Keot Jyotshna, Bora Sudipta Sankar, Das Kangabam Rajiv, Barooah Madhumita
1Department of Agricultural Biotechnology, Assam Agricultural University, Jorhat, Assam 785013 India.
2DBT-North East Centre for Agricultural Biotechnology, Assam Agricultural University, Jorhat, Assam 785013 India.
3 Biotech. 2020 Feb;10(2):64. doi: 10.1007/s13205-020-2059-z. Epub 2020 Jan 23.
This study reports the microbial quality of ethnic starter culture used for rice wine fermentation in Assam. Here, we collected 60 samples belonging to community of the state and enumerated the microorganisms using spread plate technique. Illumina-based whole genome shotgun sequencing detected the presence of microbial contaminants like , , , , , , , , , etc. Presence of major health hazards associated with spontaneous rice wine fermentation necessitated method optimization through the development of a defined mixed starter culture. For this, functionally important α-amylase producers viz, sp. ABTSJ23, ABTSJ63, ABTSJ72 and ABTSJ82 and eight yeasts viz, ABTY1J, ABTY1S, ADJ5 & ADJ1, ADJ2, ADJ3, ADJ4 and ADJ6 were retrieved using appropriate media. All the mould cultures tested negative for aflotoxins production. Among the yeasts, ABTY1S and ADJ1 decarboxylated lysine HCl and tyramine HCl, respectively, indicating their biogenic amine production ability. For defined mixed starter culture, ABT82 with α-amylase (5.92 U/ml) and glucoamylase (7.50 U/ml) activities was selected as fungal partner; while ADJ4 and ABT-Y1J with high ethanol production (up to 10.11% and 9.88% v/v, respectively) were selected as yeast partners. The mixed culture was able to produce high amount of glucose, ethanol and liquid (glucose 10.91% w/v; ethanol 7.5% w/v; liquid 51.0% w/v). Therefore, this study demonstrated the efficiency of mixed starter cultures for safe and controlled rice wine production.
本研究报告了阿萨姆邦用于米酒发酵的民族发酵剂的微生物质量。在此,我们收集了该邦60个社区的样本,并使用涂布平板技术对微生物进行计数。基于Illumina的全基因组鸟枪法测序检测到了如[具体微生物名称1]、[具体微生物名称2]、[具体微生物名称3]、[具体微生物名称4]、[具体微生物名称5]、[具体微生物名称6]、[具体微生物名称7]、[具体微生物名称8]、[具体微生物名称9]等微生物污染物的存在。与自发米酒发酵相关的主要健康危害的存在使得有必要通过开发特定的混合发酵剂来优化方法。为此,使用合适的培养基筛选出了功能上重要的α-淀粉酶产生菌,即[具体霉菌名称1]ABTSJ23、[具体霉菌名称2]ABTSJ63、[具体霉菌名称3]ABTSJ72和[具体霉菌名称4]ABTSJ82,以及8种酵母,即ABTY1J、ABTY1S、ADJ5 & ADJ1、ADJ2、ADJ3、ADJ4和ADJ6。所有霉菌培养物的黄曲霉毒素产生检测均为阴性。在酵母中,ABTY1S和ADJ1分别使赖氨酸盐酸盐和酪胺盐酸盐脱羧,表明它们具有生物胺产生能力。对于特定的混合发酵剂,选择具有α-淀粉酶(5.92 U/ml)和糖化酶(7.50 U/ml)活性的ABT82作为真菌伙伴;而选择具有高乙醇产量(分别高达10.11%和9.88% v/v)的ADJ4和ABT - Y1J作为酵母伙伴。该混合培养物能够产生大量的葡萄糖、乙醇和液体(葡萄糖10.91% w/v;乙醇7.5% w/v;液体51.0% w/v)。因此,本研究证明了混合发酵剂在安全、可控的米酒生产中的有效性。