Fermented Foods: Their Health-Promoting Components and Potential Effects on Gut Microbiota
Abstract
:1. Introduction
2. Fermented Foods
2.1. Fermented Milks
2.2. Cheese
2.3. Fermented Meat
2.4. Fermented Fishes
2.5. Fermented Legumes
2.6. Fermented Vegetables
2.7. Alcoholic Beverages
2.8. Other Fermented Foods
3. Health-Promoting Components of Fermented Foods
3.1. Antioxidant Components
3.2. Vitamin Content
3.3. Antihypertensive Properties
3.4. Antidiabetic Properties
3.5. Reducing Lactose Intolerance
3.6. Probiotic Effect
3.7. Protein Digestibility Enhancement
4. Fermented Foods and the Impact on Gut Microbiome
5. Conclusions
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Conflicts of Interest
References
- McGovern, P.E.; Zhang, J.; Tang, J.; Zhang, Z.; Hall, G.R.; Moreau, R.A.; Nuñez, A.; Butrym, E.D.; Richards, M.P.; Wang, C.-S. Fermented beverages of pre-and proto-historic China. Proc. Natl. Acad. Sci. USA 2004, 101, 17593–17598. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Tamang, J.P.; Cotter, P.D.; Endo, A.; Han, N.S.; Kort, R.; Liu, S.Q.; Mayo, B.; Westerik, N.; Hutkins, R. Fermented foods in a global age: East meets West. Compr. Rev. Food Sci. Food Saf. 2020, 19, 184–217. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Vitorino, L.C.; Bessa, L.A. Technological microbiology: Development and applications. Front. Microbiol. 2017, 8, 827. [Google Scholar] [CrossRef] [PubMed]
- Chilton, S.N.; Burton, J.P.; Reid, G. Inclusion of fermented foods in food guides around the world. Nutrients 2015, 7, 390–404. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Voidarou, C.; Antoniadou, M.; Rozos, G.; Tzora, A.; Skoufos, I.; Varzakas, T.; Lagiou, A.; Bezirtzoglou, E. Fermentative foods: Microbiology, biochemistry, potential human health benefits and public health issues. Foods 2020, 10, 69. [Google Scholar] [CrossRef] [PubMed]
- Rezac, S.; Kok, C.R.; Heermann, M.; Hutkins, R. Fermented foods as a dietary source of live organisms. Front. Microbiol. 2018, 9, 1785. [Google Scholar] [CrossRef] [PubMed]
- Marco, M.L.; Heeney, D.; Binda, S.; Cifelli, C.J.; Cotter, P.D.; Foligné, B.; Gänzle, M.; Kort, R.; Pasin, G.; Pihlanto, A. Health benefits of fermented foods: Microbiota and beyond. Curr. Opin. Biotechnol. 2017, 44, 94–102. [Google Scholar] [CrossRef]
- Pessione, E.; Cirrincione, S. Bioactive molecules released in food by lactic acid bacteria: Encrypted peptides and biogenic amines. Front. Microbiol. 2016, 7, 876. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Filannino, P.; Bai, Y.; Di Cagno, R.; Gobbetti, M.; Gänzle, M.G. Metabolism of phenolic compounds by Lactobacillus spp. during fermentation of cherry juice and broccoli puree. Food Microbiol. 2015, 46, 272–279. [Google Scholar] [CrossRef] [PubMed]
- Salazar, N.; Gueimonde, M.; De Los Reyes-Gavilán, C.G.; Ruas-Madiedo, P. Exopolysaccharides produced by lactic acid bacteria and bifidobacteria as fermentable substrates by the intestinal microbiota. Crit. Rev. Food Sci. Nutr. 2016, 56, 1440–1453. [Google Scholar] [CrossRef] [PubMed]
- Kindstedt, P. Cheese and Culture: A History of Cheese and Its Place in Western Civilization; Chelsea Green Publishing: London, UK, 2012. [Google Scholar]
- Carr, F.J.; Chill, D.; Maida, N. The lactic acid bacteria: A literature survey. Crit. Rev. Microbiol. 2002, 28, 281–370. [Google Scholar] [CrossRef]
- Smit, G.; Smit, B.A.; Engels, W.J. Flavour formation by lactic acid bacteria and biochemical flavour profiling of cheese products. FEMS Microbiol. Rev. 2005, 29, 591–610. [Google Scholar] [CrossRef] [PubMed]
- Arqués, J.L.; Rodríguez, E.; Langa, S.; Landete, J.M.; Medina, M. Antimicrobial activity of lactic acid bacteria in dairy products and gut: Effect on pathogens. BioMed Res. Int. 2015, 2015, 584183. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Bintsis, T. Lactic acid bacteria as starter cultures: An update in their metabolism and genetics. AIMS Microbiol. 2018, 4, 665. [Google Scholar] [CrossRef] [PubMed]
- Rai, R.; Shangpliang, H.N.J.; Tamang, J.P. Naturally fermented milk products of the Eastern Himalayas. J. Ethn. Foods 2016, 3, 270–275. [Google Scholar] [CrossRef]
- Robinson, R.; Lucey, J.; Tamime, A. Manufacture of Yoghurt. In Fermented Milks; Blackwell Publishing: Hoboken, NJ, USA, 2006; pp. 53–75. [Google Scholar]
- Kosikowski, F.V.; Mistry, V.V. Cheese and fermented milk foods. Volume 1: Origins and principles. In Cheese and Fermented Milk Foods; FV Kosikowski LLC: Westport, CT, USA, 1997. [Google Scholar]
- Ahmed, Z.; Wang, Y.; Ahmad, A.; Khan, S.T.; Nisa, M.; Ahmad, H.; Afreen, A. Kefir and health: A contemporary perspective. Crit. Rev. Food Sci. Nutr. 2013, 53, 422–434. [Google Scholar] [CrossRef]
- Lopitz-Otsoa, F.; Rementeria, A.; Elguezabal, N.; Garaizar, J. Kefir: A symbiotic yeasts-bacteria community with alleged healthy capabilities. Rev Iberoam Micol 2006, 23, 67–74. [Google Scholar] [CrossRef] [PubMed]
- Rosa, D.D.; Dias, M.M.; Grześkowiak, Ł.M.; Reis, S.A.; Conceição, L.L.; Maria do Carmo, G.P. Milk kefir: Nutritional, microbiological and health benefits. Nutr. Res. Rev. 2017, 30, 82–96. [Google Scholar] [CrossRef]
- Prado, M.R.; Blandón, L.M.; Vandenberghe, L.P.; Rodrigues, C.; Castro, G.R.; Thomaz-Soccol, V.; Soccol, C.R. Milk kefir: Composition, microbial cultures, biological activities, and related products. Front. Microbiol. 2015, 6, 1177. [Google Scholar] [CrossRef] [Green Version]
- Yüksekdağ, Z.; Beyatli, Y.; Aslim, B. Determination of some characteristics coccoid forms of lactic acid bacteria isolated from Turkish kefirs with natural probiotic. LWT-Food Sci. Technol. 2004, 37, 663–667. [Google Scholar] [CrossRef]
- Dimidi, E.; Cox, S.R.; Rossi, M.; Whelan, K. Fermented Foods: Definitions and Characteristics, Impact on the Gut Microbiota and Effects on Gastrointestinal Health and Disease. Nutrients 2019, 11, 1806. [Google Scholar] [CrossRef] [Green Version]
- Watanabe, K.; Makino, H.; Sasamoto, M.; Kudo, Y.; Fujimoto, J.; Demberel, S. Bifidobacterium mongoliense sp. nov., from airag, a traditional fermented mare’s milk product from Mongolia. Int. J. Syst. Evol. Microbiol. 2009, 59, 1535–1540. [Google Scholar] [CrossRef] [PubMed]
- Tamime, A.; Robinson, R. Fermented milks popular in Europe and North America. In Handbook of Food Products Manufacturing: Health, Meat, Milk, Poultry, Seafood, and Vegetables; John Wiley & Sons: Hoboken, NJ, USA, 2007; Volume 2, pp. 411–439. [Google Scholar]
- Toba, T.; Kotani, T.; Adachi, S. Capsular polysaccharide of a slime-forming Lactococcus lactis ssp. cremoris LAPT 3001 isolated from Swedish fermented milk ‘långfil’. Int. J. Food Microbiol. 1991, 12, 167–171. [Google Scholar] [CrossRef] [PubMed]
- Modler, H. Development of a continuous process for the production of Ricotta cheese. J. Dairy Sci. 1988, 71, 2003–2009. [Google Scholar] [CrossRef]
- Farkye, N.Y. Acid-Heat Coagulated Cheeses. In Cheese; Elsevier: Amsterdam, The Netherlands, 2017; pp. 1111–1115. [Google Scholar]
- Farkye, N.Y.; Vedamuthu, E.R. Microbiology of soft cheeses. In Dairy Microbiology Handbook. The Microbiology of Milk and Milk Products; Wiley Online Library: Hoboken, NJ, USA, 2002; pp. 479–513. [Google Scholar]
- Dias, F.; Santos, M.; Schwan, R. Enumeration, identification and safety proprieties of lactic acid bacteria isolated from pork sausage. Arq. Bras. De Med. Veterinária E Zootec. 2015, 67, 918–926. [Google Scholar] [CrossRef] [Green Version]
- Laranjo, M.; Elias, M.; Fraqueza, M.J. The use of starter cultures in traditional meat products. J. Food Qual. 2017, 2017, 9546026. [Google Scholar] [CrossRef] [Green Version]
- Lücke, F.-K. Quality Improvement and Fermentation Control in Meat Products. In Advances in Fermented Foods and Beverages; Elsevier: Amsterdam, The Netherlands, 2015; pp. 357–376. [Google Scholar]
- Salampessy, J.; Kailasapathy, K.; Thapa, N. Fermented fish products. In Fermented Foods Beverages World; CRC Press: Boca Raton, FL, USA, 2010; pp. 289–307. [Google Scholar]
- Jayachandran, M.; Xu, B. An insight into the health benefits of fermented soy products. Food Chem. 2019, 271, 362–371. [Google Scholar] [CrossRef]
- Cao, Z.-H.; Green-Johnson, J.M.; Buckley, N.D.; Lin, Q.-Y. Bioactivity of soy-based fermented foods: A review. Biotechnol. Adv. 2019, 37, 223–238. [Google Scholar] [CrossRef] [PubMed]
- Nout, M.R.; Kiers, J. Tempe fermentation, innovation and functionality: Update into the third millenium. J. Appl. Microbiol. 2005, 98, 789–805. [Google Scholar] [CrossRef]
- Kuligowski, M.; Jasińska-Kuligowska, I.; Nowak, J. Evaluation of bean and soy tempeh influence on intestinal bacteria and estimation of antibacterial properties of bean tempeh. Pol. J. Microbiol. 2013, 62, 189. [Google Scholar] [CrossRef]
- Abu-Salem, F.M.; Mohamed, R.; Gibriel, A.; Rasmy, N.M. Levels of some antinutritional factors in tempeh produced from some legumes and jojobas seeds. Int. Sch. Sci. Res. Innov 2014, 8, 296–301. [Google Scholar]
- Onda, T.; Yanagida, F.; Tsuji, M.; Shinohara, T.; Yokotsuka, K. Production and purification of a bacteriocin peptide produced by Lactococcus sp. strain GM005, isolated from Miso-paste. Int. J. Food Microbiol. 2003, 87, 153–159. [Google Scholar] [CrossRef] [PubMed]
- Onda, T.; Yanagida, F.; Uchimura, T.; Tsuji, M.; Ogino, S.; Shinohara, T.; Yokotsuka, K. Widespread distribution of the bacteriocin-producing lactic acid cocci in Miso-paste products. J. Appl. Microbiol. 2002, 92, 695–705. [Google Scholar] [CrossRef] [PubMed]
- Fujita, M.; Nomura, K.; Hong, K.; Ito, Y.; Asada, A.; Nishimuro, S. Purification and characterization of a strong fibrinolytic enzyme (nattokinase) in the vegetable cheese natto, a popular soybean fermented food in Japan. Biochem. Biophys. Res. Commun. 1993, 197, 1340–1347. [Google Scholar] [CrossRef]
- Kada, S.; Yabusaki, M.; Kaga, T.; Ashida, H.; Yoshida, K.-I. Identification of Two Major Ammonia-Releasing Reactions Involved in Secondary Natto Fermentation. Biosci. Biotechnol. Biochem. 2008, 72, 1869–1876. [Google Scholar] [CrossRef]
- Lanza, B.; Cellini, M.; Di Marco, S.; D’Amico, E.; Simone, N.; Giansante, L.; Pompilio, A.; Di Loreto, G.; Bacceli, M.; Del Re, P. Olive pâté by multi-phase decanter as potential source of bioactive compounds of both nutraceutical and anticancer effects. Molecules 2020, 25, 5967. [Google Scholar] [CrossRef]
- Swain, M.R.; Anandharaj, M.; Ray, R.C.; Rani, R.P. Fermented fruits and vegetables of Asia: A potential source of probiotics. Biotechnol. Res. Int. 2014, 2014, 250424. [Google Scholar] [CrossRef]
- Ehrmann, M.; Ludwig, W.; Schleifer, K. Reverse dot blot hybridization: A useful method for the direct identification of lactic acid bacteria in fermented food. FEMS Microbiol. Lett. 1994, 117, 143–149. [Google Scholar] [CrossRef]
- Nielsen, E.S.; Garnås, E.; Jensen, K.J.; Hansen, L.H.; Olsen, P.S.; Ritz, C.; Krych, L.; Nielsen, D.S. Lacto-fermented sauerkraut improves symptoms in IBS patients independent of product pasteurisation—A pilot study. Food Funct. 2018, 9, 5323–5335. [Google Scholar] [CrossRef]
- Bati, V.; Boyko, N.; Uzhhorod National University. The Microbial Diversity and Its Dynamics in the Ethnic Fermented Foods of the Black Sea Region. Mikrobiolohichnyi Zhurnal 2016, 78, 53–64. [Google Scholar] [CrossRef] [Green Version]
- Yu, Z.; Zhang, X.; Li, S.; Li, C.; Li, D.; Yang, Z. Evaluation of probiotic properties of Lactobacillus plantarum strains isolated from Chinese sauerkraut. World J. Microbiol. Biotechnol. 2013, 29, 489–498. [Google Scholar] [CrossRef]
- Ge, J.; Ping, W.; Song, G.; Du, C.; Ling, H.; Sun, X.; Gao, Y. Paracin 1.7, a bacteriocin produced by Lactobacillus paracasei HD1. 7 isolated from Chinese cabbage sauerkraut, a traditional Chinese fermented vegetable food. Wei Sheng Wu Xue Bao = Acta Microbiol. Sin. 2009, 49, 609–616. [Google Scholar]
- Patra, J.K.; Das, G.; Paramithiotis, S.; Shin, H.-S. Kimchi and other widely consumed traditional fermented foods of Korea: A review. Front. Microbiol. 2016, 7, 1493. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Jeong, S.H.; Jung, J.Y.; Lee, S.H.; Jin, H.M.; Jeon, C.O. Microbial succession and metabolite changes during fermentation of dongchimi, traditional Korean watery kimchi. Int. J. Food Microbiol. 2013, 164, 46–53. [Google Scholar] [CrossRef] [PubMed]
- Cho, N.-C.; Jhon, D.-Y.; Shin, M.-S.; Hong, Y.-H.; Lim, H.-S. Effect of garlic concentrations on growth of microorganisms during kimchi fermentation. Korean J. Food Sci. Technol. 1988, 20, 231–235. [Google Scholar]
- Jeong, S.H.; Lee, H.J.; Jung, J.Y.; Lee, S.H.; Seo, H.-Y.; Park, W.-S.; Jeon, C.O. Effects of red pepper powder on microbial communities and metabolites during kimchi fermentation. Int. J. Food Microbiol. 2013, 160, 252–259. [Google Scholar] [CrossRef]
- Chang, H.-W.; Kim, K.-H.; Nam, Y.-D.; Roh, S.W.; Kim, M.-S.; Jeon, C.O.; Oh, H.-M.; Bae, J.-W. Analysis of yeast and archaeal population dynamics in kimchi using denaturing gradient gel electrophoresis. Int. J. Food Microbiol. 2008, 126, 159–166. [Google Scholar] [CrossRef] [PubMed]
- Tamang, J.P.; Watanabe, K.; Holzapfel, W.H. Diversity of microorganisms in global fermented foods and beverages. Front. Microbiol. 2016, 7, 377. [Google Scholar] [CrossRef] [Green Version]
- Hutkins, R.W. Microbiology and Technology of Fermented Foods; John Wiley & Sons: Hoboken, NJ, USA, 2008. [Google Scholar]
- Gänzle, M.G. Enzymatic and bacterial conversions during sourdough fermentation. Food Microbiol. 2014, 37, 2–10. [Google Scholar] [CrossRef]
- Woo, H.D.; Park, S.; Oh, K.; Kim, H.J.; Shin, H.R.; Moon, H.K.; Kim, J. Diet and cancer risk in the Korean population: A meta-analysis. Asian Pac. J. Cancer Prev. 2014, 15, 8509–8519. [Google Scholar] [CrossRef] [Green Version]
- Hansen, A.; Schieberle, P. Generation of aroma compounds during sourdough fermentation: Applied and fundamental aspects. Trends Food Sci. Technol. 2005, 16, 85–94. [Google Scholar] [CrossRef]
- De Vuyst, L.; Vancanneyt, M. Biodiversity and identification of sourdough lactic acid bacteria. Food Microbiol. 2007, 24, 120–127. [Google Scholar] [CrossRef]
- Pontonio, E.; Di Cagno, R.; Mahony, J.; Lanera, A.; De Angelis, M.; van Sinderen, D.; Gobbetti, M. Sourdough authentication: Quantitative PCR to detect the lactic acid bacterial microbiota in breads. Sci. Rep. 2017, 7, 624. [Google Scholar] [CrossRef]
- Vīna, I.; Semjonovs, P.; Linde, R.; Deniņa, I. Current evidence on physiological activity and expected health effects of kombucha fermented beverage. J. Med. Food 2014, 17, 179–188. [Google Scholar] [CrossRef] [Green Version]
- Dufresne, C.; Farnworth, E. Tea, Kombucha, and health: A review. Food Res. Int. 2000, 33, 409–421. [Google Scholar] [CrossRef]
- Coton, M.; Pawtowski, A.; Taminiau, B.; Burgaud, G.; Deniel, F.; Coulloumme-Labarthe, L.; Fall, A.; Daube, G.; Coton, E. Unraveling microbial ecology of industrial-scale Kombucha fermentations by metabarcoding and culture-based methods. FEMS Microbiol. Ecol. 2017, 93, fix048. [Google Scholar] [CrossRef]
- Greenwalt, C.; Steinkraus, K.; Ledford, R. Kombucha, the fermented tea: Microbiology, composition, and claimed health effects. J. Food Prot. 2000, 63, 976–981. [Google Scholar] [CrossRef] [PubMed]
- Marsh, A.J.; O’Sullivan, O.; Hill, C.; Ross, R.P.; Cotter, P.D. Sequence-based analysis of the bacterial and fungal compositions of multiple kombucha (tea fungus) samples. Food Microbiol. 2014, 38, 171–178. [Google Scholar] [CrossRef] [PubMed]
- Elegado, F.B.; Colegio, S.M.T.; Lim, V.M.T.; Gervasio, A.T.R.; Perez, M.T.M.; Balolong, M.P.; Banaay, C.G.B.; Mendoza, B.C. Ethnic fermented foods of the Philippines with reference to lactic acid bacteria and yeasts. In Ethnic Fermented Foods and Alcoholic Beverages of Asia; Springer: Berlin/Heidelberg, Germany, 2016; pp. 323–340. [Google Scholar]
- Robinson, R.K. Encyclopedia of Food Microbiology; Academic Press: Cambridge, MA, USA, 2014. [Google Scholar]
- Fardet, A.; Rock, E. In vitro and in vivo antioxidant potential of milks, yoghurts, fermented milks and cheeses: A narrative review of evidence. Nutr. Res. Rev. 2018, 31, 52–70. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Tarfeen, N.; Nisa, Q.; Kahlief, K. Antioxidant Defense System in Plants Against Biotic Stress. In Antioxidant Defense in Plants; Springer: Berlin/Heidelberg, Germany, 2022; pp. 383–395. [Google Scholar]
- Melini, F.; Melini, V.; Luziatelli, F.; Ficca, A.G.; Ruzzi, M. Health-promoting components in fermented foods: An up-to-date systematic review. Nutrients 2019, 11, 1189. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Khan, M.K.; Karnpanit, W.; Nasar-Abbas, S.M.; Huma, Z.E.; Jayasena, V. Development of a fermented product with higher phenolic compounds and lower anti-nutritional factors from germinated lupin (Lupinus angustifolius L.). J. Food Process. Preserv. 2018, 42, e13843. [Google Scholar] [CrossRef]
- Habibi Najafi, M.B.; Fatemizadeh, S.S.; Tavakoli, M. Release of proteolysis products with ACE-inhibitory and antioxidant activities in probiotic yogurt containing different levels of fat and prebiotics. Int. J. Pept. Res. Ther. 2019, 25, 367–377. [Google Scholar] [CrossRef]
- Gholamhosseinpour, A.; Hashemi, S.M.B. Ultrasound pretreatment of fermented milk containing probiotic Lactobacillus plantarum AF1: Carbohydrate metabolism and antioxidant activity. J. Food Process Eng. 2019, 42, e12930. [Google Scholar] [CrossRef] [Green Version]
- Ramesh, V.; Kumar, R.; Singh, R.; Kaushik, J.; Mann, B. Comparative evaluation of selected strains of lactobacilli for the development of antioxidant activity in milk. Dairy Sci. Technol. 2012, 92, 179–188. [Google Scholar] [CrossRef] [Green Version]
- Grażyna, C.; Hanna, C.; Adam, A.; Magdalena, B.M. Natural antioxidants in milk and dairy products. Int. J. Dairy Technol. 2017, 70, 165–178. [Google Scholar] [CrossRef]
- Homayouni Rad, A.; Yari Khosroushahi, A.; Khalili, M.; Jafarzadeh, S. Folate bio-fortification of yoghurt and fermented milk: A review. Dairy Sci. Technol. 2016, 96, 427–441. [Google Scholar] [CrossRef] [Green Version]
- Tidona, F.; Meucci, A.; Povolo, M.; Pelizzola, V.; Zago, M.; Contarini, G.; Carminati, D.; Giraffa, G. Applicability of Lactococcus hircilactis and Lactococcus laudensis as dairy cultures. Int. J. Food Microbiol. 2018, 271, 1–7. [Google Scholar] [CrossRef] [PubMed]
- Kadiri, O. A review on the status of the phenolic compounds and antioxidant capacity of the flour: Effects of cereal processing. Int. J. Food Prop. 2017, 20, S798–S809. [Google Scholar] [CrossRef] [Green Version]
- Lorusso, A.; Verni, M.; Montemurro, M.; Coda, R.; Gobbetti, M.; Rizzello, C.G. Use of fermented quinoa flour for pasta making and evaluation of the technological and nutritional features. LWT 2017, 78, 215–221. [Google Scholar] [CrossRef] [Green Version]
- Peñas, E.; Diana, M.; Frías, J.; Quílez, J.; Martínez-Villaluenga, C. A multistrategic approach in the development of sourdough bread targeted towards blood pressure reduction. Plant Foods Hum. Nutr. 2015, 70, 97–103. [Google Scholar] [CrossRef] [Green Version]
- Jayabalan, R.; Subathradevi, P.; Marimuthu, S.; Sathishkumar, M.; Swaminathan, K. Changes in free-radical scavenging ability of kombucha tea during fermentation. Food Chem. 2008, 109, 227–234. [Google Scholar] [CrossRef] [PubMed]
- Shah, A.M.; Mohamed, H.; Song, Y. Functional Foods: An Alternative Source to Combat Viral Infection, Including COVID-19. In Functional Foods and Viral Diseases, 1st ed.; Food Science Publisher: Chicago, IL, USA, 2020; pp. 253–269. [Google Scholar]
- Devi, K.P.; Malar, D.S.; Nabavi, S.F.; Sureda, A.; Xiao, J.; Nabavi, S.M.; Daglia, M. Kaempferol and inflammation: From chemistry to medicine. Pharmacol. Res. 2015, 99, 1–10. [Google Scholar] [CrossRef] [PubMed]
- Chang, C.T.; Hsu, C.K.; Chou, S.T.; Chen, Y.C.; Huang, F.S.; Chung, Y.C. Effect of fermentation time on the antioxidant activities of tempeh prepared from fermented soybean using Rhizopus oligosporus. Int. J. Food Sci. Technol. 2009, 44, 799–806. [Google Scholar] [CrossRef]
- Yang, X.; Zhou, J.; Fan, L.; Qin, Z.; Chen, Q.; Zhao, L. Antioxidant properties of a vegetable–fruit beverage fermented with two Lactobacillus plantarum strains. Food Sci. Biotechnol. 2018, 27, 1719–1726. [Google Scholar] [CrossRef]
- Kaprasob, R.; Kerdchoechuen, O.; Laohakunjit, N.; Thumthanaruk, B.; Shetty, K. Changes in physico-chemical, astringency, volatile compounds and antioxidant activity of fresh and concentrated cashew apple juice fermented with Lactobacillus plantarum. J. Food Sci. Technol. 2018, 55, 3979–3990. [Google Scholar] [CrossRef] [PubMed]
- Sirilun, S.; Sivamaruthi, B.S.; Kesika, P.; Peerajan, S.; Chaiyasut, C. Lactobacillus paracasei hii01 mediated fermentation of Syzygium cumini l. fruits: Assessment of changes in phenolic content and antioxidant capacity. Asian J. Pharm. Clin. Res 2018, 11, 304–308. [Google Scholar] [CrossRef]
- Bujna, E.; Farkas, N.A.; Tran, A.M.; Dam, M.S.; Nguyen, Q.D. Lactic acid fermentation of apricot juice by mono-and mixed cultures of probiotic Lactobacillus and Bifidobacterium strains. Food Sci. Biotechnol. 2018, 27, 547–554. [Google Scholar] [CrossRef] [PubMed]
- Revuelta, J.L.; Serrano-Amatriain, C.; Ledesma-Amaro, R.; Jiménez, A. Formation of folates by microorganisms: Towards the biotechnological production of this vitamin. Appl. Microbiol. Biotechnol. 2018, 102, 8613–8620. [Google Scholar] [CrossRef] [Green Version]
- Saubade, F.; Hemery, Y.M.; Rochette, I.; Guyot, J.-P.; Humblot, C. Influence of fermentation and other processing steps on the folate content of a traditional African cereal-based fermented food. Int. J. Food Microbiol. 2018, 266, 79–86. [Google Scholar] [CrossRef]
- Fu, X.; Harshman, S.G.; Shen, X.; Haytowitz, D.B.; Karl, J.P.; Wolfe, B.E.; Booth, S.L. Multiple vitamin K forms exist in dairy foods. Curr. Dev. Nutr. 2017, 1, e000638. [Google Scholar] [CrossRef] [Green Version]
- Zironi, E.; Gazzotti, T.; Barbarossa, A.; Farabegoli, F.; Serraino, A.; Pagliuca, G. Determination of vitamin B12 in dairy products by ultra performance liquid chromatography-tandem mass spectrometry. Ital. J. Food Saf. 2014, 3, 4513. [Google Scholar] [CrossRef] [Green Version]
- Signorini, C.; Carpen, A.; Coletto, L.; Borgonovo, G.; Galanti, E.; Capraro, J.; Magni, C.; Abate, A.; Johnson, S.K.; Duranti, M. Enhanced vitamin B12 production in an innovative lupin tempeh is due to synergic effects of Rhizopus and Propionibacterium in cofermentation. Int. J. Food Sci. Nutr. 2018, 69, 451–457. [Google Scholar] [CrossRef]
- Chamlagain, B.; Sugito, T.A.; Deptula, P.; Edelmann, M.; Kariluoto, S.; Varmanen, P.; Piironen, V. In situ production of active vitamin B12 in cereal matrices using Propionibacterium freudenreichii. Food Sci. Nutr. 2018, 6, 67–76. [Google Scholar] [CrossRef]
- Jauhiainen, T.; Korpela, R. Milk peptides and blood pressure. J. Nutr. 2007, 137, 825S–829S. [Google Scholar] [CrossRef] [Green Version]
- Beltrán-Barrientos, L.M.; Hernández-Mendoza, A.; González-Córdova, A.F.; Astiazarán-García, H.; Esparza-Romero, J.; Vallejo-Córdoba, B. Mechanistic pathways underlying the antihypertensive effect of fermented milk with Lactococcus lactis NRRL B-50571 in spontaneously hypertensive rats. Nutrients 2018, 10, 262. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Nejati, F.; Rizzello, C.G.; Di Cagno, R.; Sheikh-Zeinoddin, M.; Diviccaro, A.; Minervini, F.; Gobbetti, M. Manufacture of a functional fermented milk enriched of Angiotensin-I Converting Enzyme (ACE)-inhibitory peptides and γ-amino butyric acid (GABA). LWT-Food Sci. Technol. 2013, 51, 183–189. [Google Scholar] [CrossRef]
- Chen, L.; Alcazar, J.; Yang, T.; Lu, Z.; Lu, Y. Optimized cultural conditions of functional yogurt for γ-aminobutyric acid augmentation using response surface methodology. J. Dairy Sci. 2018, 101, 10685–10693. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Gobbetti, M.; De Angelis, M.; Di Cagno, R.; Calasso, M.; Archetti, G.; Rizzello, C.G. Novel insights on the functional/nutritional features of the sourdough fermentation. Int. J. Food Microbiol. 2019, 302, 103–113. [Google Scholar] [CrossRef]
- Tarfeen, N.; Nisa, K.U.; Ahmad, M.B.; Waza, A.A.; Ganai, B.A. Metabolic and Genetic Association of Vitamin D with Calcium Signaling and Insulin Resistance. Indian J. Clin. Biochem. 2022, 1–11. [Google Scholar] [CrossRef]
- Sivamaruthi, B.S.; Kesika, P.; Prasanth, M.I.; Chaiyasut, C. A mini review on antidiabetic properties of fermented foods. Nutrients 2018, 10, 1973. [Google Scholar] [CrossRef] [Green Version]
- Deng, Y.; Misselwitz, B.; Dai, N.; Fox, M. Lactose intolerance in adults: Biological mechanism and dietary management. Nutrients 2015, 7, 8020–8035. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Perna, A.; Intaglietta, I.; Simonetti, A.; Gambacorta, E. Donkey milk for manufacture of novel functional fermented beverages. J. Food Sci. 2015, 80, S1352–S1359. [Google Scholar] [CrossRef] [PubMed]
- Hertzler, S.R.; Clancy, S.M. Kefir improves lactose digestion and tolerance in adults with lactose maldigestion. J. Am. Diet. Assoc. 2003, 103, 582–587. [Google Scholar] [CrossRef] [PubMed]
- Frias, J.; Martinez-Villaluenga, C.; Peñas, E. Fermented Foods in Health and Disease Prevention; Elsevier: Amsterdam, The Netherlands, 2016. [Google Scholar]
- Bull, M.; Plummer, S.; Marchesi, J.; Mahenthiralingam, E. The life history of Lactobacillus acidophilus as a probiotic: A tale of revisionary taxonomy, misidentification and commercial success. FEMS Microbiol. Lett. 2013, 349, 77–87. [Google Scholar] [CrossRef] [Green Version]
- Champagne, C.P.; Raymond, Y.; Guertin, N.; Martoni, C.J.; Jones, M.L. Growth of Lactobacillus reuteri NCIMB 30242 during yogurt fermentation and bile salt hydrolysis activity in the product. Dairy Sci. Technol. 2016, 96, 173–184. [Google Scholar] [CrossRef]
- Mustafa, S.M.; Chua, L.S.; El-Enshasy, H.A.; Abd Majid, F.A.; Hanapi, S.Z.; Abdul Malik, R. Effect of temperature and pH on the probiotication of Punica granatum juice using Lactobacillus species. J. Food Biochem. 2019, 43, e12805. [Google Scholar] [CrossRef]
- Peres, C.M.; Peres, C.; Hernández-Mendoza, A.; Malcata, F.X. Review on fermented plant materials as carriers and sources of potentially probiotic lactic acid bacteria–with an emphasis on table olives. Trends Food Sci. Technol. 2012, 26, 31–42. [Google Scholar] [CrossRef]
- Wagner, R.D.; Warner, T.; Roberts, L.; Farmer, J.; Balish, E. Colonization of congenitally immunodeficient mice with probiotic bacteria. Infect. Immun. 1997, 65, 3345–3351. [Google Scholar] [CrossRef] [Green Version]
- Goldin, B.R.; Gualtieri, L.J.; Moore, R.P. The effect of Lactobacillus GG on the initiation and promotion of DMH-induced intestinal tumors in the rat. Nutr. Cancer 1996, 25, 197–204. [Google Scholar] [CrossRef]
- Surono, I.S.; Koestomo, F.P.; Novitasari, N.; Zakaria, F.R. Novel probiotic Enterococcus faecium IS-27526 supplementation increased total salivary sIgA level and bodyweight of pre-school children: A pilot study. Anaerobe 2011, 17, 496–500. [Google Scholar] [CrossRef]
- Surono, I.S.; Martono, P.D.; Kameo, S.; Suradji, E.W.; Koyama, H. Effect of probiotic L. plantarum IS-10506 and zinc supplementation on humoral immune response and zinc status of Indonesian pre-school children. J. Trace Elem. Med. Biol. 2014, 28, 465–469. [Google Scholar] [CrossRef] [PubMed]
- Çabuk, B.; Nosworthy, M.G.; Stone, A.K.; Korber, D.R.; Tanaka, T.; House, J.D.; Nickerson, M.T. Utjecaj fermentacije na probavljivost proteina i udjel nenutritivnih sastojaka u koncentratu proteina graška. Food Technol. Biotechnol. 2018, 56, 257–264. [Google Scholar]
- Lim, S.-M. Microbiological, physicochemical, and antioxidant properties of plain yogurt and soy yogurt. Korean J. Microbiol. 2013, 49, 403–414. [Google Scholar] [CrossRef] [Green Version]
- Tavakoli, M.; Najafi, M.B.H.; Mohebbi, M. Effect of the milk fat content and starter culture selection on proteolysis and antioxidant activity of probiotic yogurt. Heliyon 2019, 5, e01204. [Google Scholar] [CrossRef] [Green Version]
- Qian, B.; Xing, M.; Cui, L.; Deng, Y.; Xu, Y.; Huang, M.; Zhang, S. Antioxidant, antihypertensive, and immunomodulatory activities of peptide fractions from fermented skim milk with Lactobacillus delbrueckii ssp. bulgaricus LB340. J. Dairy Res. 2011, 78, 72–79. [Google Scholar] [CrossRef]
- Widodo, K.; Sukarno, A.; Estancia, K.; Widianto, D. Conjugated Linoleic Acid Synthesis in Milk Fermented with Lactobacillus casei strain AG. Pak. J. Nutr 2018, 17, 524–529. [Google Scholar]
- Solieri, L.; Rutella, G.S.; Tagliazucchi, D. Impact of non-starter lactobacilli on release of peptides with angiotensin-converting enzyme inhibitory and antioxidant activities during bovine milk fermentation. Food Microbiol. 2015, 51, 108–116. [Google Scholar] [CrossRef] [Green Version]
- Rocchetti, G.; Miragoli, F.; Zacconi, C.; Lucini, L.; Rebecchi, A. Impact of cooking and fermentation by lactic acid bacteria on phenolic profile of quinoa and buckwheat seeds. Food Res. Int. 2019, 119, 886–894. [Google Scholar] [CrossRef]
- Đorđević, T.M.; Šiler-Marinković, S.S.; Dimitrijević-Branković, S.I. Effect of fermentation on antioxidant properties of some cereals and pseudo cereals. Food Chem. 2010, 119, 957–963. [Google Scholar] [CrossRef]
- Amaya Villalva, M.F.; González-Aguilar, G.; Sández, O.R.; Astiazarán García, H.; Ledesma Osuna, A.I.; López-Ahumada, G.A.; Robles-Sánchez, R.M. Bioprocessing of wheat (Triticum aestivum cv. Kronstad) bran from Northwest Mexico: Effects on ferulic acid bioaccessibility in breads. CyTA-J. Food 2018, 16, 570–579. [Google Scholar] [CrossRef] [Green Version]
- Ryan, E.P.; Heuberger, A.L.; Weir, T.L.; Barnett, B.; Broeckling, C.D.; Prenni, J.E. Rice bran fermented with Saccharomyces boulardii generates novel metabolite profiles with bioactivity. J. Agric. Food Chem. 2011, 59, 1862–1870. [Google Scholar] [CrossRef] [PubMed]
- Nur, Y.; Dang, L.; Anisah, J.; Shaiful, A.S.; Long, K. Bioactive compounds and antioxidant activity of rice bran fermented with lactic acid bacteria. Malays. J. Microbiol. 2015, 11, 156–162. [Google Scholar]
- Mantzourani, I.; Terpou, A.; Alexopoulos, A.; Kimbaris, A.; Bezirtzoglou, E.; Koutinas, A.A.; Plessas, S. Production of a potentially synbiotic pomegranate beverage by fermentation with Lactobacillus plantarum ATCC 14917 adsorbed on a prebiotic carrier. Appl. Biochem. Biotechnol. 2019, 188, 1096–1107. [Google Scholar] [CrossRef]
- Bah, A.; Ferjani, R.; Fhoula, I.; Gharbi, Y.; Najjari, A.; Boudabous, A.; Ouzari, H.I. Microbial community dynamic in tomato fruit during spontaneous fermentation and biotechnological characterization of indigenous lactic acid bacteria. Ann. Microbiol. 2019, 69, 41–49. [Google Scholar] [CrossRef]
- Cusano, E.; Simonato, B.; Consonni, R. Fermentation process of apple juice investigated by NMR spectroscopy. LWT 2018, 96, 147–151. [Google Scholar] [CrossRef]
- Wiczkowski, W.; Szawara-Nowak, D.; Romaszko, J. The impact of red cabbage fermentation on bioavailability of anthocyanins and antioxidant capacity of human plasma. Food Chem. 2016, 190, 730–740. [Google Scholar] [CrossRef]
- Beltrán-Barrientos, L.M.; González-Córdova, A.F.; Hernández-Mendoza, A.; Torres-Inguanzo, E.H.; Astiazarán-García, H.; Esparza-Romero, J.; Vallejo-Cordoba, B. Randomized double-blind controlled clinical trial of the blood pressure–lowering effect of fermented milk with Lactococcus lactis: A pilot study. J. Dairy Sci. 2018, 101, 2819–2825. [Google Scholar] [CrossRef] [Green Version]
- Tarvainen, M.; Fabritius, M.; Yang, B. Determination of vitamin K composition of fermented food. Food Chem. 2019, 275, 515–522. [Google Scholar] [CrossRef]
- Lorusso, A.; Coda, R.; Montemurro, M.; Rizzello, C.G. Use of selected lactic acid bacteria and quinoa flour for manufacturing novel yogurt-like beverages. Foods 2018, 7, 51. [Google Scholar] [CrossRef] [Green Version]
- Angelov, A.; Yaneva-Marinova, T.; Gotcheva, V. Oats as a matrix of choice for developing fermented functional beverages. J. Food Sci. Technol. 2018, 55, 2351–2360. [Google Scholar] [CrossRef]
- Taylor, B.C.; Lejzerowicz, F.; Poirel, M.; Shaffer, J.P.; Jiang, L.; Aksenov, A.; Litwin, N.; Humphrey, G.; Martino, C.; Miller-Montgomery, S. Consumption of fermented foods is associated with systematic differences in the gut microbiome and metabolome. Msystems 2020, 5, e00901–e00919. [Google Scholar] [CrossRef] [Green Version]
- Veiga, P.; Pons, N.; Agrawal, A.; Oozeer, R.; Guyonnet, D.; Brazeilles, R.; Faurie, J.-M.; van Hylckama Vlieg, J.E.; Houghton, L.A.; Whorwell, P.J. Changes of the human gut microbiome induced by a fermented milk product. Sci. Rep. 2014, 4, 6328. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Unno, T.; Choi, J.-H.; Hur, H.-G.; Sadowsky, M.J.; Ahn, Y.-T.; Huh, C.-S.; Kim, G.-B.; Cha, C.-J. Changes in human gut microbiota influenced by probiotic fermented milk ingestion. J. Dairy Sci. 2015, 98, 3568–3576. [Google Scholar] [CrossRef] [Green Version]
- Yılmaz, İ.; Dolar, M.E.; Özpınar, H. Effect of administering kefir on the changes in fecal microbiota and symptoms of inflammatory bowel disease: A randomized controlled trial. Turk. J. Gastroenterol. 2019, 30, 242. [Google Scholar] [CrossRef] [PubMed]
- Lisko, D.J.; Johnston, G.P.; Johnston, C.G. Effects of dietary yogurt on the healthy human gastrointestinal (GI) microbiome. Microorganisms 2017, 5, 6. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Han, K.; Bose, S.; Wang, J.h.; Kim, B.S.; Kim, M.J.; Kim, E.J.; Kim, H. Contrasting effects of fresh and fermented kimchi consumption on gut microbiota composition and gene expression related to metabolic syndrome in obese Korean women. Mol. Nutr. Food Res. 2015, 59, 1004–1008. [Google Scholar] [CrossRef]
- Inoguchi, S.; Ohashi, Y.; Narai-Kanayama, A.; Aso, K.; Nakagaki, T.; Fujisawa, T. Effects of non-fermented and fermented soybean milk intake on faecal microbiota and faecal metabolites in humans. Int. J. Food Sci. Nutr. 2012, 63, 402–410. [Google Scholar] [CrossRef] [PubMed]
- Cheng, I.-C.; Shang, H.-F.; Lin, T.-F.; Wang, T.-H.; Lin, H.-S.; Lin, S.-H. Effect of fermented soy milk on the intestinal bacterial ecosystem. World J. Gastroenterol. WJG 2005, 11, 1225. [Google Scholar] [CrossRef]
- Lan, A.; Bruneau, A.; Philippe, C.; Rochet, V.; Rouault, A.; Hervé, C.; Roland, N.; Rabot, S.; Jan, G. Survival and metabolic activity of selected strains of Propionibacterium freudenreichii in the gastrointestinal tract of human microbiota-associated rats. Br. J. Nutr. 2007, 97, 714–724. [Google Scholar] [CrossRef] [Green Version]
- Zhang, Y.-J.; Li, S.; Gan, R.-Y.; Zhou, T.; Xu, D.-P.; Li, H.-B. Impacts of gut bacteria on human health and diseases. Int. J. Mol. Sci. 2015, 16, 7493–7519. [Google Scholar] [CrossRef]
- Gan, R.Y.; Shah, N.P.; Wang, M.F.; Lui, W.Y.; Corke, H. Fermentation alters antioxidant capacity and polyphenol distribution in selected edible legumes. Int. J. Food Sci. Technol. 2016, 51, 875–884. [Google Scholar] [CrossRef]
- Zhai, F.-H.; Liu, H.-Y.; Han, J.-R. Protein nutritional value, polyphenols and antioxidant properties of corn fermented with Agaricus brasiliensis and Agaricus bisporus. World J. Microbiol. Biotechnol. 2018, 34, 36. [Google Scholar] [CrossRef] [PubMed]
- Yadav, S.; Khetarpaul, N. Indigenous legume fermentation: Effect on some antinutrients and in-vitro digestibility of starch and protein. Food Chem. 1994, 50, 403–406. [Google Scholar] [CrossRef]
- Wu, T.; Chu, X.; Cheng, Y.; Tang, S.; Zogona, D.; Pan, S.; Xu, X. Modulation of gut microbiota by lactobacillus casei fermented raspberry juice in vitro and in vivo. Foods 2021, 10, 3055. [Google Scholar] [CrossRef] [PubMed]
- Duda-Chodak, A.; Tarko, T.; Satora, P.; Sroka, P. Interaction of dietary compounds, especially polyphenols, with the intestinal microbiota: A review. Eur. J. Nutr. 2015, 54, 325–341. [Google Scholar] [CrossRef] [Green Version]
- Zhou, F.; Li, Y.-L.; Zhang, X.; Wang, K.-B.; Huang, J.-A.; Liu, Z.-H.; Zhu, M.-Z. Polyphenols from Fu Brick tea reduce obesity via modulation of gut microbiota and gut microbiota-related intestinal oxidative stress and barrier function. J. Agric. Food Chem. 2021, 69, 14530–14543. [Google Scholar] [CrossRef]
- Lee, H.C.; Jenner, A.M.; Low, C.S.; Lee, Y.K. Effect of tea phenolics and their aromatic fecal bacterial metabolites on intestinal microbiota. Res. Microbiol. 2006, 157, 876–884. [Google Scholar] [CrossRef] [PubMed]
- Hervert-Hernández, D.; Pintado, C.; Rotger, R.; Goñi, I. Stimulatory role of grape pomace polyphenols on Lactobacillus acidophilus growth. Int. J. Food Microbiol. 2009, 136, 119–122. [Google Scholar] [CrossRef]
- Nash, V.; Ranadheera, C.S.; Georgousopoulou, E.N.; Mellor, D.D.; Panagiotakos, D.B.; McKune, A.J.; Kellett, J.; Naumovski, N. The effects of grape and red wine polyphenols on gut microbiota–A systematic review. Food Res. Int. 2018, 113, 277–287. [Google Scholar] [CrossRef]
- Hervert-Hernández, D.; Goñi, I. Dietary polyphenols and human gut microbiota: A review. Food Rev. Int. 2011, 27, 154–169. [Google Scholar] [CrossRef]
- Champ, C.E.; Kundu-Champ, A. Maximizing polyphenol content to uncork the relationship between wine and cancer. Front. Nutr. 2019, 6, 44. [Google Scholar] [CrossRef] [Green Version]
- Leeuwendaal, N.K.; Stanton, C.; O’Toole, P.W.; Beresford, T.P. Fermented Foods, Health and the Gut Microbiome. Nutrients 2022, 14, 1527. [Google Scholar] [CrossRef] [PubMed]
- Queipo-Ortuño, M.I.; Boto-Ordóñez, M.; Murri, M.; Gomez-Zumaquero, J.M.; Clemente-Postigo, M.; Estruch, R.; Cardona Diaz, F.; Andres-Lacueva, C.; Tinahones, F.J. Influence of red wine polyphenols and ethanol on the gut microbiota ecology and biochemical biomarkers. Am. J. Clin. Nutr. 2012, 95, 1323–1334. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Barroso, E.; Muñoz-González, I.; Jimenez, E.; Bartolome, B.; Moreno-Arribas, M.V.; Pelaez, C.; del Carmen Martínez-Cuesta, M.; Requena, T. Phylogenetic profile of gut microbiota in healthy adults after moderate intake of red wine. Mol. Nutr. Food Res. 2017, 61, 1600620. [Google Scholar] [CrossRef]
- Clemente-Postigo, M.; Queipo-Ortuno, M.I.; Boto-Ordonez, M.; Coin-Aragüez, L.; Roca-Rodriguez, M.d.M.; Delgado-Lista, J.; Cardona, F.; Andres-Lacueva, C.; Tinahones, F.J. Effect of acute and chronic red wine consumption on lipopolysaccharide concentrations. Am. Clin. Nutr. 2013, 97, 1053–1061. [Google Scholar] [CrossRef] [Green Version]
- Moreno-Indias, I.; Sánchez-Alcoholado, L.; Pérez-Martínez, P.; Andrés-Lacueva, C.; Cardona, F.; Tinahones, F.; Queipo-Ortuño, M.I. Red wine polyphenols modulate fecal microbiota and reduce markers of the metabolic syndrome in obese patients. Food Funct. 2016, 7, 1775–1787. [Google Scholar] [CrossRef] [Green Version]
- Zhao, L.; Zhang, Q.; Ma, W.; Tian, F.; Shen, H.; Zhou, M. A combination of quercetin and resveratrol reduces obesity in high-fat diet-fed rats by modulation of gut microbiota. Food Funct. 2017, 8, 4644–4656. [Google Scholar] [CrossRef] [PubMed]
- Etxeberria, U.; Arias, N.; Boqué, N.; Macarulla, M.; Portillo, M.; Martínez, J.; Milagro, F. Reshaping faecal gut microbiota composition by the intake of trans-resveratrol and quercetin in high-fat sucrose diet-fed rats. J. Nutr. Biochem. 2015, 26, 651–660. [Google Scholar] [CrossRef]
- Korcz, E.; Kerényi, Z.; Varga, L. Dietary fibers, prebiotics, and exopolysaccharides produced by lactic acid bacteria: Potential health benefits with special regard to cholesterol-lowering effects. Food Funct. 2018, 9, 3057–3068. [Google Scholar] [CrossRef]
- Voreades, N.; Kozil, A.; Weir, T.L. Diet and the development of the human intestinal microbiome. Front. Microbiol. 2014, 5, 494. [Google Scholar] [CrossRef] [Green Version]
- De Vadder, F.; Kovatcheva-Datchary, P.; Goncalves, D.; Vinera, J.; Zitoun, C.; Duchampt, A.; Bäckhed, F.; Mithieux, G. Microbiota-generated metabolites promote metabolic benefits via gut-brain neural circuits. Cell 2014, 156, 84–96. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Pessione, E. Lactic acid bacteria contribution to gut microbiota complexity: Lights and shadows. Front. Cell. Infect. Microbiol. 2012, 2, 86. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Marques, F.Z.; Nelson, E.; Chu, P.-Y.; Horlock, D.; Fiedler, A.; Ziemann, M.; Tan, J.K.; Kuruppu, S.; Rajapakse, N.W.; El-Osta, A. High-fiber diet and acetate supplementation change the gut microbiota and prevent the development of hypertension and heart failure in hypertensive mice. Circulation 2017, 135, 964–977. [Google Scholar] [CrossRef] [PubMed]
- Burger-van Paassen, N.; Vincent, A.; Puiman, P.J.; van der Sluis, M.; Bouma, J.; Boehm, G.; Van Goudoever, J.B.; Van Seuningen, I.; Renes, I.B. The regulation of intestinal mucin MUC2 expression by short-chain fatty acids: Implications for epithelial protection. Biochem. J. 2009, 420, 211–219. [Google Scholar] [CrossRef] [Green Version]
- Tassell, M.L.V.; Miller, M.J. Lactobacillus adhesion to mucus. Nutrients 2011, 3, 613–636. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Sicard, J.-F.; Le Bihan, G.; Vogeleer, P.; Jacques, M.; Harel, J. Interactions of intestinal bacteria with components of the intestinal mucus. Front. Cell. Infect. Microbiol. 2017, 7, 387. [Google Scholar] [CrossRef] [Green Version]
- Shimotoyodome, A.; Meguro, S.; Hase, T.; Tokimitsu, I.; Sakata, T. Short chain fatty acids but not lactate or succinate stimulate mucus release in the rat colon. Comp. Biochem. Physiol. Part A Mol. Integr. Physiol. 2000, 125, 525–531. [Google Scholar] [CrossRef]
- Willemsen, L.; Koetsier, M.; Van Deventer, S.; Van Tol, E. Short chain fatty acids stimulate epithelial mucin 2 expression through differential effects on prostaglandin E1 and E2 production by intestinal myofibroblasts. Gut 2003, 52, 1442–1447. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- van Hylckama Vlieg, J.E.; Veiga, P.; Zhang, C.; Derrien, M.; Zhao, L. Impact of microbial transformation of food on health—From fermented foods to fermentation in the gastro-intestinal tract. Curr. Opin. Biotechnol. 2011, 22, 211–219. [Google Scholar] [CrossRef]
- Darzi, J.; Frost, G.S.; Montaser, R.; Yap, J.; Robertson, M.D. Influence of the tolerability of vinegar as an oral source of short-chain fatty acids on appetite control and food intake. Int. J. Obes. 2014, 38, 675–681. [Google Scholar] [CrossRef] [Green Version]
- de la Fuente, M.A.; Fontecha, J.; Juárez, M. Fatty acid composition of the triglyceride and free fatty acid fractions in different cows-, ewes-and goats-milk cheeses. Z. Für Lebensm. -Unters. Und Forsch. 1993, 196, 155–158. [Google Scholar] [CrossRef]
- Collins, Y.F.; McSweeney, P.L.; Wilkinson, M.G. Lipolysis and free fatty acid catabolism in cheese: A review of current knowledge. Int. Dairy J. 2003, 13, 841–866. [Google Scholar] [CrossRef]
- Moslemi, M.; Mazaheri Nezhad Fard, R.; Hosseini, S.; Homayouni-Rad, A.; Mortazavian, A.M. Incorporation of propionibacteria in fermented milks as a probiotic. Crit. Rev. Food Sci. Nutr. 2016, 56, 1290–1312. [Google Scholar] [CrossRef] [PubMed]
Health Promoting Property | Food to Be Fermented | Fermenting Microbes | References |
---|---|---|---|
Antioxidant property | Milk Quinoa and buckwheat Quinoa fermented Wheat germ, barley, rye, and buckwheat Bread supplemented with bioprocessed bran Rice bran Rice bran Bread prepared with wheat Sourdough Cashew-apple-juice Pomegranate juice fermented Syzygium cumini L fruit juice Tomato Apple juice Red cabbage | Lactobacillus acidophilus strain PC16 L. acidophilus Lactobacillus delbrueckii spp. bulgaricus strain LB340 L. casei strain AG Lactobacillus casei strain PRA205 Lactobacillus plantarum strain AF1 Pediococcus pentosaceus Lactobacillus rhamnosus strain PTCC 1637 P. pentosaceus and Lactobacillus paracasei L. plantarum strain T6B10 and Lactobacillus rossiae strain T0B10 L. rhamnosus and S. cerevisiae Yeast, xylanase enzyme and combinationthereof Saccharomyces boulardii Pediococcus acidilactici, L. lactis and Pediococcus pentoseous L. brevis CECT 8183 and a commercial protease L. plantarum L. plantarum strain ATCC 14917 L. paracasei strain HII01 LAB - - | [117] [118] [119] [120] [121] [75] [70] [70] [122] [81] [123] [124] [125] [126] [82] [88] [127] [89] [128] [129] [130] |
Antihypertensive property | Milk Sourdough | Lactococcus lactis strain NRRL B-50571 Streptococcus salivarius subsp. thermophilus strain fmb5 Lactobacillus spp. L. brevis CECT 8183 and protease | [131] [100] [99] [82] |
Vitamin Content | Milk Lupin—tempeh Natto Cereal-based matrices (wheat aleurone, malted barley flour, barley flour) Kimchi Cashew apple juice | LAB and Bifidobacteria species Rhizopus oryzae and Propionibacterium freudenreichii P. freudenreichii strains P. freudenreichii strains 5 probiotic strains (L. acidophilus, L. mesenteroides L. plantarum, L. casei and B. longum) | [91] [95] [132] [96] [132] [88] |
Antidiabetic properties | Fermented quinoa flour | P. freudenreichii strains | [81] |
Reduce lactose intolerance | Milk | L. casei and L. acidophilus | [105] |
Enhancement of protein digestibility- | Kefir | L. rhamnosus SP1, L. plantarum Weissella confusa DSM 20194 | [133] |
Probiotic properties | Milk Oat-based dairy-fermented beverages | Lactobacillus reuteri | [109] [134] |
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Shah, A.M.; Tarfeen, N.; Mohamed, H.; Song, Y. Fermented Foods: Their Health-Promoting Components and Potential Effects on Gut Microbiota. Fermentation 2023, 9, 118. https://doi.org/10.3390/fermentation9020118
Shah AM, Tarfeen N, Mohamed H, Song Y. Fermented Foods: Their Health-Promoting Components and Potential Effects on Gut Microbiota. Fermentation. 2023; 9(2):118. https://doi.org/10.3390/fermentation9020118
Chicago/Turabian StyleShah, Aabid Manzoor, Najeebul Tarfeen, Hassan Mohamed, and Yuanda Song. 2023. "Fermented Foods: Their Health-Promoting Components and Potential Effects on Gut Microbiota" Fermentation 9, no. 2: 118. https://doi.org/10.3390/fermentation9020118
APA StyleShah, A. M., Tarfeen, N., Mohamed, H., & Song, Y. (2023). Fermented Foods: Their Health-Promoting Components and Potential Effects on Gut Microbiota. Fermentation, 9(2), 118. https://doi.org/10.3390/fermentation9020118