. etc. Specifically, L. plantarum CIDCA 83114 seems to have a protective effect against pathogen invasion of cultured human cells, with pre-incubation of the strain with Caco-2 or HT-29 colon cell lines [113]. The same strain was capable to protect Vero cells from the effects of E. coli O157:H7 containing type-II Shiga toxin and was effective against pathogenic E. coli in various in vivo studies [114]. L. plantarum CIDCA 8337 exhibited very high adhesion to Caco-2 cells and inhibition of E. coli and S. typhimurium cells [115]. In other studies, L. plantarum C4 displayed significant adhesion to Caco-2 cells, as well as antimicrobial activity, against L. monocytogenes, Y. enterocolitica, S. typhimurium, and E. coli in a spot assay test [116]. L. plantarum MA2, isolated from kefir grains, showed that total cholesterol (TC), low-density lipoprotein cholesterol (LDL-C) and triglycerides (TG) were determined in significantly lower levels in treated rats, with high-density lipoprotein cholesterol (HDL-C) [117]. L. plantarum B23 exhibited high-level adhesion to Caco-2 cells and was susceptible to a range of antibiotics [91].

5. Conclusions

L. plantarum is considered as a versatile species, with advantageous properties. It possesses a wide portfolio of enzymes and it can biosynthesize many bioactive compounds, bacteriocins and EPS, which exert antimicrobial, antioxidant and probiotic properties. Consequently, application of probiotic strains of L. plantarum in the fermentation of fruit juices is very attractive, since it could lead to final products with extended self-life, enhanced nutritional value, better sensorial characteristics and health benefits. Moreover, L. plantarum is widely employed in industrial fermentation and processing of raw foods and has qualified presumption of safety (QPS) status [118]. Currently, specific sectors of Food industry, involved with functional food production, including fruit matrices, are broadly using probiotic L. plantarum strains. Nevertheless, updated knowledge is paramount, in order specific variation of L. plantarum strains to be clarified, particularly in relation to probiotic characteristics and conveyed health benefits.

Author Contributions

Conceptualization, S.P.; methodology, S.P.; investigation, S.P.; writing—original draft preparation, S.P.; writing—review and editing, S.P. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

The author declares that there are no conflict of interest.

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Figure 1. Proposed scale-up route for fruit juice fermentation by probiotic L. plantarum strains.
Figure 1. Proposed scale-up route for fruit juice fermentation by probiotic L. plantarum strains.
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Table 1. Examples of fermented fruit juices with various LAB strains (including L. plantarum) in single or mixed cultures with the respective effects.
Table 1. Examples of fermented fruit juices with various LAB strains (including L. plantarum) in single or mixed cultures with the respective effects.
Fruit JuicesStrainsMain Positive EffectsReferences
Mulberry juice
(Morus nigra)
L. plantarum, L. acidophilus,
L. paracasei
Increase in total anthocyanin, phenolic, antioxidant activity.[22]
Pomegranate juice
(Punica granatum L.)
L. plantarumIncrease in antimicrobial activity. Volatile free fatty acids content increased. Better organoleptic properties and composition of volatile compounds.[23]
Pomegranate juice
(Punica granatum L.)
L. plantarumImproved sensorial characteristics. improved TPC and antioxidant activity.[24]
Pomegranate juice
(Punica granatum L.)
L. paracaseiImproved sensorial characteristics. Improved TPC and antioxidant activity.[13,25]
Cornelian cherry
(Cornus mas L.)
L. paracaseiImproved TPC and antioxidant activity.[26]
Cashew apple juice
(Anacardium occidentale L.)
B. bifdum, B. longum subsp. infantis, L. plantarum,
L. acidophilus,
L. mesenteroides, L. johnsonii
Improved antioxidant activity. Modification of the type and content of phenolic. Possible prebiotic action of phenolics to lactic acid bacteria.
Contained prebiotic oligosaccharides mesenteroides) enhanced the growth of L. johnsonii.
[27]
Cantaloupe melon
(Cucumis melo L.) and cashew apple juice (Anacardium occidentale L.)
L. caseiEmergence of new volatile compounds.[28]
Apple juice
L. acidophilus, L. rhamnosus,
L. casei, L. plantarum
Generation of new aromatic compounds.[29]
Apple juice
L. plantarumEnhanced antioxidant capacity and bioavailability of polyphenols. [30]
Elderberry juice
(Sambucus nigra L.)
L. plantarumImproved composition of volatile compounds.[20]
Jujube juice
(Ziziphus jujuba Mill.)
L. plantarumEnhanced sensorial features.[31]
Noni juice
(Morinda citrifolia)
L. casei, L. plantarum, B. longum, L. acidophilusSlight increase in total antioxidant activity. ACE inhibitory potential decreased during fermentation. The content of ascorbic acid and antioxidant activity remained stable.[32]
Cranberry juice
(Vaccinium macrocarpon)
L. paracaseiSynergistic and additive antibacterial effects of the combination of fermented cranberry juice and antibiotics.[33]
Phyllanthus emblica
fruit juice
L. paracaseiIncreased Total polyphenol content and antioxidant activity.[34]
Jujube juice
(Ziziphus jujuba Mill.)
L. rhamnosus, L. plantarum,
L. paracasei, L. mesenteroides,
L. plantarum
Increased flavonoid content.[35]
Cactus pear juice
(Opuntia fcus-indica)
L. plantarumAmeliorated insulin resistance.[36]
Table 2. Global commercial probiotic products based on fruit matrices fermented by probiotic L. plantarum. Source: [90].
Table 2. Global commercial probiotic products based on fruit matrices fermented by probiotic L. plantarum. Source: [90].
Food MatrixCommercial NameOriginActive Probiotic Culture
Fruit drinkProbi-Bravo FriscusSwedenL. plantarum, L. paracasei
Fruit drinkDanone-ProVivaSweden, FinlandL. plantarum
Raw organic fruits and vegetable blendGarden of Life RAW Organic Kids ProbioticFlorida, USAL. gasseri, L. plantarum, L. casei, L. acidophilus
Fruit juice drinkGoodBellyColorado, USALb. plantarum 299v
Fruit- and vegetable-basedKeVita active probiotic drinkOxnard, USAB. coagulans, L. rhamnosus, L. plantarum
Fruit juiceHealthy Life Probiotic juiceAustraliaL. plantarum, L. casei
Table 3. Various L. plantarum strains producing EPS with respective biological activities.
Table 3. Various L. plantarum strains producing EPS with respective biological activities.
L. plantarum StrainsEPS Biological ActivityReferences
DM5Prebiotic potential.[99]
NTU 102Antioxidant and immunomodulation activities.[100]
KF5Cholesterol-reducing ability.[101]
CIDCA 8327Prebiotic potential.[96]
CGMCC 1557Cholesterol assimilation, nitrite-depleting property; antibacterial, immunomodulatory, antioxidative activities; antibiotic resistance.[102]
C88Antioxidant activities.[94]
NTMI05 Antioxidant activities.[103]
RJF4Antioxidant activity and inhibition of cancer cells lines.[104]
70810Antioxidant and antitumor activities.[101]
CNPC003Antioxidant activities.[92]
12Bioactive macromolecules with the potential ability to act against S. flexneri infections.[105]
C70Potential bioactivities, including anticancer. antidiabetic, and antioxidant activities. Possible improvements of food texture.[106]
YW11Dairy products with enhanced textural stability and bioactivities (cholesterol-lowering, antioxidant, antibiofilm).[107]
SP8Antioxidant activities.[108]
GA06, GA1Cholesterol removal and glycocholate deconjugation.[109]
LPC-1Antioxidant activities.[110]
LBIO1, LBIO14, LBIO2Improved rheological properties[111]
47FEAntimicrobial, anticoagulant, antioxidant, and emulsification activities.[112]
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Plessas, S. Advancements in the Use of Fermented Fruit Juices by Lactic Acid Bacteria as Functional Foods: Prospects and Challenges of Lactiplantibacillus (Lpb.) plantarum subsp. plantarum Application. Fermentation 2022, 8, 6. https://doi.org/10.3390/fermentation8010006

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Plessas S. Advancements in the Use of Fermented Fruit Juices by Lactic Acid Bacteria as Functional Foods: Prospects and Challenges of Lactiplantibacillus (Lpb.) plantarum subsp. plantarum Application. Fermentation. 2022; 8(1):6. https://doi.org/10.3390/fermentation8010006

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Plessas, Stavros. 2022. "Advancements in the Use of Fermented Fruit Juices by Lactic Acid Bacteria as Functional Foods: Prospects and Challenges of Lactiplantibacillus (Lpb.) plantarum subsp. plantarum Application" Fermentation 8, no. 1: 6. https://doi.org/10.3390/fermentation8010006

APA Style

Plessas, S. (2022). Advancements in the Use of Fermented Fruit Juices by Lactic Acid Bacteria as Functional Foods: Prospects and Challenges of Lactiplantibacillus (Lpb.) plantarum subsp. plantarum Application. Fermentation, 8(1), 6. https://doi.org/10.3390/fermentation8010006

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