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利用分泌真菌淀粉酶的工业酿酒酵母菌株将淀粉质底物整合生物加工为乙醇。

Consolidated bioprocessing of starchy substrates into ethanol by industrial Saccharomyces cerevisiae strains secreting fungal amylases.

作者信息

Favaro Lorenzo, Viktor Marko J, Rose Shaunita H, Viljoen-Bloom Marinda, van Zyl Willem H, Basaglia Marina, Cagnin Lorenzo, Casella Sergio

机构信息

Department of Agronomy Food Natural resources Animals and Environment (DAFNAE), Università di Padova, Agripolis, Viale dell'Università 16, 35020, Legnaro (PD), Italy.

Department of Microbiology, Stellenbosch University, Stellenbosch, South Africa.

出版信息

Biotechnol Bioeng. 2015 Sep;112(9):1751-60. doi: 10.1002/bit.25591. Epub 2015 Jul 14.

Abstract

The development of a yeast strain that converts raw starch to ethanol in one step (called Consolidated Bioprocessing, CBP) could significantly reduce the commercial costs of starch-based bioethanol. An efficient amylolytic Saccharomyces cerevisiae strain suitable for industrial bioethanol production was developed in this study. Codon-optimized variants of the Thermomyces lanuginosus glucoamylase (TLG1) and Saccharomycopsis fibuligera α-amylase (SFA1) genes were δ-integrated into two S. cerevisiae yeast with promising industrial traits, i.e., strains M2n and MEL2. The recombinant M2n[TLG1-SFA1] and MEL2[TLG1-SFA1] yeast displayed high enzyme activities on soluble and raw starch (up to 8118 and 4461 nkat/g dry cell weight, respectively) and produced about 64 g/L ethanol from 200 g/L raw corn starch in a bioreactor, corresponding to 55% of the theoretical maximum ethanol yield (g of ethanol/g of available glucose equivalent). Their starch-to-ethanol conversion efficiencies were even higher on natural sorghum and triticale substrates (62 and 73% of the theoretical yield, respectively). This is the first report of direct ethanol production from natural starchy substrates (without any pre-treatment or commercial enzyme addition) using industrial yeast strains co-secreting both a glucoamylase and α-amylase.

摘要

开发一种能将生淀粉一步转化为乙醇的酵母菌株(称为整合生物加工,CBP)可显著降低淀粉基生物乙醇的商业成本。本研究中开发了一种适用于工业生物乙醇生产的高效淀粉分解酿酒酵母菌株。嗜热栖热菌葡糖淀粉酶(TLG1)和扣囊复膜孢酵母α-淀粉酶(SFA1)基因的密码子优化变体通过δ整合到两种具有良好工业特性的酿酒酵母中,即M2n和MEL2菌株。重组M2n[TLG1-SFA1]和MEL2[TLG1-SFA1]酵母在可溶性淀粉和生淀粉上表现出高酶活性(分别高达8118和4461 nkat/g干细胞重量),并在生物反应器中从200 g/L的生玉米淀粉中产生约64 g/L乙醇,相当于理论最大乙醇产量(乙醇克数/可用葡萄糖当量克数)的55%。它们在天然高粱和小黑麦底物上的淀粉到乙醇的转化效率甚至更高(分别为理论产量的62%和73%)。这是首次报道使用共分泌葡糖淀粉酶和α-淀粉酶的工业酵母菌株从天然淀粉底物直接生产乙醇(无需任何预处理或添加商业酶)。

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