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Review

Fermented Beverages from Amazonian Fruits: Nutritional Characteristics and Bioactive Compounds

by
Bárbara N. Batista
1,2,
Ana Cristina Correia
3,
António M. Jordão
2,3,* and
Patrícia M. Albuquerque
1,2,*
1
Laboratory of Chemistry Applied to Technology, School of Technology, Amazonas State University, Manaus 69050-020, Brazil
2
Post-Graduate Program in Biotechnology and Natural Resources, School of Health Sciences, Amazonas State University, Manaus 69050-010, Brazil
3
CERNAS Research Center, Agrarian School, Polytechnic University of Viseu, 3500-606 Viseu, Portugal
*
Authors to whom correspondence should be addressed.
Beverages 2025, 11(5), 152; https://doi.org/10.3390/beverages11050152
Submission received: 8 August 2025 / Revised: 14 September 2025 / Accepted: 16 September 2025 / Published: 21 October 2025
(This article belongs to the Special Issue Bioactive Compounds in Fermented Beverages)

Abstract

Fermented beverages are drinks that undergo a fermentation process involving yeasts, bacteria, or other microbial groups, leading to the conversion of natural sugars into alcohol, acids, and gases. Beer, wine, kombucha, kefir, and cider are examples of fermented beverages produced and consumed worldwide, representing a rapidly growing market. However, demands for these products have expanded beyond aspects such as size, shape, and storage conditions. There is an increasing demand for eco-sustainable, fresh products tailored to individuals with dietary restrictions and/or enriched with nutrients and health-promoting compounds. In this context, the market has witnessed a surge in alternative fermented beverages made from nutrient-rich or exotic-flavored raw materials, highlighting their versatility. A noteworthy example is the application of Amazonian fruits, which, despite being primarily consumed fresh by local populations, have been extensively characterized in scientific studies for their abundance of molecules with beneficial effects and their use in products like juices, ice creams, and fermented beverages. Thus, this review aims to explore the nutritional composition and microbiological aspects of different fermented beverages produced from several Amazonian fruits.

1. Introduction

The Amazon region spans parts of Bolivia, Brazil, Colombia, Ecuador, Guyana, Peru, Suriname, and Venezuela, covering approximately 7.4 million km2 of South America and representing about 4.9% of the planet’s land surface [1]. In line with the Chico Mendes Institute for Biodiversity Conservation (ICMBio), approximately 300 animal species, 1300 bird species, and around 40,000 plant species have been cataloged in this region [2]. Among these plant species, there are medicinal, food, fiber, and oil plants, whose uses stem from ancient traditions. Seeds, flowers, fruits, leaves, roots, bark, latex, vegetable and essential oils, dyes, and fibers have all been integral to rituals, celebrations, and daily life among Indigenous communities and were eventually adopted by riverside populations as well [3].
Another example of knowledge passed down through indigenous populations is fermentation. Recognized as part of the oldest methods for food preservation practiced by humans, fermentation is a biological process driven by microbial activity that transforms the flavor and appearance of food while extending its shelf life. In some cases, fermentation also enhances digestibility and improves the nutritional and functional properties of produce [4,5]. These benefits have contributed to the growing consumer interest in fermented beverages.
Beyond cassava, fermented beverages in the Amazon region are also produced from native Amazonian fruits [6,7]. The scientific literature has documented the fermentation of several regional species, including cupuaçu (Theobroma grandiflorum) [8], açaí (Euterpe oleracea) [9], buriti (Mauritia flexuosa) [10], taperebá (Spondias mombin) [11], bacuri (Platonia insignis) [12], bacaba (Oenocarpus bacaba) [13], murici (Byrsonima crassifolia and B. verbascifolia) [14], pupunha (Bactris gasipaes) [15], graviola (Annona muricata) [16], and camu-camu (Myrciaria dubia) [17], among others. These fruits are widely recognized by Amazonian riverine communities for their nutritional and, in many cases, medicinal properties. They are also commercialized in local markets, highlighting their economic and cultural importance.
The development of fermented beverages from Amazonian fruits represents a valuable strategy for enhancing the value of native species and driving innovation in the beverage industry. Both Amazonian fruits and fermented beverages are known to be fundamental sources of nutrients and bioactive compounds with numerous potential health benefits, including support for immune function, improvements in gut and cardiovascular health, and assistance in weight management [18].
With technological advancements, the beverage industry has garnered increasing attention. For instance, the global fermented beverage market is projected to reach USD 2.41 trillion by the end of 2025 and USD 3.26 trillion by 2030, with a compound annual growth rate (CAGR) of 6.2% between 2025 and 2030 [19]. This growth underscores the rising demand for functional beverages and the need for further exploration of this sector.
In South America, awareness of the connection between diet and health is growing. Brazil and Argentina lead the regional market, with a huge consumption of both alcoholic fermented beverages, such as beer and wine, and non-alcoholic options, such as kombucha and kefir [20].
In this context, the present review aims to explore the biodiversity of Amazonian fruits and their promising application in the production of fermented products. It highlights the nutritional value and feasibility of using native Amazonian fruits to develop fermented products, promoting the enhancement of unique and culturally significant resources, stimulating the regional economy, and promoting the preservation of traditional practices. Furthermore, this review underscores the importance of advancing research on the nutritional and phytochemical profiles of these and other Amazonian fruits, while also exploring alternative strategies to enhance nutrient intake through the development of nutritious fermented beverages.

2. Fermented Beverages from Different Amazonian Fruits

The Amazon region hosts one of the richest biodiversities on Earth, comprising over 13,000 tree species, of which approximately 2956 are endemic. Some of these species produce edible fruits that are commercially valuable and contribute significantly to the daily intake of nutrients, fiber, energy, and bioactive compounds, especially for riverine populations [21].
The regular consumption of Amazonian fruits has been associated with the prevention of chronic diseases such as cancer, cardiovascular disorders, and diabetes. These health benefits are often attributed to the presence of bioactive compounds, including antioxidants, carotenoids, phenolic compounds, steroids, minerals, essential amino acids, and vitamins [22]. Traditionally, these fruits have been used in indigenous medicine for a variety of treatments. Graviola, for example, is used in ethnobotanical practices in tropical regions to treat conditions such as diabetes, headaches, and hypertension [23]. Another example is bacuri, which is traditionally used to treat various ailments, including skin problems, spider and snake bites, rheumatism, and arthritis [24].
The following sections will explore various Amazonian fruits and the fermented beverages derived from them, with a focus on their nutritional properties and the presence of active substances, thereby highlighting the capacity of these species for the formulation of new nutritious and functional beverages.

2.1. Cupuaçu (Theobroma grandiflorum)

Popularly known as “cupuaçuzeiro”, “copoasu”, or “copuazú”, the species Theobroma grandiflorum is a component of the Sterculiaceae family and is a tree that can grow between 15 and 20 m in height. Its fruit, cupuaçu (Figure 1), has an oblong to ellipsoidal shape, with a light to dark brown peel [25].
With a pH ranging between 3.4 and 3.7 and notable antioxidant activity (1.7–2.0 µM trolox/g), cupuaçu pulp is yellowish-white and, in addition to its seeds, accounts for approximately 57% of the total fruit weight. It is rich in antioxidants such as vitamin C (ascorbic acid) and vitamin E (tocopherols), as well as flavonoids, anthocyanins, and polyphenols. Additionally, it is a source of proteins, fats, carbohydrates, and minerals, including sodium, potassium, magnesium, phosphorus, and calcium (Table S1) [26,27,28,29,30,31].
Among the main essential amino acids found in cupuaçu pulp are leucine, valine, and threonine (8.44 ± 0.15, 7.26 ± 0.15, and 5.92 ± 0.04 g/100 g of protein, respectively), while the predominant non-essential amino acids are glutamic and aspartic acids (14.83 ± 0.1 and 12.38 ± 0.26 g/100 g of protein, respectively) [27]. The pulp also contains native starch with a prominent amylose content (71%), distinguishing it from starches present in fruits such as an apple (Malus domestica) [28].
Cupuaçu pulp also contains citric acid, which contributes not only to its sensory qualities but also to a more natural and effective preservation process by inhibiting microbial contamination and extending product shelf life [29]. Moreover, the ascorbic acid content of the pulp represents approximately 30% of the recommended daily intake for individuals under the age of 18 (75 mg for men and 65 mg for women) and about 25% for those over 19 (90 mg for men and 95 mg for women). This makes cupuaçu a nutritious option for achieving recommended ascorbic acid levels, especially for individuals allergic to the dyes found in effervescent ascorbic acid supplements [30].
The pulp of cupuaçu exhibits a notable lipid content of 12.7% on a dry matter basis, with palmitic acid (55.2%) and oleic acid (18.8%) constituting the dominant fatty acids. Remarkably, α-linolenic acid, an omega-3 fatty acid of nutritional relevance, accounts for 18% of total fatty acids, underscoring the pulp’s potential as a dietary source of essential polyunsaturated fats. Regarding mineral composition, cupuaçu pulp contains appreciable amounts of potassium (34.3 mg/100 g), phosphorus (15.7 mg/100 g), and magnesium (13.1 mg/100 g), along with trace elements such as zinc (0.53 mg/100 g), copper (0.26 mg/100 g), and manganese (0.21 mg/100 g). These findings highlight the nutritional level of cupuaçu pulp, particularly for its balanced lipid profile and mineral richness [31].
In Brazil, cupuaçu pulp is consumed fresh or processed into juices, ice creams, popsicles, jams, and sweets due to its acerbity and strong aroma. Furthermore, it has attracted interest in the food service industry for its ability to enhance the physicochemical properties of dairy beverages, such as viscosity, water retention capacity, carbohydrate content, fatty acid profile, ascorbic acid, soluble fiber, and phenolic compounds, thereby improving their overall nutritional value [32].
As a strategy to improve the sensory and dietary value of beverages, cupuaçu pulp and its derivatives have been incorporated into dairy and fermented drinks. Studies have demonstrated the use of cupuaçu in the formulation of a probiotic beverage fermented with Lacticaseibacillus casei NRRL B-442. Under initial conditions of 34% (w/v) pulp, pH 5.8, and fermentation at 30 °C for approximately 18 h, the resulting beverage showed enhanced antioxidant activity (Table 1) and was well accepted in sensory evaluations, highlighting its potential as a functional food alternative [33].
As shown in Table 1, among the carbohydrates present in cupuaçu pulp, fructose was the most consumed (a difference of 84.76%), followed by sucrose (62.10%) [33]. During lactic fermentation, homofermentative lactic acid bacteria (LAB) convert sugars into lactic acid, whereas heterofermentative LAB produce lactic acid along with acetic acid, ethanol, and carbon dioxide. This microbial activity is required to produce fermented dairy products, such as yogurt and kefir [34].
Furthermore, both cupuaçu pulp and flour have been investigated for use in the production of artisanal fermented dairy beverages. Initially, pasteurized whey and milk were employed as the liquid base, to which sugar and a starter culture composed of Streptococcus thermophilus and Lactobacillus delbrueckii subsp. bulgaricus were added. Fermentation was carried out in a water bath for five hours at 42 °C until the pH reached 4.6. Depending on the treatment, cupuaçu pulp and/or flour were then incorporated into the fermented matrix. The study reported that higher pulp concentrations (10%) yielded a beverage with the characteristics summarized in Table 2 [35].

2.2. Açaí (Euterpe oleracea)

The term “açaí” is generally used to refer to the berries of the Euterpe genus, yet it is primarily associated with Euterpe oleracea Mart., commonly known as “açaizeiro”, “juçara”, or “açaí-de-touceiras”. E. oleracea is associated with the Aceraceae family and is endemic to the eastern Amazon but also grows in Panama, Ecuador, Colombia, Venezuela, the Guianas, Suriname, and Brazil [36].
The açaí fruit (Figure 2) is spherical, measuring 0.9 to 1.3 cm in diameter, with a fibrous seed, a thin mesocarp (pulp), and a dark purple-black skin when ripe. Its pulp is rich in active products and antioxidants, mainly anthocyanins, proanthocyanidins, and other flavonoids [37], some of which are mentioned in Table S2.
Among the active substances that were identified in the edible portion of E. oleracea, anthocyanins such as cyanidin-3-glucoside and cyanidin-3-rutinoside predominate. These anthocyanins are also predominant in the pap of another species of the Euterpe genus, E. precatoria. Although both species are commonly used to produce açaí, they exhibit distinct observable and chemical characteristics. One key difference is in the total anthocyanin content, which is 50% higher in E. precatoria compared to E. oleracea. Additionally, E. precatoria contains pelargonidin-3-glucoside (319 mg/kg), while E. oleracea contains peonidin-3-rutinoside (44 mg/kg) [38].
Studies characterizing freeze-dried E. oleracea pulp have reported a high presence of oleic acid (52.7%) and palmitic acid (25.56%), with levels similar to those found in açaí juices collected in the Brazilian State or region of Pará (60% and 22%, respectively). Notably, the oleic acid content in açaí pulp is higher than in cupuaçu. While palmitic acid is considered one of the most harmful saturated fatty acids in terms of cardiovascular disease risk, oleic acid is regarded as a neuroprotective agent [31]. Among the minerals present in the freeze-dried pulp, potassium is the most plentiful, followed by calcium. The recommended daily intake for healthy adults is 4.7 g of potassium and 1000 mg of calcium, which may be easily met by consuming 200 g of freeze-dried açaí pulp [39].
Consumption of açaí pulp has been associated with the prevention and management of various diseases, including diabetes, dyslipidemia, and cardiovascular conditions, by virtue of its high antioxidant activity, nutritional richness, and therapeutic benefits. Açaí can be consumed in various forms, such as jelly, liqueur, frozen pulp, syrup, cream, ice cream, and as an exotic beverage outside of Brazil [40]. Given its nutritional properties, açaí has gained considerable economic value, particularly in the food sector. It is incorporated into energy drinks, shakes, smoothies, isotonic beverages, juices, and dietary supplements exported worldwide. Fermented beverages have also gained attention on account of their functional properties and high nutritional value [41].
For example, a study on açaí pulp demonstrated the successful generation of a fermented beverage using Lacticaseibacillus paracasei, Leuconostoc mesenteroides, and Lactiplantibacillus plantarum in a ratio of 0.5:1.0:1.5, under fermentation conditions of 6 days, with a nitrogen source supplementation of 2.5% and a temperature of 27 °C. This combination resulted in increased ash and protein contents. The raw açaí liquid showed changes in its basic physicochemical composition, as reflected in Table 3, with protein content rising from 1.30 g/100 g to 2.77 g/100 g in the fermented açaí beverage. Changes also occurred in the amino acid profile. In the wine açaí liquid, glutamic acid, aspartic acid, leucine, lysine, and proline were detected (0.123, 0.108, 0.095, 0.072, and 0.066 g/100 g, respectively). After fermentation, elevated levels of glutamic acid, proline, leucine, valine, and phenylalanine were observed (0.614, 0.207, 0.109, 0.091, and 0.082 g/100 g, respectively), which provide a bittersweet flavor profile in the final product [42].
As presented in Table 3, seven volatile aroma compounds were produced following the fermentation process: n-propanol, isoamyl alcohol, acetaldehyde, isobutanol, ethyl acetate, ethyl formate, and dimethyl sulfur. Overall, the content of volatile compounds increased after fermentation, which can enhance the flavor of the fermented beverage. The oxygen radical absorbance capacity (ORAC), an indicator of antioxidant capacity, was measured in both raw and fermented açaí liquids. The values were 453.64 µmol/g trolox and 708.77 µmol/g trolox, respectively. These levels are comparable to those in sage spice (987.14 µmol/g trolox) and approximately 60 times higher than those in red grapes (16.40 µmol/g trolox), indicating a significant nutritional enhancement and the potential for development of highly nutritious formulations using açaí [42].
Açaí-based liqueurs demonstrated high anthocyanin content, reaching 203 mg/L-significantly higher than levels typically found in grape juice (17.31 mg/L) and red wines (11–31.57 mg/L). This indicates the beverage’s potential as a rich source of phenolic compounds [43].

2.3. Buriti (Mauritia flexuosa)

Analogous to the açaí palm, Mauritia flexuosa (Kunth) McVaugh is a species in the Aceraceae family. Commonly known as “buritizeiro” or “miriti”, M. flexuosa is the most copious palm in Brazil, restricted to South America and widely dispersed throughout the Amazon region. Almost everything in the buritizeiro is useful, but the most utilized part is its fruit (Figure 3), buriti, which is characterized by a reddish-brown peel and yellowish pulp [44].
Buriti pulp has a high moisture content (50.5 g/100 g) and fat content (19.0 g/100 g), with a lipid concentration higher than that of patauá (Oenocarpus bataua), a species known for its oil-rich products. However, buriti contains linoleic acid that is sparsely distributed (2.1 g/100 g). With a tocopherol content of 1169 µg/g, buriti pulp is rich in α-tocopherol (37.2% w/w) and is recognized as an excellent source of vitamins A and E [45]. Manhães and Sabaa-Srur [46] also indicate a considerable presence of minerals, with potassium the prevailing element (218.00 mg/100 g), followed by calcium (80.49 mg/100 g) and manganese (40.34 mg/100 g). In addition, buriti pulp contains a high amount of total aromatic amino acids, which are important for human physiological functions as cofactors (Table S3).
The concentration of phenolic compounds in buriti pulp varies with ripeness, with the notable presence of quinic acid, caffeic acid, chlorogenic acid, ferulic acid, p-coumaric acid, and protocatechuic acid, along with flavonoids such as (+)-catechin, (−)-epicatechin, and luteolin, which are also abundant [10]. Although the pulp contains lower levels of total phenolics, flavonoids, carotenoids, hydrolysable and condensed tannins, and ascorbic acid compared to the peel, it still retains significant amounts and exhibits high antioxidant capacity. Therefore, buriti pulp can be easily incorporated into the human diet to help meet daily nutritional requirements and can be consumed in processed forms such as sweets, ice creams, juices, jams, and wines [10,47].
The Kichwa tribe of the Ecuadorian Amazon and the Guahibo people from the eastern plains of Colombia and Venezuela ferment buriti juice to produce chicha de morete [48]. Chicha is a traditional beverage that may be either fermented (alcoholic, with an alcohol content ranging from 1 to 12% v/v) or non-fermented (non-alcoholic), and it is often used in rituals and religious practices [49].
Although no detailed studies exist on the process of producing chicha from buriti pulp, available reports indicate that both fermented and non-fermented versions are made by crushing the fruit. In the alcoholic version, the pureed fruit is left to ferment for 3 to 4 days, with the addition of liquid obtained from chewed sweet potatoes, which serves as a source of amylase and microorganisms [49]. Microbiological analyses report the presence of yeasts—especially Saccharomyces cerevisiae—as well as bacteria of the genera Leuconostoc, Acetobacter, and Lactobacillus, in combination with various molds such as Aspergillus spp., as the primary fermentative microorganisms in this traditional beverage [50].
Additionally, buriti pulp has been evaluated for use in fermented milk production with L. casei SJRP38, showing promising functional potential. The formulation involved reconstituted milk (12% total solids [w/v]) and 1% buriti pulp, subjected to heat treatment at 90 °C for 10 min, cooled to 42 °C, followed by inoculation with L. casei SJRP38 (8 log CFU/mL), and fermented at 42 °C until reaching a pH of 4.6. Table 4 shows that the fermented product made with buriti presented a high lipid content and minimal variation in total solids and ash contents, values close to those observed in passion fruit (11.65 and 1.28 g/100 g, respectively) [51].

2.4. Taperebá (Spondias mombin)

Another Amazonian fruit with a distinctive flavor is Spondias mombin (Figure 4). Commonly known in Brazil as “cajazeiro”, “taperebá”, “cajá-mirim”, “cajazinho”, or “cajá” depending on the region, S. mombin is a fruit-bearing species native to Brazil and distributed throughout tropical regions of the Americas, from southern Mexico to Brazil, including some Caribbean islands. The fruit is the primary edible part. It has an elliptical shape, a yellow-orange color, smooth fibrous skin, and a sweet-sour taste. The flesh and skin together account for approximately 38% of the total fruit weight, while the seed constitutes the majority [52].
Beyond the fruit, the leaves, flowers, seeds, and bark of taperebá also have nutritional and ethnomedicinal applications, including treatments for abortion, fever, gonorrhea, postpartum hemorrhage, digestive pain, and wounds. Approximately 102 compounds have been isolated from several parts of the plant, highlighting its pharmacological importance. Table S4 shows the physicochemical and nutritional aspects of S. mombin pulp [53].
Although S. mombin pulp has low sodium and calcium contents, it is rich in magnesium, phosphorus, and potassium. Potassium levels are comparable to those observed in Genipa americana (jenipapo) and Hancornia speciosa (mangaba), and phosphorus levels are similar to those in S. purpurea (seriguela), Caryocar brasiliense (pequi), and passion fruit [53]. Notably, to prepare 300 mL of juice from S. mombin, 100 g of pulp is required, which provides approximately 5.8% of the recommended daily intake (RDI) of magnesium, 4.6% of phosphorus, 8.2% of potassium, and 4% of iron for adults [54].
Cajá pulp has an elevated antioxidant capacity (17.47 mmol trolox/g), placing it among fruits with above-average antioxidant activity. It ranks alongside guava, plum, and strawberry and outperforms other Brazilian fruits such as umbu (S. tuberosa) (1.07 mmol trolox/g), graviola (6.09 mmol trolox/g), sapoti (Manilkara zapota) (0.99 mmol trolox/g), papaya (7.6 mmol trolox/g), and pineapple (3.78 mmol trolox/g) [55].
Spondias mombin pulp is often employed in the preparation of juices, ice creams, and liqueurs owing to its content of carbohydrates, proteins, fibers, essential minerals, and bioactive compounds—particularly tannins (299.81 mg/100 g) and carotenoids (28.30 µg/g) [56].
According to Alves et al. [57], a formulation containing taperebá pulp (50%), sucrose, stevia, and fermented Talinum triangulare (50% infusion at 10% w/v), fermented at 30 °C for 14 h, showed satisfactory sensory acceptance. Fermentation with L. casei NRRL B-442 (7.00 log CFU/mL) was tested using T. triangulare leaf tea and cajá pulp. Beverages containing blends of cajá pulp and T. triangulare leaf tea sweetened with sucrose showed the highest microbial growth rates—45.43% and 40.45%, respectively—at initial pH values of 6.1 and 6.0. Over a 42-day storage period, these beverages showed minimal reductions in phenolic composition and free radical scavenging activity, with stevia-containing formulations exhibiting greater losses. The phenolic content of the beverage containing blends of cajá pulp showed a decrease from 2.90 to 2.75 mg/100 mL after 7 days and to 2.00 mg/100 mL after 42 days. Conversely, the beverage containing T. triangulare leaf tea sweetened with sucrose showed a decrease from 1.90 to 1.85 mg/100 mL on day 7 and to 1.60 mg/100 mL on day 42. A comparable pattern was noted in DPPH antioxidant activity: the first beverage exhibited a 33.09% reduction, while the second beverage showed a 27.61% reduction over the 42-day storage period.
Taperebá pulp was also used as a substrate for L. plantarum NRRL B-4496 to produce a synbiotic drink. The fermentation was carried out at 30 °C for 18 h with an initial pH of 4.5. A formulation using 100 g of frozen pulp per 200 mL beverage and 10% (v/v) of L. plantarum showed pH stability over 28 days (ranging from 2.3 to 2.5) and a slight decrease in acidity (from 0.79 to 0.76 mg citric acid/mL), possibly due to citric acid degradation or reduced production (Table 5). The soluble solids content peaked at day 21 (ranging from 7.73 to 8.80 °Brix), which may result from the acid hydrolysis of complex sugars. Total phenolic compounds increased from 271.7 to 320.5 mg GAE/L, comparable to an apple (339 mg GAE/L) and pineapple juice (358 mg GAE/L) [58].
The proximate composition of taperebá mombin-based beverages, including fermented ones, was also determined (Table 6). These drinks can be regarded as low-calorie and suitable for individuals with caloric restrictions [58].
A successful application of taperebá pulp was likewise found in the production of ginger beer. The formulation included 4% grated ginger (w/v), mineral water, 1% lemon juice (v/v), 15% sugar (w/v), 15% taperebá pulp (w/v), and 25% ginger bug (v/v). The mixture was homogenized, filtered, and incubated at 25 °C for 14 days (Table 7) [59].
The taperebá-based fermented beverage showed high initial concentrations of organic acids such as malic (2.40 g/L), citric (0.57 g/L), lactic (0.09 g/L), succinic (0.08 g/L), acetic (0.11 g/L), formic (0.02 g/L), and butyric (0.46 g/L), indicating that the fruit contributed significantly to the beverage’s acidity. During fermentation, succinic and acetic acid levels increased, with succinic acid being an important stimulant of gastric acid production (Table 7). Regarding alcohol content, the beverage was classified as low alcohol by Brazilian standards, with an alcohol content of approximately 2.3% after 14 days of fermentation. Several phenolic compounds, including procyanidin B1, gallic acid, (+)-catechin, procyanidin A2, trans-caftaric acid, and rutin, were detected at high concentrations, helping to increase the beverage’s functional potential through their significant antioxidant effects and possible benefits in preventing chronic diseases [59].

2.5. Bacuri (Platonia insignis)

The bacurizeiro (Platonia insignis Mart.) is a unique fruit-bearing species within its genus. This multifunctional tree provides high-quality timber, medicinal exudates, seed-derived butter, and the highly valued fruit known as bacuri, which holds significant cultural and economic importance for certain Amazonian communities. The bacuri fruit is ovoid in shape (Figure 5), weighs between 200 and 500 g, and is enclosed in a thick pale yellow to brown rind that accounts for approximately 65–75% of the total fruit weight [60].
The pulp, which accounts for less than 15% of the fruit’s weight, is a source of essential minerals—such as sodium, potassium, calcium, magnesium, phosphorus, iron, zinc, and copper—as well as carbohydrates, bioactive compounds with antioxidant properties, dietary fiber, and amino acids, despite its low protein content [61]. Although bacuri pulp has a lower total phenolic content (0.2–23.8 mg GAE/100 g) compared to taperebá (S. mombin) (391.69 mg GAE/100 g), murici (Byrsonima crassifolia) (271.60 mg GAE/100 g), and açaí (E. oleracea) (708.22 mg GAE/100 g), it contains higher flavonoid levels (15.34–16.9 mg QE/100 g) than taperebá (14.949 mg QE/100 g), cupuaçu (T. grandiflorum) (4.879 mg QE/100 g), and orange (Citrus sinensis) (10.579 mg QE/100 g) [62] (Table S5).
Bacuri is typically consumed fresh but can also be processed into juices, ice cream, sweets, liqueurs, and milk-based beverages. A brewery located in Pará (Brazil), for example, won the “International Beer Challenge 2014” with a craft beer made with bacuri. Although the specific brewing parameters are not publicly disclosed, the 3.8% ABV beer is described as a fruit beer style—clear, light, with a good, persistent foam, and a fruity aroma attributed to maturation with bacuri [63].
Bacuri pulp juice has also been evaluated for kombucha production. A green tea infusion (2 L of water with 14 g of Camellia sinensis) and 40 g of sugar were used. The Symbiotic Culture of Bacteria and Yeast (SCOBY) was inoculated and incubated at 25 °C for 7 days before the addition of 20% of a formulation consisting of bacuri pulp (100 g pulp, 150 mL water, and 10 g sugar). The mixture was then bottled and stored away from light for 24 to 36 h. The resulting kombucha met safety and quality standards for this type of beverage. It contained 0.16 g/L of reducing sugars, 2.27 g/L of ethanol, and 318.3 mg GAE/L of total phenolic compounds—higher than those found in kombuchas produced with taperebá (34.92 mg GAE/L) and cupuaçu (33.40 mg GAE/L). The beverage also presented antioxidant activity of 307.98 μmol TE/mL and a vitamin C content of 375.25 mg/100 mL, exceeding values found in kombucha from cupuaçu (360.57 mg/100 mL), suggesting that bacuri is a promising raw material for developing nutritious beverages (Table 8) [64].
Bacuri pulp has also shown potential in the development of whole, semi-skimmed, and skimmed yogurts. The process involved heating the milk (whole, semi-skimmed, or skimmed) to 45 °C, followed by the addition of 3% (w/w) lactic starter cultures (Streptococcus salivarius subsp. thermophilus and L. delbrueckii subsp. bulgaricus) and 15% (w/w) sucrose. The mixture was incubated at 43 °C until the acidity reached between 0.87% and 0.90% lactic acid. After breaking the curd by stirring and cooling, bacuri pulp was added at 15% (w/w), followed by filling and storage at 6–8 °C [65].
As shown in Table 9, the yogurts formulated with bacuri pulp displayed lipid contents within the limits established by the Brazilian Health Regulatory Agency (ANVISA): 3–5.9% for whole yogurt, 0.6–2.9% for semi-skimmed, and a maximum of 0.5% for skimmed yogurt. The addition of bacuri pulp led to fat reductions of 75% and 79.16% in semi-skimmed and skimmed yogurts, respectively, compared to whole milk yogurts. These products can thus be classified as light or low-fat, offering innovative flavors while promoting health benefits for consumers [66].

2.6. Bacaba (Oenocarpus bacaba)

Native to the Amazon rainforest, bacaba (Oenocarpus bacaba Mart.), also known as “red bacaba”, “bacaba-açu”, or “bacabão”, is a palm species found in both the Amazon and Cerrado biomes of Brazil. This species has a variety of traditional uses: its seed oil is used in cooking; its palm heart juice is employed by the Yagua people to treat scorpion and venomous spider bites; its wood is utilized by the Yanomami native people for making bows, posts, and beams; and its leaf petioles are woven into tapetis used for pressing cassava. Additionally, its fruits (Figure 6) are an important source of bioactive compounds with potential biotechnological relevance [48,67].
Bacaba fruits grow in dense clusters and are approximately 1.5 cm in diameter, with a dark purple hue. They have a high lipid content (38.3% of pulp) [3]—greater than that found in fruits such as bacuri (Platonia insignis, 1.46 g/100 g) and açaí (E. oleracea, 6.12 g/100 g)—along with a significant concentration of phenolic compounds, surpassing those detected in açaí pulp. Table S6 shows some of the major characteristics of bacaba pulp.
The fruit is also rich in bioactive compounds, pigments, and natural antioxidants, making it a promising ingredient for dietary and functional food applications. Phenolic compounds reported in bacaba pulp include C-glycosides, flavonoids, C-hexosides, C-glycosylflavones, isorhamnetin hexoside, quercetin hexoside, and quercetin diglycoside. Among the anthocyanins detected are cyanidin glycoside and cyanidin hexoside, identified by HPLC-DAD-ESI-MS. It is worth noting that the pulp has not yet been fully characterized, and detailed compositional data remain scarce [68].
By virtue of its fibrous and lipid-rich pulp, bacaba is primarily consumed in beverage form, but it is also used in jellies, ice creams, and fermented drinks. The Umutina Indigenous people traditionally prepare a fermented bacaba beverage known as chicha de bacaba. This beverage can be prepared with cereals and fruits via spontaneous fermentation or consumed immediately as a non-fermented version. The preparation involves selecting the fruits, boiling them, allowing them to rest for 30 min, and replacing the water. The fruits are then mashed in a wooden mortar, and the skins and seeds are removed using a sieve. Sugarcane juice is then added, and the beverage can be consumed fresh or fermented for approximately 30 h at room temperature [69]. The resulting beverage has been characterized for microbial and physicochemical parameters, showing the appearance of mesophilic bacteria, lactic acid bacteria, and yeasts at concentrations of 4.8, 4.9, and 4.8 log CFU/mL, respectively. The final beverage had a pH of 6.2 and an energy value of 76.7 kcal/100 mL, as shown in Table 10 [69].
“Chicha de bacaba” is notable for its high lipid and protein contents and is consumed by Indigenous communities in the Colombian Amazon, including the Huitoto, Andoque, Yukuna, Muinane, and Miraña peoples. It contributes significantly to their intake of fats and carbohydrates [69]. Among the fatty acids identified in bacaba pulp are palmitic, oleic, and linoleic acids, accounting for approximately 22%, 61%, and 12% of total lipids, respectively [70].
Furthermore, significant concentrations of succinic, acetic, and citric acids have been detected. The beverage has a low ethanol content (0.52 g/L), and the absence of methanol classifies chicha de bacaba as a non-alcoholic beverage. These features underscore the nutritional value of bacaba as a dietary supplement and highlight its potential for broader application despite its current underutilization [69].

2.7. Murici (Byrsonima crassifolia and B. verbascifolia)

Commonly known as “murici” or “beach murici”, Byrsonima crassifolia (L.) Kunth and Byrsonima verbascifolia (L.) DC. are members of the Malpighiaceae family and are predominantly found in the northern and northeastern regions of Brazil. The most consumed part of these species is their small yellow fruit (Figure 7), approximately 2 cm in diameter, which is mainly collected by local populations [71].
Murici fruits have a high moisture content (77.4%), which is greater than that of other Amazonian fruits such as buriti (M. flexuosa, 50.5%) [72]. This high moisture contributes to the fruit’s susceptibility to enzymatic and microbial deterioration, necessitating prompt processing. The fruit also contains significant amounts of crude fiber and lipids, about 63% of which are unsaturated fatty acids. Oleic acid is the predominant fatty acid, followed by palmitic and linoleic acids [73] (Table S7).
Headspace analysis identified 12 volatile compounds in murici pulp, with esters of hexanoic and butanoic acids contributing significantly to its characteristic aroma [71]. Another noteworthy attribute is its substantial vitamin E content, which surpasses that found in fruits such as kiwi (1.450 µg/100 g) and peach (1.230 µg/100 g) [72].
The consumption of 86 g of pulp (approximately 70 kcal) can fulfill about 40% of the recommended daily fiber intake for children, adults, and pregnant women. Additionally, one portion provides around 93.7% and 26% of the daily vitamin C requirements for children and adults, respectively [74]. Despite its economic and nutritional relevance, murici remains underexplored, particularly regarding its physiological and chemical behavior under different environmental conditions. Most current applications involve extracts for pharmaceutical and cosmetic purposes, with relatively few studies investigating the fruit’s use in beverages, pastes, purées, and jams [75].
A study carried out by Couto et al. [76] that fermented dairy beverages incorporating murici pulp (5% w/v) and passion fruit peel flour (Passiflora edulis Sims) at varying concentrations (0.0%, 0.5%, 1.0%, and 1.5% w/v) used a 2.5-L dairy base composed of 30% skimmed whey and 70% whole milk. The mixture included 10% sucrose and was pasteurized at 90 °C for 3 min. After cooling to 42 °C, cultures of S. thermophilus, Lacticaseibacillus acidophilus, and Bifidobacterium lactis were inoculated. Once fermentation reduced the pH to 4.5, murici pulp and passion fruit peel flour were added, resulting in a beverage suitable for high-protein diets. These authors reported an increase in antioxidant activity. The beverage without passion fruit peel flour exhibited an EC50 of 238.244 g/L, while the beverage with 1.5% flour showed an EC50 of 224.302 g/L, attributed to the contribution of the passion fruit component (Table 11). Although the authors did not evaluate other concentrations of murici pulp, the version without passion fruit peel flour received the highest sensory evaluation scores, indicating a clear preference for the murici flavor [76].
Other research has focused on murici-based yogurt formulations [77]. One successful formulation used whole pasteurized milk (3% fat) and 10% crystalline sugar per liter. After inoculation with S. thermophilus, L. acidophilus, and Bifidobacterium spp., fermentation was carried out at 43 °C for 6–7 h until gel formation. After cooling, 5–15% murici pulp was added, followed by homogenization and packaging for storage at 5 °C. Although the associated patent did not provide detailed information on the final product characteristics, it highlights the potential for using murici as a flavoring agent and its growing appreciation as a native Amazonian fruit in dairy beverages.

2.8. Pupunha (Bactris gasipaes)

The peach palm (Bactris gasipaes Kunth) is a tropical palm tree reaching up to 20 m in height and is distributed from southern Mexico to Brazil and Paraguay. It is valued for both its heart of palm and its fruit (known as pupunha) (Figure 8), which are widely consumed in local cuisine [78]. The skin of pupunha varies in color—red, orange, or yellow—and its pulp is highly nutritious. The fruits typically measure 4–6 cm in length and 3–5 cm in width. The fruit pulp exhibits a high carbohydrate content (an average of 86.35 g/100 g of dry matter), followed by notable amounts of lipids, proteins, and dietary fiber [79] (Table S8).
Daily intakes of 2000 mg of potassium, 2–5 mg of manganese, and 10 mg of iron are recommended, all of which can be supplied by consuming a 250 g portion of pupunha fruit [79]. In addition, the content of phenolic compounds in pupunha (2.11 mg GAE/g dry matter) is higher than that found in rice (0.90 mg GAE/g dry matter) and guava (0.84 mg GAE/g dry matter), highlighting its potential as a source of phenolics for dietary intake [80].
Carotenoid-rich extracts have also been successfully obtained from pupunha pulp using supercritical CO2 extraction. The antioxidant activity of these extracts (10.3%) was statistically similar to that of caffeic acid [81]. Carotenoids are a class of pigments responsible for the red, yellow, and orange colors in fruits and vegetables, and they also occur in green vegetables. These compounds are known for their health-promoting effects and are abundantly present in pupunha, which exists in a wide range of varieties [82]. Among the carotenoids already identified in raw pupunha pulp are all-trans-β-carotene, all-trans-δ-carotene, cis-γ-carotene 2, and all-trans-γ-carotene. An interesting fact is that to be consumed, pupunha needs to undergo heat treatment, which in turn favors the appearance of new carotenoids such as all-trans α-cryptoxanthin, 15-cis-β-carotene, cis-δ-carotene, cis-γ-carotene 1, and lycopene. Table S8 also shows that the total carotenoid content in cooked pupunha pulp—its traditional form of consumption—is 115.6 μg β-carotene/g fresh weight. This exceeds the values found in fruits such as banana (10.62 μg/g), guava (42.98 μg/g), and watermelon (40.09 μg/g) [83].
Raw pupunha should not be consumed on account of the presence of antinutritional factors such as calcium oxalate crystals, lectins, specific polyphenols, saponins, and inhibitors of amylase and trypsin. It must be boiled in salted water for 30 to 60 min prior to consumption [84]. Beyond direct consumption, pupunha fruit is used to produce flour, oils, ice cream, and fermented beverages. Usage of pupunha in fermented drinks has its roots in Indigenous traditions from the Amazon and Andes, where such beverages were prepared for ceremonial purposes. Depending on the region and ethnic group, variations exist in the raw materials used and fermentation times, with the common addition of salivary ptyalin (amylase) to aid in starch hydrolysis [85].
One example is chicha or masato, traditional South American beverages sourced from the spontaneous fermentation of various starchy substrates. These drinks may have probiotic properties, as certain species of lactic acid bacteria isolated from them have shown antagonistic activity against pathogenic microorganisms [86].
One method of producing a fermented pupunha beverage involves boiling the fruit and mashing the pulp. Simultaneously, a portion of the pulp is chewed—typically by women—to introduce salivary enzymes and then mixed with the mashed pulp. The mixture is left to ferment for several days, during which alcohol content can rise to 2–5%. After fermentation, the mass is diluted with water and sieved to remove fibers [48,86].
A successful formulation included 1 kg of fruit, 4 L of sucrose solution, and 1% Saccharomyces cerevisiae. The fermentation at 27 °C for seven days produced a uniform orange beverage with 12.74% alcohol. Carotenoid levels stabilized at 2.2 mg/100 mL of must during fermentation. The pH dropped from 6.0 to 3.5, and the beverage was described as having a pleasant flavor and aroma, with a high acceptability rate of 81.9% (Table 12) [85].
Therefore, similar to other Arecaceae family fruits such as açaí (Euterpe spp.) and bacaba (Oenocarpus bacaba Mart.), pupunha fruits hold strong potential for the development of nutritious fermented beverages. The high carotenoid content of the pulp further supports pupunha’s value as a primary dietary source of vitamin A precursors [87].

2.9. Graviola (Annona muricata)

Known as “guanabana”, “sauersak”, “guayabano”, or “soursop”, Annona muricata belongs to the Annonaceae family and is native to tropical regions, being widely distributed across the Caribbean and Southeast Asia. The pulp, leaves, and seeds of A. muricata are rich in phenolic compounds (Table S9), making the plant a promising source of bioactive substances with potential applications in the pharmaceutical, cosmetic, and food industries [88,89,90,91,92].
One important bioactive compound identified in graviola pulp is 5-caffeoylquinic acid, which is also found in coffee and exhibits antioxidant, antibacterial, anticancer, antihistaminic, and other biological activities. Another compound of interest is p-coumaric acid, with levels reaching 0.94 mg/100 g fresh weight (FW), comparable to those found in orange juice (1.0 mg/100 g FW) and apple juice (1.2 mg/100 g FW) [93].
Graviola fruit has a heart-like shape with a green, spiny rind, measuring 10–20 cm in diameter and weighing up to 15 kg (Figure 9) [94]. As shown in Table 13, its pulp juice is characterized by a high moisture content and elevated levels of phosphorus and carbohydrates. Table S10 shows notable concentrations of vitamin A (14.45 mg/100 g) and ascorbic acid (19.4 mg/100 g), the latter being a compound with well-documented antioxidant properties [95]. The pulp is white, aromatic, and has a distinctive, mildly acidic, and sweet flavor. Additionally, soursop has been associated with a range of biological activities, including thrombolytic, antidiarrheal, cytotoxic, and antioxidant effects [96].
In vitro studies using methanol-soluble fractions of the graviola pulp have demonstrated thrombolytic, antibacterial, and antidiarrheal activities. Thrombolytic assays showed that a concentration of 10 mg/mL induced maximum clot lysis of 18.33%, compared to 55.50% for the standard streptokinase. For antidiarrheal evaluation, diarrhea was induced in albino mice using castor oil, and all tested doses (100, 200, and 400 mg/kg body weight) showed significant effects, with 400 mg/kg achieving 58.38% inhibition [97].
Further investigation into the cytotoxic and antioxidant properties of aqueous and alcoholic extracts from freeze-dried graviola pulp revealed significant activity against human tumor cell lines. The most potent cytotoxic effects were observed against PC3 (prostate carcinoma) (0.8460 µg/mL) and HeLa (cervical carcinoma) (7.1940 µg/mL) cells. In antioxidant assays using the DPPH method, the extract demonstrated a 69.77% radical scavenging activity. These findings are particularly important given the insufficient data on the antioxidant potential of different graviola tissues [98].
Graviola pulp constitutes approximately 83–85% of the total fruit weight and is commonly consumed as juice. It is also used in the production of nectar, ice cream, and jams. A study investigating the production of wine from graviola pulp using propagated indigenous yeast yielded a beverage with 16% (v/v) alcohol [99]. The indigenous yeast was obtained from soursop juice fermented for two days, which was aseptically inoculated using the streak plate technique on SDA (Sabouraud Dextrose Agar) containing 500 mg of chloramphenicol per plate. The pasteurized pulp was fermented with 15 g/100 mL of sucrose and nutrients (0.08 g KH2PO4, 0.06 g ammonium sulfate, and 0.02 g sodium metabisulfite) for 10 days. The wine reached a pH of 4.5 and showed an increase in alcohol content from the initial stages of fermentation. The indigenous yeast contributed to the fermentation process, which resulted in several changes in the physicochemical properties of the pulp (Table 14).
Additionally, fermentation resulted in increases in titratable acidity, lipid, and alcohol content, while reducing fiber, protein, carbohydrate, pH, vitamin C, and ° Brix values. Despite these reductions, the fermented product retained several nutritionally important components [99].
Graviola has also been used in beer production. For this, 3.7 kg of Pilsen malt and 0.3 kg of Vienna malt were milled and mixed with 16 L of water at 70 °C, then transferred to a mash tun at 68 °C for 60 min [100]. After a 15-min mash-out at 78 °C, the wort was clarified via gravity recirculation. Boiling was performed with 15.4 g of hops added after 40 min, and the total boiling time was 60 min. After resting at 29 °C, the wort was transferred to a fermentation tank and inoculated with 8.05 g of yeast previously hydrated in 100 mL of mineral water. Fermentation proceeded at 19 °C for 7 days, followed by maturation at 0 °C for 10 days. The final product was filtered and bottled with 12 mL of priming solution (Table 15).

2.10. Camu-Camu (Myrciaria dubia)

Commonly known as “camu-camu,” “caçari,” “araçá d’água,” or “sarão,” Myrciaria dubia (HBK) McVaugh belongs to the Myrtaceae family and is native to northern Brazil, as well as neighboring countries such as Peru, Colombia, and Venezuela [101]. It typically grows along the banks of rivers and lakes in the Amazon basin, particularly during seasonal floods. Camu-camu produces globose fruits measuring approximately 2.5 cm in diameter (Figure 10), which are renowned for their exceptionally high vitamin C content, ranging from 0.96 to 2.99 g/100 g, significantly higher than other common sources such as orange juice, thus highlighting its substantial nutritional and economic potential (Table S11) [102].
Beyond its remarkable vitamin C concentration, another notable feature of camu-camu is the peak in antioxidant activity and bioactive compound content—such as ascorbic acid (4752.23 mg/100 g of pulp), anthocyanins (52.6 mg/100 g of pulp), and total phenolics (12,798.80 mg GAE/100 g of pulp)—observed during the intermediate stage of ripening, when the peel exhibits a green-reddish coloration. These levels tend to decline as ripening progresses [103].
Camu-camu contains a diverse array of phytochemicals, amino acids, essential fatty acids, and minerals such as potassium, iron, selenium, calcium, and magnesium (Table S11). It is internationally recognized as a “superfruit” because of its numerous health-promoting properties, and its bioactive compounds can contribute to the prevention or delay of various diseases [104]. Schwertz et al. [105] investigated the hypolipidemic effect of camu-camu juice in rats and demonstrated its potential to modulate lipid profiles. After inducing dyslipidemia with a high-fat diet for 21 days, rats were treated with different concentrations of camu-camu juice (0.4 mL/kg, 4.0 mL/kg, and 10 mL/kg) for 14 days. A control group received quercetin (10 mL/kg). The most effective treatment was the 10 mL/kg dosage, which reduced triacylglycerol levels from 166.4 mg/dL to 56.1 mg/dL and total cholesterol from 178.9 mg/dL to 147.4 mg/dL. Although quercetin produced slightly stronger effects, the juice still showed considerable potential and provided a useful concentration reference for future studies.
Due to its high acidity (pH 2.51–2.54), camu-camu is most often consumed in processed forms such as frozen pulp, which facilitates its use in juices, ice creams, jams, and other formulations that allow dilution of the fruit’s acidity [106]. Additionally, M. dubia pulp has proven suitable for producing fermented beverages. According to Maeda and Andrade [107], to reduce the bitterness, the pulp is blanched at 90 °C for 7 min. To obtain a final alcohol content of 12 °GL, sugar is added to the must, which is then mixed with the pulp and transferred to a fermentation vat. A total of 18 L of potable water and Saccharomyces cerevisiae (20 g of baker’s yeast per 2 L of must) is added, and fermentation proceeds for 25 days at 25 °C. Following fermentation, the beverage is bottled, pasteurized (70 °C for 15 min), cooled, and filtered.
As shown in Table 16, the fermentation process yielded good alcohol production (44.5%) and high fermentation efficiency (87%), demonstrating the suitability of the selected medium and conditions. The final beverages reached an alcohol content of 11%, regardless of whether the pulp was blanched. Sensory analysis revealed acceptability rates of 69.2% and 70.1% for beverages made with blanched and unblanched pulp, respectively [107].
Another study highlighted the successful application of camu-camu in a fermented dairy beverage [108]. Thus, milk is heated (90 °C for 15 min), cooled, and inoculated with a dairy starter culture (S. salivarius subsp. thermophilus and L. delbrueckii subsp. bulgaricus), then fermented at 42 °C until the pH drops from 6.0 to 4.5 and titratable acidity exceeds 0.90% lactic acid. After fermentation, camu-camu pulp is added at concentrations of 10%, 13%, and 15%. As shown in Table 17, the final product has an average pH of 4.08 and a titratable acidity of 1.01%, suggesting a high organic acid content. The lactic acid levels are within the legal range for fermented dairy beverages (0.60–2.00%).

2.11. Other Fruits from the Amazon Region

In addition to the fruit species discussed throughout this review, the potential of using other Amazonian species to produce fermented beverages should be highlighted, as many other fruits could be used in a sustainable approach to provide innovative beverage products. One such example is tucumã (Astrocaryum aculeatum), a palm native to northern Brazil, primarily found in the states of Acre, Amazonas, Rondônia, and Roraima. Its ellipsoid, globose, and smooth fruits measure approximately 5 to 6 cm in diameter, weigh around 70 to 75 g, and vary in color from yellow to orange or red [109]. The pulp is highly valued for its high oil content (around 30%) and is composed predominantly of unsaturated fatty acids (approximately 70%), with oleic acid accounting for 63.5% and palmitic acid for 25%. In addition to its promising composition of bioactive compounds, tucumã pulp contains significant levels of α-tocopherol (142.4 μg/g of oil), β-tocopherol (5.6 μg/g of oil), carotenoids (1637.1 μg/g of oil), quercetin (14.51 mg/100 g of pulp), and gallic acid (10 mg/100 g of pulp) [110].
Another potential raw material for fermented beverages is araçá-boi (Eugenia stipitata McVaugh). This fruit can be consumed fresh or processed into jam, jelly, juice, ice cream, or mousse [31]. Its pulp contains relevant nutritional compounds, including proteins (0.6 to 1.0 g/100 g), nitrogen (152.7 mg/100 g), potassium (215.3 mg/100 g), iron (87 ppm/100 g), vitamin A (7.8 µg/100 g), vitamin B1 (9.8 µg/100 g), vitamin C (0.2 to 101.1 mg/100 g), and total phenolics (0.6 to 274.12 mg/100 g), positioning the fruit as a nutraceutical ingredient suitable for functional beverages [111].
Best known for its high caffeine content (ranging from 2.7 to 5.8%) and its use in the energy drink industry, guaraná (Paullinia cupana) is a species domesticated by the Sateré-Mawé people from the lower Madeira River in the Amazon region. It is considered a strategic crop for supplementing the income of small farmers in the Amazon basin. Guaraná is commonly consumed in the form of extracts, syrups, energy drinks, or soft drinks [3,112]. One of the few studies to investigate the production of fermented beverages using guaraná reported that the combination of kefir (0.2 mL/100 g) with a hydroethanolic extract of guaraná (300 mg/kg; extracted at a ratio of 100 g per 1 L of 70% ethanol) was effective in preventing hyperglycemia in diabetic rats. The treatment significantly reduced serum levels of liver enzymes: diabetic rats had AST and ALT levels of 90 U/L and 140 U/L, respectively, while treated rats showed reductions to 65 U/L (AST) and 50 U/L (ALT). These findings suggest that the combined extract offers therapeutic benefits for diabetic individuals and reinforce the potential of guaraná as a functional ingredient, encouraging further exploration of this widely recognized raw material [113].
Therefore, expanding research on these and other Amazonian fruits not only broadens the range of possibilities for the beverage industry but also contributes to the valorization of native species and deepens scientific knowledge of their nutritionally advantageous properties. It is thus essential to invest in and advance studies that integrate biotechnology, sustainability, and traditional knowledge in order to better harness the health benefits of these fruits and establish them as innovative alternatives in the global fermented beverage market.

3. Conclusions

The growing demand for fermented beverages, driven by health benefits and the search for natural and sustainable alternatives, has led research to focus on identifying new microbial sources, optimizing production processes, and formulating beverages with unique flavors and added functional value. Within this context, fermented beverages derived from Amazonian fruits offer significant potential for both regional and international markets, providing a concrete opportunity to boost the local economy by promoting cultural heritage and ancestral knowledge of Amazonian populations, while simultaneously supporting biodiversity conservation and the sustainable use of natural resources in northern Brazil.
Fruits such as cupuaçu, açaí, buriti, taperebá, bacuri, bacaba, murici, pupunha, graviola, and camu-camu not only result in beverages with diverse sensory profiles, high nutritional value, and functional properties but also represent a strategic opportunity to foster a bioeconomy based on socio-biodiversity, with positive impacts on income generation, the strengthening of local economies, and the socio-productive inclusion of traditional communities.
Therefore, the development of this sector must be guided by a sustainability-oriented approach, involving practices that ensure ecosystem conservation, the responsible use of natural resources, and respect for local socio-cultural structures. The consolidation of a production chain for Amazonian fermented beverages may thus represent not only scientific and technological progress but also a powerful vector for sustainable regional development.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/beverages11050152/s1, Table S1: Physicochemical and nutritional aspects of cupuaçu (Theobroma grandiflorum) pulp; Table S2: Physicochemical and nutritional aspects of açaí (Euterpe olearacea) pulp; Table S3: Physicochemical and nutritional aspects of buriti (Mauritia flexuosa) pulp; Table S4: Physicochemical and nutritional aspects of taperebá (Spondias mombin) pulp; Table S5: Physicochemical and nutritional aspects of bacuri (Platonia insignis) pulp; Table S6: Physicochemical and nutritional aspects of bacaba (Oenocarpus bacaba) pulp; Table S7: Physicochemical and nutritional aspects of Murici (Byrsonima crassifolia and B. verbascifolia) pulp; Table S8: Physicochemical and nutritional aspects of Pupunha (Bactris gasipaes) pulp; Table S9: Bioactive compounds of graviola (Annona muricata) leaf, peel, pulp and seed; Table S10: Physicochemical and nutritional aspects of Graviola (Annona muricata) pulp; Table S11: Physicochemical and nutritional aspects of Camu-camu (Myrciaria dubia) fresh pulp.

Author Contributions

Conceptualization, P.M.A. and A.M.J.; writing—original draft preparation, B.N.B.; writing—review and editing, P.M.A., A.M.J. and A.C.C. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by Fundação de Amparo à Pesquisa do Estado do Amazonas (FAPEAM) (grant numbers 01.02.016301.00568/2021-05 and 01.02.016301.00101/2024-08) and by Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) (finance code 001 and grant number 88881.510151/2020-01—PDPG Amazônia Legal).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Acknowledgments

We would like to thank Universidade do Estado do Amazonas—UEA, Instituto Politécnico de Viseu—IPV, Fundação de Amparo à Pesquisa do Estado do Amazonas (FAPEAM), and Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) for supporting this research and Ruth Jucá, Julcéia Camillo, and Walnice Maria, who provided some of the photographs used in the review.

Conflicts of Interest

The authors declare no conflicts of interest.

Abbreviations

The following abbreviations are used in this manuscript:
ICMBioChico Mendes Institute for Biodiversity Conservation
CAGRCompound Annual Growth Rate
ORACOxygen Radical Absorbance Capacity
CFUEquivalent Colony-forming Unit
RDIRecommended Daily Intake
GAEGallic Acid Equivalent
QEQuercetin Equivalent
SCOBYSymbiotic Culture of Bacteria and Yeast
SDASabouraud Dextrose Agar
ANVISABrazilian Health Regulatory Agency
mEqMilliequivalent
EC50Effective Concentration
FWFresh Weight
PC3Prostate Carcinoma
HeLaCervical Carcinoma
LABLactic Acid Bacteria
ADS-AMAgência de Desenvolvimento Sustentável do Amazonas

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Figure 1. Cupuaçu (Theobroma grandiflorum) fruits. Photo: Ruth Jucá—Agência de Desenvolvimento Sustentável do Amazonas (ADS—AM).
Figure 1. Cupuaçu (Theobroma grandiflorum) fruits. Photo: Ruth Jucá—Agência de Desenvolvimento Sustentável do Amazonas (ADS—AM).
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Figure 2. Açaí (Euterpe oleracea) fruits. Photo: Ruth Jucá—Agência de Desenvolvimento Sustentável do Amazonas (ADS—AM).
Figure 2. Açaí (Euterpe oleracea) fruits. Photo: Ruth Jucá—Agência de Desenvolvimento Sustentável do Amazonas (ADS—AM).
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Figure 3. Buriti (Mauritia flexuosa) fruits. Photo reproduced with permission from Julcéia Camillo [3].
Figure 3. Buriti (Mauritia flexuosa) fruits. Photo reproduced with permission from Julcéia Camillo [3].
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Figure 4. Taperebá (Spondias mombin) fruit. Photo reproduced with permission from Walnice Maria Oliveira do Nascimento [3].
Figure 4. Taperebá (Spondias mombin) fruit. Photo reproduced with permission from Walnice Maria Oliveira do Nascimento [3].
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Figure 5. Bacuri (Platonia insignis) fruit. Photo reproduced with permission from Julcéia Camillo [3].
Figure 5. Bacuri (Platonia insignis) fruit. Photo reproduced with permission from Julcéia Camillo [3].
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Figure 6. Bacaba (Oenocarpus bacaba) fruits. Photo reproduced with permission from Julcéia Camillo [3].
Figure 6. Bacaba (Oenocarpus bacaba) fruits. Photo reproduced with permission from Julcéia Camillo [3].
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Figure 7. Murici (Byrsonima crassifolia and B. verbascifolia) fruit. Photo reproduced with permission from Julcéia Camillo [3].
Figure 7. Murici (Byrsonima crassifolia and B. verbascifolia) fruit. Photo reproduced with permission from Julcéia Camillo [3].
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Figure 8. Pupunha (Bactris gasipaes) fruit. Photo: Ruth Jucá—Agência de Desenvolvimento Sustentável do Amazonas (ADS—AM).
Figure 8. Pupunha (Bactris gasipaes) fruit. Photo: Ruth Jucá—Agência de Desenvolvimento Sustentável do Amazonas (ADS—AM).
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Figure 9. Graviola (Annona muricata) fruits. Adapted from [16].
Figure 9. Graviola (Annona muricata) fruits. Adapted from [16].
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Figure 10. Camu-camu (Myrciaria dubia) fruits. Adapted from [102].
Figure 10. Camu-camu (Myrciaria dubia) fruits. Adapted from [102].
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Table 1. Characteristics of a prebiotic beverage produced with cupuaçu (Theobroma grandiflorum) pulp. Adapted from Pereira et al. [33].
Table 1. Characteristics of a prebiotic beverage produced with cupuaçu (Theobroma grandiflorum) pulp. Adapted from Pereira et al. [33].
ComponentsBefore FermentationAfter Fermentation
Citric acid (g/L)8.456.02
Ascorbic acid (mg/L)9030
Quinic acid (g/L)0.630.26
Fructose (g/L)105.9716.23
Sucrose (g/L)53.6820.35
Glucose (g/L)39.3725.78
Antioxidant activity (µM trolox/mL)0.5021.00
Table 2. Characteristics of a fermented milk beverage produced with cupuaçu (Theobroma grandiflorum) 10% (w/v) pulp and S. thermophilus and L. delbrueckii subsp. Bulgaricus. Adapted from Gutiérrez-Álzate et al. [35].
Table 2. Characteristics of a fermented milk beverage produced with cupuaçu (Theobroma grandiflorum) 10% (w/v) pulp and S. thermophilus and L. delbrueckii subsp. Bulgaricus. Adapted from Gutiérrez-Álzate et al. [35].
Variables/ComponentsContent
Moisture (%)93.02 ± 0.20
Ashes (%)0.63 ± 0.01
Protein (%)0.94 ± 0.01
Fat (%)0.80 ± 0.01
Fiber (%)0.12 ± 0.01
Carbohydrates (%)4.48 ± 0.18
Table 3. Characteristics of raw açaí (Euterpe oleracea) and of a fermented beverage with açaí (average values). Adapted from Liu et al. [42].
Table 3. Characteristics of raw açaí (Euterpe oleracea) and of a fermented beverage with açaí (average values). Adapted from Liu et al. [42].
Components (g/100 g)Before FermentationAfter Fermentation
Moisture88.9989.09
Ash0.020.26
Protein1.302.77
Fat3.602.99
Polyphenols0.820.50
Procyanidins0.440.12
Total amino acids10121727
3′,4′OH-Nobiletin0.0900.197
3′OH-Nobiletin0.0110.009
4′OH-Nobiletin0.2270.020
Sinensetin0.2030.281
4′OH-Tan0.0530.044
Nobiletin0.0290.013
Tangeretin0.1530.208
5′OH-Nobiletin0.1220.155
5′OH-Tan0.1690.082
Total flavonoids *1.0581.007
Acetaldehyde0.240.94
Dimethyl sulfur0.000.07
Ethyl formate0.000.09
Ethyl acetate0.070.22
N-propanol0.191.33
Isobutanol0.000.38
Isoamyl alcohol0.141.20
* Values expressed in mg/L.
Table 4. Characteristics of buriti (Mauritia flexuosa) pulp and a fermented beverage with buriti. Adapted from Borgonovi et al. [51].
Table 4. Characteristics of buriti (Mauritia flexuosa) pulp and a fermented beverage with buriti. Adapted from Borgonovi et al. [51].
ComponentsFermented MilkFermented Milk with Buriti Pulp
Total solids (° Brix) (g/100 g)11.06 ± 0.2811.85 ± 0.10
Total protein (g/100 g)3.6 ± 0.104.00 ± 0.05
Ashes (g/100 g)1.17 ± 0.191.21 ± 0.01
Lipids (g/100 g)0.000.2 ± 0.1
Carbohydrates (g/100 g)5.936.44
Table 5. Physicochemical and antioxidant stability evolution of the taperebá (Spondias mombin) fermented beverage during 28 days of storage. Adapted from Ribeiro et al. [58].
Table 5. Physicochemical and antioxidant stability evolution of the taperebá (Spondias mombin) fermented beverage during 28 days of storage. Adapted from Ribeiro et al. [58].
ParameterStorage (Days)
07142128
pH2.3 ± 0.12.4 ± 0.12.5 ± 0.12.5 ± 0.12.4 ± 0.0
Titratable acidity (mg citric acid/mL)0.79 ± 0.010.80 ± 0.020.73 ± 0.040.76 ± 0.000.76 ± 0.02
Total soluble solids (° Brix)7.73 ± 0.068.63 ± 0.428.77 ± 0.068.80 ± 0.267.80 ± 0.00
Total phenolic compounds (mg GAE/L)271.7 ± 29.9309.8 ± 32.2296.2 ± 16.8337.9 ± 17.8320.5 ± 32.2
Antioxidant activity (µM trolox)61.9 ± 3.050.6 ± 3.453.4 ± 2.158.6 ± 5.161.4 ± 4.5
Table 6. Characteristics of a fermented beverage with taperebá (Spondias mombin) pulp. Adapted from Ribeiro et al. [58].
Table 6. Characteristics of a fermented beverage with taperebá (Spondias mombin) pulp. Adapted from Ribeiro et al. [58].
ComponentsContent
Moisture (g/100 g)92.3 ± 0.6
Lipid (g/100 g)1.3 ± 0.6
Protein (g/100 g)0.4 ± 0.2
Ash (g/100 g)0.3 ± 0.0
Fiber (g/100 g)3.0
Carbohydrates (g/100 g)2.7
Caloric value (kcal/200 mL)49
Table 7. Characteristics of a fermented beverage with taperebá (Spondias mombin) pulp and ginger during the fermentation process. Adapted from Ribeiro et al. [59].
Table 7. Characteristics of a fermented beverage with taperebá (Spondias mombin) pulp and ginger during the fermentation process. Adapted from Ribeiro et al. [59].
Components (g/L)Contents
0 Days7 Days14 Days
Citric acid0.57 ± 0.030.49 ± 0.020.53 ± 0.02
Malic acid2.40 ± 0.13<LOD<LOD
Succinic acid0.08 ± 0.030.14 ± 0.010.14 ± 0.02
Latic acid0.09 ± 0.010.09 ± 0.010.08 ± 0.01
Formic acid0.02 ± 0.00<LOD<LOD
Acetic acid0.11 ± 0.020.27 ± 0.040.21 ± 0.02
Propionic acid<LOD0.05 ± 0.01<LOD
Butyric acid0.46 ± 0.030.79 ± 0.100.50 ± 0.07
Maltose54.93 ± 0.885.00 ± 0.250.75 ± 0.12
Glucose59.76 ± 1.0444.32 ± 0.7838.91 ± 0.69
Fructose25.35 ± 0.4736.55 ± 0.9430.67 ± 0.59
Ethanol0.93 ± 0.057.28 ± 0.3723.78 ± 1.24
Glycerol0.12 ± 0.040.63 ± 0.071.72 ± 0.12
Gallic acid1.37 ± 0.165.77 ± 0.236.42 ± 0.18
Syringic acid0.18 ± 0.03<LOD<LOD
Hesperidin0.56 ± 0.03<LOD0.45 ± 0.04
Procyanidin B10.26 ± 0.03<LOD<LOD
(+)-Catechin0.63 ± 0.05<LOD<LOD
Procyanidin B20.23 ± 0.02<LOD<LOD
(−)-Epicatechin0.19 ± 0.01<LOD<LOD
Epigallocatechin gallate0.19 ± 0.02<LOD<LOD
Epicatechin gallate0.57 ± 0.040.81 ± 0.140.81 ± 0.09
Procyanidin A237.59 ± 0.2820.75 ± 0.6618.63 ± 0.44
Trans-caftaric acid5.23 ± 0.10<LOD<LOD
Chlorogenic acid0.83 ± 0.030.23 ± 0.050.26 ± 0.04
Caffeic acid0.10 ± 0.02<LOD<LOD
Myricetin2.70 ± 0.09<LOD<LOD
Rutin0.96 ± 0.070.75 ± 0.030.71 ± 0.02
Quercetin2.80 ± 0.051.43 ± 0.151.48 ± 0.11
Kaempferol0.75 ± 0.05<LOD<LOD
Delphinidin 3-glucoside0.12 ± 0.00<LOD<LOD
Cyanidin 3-glucoside8.34 ± 0.18<LOD<LOD
Pelargonidin 3-glucoside3.39 ± 0.10<LOD<LOD
Peonidin 3-glucoside1.76 ± 0.06<LOD<LOD
Malvidin 3-glucoside9.68 ± 0.22<LOD<LOD
Total Soluble Solids *12.00 ± 0.0012.00 ± 0.009.00 ± 0.00
pH2.67 ± 0.042.61 ± 0.022.76 ± 0.01
<LOD = Below the limit of detection. * Values expressed in ° Brix.
Table 8. Characteristics of kombucha flavored and not flavored with bacuri (Platonia insignis). Adapted from Crispino et al. [64].
Table 8. Characteristics of kombucha flavored and not flavored with bacuri (Platonia insignis). Adapted from Crispino et al. [64].
ComponentsKombucha Without BacuriKombucha with Bacuri Pulp
Total soluble solids (° Brix)1.0 ± 0.002.11 ± 0.00
Titratable acidity (mEq NaOH/100 mL)65.3 ± 0.6070.04 ± 1.00
Titratable acidity (g acetic acid/mL)0.39 ± 0.000.41 ± 0.01
Reducing sugars (g/L)0.09 ± 0.000.16 ± 0.00
Ethanol (g/L)0.54 ± 0.022.27 ± 0.21
Table 9. Characteristics of bacuri (Platonia insignis) yogurts. Adapted from Braga et al. [65].
Table 9. Characteristics of bacuri (Platonia insignis) yogurts. Adapted from Braga et al. [65].
ComponentsWholeSemi-SkimmedSkimmed
Moisture (g/100 g)74.83 ± 0.0276.57 ± 0.0077.46 ± 0.03
Ashes (g/100 g)0.72 ± 0.030.76 ± 0.000.75 ± 0.02
Proteins (g/100 g)2.53 ± 0.012.61 ± 0.000.50 ± 0.03
Lipids (g/100 g)2.40 ± 0.040.60 ± 0.012.58 ± 0.05
Acidity (% lactic acid)1.04 ± 0.081.05 ± 0.010.97 ± 0.07
Table 10. Characteristics of “chicha de bacaba” (Oenocarpus bacaba). Adapted from Puerarui et al. [69].
Table 10. Characteristics of “chicha de bacaba” (Oenocarpus bacaba). Adapted from Puerarui et al. [69].
ComponentsContent
Moisture (g/100 mL)83.58 ± 0.70
Ashes (g/100 mL)0.18 ± 0.0
Proteins (g/100 mL)3.36 ± 0.44
Lipids (g/100 mL)2.20 ± 0.0
Fiber (g/100 mL)1.68 ± 0.13
Carbohydrate (g/100 mL)10.87 ± 0.26
Energy (kcal/100 mL)76.70
Succinic acid (g/L)2.69
Acetic acid (g/L)0.90
Citric acid (g/L)0.49
Ethanol (g/L)0.52
Table 11. Characteristics of the murici (Byrsonima crassifolia and B. verbascifolia) pulp and passion fruit peel flour (Passiflora edulis) fermented dairy beverage. Adapted from Couto et al. [76].
Table 11. Characteristics of the murici (Byrsonima crassifolia and B. verbascifolia) pulp and passion fruit peel flour (Passiflora edulis) fermented dairy beverage. Adapted from Couto et al. [76].
Components
(g/100 g)
Passion Fruit Bark Flour Concentrations (%)
0.00.51.01.5
Moisture82.12 ± 0.0881.73 ± 0.0381.65 ± 0.3280.77 ± 0.33
Ashes0.54 ± 0.140.67 ± 0.020.69 ± 0.030.78 ± 0.01
Protein1.97 ± 0.042.01 ± 0.072.10 ± 0.052.26 ± 0.02
Lipids2.0 ± 0.201.73 ± 0.641.23 ± 0.310.93 ± 0.92
Carbohydrates13.37 ± 0.2513.84 ± 0.814.31 ± 0.5515.25 ± 0.97
Table 12. Evolution of the general chemical parameters of pupunha (Bactris gasipaes) during the fermentation process. Adapted from Andrade et al. [85].
Table 12. Evolution of the general chemical parameters of pupunha (Bactris gasipaes) during the fermentation process. Adapted from Andrade et al. [85].
ComponentsFermentation’s Time (Hours)
024487296120144168
Moisture (%)76.3176.6184.3186.6688.7487.3587.7388.68
pH5.863.483.473.483.473.503.513.62
Acidity (%)0.170.230.330.370.400.310.450.43
Starch (%)4.114.214.335.114.595.334.534.12
Sugars (%)0.0318.029.116.734.412.520.961.07
Soluble solids (° Brix)26.1618.0012.1610.167.836.836.666.60
Carotenoids (g/100 g)2.352.132.122.112.202.172.212.18
Alcohol (%)0.002.464.7310.3210.7412.3212.2612.74
Table 13. Physicochemical and nutritional aspects of Graviola (Annona muricata) pulp. Adapted from Babaji and Bakar [96].
Table 13. Physicochemical and nutritional aspects of Graviola (Annona muricata) pulp. Adapted from Babaji and Bakar [96].
ComponentsContent
Water (g/100 g)81.0 ± 2.5
Proteins (g/100 g)1.0 ± 0.6
Lipids (g/100 g)0.6 ± 0.3
Carbohydrates (g/100 g)17.25 ± 0.1
Phosphorus (mg/100 g)28 ± 1
Table 14. Characteristics of graviola (Annona muricata) juice and a fermented beverage produced with graviola pulp. Adapted from Okigbo and Obire [99].
Table 14. Characteristics of graviola (Annona muricata) juice and a fermented beverage produced with graviola pulp. Adapted from Okigbo and Obire [99].
ComponentsGraviola JuiceGraviola Wine
Moisture (%)87.4997.9
Ash (%)0.500.23
Fiber (%)3.290.58
Fat (%)0.030.2
Protein (%)0.630.31
Carbohydrate (%)8.060.78
Alcohol (%)0.0014.5
Vitamin C (mg/100 mL)46.216.0
pH4.84.5
Titratable acidity (g citric acid/100 g)0.030.06
Total solids (° Brix)14.975.03
Specific gravity1.031.01
Table 15. Characteristics of graviola (Annona muricata) beer. Adapted from Santos et al. [100].
Table 15. Characteristics of graviola (Annona muricata) beer. Adapted from Santos et al. [100].
ComponentsGraviola PulpGraviola Beer
Moisture (g/100 g)90.65 ± 1.2994.99 ± 0.06
Ash (g/100 g)0,46 ± 0.060.2 ± 0.04
Lipids (g/100 g)0.03 ± 0.000.02 ± 0.00
Protein (g/100 g)0.95 ± 0.020.14 ± 0.02
Total carbohydrates (g/100 g)7.90 ± 0.984.60 ± 0.04
Calories (kcal/g)35.7 ± 4.0219.3 ± 0.1
Calcium (mg/L)<LOD1.18
Magnesium (mg/L)<LOD1.13
Potassium (mg/L)<LOD0.17
Sodium (mg/L)<LOD1.3
<LOD = Below the limit of detection.
Table 16. Characteristics of a camu-camu (Myrciaria dubia) fermented beverage with and without pulp blanching. Adapted from Maeda and Andrade [107].
Table 16. Characteristics of a camu-camu (Myrciaria dubia) fermented beverage with and without pulp blanching. Adapted from Maeda and Andrade [107].
ComponentsFermented Camu-Camu
Beverage with Blanched Pulp
Fermented Camu-Camu
Beverage
Moisture (%)94.35 ± 0.7092.75 ± 0.57
pH3.202.70
Acidy (% in citric acid)2.91 ± 0.044,40 ± 0.16
Soluble solids (° Brix)5.57 ± 0.306.77 ± 0.20
° Brix/acidity1.911.54
reducing sugars (%)1.40 ± 0.192.05 ± 0.12
Ascorbic acid (%)0.80 ± 0.051.20 ± 0.06
Alcohol (°GL)11.0011.00
Phenolic compounds (mg/100 g)983.3 ± 4.24978.0 ± 5.2
Total anthocyanins (mg/100 g)1.92 ± 0.232.12 ± 0.08
Total flavonoids (mg/100 g)16.93 ± 0.0316.38 ± 0.11
Table 17. Characteristics of camu-camu (Myrciaria dubia) yogurt. Adapted from Aguiar and Souza [108].
Table 17. Characteristics of camu-camu (Myrciaria dubia) yogurt. Adapted from Aguiar and Souza [108].
ComponentsCamu-Camu Pulp Concentration (%)
101315
pH4.07 ± 0.04.09 ± 0.04.1 ± 0.0
Acidity (%)0.97 ± 0.01.04 ± 0.01.03 ± 0.0
Total solids (° Brix) (%)24.2 ± 0.625.6 ± 1.526.6 ± 2.0
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Batista, B.N.; Correia, A.C.; Jordão, A.M.; Albuquerque, P.M. Fermented Beverages from Amazonian Fruits: Nutritional Characteristics and Bioactive Compounds. Beverages 2025, 11, 152. https://doi.org/10.3390/beverages11050152

AMA Style

Batista BN, Correia AC, Jordão AM, Albuquerque PM. Fermented Beverages from Amazonian Fruits: Nutritional Characteristics and Bioactive Compounds. Beverages. 2025; 11(5):152. https://doi.org/10.3390/beverages11050152

Chicago/Turabian Style

Batista, Bárbara N., Ana Cristina Correia, António M. Jordão, and Patrícia M. Albuquerque. 2025. "Fermented Beverages from Amazonian Fruits: Nutritional Characteristics and Bioactive Compounds" Beverages 11, no. 5: 152. https://doi.org/10.3390/beverages11050152

APA Style

Batista, B. N., Correia, A. C., Jordão, A. M., & Albuquerque, P. M. (2025). Fermented Beverages from Amazonian Fruits: Nutritional Characteristics and Bioactive Compounds. Beverages, 11(5), 152. https://doi.org/10.3390/beverages11050152

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