Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/54158
Title: Selection of Bacillus spp. for isoflavone aglycones enriched Thua-nao, a traditional Thai fermented soybean
Authors: Rewat Phongphisutthinant
Pairote Wiriyacharee
Sakda Preunglampoo
Posri Leelapat
Pattama Kanjanakeereetumrong
Saisamorn Lamyong
Keywords: Biochemistry, Genetics and Molecular Biology
Immunology and Microbiology
Issue Date: 1-Jan-2015
Abstract: © 2015, Journal of Pure and Applied Microbiology. All rights reserved. This study aimed to select the strain of Bacillus spp. as a starter culture for enriching isoflavone aglycones in traditional Thai fermented soybean (thua-nao) production. Forty-one strains of Bacillus spp. from Thai thua-nao and Japanese natto were characterized and divided into 5 groups; Bacillus licheniformis, Bacillus coagulans, Bacillus subtilis, Bacillus pumilus and Bacillus megaterium. Each strain was used to produce thua-nao. As a result, Bacillus PR03 produced the highest amount of isoflavone aglycones (146 mg/100g dry weight; 3.81 times higher than the amount in soybean) and was selected as the starter culture. According to 16S rDNA sequencing, Bacillus PR03 was identified as B. coagulans with 99.93% identical to IAM12463 strain. B. coagulans have never been reported as predominant bacteria in soybean fermentation. Therefore, this is the first research using B. coagulans as predominant bacteria for producing thua-nao. To enrich isoflavone aglycones in thua-nao production by B. coagulans PR03, it was found that the fermentation time of 5 d resulted in the optimal contents of daidzein, genistein, glycitein and total aglycones; 94.16, 68.29, 6.33 and 168.77 mg/100 g dry weight, respectively. With improved functional properties, the enriched isoflavone aglycones thua-nao could be applied as an ingredient in functional food development.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85037066433&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/54158
ISSN: 09737510
Appears in Collections:CMUL: Journal Articles

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