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Different types of tea, including black, green, white, oolong, dark, and summer teas, serve as the primary raw materials in the production of fermented beverages such as kombucha, tea wine, and tea vinegar[15,21,22,30−33,35−39,55,72] (Table 1). Generally, fermentation enhances the phenolic content and antioxidant capacity of these drinks[58]. In the case of kombucha, the fermentation process notably affects polyphenols when using black tea, leading to a greater variety of phenolic compounds[51]. Specifically, phenolic compounds newly formed in black tea kombucha represent 42.72% of the total phenolics, compared to a mere 0.97% in green tea kombucha[30]. Moreover, green tea kombucha features elevated levels of epicatechin, catechin, and kaempferol relative to its black tea kombucha[91]. The abundant amino acids in green tea promote sugar consumption, boosting alcohol production and enhancing yeast fermentation. Consequently, wines derived from green tea display higher concentrations of total and specific catechins (EC, EGC, ECG, and EGCG) than those produced from black, oolong, and dark teas[31].
Table 1. Kombucha, tea wine, and tea vinegar prepared from different types of tea.
Beverage Fermentation conditions Substrate Results Ref. Kombucha 3% (w/v) SCOBY,
100 mL/L kombucha,
fermented at 25 °C for 10 d.Green tea pH = 3.2, total acid: 0.36% (w/v acetic acid), alcohol: 7.29 g/L,
total phenols: 0.70 mg GAE/mL, theaflavin: 0.028 (% w/v),
theobromine: 1.330 (% w/v).[30] Black tea pH = 3.5, total acid: 0.32% (w/v acetic acid), alcohol: 4.90 g/L,
total phenol: 1.09 mg GAE/mL, theaflavin: 0.151 (% w/v), theobromine: 1.998 (% w/v).Kombucha 30 g SCOBY, 100 mL kombucha, fermented at 27 °C for 14 d. Black tea Days 7 and 14 of fermentation: acetic acid: 3.18, 9.18 (mg/mL),
Alcohol: 4.69, 5.83(mg/mL).
Days 0, 7 and 14 of fermentation:
polyphenolics: 79.38, 64.81, 67.20 (mg/g DW),
flavonoids: 17.97, 14.46, 13.87 (mg/g DW), and
total catechins: 2.184 ,0.99, 0.464 (mg/g DW).[33] Green tea Days 7 and 14 of fermentation: acetic acid: 4.22, 7.65 (mg/mL),
alcohol: 2.81, 4.18 (mg/mL).
Days 0, 7 and 14 of fermentation:
polyphenolic compounds: 74.40, 100.33, 67.40 (mg/g DW),
flavonoids: 16.57, 18.49, 15.11 (mg/g DW),
total catechins: 18.253, 9.770, 11.844 (mg/g DW).Kombucha 10% SCOBY and kombucha,
28 ° C fermented for 1, 7, 14 d.Green tea Tea soup: pH = 5.54, alcohol: 0, acidity: 20.12 (mg acetic acid/L),
TFC: 254.1 (mg/L), TPC: 269.0 (mg/L).
At 1, 7, 14 d fermentation:
pH = 3.50, 2.61, 2.49, alcohol: 0.2%, 3.0%, 2.75%,
acidity: 610.34, 7,039.21, 9,147.4 (mg acetic acid/L),
TFC: 196.2, 146.8, 181.3 (mg/L), TPC: 277.6, 299.6, 320.1 (mg/L).[29] Black tea Tea soup: pH = 5.34, Alcohol: 0, acidity: 23.5 (mg acetic acid/L),
TFC: 231.7 (mg/L), TPC:183.1 (mg/L),
At 1, 7, 14 d fermentation: pH = 3.54, 2.62, 2.53,
Saccharose: 10.88, 9.5, 7.5 (Brix-g/100 mL),
alcohol: 0.3%, 3.25%, 2.0%,
acidity: 501.02, 7,039.08, 9,083.03 (mg acetic acid/L),
TFC: 149.1, 90.5, 126.7 (mg/L), TPC: 201.0, 219.5, 206.0 (mg/L).White tea Tea soup: pH = 6.53, alcohol: 0, acidity: 21.09 (mg acetic acid/L)
TFC: 209.3 (mg/L), TPC: 184.6 (mg/L);
At 1, 7, 14 d fermentation: pH = 3.56, 2.53, 2.37,
saccharose: 10.13, 10.13, 9.5 (°Brix-g/100 mL),
alcohol: 0.4%, 3.5%, 3.0%,
acidity: 620.13, 7,048.06, 9,132.20 (mg acetic acid/L)
TFC: 132.6 (mg/L), 83.8 (mg/L),111.6 (mg/L),
TPC: 200.8 (mg/L), 205.6 (mg/L), 228.1 (mg/L).Pu'er tea Tea soup: pH = 5.58, alcohol: 0, acidity: 20.42 (mg acetic acid/L),
TFC: 359.9 (mg/L), TPC: 229.5 (mg/L),
At 1, 7, 14 d fermentation: pH = 3.62, 2.38, and 2.32,
alcohol: 0.4%, 3.5%, 3.0%,
acidity: 600.09, 7,059.47, 9,071.02 (mg acetic acid/L),
TFC: 292.5, 198.1, 242.5 (mg/L), TPC: 219.8, 270.5, 271.9 (mg/L).Kombucha 10% (v/v) kombucha, fermented at room temperature for 15 d. Green tea pH = 2.94, total acid: 11.72 g/L,
alcohol free, glucuronic acid: 1.37 g/L, gluconic acid: 41.42 g/L, DSL: 3.44 g/L, ascorbic acid: 0.61 g/L, acetic acid: 10.42 g/L, succinic acid: none.[35] Black tea pH = 2.70, total acid: 16.75 g/L,
alcohol free, glucuronic acid: 1.58 g/L, gluconic acid: 70.11 g/L, DSL: 5.23 g/L, ascorbic acid: 0.70 g/L, acetic acid: 11.15 g/L, succinic acid: 3.05 g/L.Oolong tea pH = 2.89, Total acid: 12.24 g/L, no alcohol,
glucuronic acid: 0.07 g/L, gluconic acid: 48.75 g/L, DSL: 4.02 g/L, ascorbic acid: 0.60 g/L, acetic acid: 10.48 g/L, succinic acid: none.Tea wine 25°Brix, 0.5% yeast,
fermentation at 25 °C.Black tea Alcohol 14.0% vol, theanine content: 0.241 mg/mL. [38] Tea wine The sugar level was 17 °Bx, 0.3 % yeast, fermentation at 24 °C for 13 d. Green tea The alcohol content was 8.5 %vol, the concentration of tea polyphenols was 2,902.35 mg/L. [36] Tea vinegar 4% alcohol by total volume, 5% acetic acid strain, 30 °C for 9 d. Black tea Theaflavins were significantly decreased, thearubigins were decreased, and theabrownines were increased. [22] Tea vinegar 0.9% yeast, initial sugar 15%. The initial alcohol content was 6% vol,
9% acetic acid bacteria, fermentation at 28 °C for 12 d.Summer and
fall green
tea fragmentsThe acidity content was 59.10 g/L, tea polyphenol content was 2.95 g/L, alcohol content was 0.08% vol, amino acid nitrogen content was 0.14 g/dL, and caffeine content was 0.80%. [72] GAE: Gallic acid equivalent, DW: Dry Weight, TPC: total polyphenols content, TFC: total flavonoids content. Overall, while kombucha, tea wine, and tea vinegar can be produced from six predominant tea types, an assessment of factors such as taste, fermentation duration, and polyphenol content highlights specific advantages of black tea. Nevertheless, green tea is distinguished by its higher catechin levels and superior antioxidant properties, making its transition from tea soup to fermented tea beverages during microbial fermentation (Fig. 2).
Figure 2.
Fermentation processes in tea beverages: from raw materials to finished products. (1) In the production of kombucha, tea wine, and tea vinegar, commonly used tea leaf raw materials include various types of tea such as green, black, oolong, dark, and white teas, processed differently, as well as seasonally surplus summer tea leaves. (2) These teas provide the substrate for fermentation. For kombucha, sugar tea soup, yeast, and a mix of acetic acid bacteria are added to initiate fermentation. In contrast, the addition of yeast alone ferments into tea wine while combining the ethanol from yeast fermentation with acetic acid bacteria further produces tea vinegar[16]. (3) During fermentation, glucose and fructose are converted into ethanol by yeast and transformed into gluconic and glucuronic acid by acetic acid bacteria. Additionally, ethanol is oxidized to acetic acid[14,27]. Throughout the microbial metabolism process, various compounds such as alcohols, ketones, aldehydes, acids, amino acids, caffeine, and polyphenols in the tea undergo transformations, being preserved, increased, or decreased. Caffeine is converted into theobromine and theophylline, serving as nitrogen sources for the microbes. Amino acids provide nitrogen and are transformed into alcohols, while aldehydes convert into alcohols and acids. Reactions between alcohols and acids with ethanol and acetic acid result in the formation of new ethyl esters and acetate compounds[15,30,31,33,35,55,72]. Tea polyphenols, predominantly flavonoids, and phenolic acids[67], undergo significant changes: catechin ester bonds break, (–)epigallocatechin gallate hydrolyzes into epigallocatechin and gallic acid, and chlorogenic acid converts into caffeic acid and quinic acid[19]. This intricate fermentation process not only alters the chemical composition of the raw materials but also enhances the flavor and nutritional value of the final products, underscoring the uniqueness and complexity of tea beverage fermentation.
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Fermented tea beverages, including kombucha, tea wine, and tea vinegar, owe their health benefits to bioactive compounds that are produced during the fermentation process. These health benefits encompass antioxidant properties, antibacterial activity, anti-inflammatory effects, and blood sugar regulation. Additionally, these beverages contribute to gut health by promoting the growth of beneficial bacteria (Table 2). Fermented tea beverages may also aid in detoxification and support liver health, attributed to the increased levels of polyphenols, organic acids, and other metabolites produced by microbial fermentation.
Table 2. Healthy benefits of fermented tea beverage kombucha in vivo.
Model Intervention and dosage Significant results and biological activity Ref. Glycemic index and insulin index after a standard carbohydrate meal Sample: 11 healthy adults (four males and seven females),
Period: 120 min after test meals
Group 1: 330 ml of soda water;
Group 2: diet lemonade soft drink;
Group 3: organic kombucha.
Additional capillary blood samples were collected at regular intervals
(15, 30, 45, 60, 90, and 120 min) after commencement of the reference solution or test meal.Soda water (GI: 86 and II: 85)
soft drink (GI: 84 and II: 81)
kombucha (GI: 68, and II: 70)
↓GI (Glycemic index)
↓II (insulin index).[92] HFHF Sample: 40 wistar rats,
Period: 10 weeks,
n = 10 for all groups, ad libitum consume,
Group 1: standard diet (AIN-93M);
Group 2: high-fat and high-fructose diet (HFHF);
Group 3: HFHF + GTK diluted in water (30% v/v);
Group 4: HFHF + BTK diluted in water (30% v/v).GTK, BTK: ↑propionic acid
↑Firmicutes: Bacteroidetes,
↑Erysipelotrichaceae,
↓Bacteroidaceae ,
↓S24-7, Desulfovibrionaceae.
GTK: ↓Proteobacteria.
BTK: ↑Euryarchaeota, Lachnospiraceae.[93] HFHF Sample: 32 wistar rats,
Period: 10 weeks, ad libitum consume,
Group 1: AIN-93M: standard diet (n = 8);
Group 2: HFHF (n = 24);
then regroup as follows: HFHF; HFHF + GTK diluted in water (30% v/v);
HFHF + BTK diluted in water (30% v/v).GTK, BTK: improving the insulin sensitivity, reduced the percentage of lipid vesicles in the liver, reverting the liver steatosis from grade 2 to 1, active CPT1 express,
↑glucose tolerance, TAC in plasma and liver, SOD and CAT in liver,
↓ALT, NO, NLR,
GTK: ↑ADIPO-R2, BTK: ↑SREBP1c.[94] LPS-induced sepsis Sample: Specific pathogen-free C57BL/6 adult mice,
Period: 60 d,
n = 10 per group, with equal numbers of male and female.
Group 1: free-drinking water, the sham;
Group 2: free-drinking kombucha (FD), (replaced every 2 d);
Group 3: intragastric administration (IA) of kombucha (100 μL/100 g daily);
Group 4: free-drinking water, LPS-induced sepsis (LPS);
Group 5: FD + LPS;
Group 6: IA + LPS.
At day 60, Group 1−3 injected phosphate-buffered saline, Group 4−6 injected LPS (20 mg/kg).
Kombucha was added to drinking water at a volume ratio of 1:20.↑CD4+ T cells, B cell, macrophages,
↓CD8+ T cells,
↓IL-1β, TNF-α, CCL-2, IL-10, and CXCL10 in the lung tissues, alleviated the symptoms of lung histopathological damage
↓pIκBα, p-NF-κB expression.
inhibits LPS-induced NF-κB activation.
↓Bacteroidetes,
↑Cyanobacteria and Alistipes,
Prevotellaceae enrich in IA and FD group.[95] High fat high sugar diet injected with Streptozotocin to Type 2 Diabetes Sample: 60 Kunming mice,
Period: day 40 to 68 (4 weeks), randomly divided into five groups ( n = 12). The mice feed with HFHSD was intraperitoneally injected with STZ (50 mg/kg·bw) 4 times (day 28, day 31, day 34 and day 37) to induce T2DM.
Group 1: the normal control (NC), normal diet and gavage administration with 11.1 mL/kg·bw saline;
Group 2: DC, HFHSD and gavage administration with 11.1 mL/kg·bw saline;
Group 3: MET, HFHSD and gavage administration with 0.13 g/kg·bw metformin;
Group 4: KT, HFHSD and gavage administration with 11.1 mL/kg·bw kombucha;
Group 5: tea soup (TS), HFHSD and gavage administration with 11.1 mL/kg·bw tea soup.↓HOMA-IR, ↑HOMA- β, ↓AST, ALT.
↑liver glycogen content,
↓pancreatic index,
↑GPR41/GPR43 mRNA express,
↑GLP-1, PYY,
↑ZO-1, Claudin-1, Occludin,Muc2,
↓IL-1β, IL-6, TFN-α mRNA in intestinal inflammation,
↓LPS, TNF-α and IL-6 in serum.
↑Firmicutes, Lactobacillus, Butyricicoccus, Bifidobacterium,
↓Proteobacteria.
↑acetic acid and butyric acid in SCFAs.[96] NAFLD Sample: 12 male C57BLKS db/db mice,
Group 1: Control, the control diet (n = 4); MCD, the methionine/choline-deficient (MCD) diet (n = 8) for 4 weeks;
Group 2: MCD + water (n = 4);
Group 3: MCD + KT, Kombucha powder 2 g/kg by oral administration,
every 24 h for 3 weeks (n = 4).↓Fat accumulation in the livers.
↓Firmicutes,
↓Erysipelotrichia,
↓Allobaculum,
Turicibacter and Clostridium, ↑Bacteroidetes, ↑Lactobacillus, ↑Mucispirillum.[97] High-fat diet NAFLD Sample: 20 male C57BL/6 mice,
Period: 12 weeks (At the end of the 10th week, for nine consecutive days),
n = 5 for all groups.
Group 1: RC, the control group + tap water;
Group 2: RC + K, control group + kombucha (0.2 mL containing 107–108 microorganisms/mL);
Group 3: HFD, HFD + tap water;
Group 4: HFD + kombucha (HFD + K).Reduced the presence of intra hepatocyte lipid droplets, collagen deposition in the liver's perivascular spaces, and hepatic FXR gene expression. [98] DSS induced the leaky gut syndrome Sample:16 male NMR mice,
Period: day 7 to 21 (14 d);
Old mice: normal group (n = 8); DSS colitis induction group (n = 8): DSS no treatment group and DSS + fKT.
Young mice: normal group (n = 8); DSS colitis induction group (n = 8): DSS no treatment group and DSS + fKT.Ameliorates tissue changes associated with PMNs infiltration, crypt loss, epithelial defects, mucosal destruction, apoptosis, edema, and increased mucosal thinness due to DSS.
↑ZO-1 and ZO-2 express.[99] Antioxidant properties
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Fermentation generally increases phenolic content and antioxidant activity[58]. Kombucha, for example, demonstrates strong antioxidant properties[35]. Green tea kombucha, after seven days of fermentation, exhibits less DPPH radical inhibition than unfermented green tea, while black tea kombucha has higher antioxidant activity compared to its unfermented counterpart[34,48,100]. This may be due to the higher phenolic content in black tea kombucha[93]. Green tea kombucha is found to have the highest antioxidant capability among kombuchas made from different tea types[29,47]. Similarly, with green tea wine having significantly higher ABTS values compared to other tea wines[31]. Tea vinegar's antioxidant and antibacterial functions surpass those of tea soup and conventional food vinegar[101], likely due to its rich phenolic and organic acid content[22].
Anti-inflammatory effects
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Kombucha intervention significantly reduces serum levels of lipopolysaccharide (LPS), interleukin (IL)-6, IL-1β, and tumor necrosis factor (TNF)-α cytokines, and markedly decreases the expression levels of inflammatory factors IL-1β, IL-6, and TNF-α mRNA in the colon[95,96]. It significantly restores T cell levels and macrophage counts, elevates CD4+ T cell and B cell levels, significantly lowers CD8+ T cell levels, markedly suppresses the upregulation of CCL-2, IL-10, and CXCL10, decreases phosphorylated-IκBα (pIκBα)expression levels and inhibits nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB)signal transduction[95].
Blood sugar regulation
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In human clinical trials, consuming unpasteurized kombucha significantly reduces Glycemic Index (GI ) and Insulin Index (II) after a standard high-GI diet for 2 h[92]. In animal models induced by a high-fat diet, kombucha can reduce weight, significantly decrease fasting blood glucose (FBG) and food intake, reduce HOMA-IR, increase HOMA-β, raise glucagon-like peptide-1 (GLP-1) and peptide YY (PYY) levels in the intestine, significantly repair pancreatic damage, and protect the pancreas[95,96]. It improves insulin sensitivity, lowers insulin resistance, and enhances glucose tolerance[94,98].
Liver protection
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Kombucha intervention can reduce total fat tissue in high-fat, high-sugar diet mice, decrease serum triglyceride levels, significantly reduce AST levels, enhance glycogen synthesis, and effectively improve liver function[96]. It restores liver fat degeneration from grade 2 to grade 1, increases plasma and liver total antioxidant capacity (TAC), reduces the neutrophil/lymphocyte ratio (NLR), and inflammatory marker levels. Black tea kombucha reduces SREBP1c expression, while green tea kombucha increases ADIPO-R2 expression[94]. Kombucha decreases citrate synthase and phosphofructokinase-1 enzyme activity, downregulates G protein-coupled bile acid receptor (Gpbar1, also known as TGR5) and farnesol X receptor (FXR) gene expression, reduces liver collagen fiber deposition, and liver fat accumulation[97,98].
Regulation of gut microbiota
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Both green tea and black tea kombucha can regulate the intestinal microbiota, improving intestinal health in Wistar rats fed a high-fat, high-fructose (HFHF) diet[93]. Kombucha can restore colon damage in Type 2 diabetes mellitus (T2DM) mice, significantly increase the relative expression levels of tight junction proteins (ZO-1, Claudin-1, Occludin), and mucin proteins (Muc2), improving intestinal barrier damage[96]. Kombucha can improve tissue changes associated with "leaky gut syndrome" induced by dextran sodium sulfate (DSS), such as polymorphonuclear cells (PMNs) infiltration, crypt loss, epithelial defects, upregulating ZO-1 and ZO-2 expression[99].
In HFHF and T2DM animal models, kombucha can increase the ratio of Firmicutes to Bacteroidetes, decrease Proteobacteria, significantly increase intestinal microbial richness, such as Lactobacillus, Butyricicoccus, Lachnospiraceae, Bifidobacterium, and others[93,96,97]. It can significantly increase the content of short-chain fatty acids (SCFAs) acetate, butyrate, and propionate, and promote the growth of bacteria producing propionate, thereby exerting anti-inflammatory effects[93,95,96].
Antibacterial effects
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The antibacterial activity of kombucha is similar to that of acetic acid, exhibiting inhibitory effects on intestinal pathogenic bacteria (Escherichia coli, Shigella dysenteriae, Salmonella Typhi, and Vibrio cholerae)[35,102]. Black tea kombucha shows strong inhibitory effects on Candida krusei, C. glabrata, C. albicans, C. tropicalis, and Hemophilus influenzae[34]. The main antibacterial compounds present in the polyphenolic fraction of kombucha were catechin and isorhamnetin[102]. These findings suggest that acetic acid and polyphenols in kombucha offer significant potential health benefits in inhibiting intestinal pathogenic bacteria.
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All data generated or analyzed during this study are included in this published article.
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About this article
Cite this article
Guo Q, Yuan J, Ding S, Nie Q, Xu Q, et al. 2024. Microbial fermentation in fermented tea beverages: transforming flavor and enhancing bioactivity. Beverage Plant Research 4: e029 doi: 10.48130/bpr-0024-0026
Microbial fermentation in fermented tea beverages: transforming flavor and enhancing bioactivity
- Received: 21 February 2024
- Revised: 10 June 2024
- Accepted: 24 June 2024
- Published online: 09 August 2024
Abstract: This study mainly explores three types of fermented tea beverages: kombucha, known for its distinctive sweet and sour flavor; tea wine, valued for its rich taste and low alcohol content; and tea vinegar, notable for its unique vinegar aroma. These beverages are produced through fermentation using teas as a base, facilitated by yeast and acetic acid bacteria. The research investigates how these microbes utilize tea as a nitrogen source, enhancing the content of tea polyphenols, reducing caffeine, and generating a rich array of organic acids and volatile compounds. This process imparts fermented tea beverages with unique flavors and augmented health benefits. Moreover, the bacterial cellulose film created by the symbiotic relationship between yeast and acetic acid bacteria opens up innovative avenues for the deep processing and high-value utilization of tea leaves.