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Research Article | Open Access

Fermented soy whey induced changes on intestinal microbiota and metabolic influence in mice

Wei Hana( )Xuhui ZhuangaQian LiubBo SunaHaijiang MiaoaXiaolin Zhangc
Academy of State Administration of Grain, Beijing 100037, China
Beijing Key Laboratory of Bioactive Substances and Functional Foods, Beijing Union University, Beijing 100191, China
COFCO Nutrition and Health Institute, Beijing 102209, China

Peer review under responsibility of KeAi Communications Co., Ltd.

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Abstract

Soy whey (SW) is generated as process waste while preparing soy protein isolates (SPI), and causing severe environmental pollution. Therefore, its value-added utilization is of prime importance for transforming and upgrading traditional industry. This study aims to utilize SW as a substrate for the growth of probiotics and produce a SW based synbiotics. By a series of trials, the effect of the dietary supplementation with this fermented SW (FSW) was analyzed on ICR mice's body weight, metabolites, and intestinal microbiota in 4 weeks. The results showed that, when SW was concentrated 15 times, the count of viable Lactobacillus casei reached 3.4 × 109 CFU/mL by liquid fermentation method, which was the highest viable cell count among all test strains. In this FSW, the protein, amino acid, total dietary fibre, soluble dietary fibre, and oligosaccharide were 2.10%, 1.63%, 0.52%, 0.51% and 0.79%, respectively. Compared to two control group, the total yields of the short chain fatty acids (SCFAs) were significantly improved (75%–125% at average), while the SCFAs structure was also significantly changed (especially acetic acid and butyrate) in the faeces of mice fed FSW. Meanwhile, FSW dietary addition was associated with the diversity and richness of the intestinal microbiota. Obviously, with mice's body weight loss, Firmicutes/Bacteroides ratio reduced accordingly (< 1.21), and the abundance of Akkermansia muciniphila was significantly increased (the maximum amount was about 0.013%). In summary, our results indicated that the dietary supplementation of FSW affected mice's intestinal microbiota and metabolism and improved their health profile.

References

[1]
X.F. Li, Soybean whey proteins-polysaccharide complexation and the selective extraction of proteins, Jiang Nan University. (2016) (In Chinese)
[2]

W. Liu, H.X. Zhang, Z.L. Wu, et al., Recovery of isoflavone aglycones from soy whey waste water using foam fractionation and acidic hydrolysis, J. Agr. Food Chem. 61(30) (2013) 7366-7372. https://doi.org/10.1021/jf401693m.

[3]

A.N. Roopashri, M.C. Varadaraj, Soy whey based medium for optimized phytase activity in Saccharomyces cerevisiae MTCC 5421 and α-D-galactosidase and antibacterial activities in Lactobacillus plantarum MTCC 5422 by response surface methodology, J. Food Sci. Tech. 51(3) (2014) 519-526. https://doi.org/10.1007/s13197-011-0527-5.

[4]

A. Singh, R. Banerjee, Peptide enriched functional food adjunct from soy whey: a statistical optimization study, Food Sci. Biotech. 22 (2013) 65-71. https://doi.org/10.1007/s10068-013-0050-8.

[5]

D. Mitra, A.L. Pometto, S.K. Khanal, et al., Value-added production of nisin from soy whey, Appl. Biochem. Biotech. 162 (2010) 1819-1833. https://doi.org/10.1007/s12010-010-8951-y.

[6]
Food and Agricultural Organization of the United Nations/World Health Organization (FAO/WHO), Guidelines for the evaluation of probiotics in food. Food and health agricultural organization of the United Nations-World health organization working group report. (2002) http://www.indiaenvironmentportal.org.in/files/PROBIOTICS_GUIDELINES.pdf.
[7]

C. Hill, F. Guarner, G. Reid, et al., The international scientific association for probiotics and prebiotics consensus statement on the scope and appropriate use of the term probiotic, Nat. Rev. Gastro. Herpet. 11 (2014) 506-514. https://doi.org/10.1038/nrgastro.2014.66.

[8]

G.R. Gibson, R. Hutkins, M.E. Sanders, et al., The international scientific association for probiotics and prebiotics (ISAPP) consensus statement on the definition and scope of prebiotics, Nat. Rev. Gastro. Herpet. 14 (2017) 491-502. https://doi.org/10.1038/nrgastro.2014.66.

[9]

J.J. Mosher, E.L. Bernberg, O. Shevchenko, et al., Efficacy of a 3rd generation high-throughput sequencing platform for analyses of 16S rRNA genes from environmental samples, J. Microbiol. Meth. 95 (2013) 175-181. https://doi.org/10.1016/j.mimet.2013.08.009.

[10]

W. Han, X.L. Zhang, D.W. Wang, et al., Effects of microencapsulated Enterococcus fecalis CG1.0007 on growth performance, antioxidation activity, and intestinal microbiota in broiler chickens, J. Anim. Sci. 91(9) (2013) 4374-4382. https://doi.org/10.2527/jas.2012-5956.

[11]
GB 5009.5–2010. National food safety standard-Determination of protein in food. (Chinese national standard)
[12]
GB/T 5009.124–2003. Determination of amino acids in foods. (Chinese national standard)
[13]
GB 5009.88–2014. National food safety standard-Determination of dietary fibers in foods. (Chinese national standard)
[14]
GB/T 22491–2008. Soybean oligosaccharide. (Chinese national standard)
[15]

H. Lee, G. Ko, Effect of metformin on metabolic improvement and gut microbiota, Appl. Environ. Microbiol. 80(19) (2014) 5935-5943. https://doi.org/10.1128/AEM.01357-14.

[16]

N.R. Shin, J.C. Lee, H.Y. Lee, et al., An increase in the Akkermansia spp. population induced by metformin treatment improves glucose homeostasis in diet-induced obese mice, Gut 63 (2014) 727-735. http://dx.doi.org/10.1136/gutjnl-2012-303839.

[17]

E. Zubaidah, M. Nurcholis, S.N. Wulan, Comparative study on synbiotic effect of fermented rice bran by probiotic lactic acid bacteria Lactobacillus casei and newly isolated Lactobacillus plantarum B2 in wistar rats, APCBEE Procedia 2 (2012) 170-177. https://doi.org/10.1016/j.apcbee.2012.06.031.

[18]

K.R. Amato, C.J. Yeoman, A. Kent, et al., Habitat degradation impacts black howler monkey (Alouattapigra) gastrointestinal microbiomes, ISME J. 16 (2013) 1344-1353. https://doi.org/10.1038/ismej.2013.16.

[19]

D.E. Fouts, S. Szpakowski, J. Purushe, et al., Next generation sequencing to define prokaryotic and fungal diversity in the bovine rumen, PLoS One 7(11) (2012) e48289. https://doi.org/10.1371/journal.pone.0048289.

[20]

E. Jami, A. Israel, A. Kotser, et al., Exploring the bovine rumen bacterial community from birth to adulthood. ISME J. 7(6) (2013) 1069-1079. https://doi.org/10.1038/ismej.2013.2.

[21]

O. Lisa, Z. Christin, L. Stefan, et al., The ignored diversity: complex bacterial communities in intensive care units revealed by 16S pyrosequencing, Sci. Rep. 3 (2013) 1413. https://doi.org/10.1038/srep01413.

[22]

S.T. Bates, J.C. Clemente, G.E. Flores, et al., Global biogeography of highly diverse protistan communities in soil, ISME J. 7 (2013) 652-659. https://doi.org/10.1038/ismej.2012.147.

[23]

S. Srinivasan, N.G. Hoffman, M.T. Morgan, et al., Bacterial communities in women with bacterial vaginosis: high resolution phylogenetic analyses reveal relationships of microbiota to clinical criteria, PLoS One 7(6) (2012) e37818. https://doi.org/10.1371/journal.pone.0037818.

[24]

J.Y. Chua, S.Q. Liu, Soy whey: more than just wastewater from tofu and soy protein isolate industry, Trends Food Sci. Tech. 91 (2019) 24-32. https://doi.org/10.1016/j.tifs.2019.06.016.

[25]

M.J. Barratt, C. Lebrilla, H.Y. Shapiro, et al., The gut microbiota, food science, and human nutrition: a timely marriage, Cell Host & Microbe. 22 (2017) 134-141. https://dx.doi.org/10.1016/j.chom.2017.07.006.

[26]

Y. Belkaid, T.W. Hand, Role of the microbiota in immunity and inflammation, Cell 157 (2014) 121-141. https://doi.org/10.1016/j.cell.2014.03.011.

[27]

J.R. Brestoff, D. Artis, Commensal bacteria at the interface of host metabolism and the immune system, Nat. Immunol. 14 (2013) 676-684. https://doi.org/10.1038/ni.2640.

[28]

R. Jumpertz, D.S. Le, P.J. Turnbaugh, et al., Energy-balance studies reveal associations between gut microbes, caloric load and nutrient absorption in humans, Am. J. Clini. Nutri. 94 (2011) 58-65. https://doi.org/10.3945/ajcn.110010132.

[29]

P.J. Turnbaugh, R.E. Ley, M.A. Mahowald, et al., An obesity-associated gut microbiome with increased capacity for energy harvest, Nature 444 (2006) 1027-1031. https://doi.org/10.1038/nature05414.

[30]

R.E. Ley, P.J. Turnbaugh, S. Klein, et al., Microbial ecology: human gut microbes associated with obesity, Nature 444 (2006) 1022-1023. https://doi.org/10.1038/4441022a.

[31]

A. Everard, C. Belzer, Geurts L, et al., Cross-talk between Akkermansia muciniphila and intestinal epithelium controls diet-induced obesity, PNAS 110(22) (2013) 9066-9071. https://doi.org/10.1073/pnas.1219451110.

[32]

C.H.F. Hansen, L. Krych, D.S. Nielsen, et al., Early life treatment with vancomycin propagates Akkermansia muciniphila and reduces diabetes incidence in the NOD mouse, Diabetologia 55 (2012) 2285-2294. https://doi.org/10.1007/s00125-012-2564-7.

[33]

C.L.J. Karlsson, J. Önnerfält, J. Xu, et al., The microbiota of the gut in preschool children with normal and excessive body weight, Pediatr. Obes. 11 (2012) 2257-2261. https://doi.org/10.1038/oby.2012.110.

[34]

A.M. Neyrinck, U. Etxeberria, B. Taminiau, et al., Rhubarb extract prevents hepatic inflammation induced by acute alcohol intake, an effect related to the modulation of the gut microbiota, Mol. Nutr. Food Res. 61(1) (2017) 1500899. https://doi.org/10.1002/mnfr.201500899.

[35]

S.S. Sereqin, N. Golovchenko, B. Schaf, et al., NLRP6 protects Il10–/– mice from colitis by limiting colonization of Akkermansia muciniphila, Cell Rep. 19 (2017) 733-745. https://doi.org/10.1016/j.celrep.2017.03.080.

[36]

L.V. Wang, C.T. Christophersen, M.J. Sorich, et al., Low relative abundances of the mucolytic bacterium Akkermansia muciniphila and Bifidobacterium spp. in faces of children with autism, Appl. Environ. Microbiol. 77(18) (2011) 6718-6721. https://doi.org/10.1128/AEM.05212-11.

[37]
J.X. Ye, Intestinal bacteria associated with colitis and inflammatory bowel disease, University of California riverside. (2009)
[38]

A. Everard, C. Belzerm, L. Geurtsm, et al., Akkermansia muciniphila communique avec l' épithélium intestinal pour contrôler le développement de l'obésitéet du diabète de type 2, Diabetes Metab. 39 (2013) A1-A20. https://doi.org/10.1016/S1262-3636(13)71692-6.

[39]

P.P. Ti, J.M. Wang, X.Y. Pang, et al., Effects of Lactobacillus casei SY13 and its symbiotic on the abundance of Akkermansia muciniphila in mice intestine tract, Sci. Tech. Food Ind. 39(10) (2018) 308-314. (In Chinese)

[40]

Y. Zhao, Wu J, J.V. Li, et al., Gut microbiota composition modifies fecal metabolic profiles in mice, J. Proteome. Res. 12(6) (2013) 2987-2999. https://doi.org/10.1021/pr400263n.

[41]

E.E. Canfora, J.W. Jocken, E.E. Blaak, Short-chain fatty acids in control of body weight and insulin sensitivity, Nat. Rev. Endocrinol. 11(10) (2015) 577-591. https://doi.org/10.1038/nrendo.2015.128.

[42]
S. Karppinen, Dietary fiber component of rye bran and the fermentation in vitro, Biotech Faculty of Science University of Helsinki. (2003)
Food Science and Human Wellness
Pages 41-48
Cite this article:
Han W, Zhuang X, Liu Q, et al. Fermented soy whey induced changes on intestinal microbiota and metabolic influence in mice. Food Science and Human Wellness, 2022, 11(1): 41-48. https://doi.org/10.1016/j.fshw.2021.07.005

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Received: 25 December 2019
Revised: 02 August 2020
Accepted: 03 August 2020
Published: 11 September 2021
© 2021 Beijing Academy of Food Sciences. Publishing services by Elsevier B.V. on behalf of KeAi Communications Co., Ltd.

This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

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