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Engineering Bacillus subtilis for isobutanol production by heterologous Ehrlich pathway construction and the biosynthetic 2-ketoisovalerate precursor pathway overexpression

机译:工程化枯草芽孢杆菌通过异源Ehrlich途径构建和生物合成2-酮异戊酸前体途径过表达来生产异丁醇

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In the present work, Bacillus subtilis was engineered as the cell factory for isobutanol production due to its high tolerance to isobutanol. Initially, an efficient heterologous Ehrlich pathway controlled by the promoter P43 was introduced into B. subtilis for the isobutanol biosynthesis. Further, investigation of acetolactate synthase of B. subtilis, ketol-acid reductoisomerase, and dihydroxy-acid dehydratase of Corynebacterium glutamicum responsible for 2-ketoisovalerate precursor biosynthesis showed that acetolactate synthase played an important role in isobutanol biosynthesis. The overexpression of acetolactate synthase led to a 2.8-fold isobutanol production compared with the control. Apart from isobutanol, alcoholic profile analysis also confirmed the existence of 1.21 g/L ethanol, 1.06 g/L 2-phenylethanol, as well as traces of 2-methyl-1-butanol and 3-methyl-1-butanol in the fermentation broth. Under microaerobic condition, the engineered B. subtilis produced up to 2.62 g/L isobutanol in shake-flask fed-batch fermentation, which was 21.3% higher than that in batch fermentation.
机译:在目前的工作中,枯草芽孢杆菌由于对异丁醇的高度耐受性而被设计为生产异丁醇的细胞工厂。最初,由启动子P 43 控制的有效异源Ehrlich途径被引入枯草芽孢杆菌中,用于异丁醇的生物合成。此外,对枯草芽孢杆菌的乙酰乳酸合酶,谷氨酸棒杆菌的酮醇酸还原异构酶和谷氨酸棒状杆菌的二羟基酸脱水酶负责2-酮异戊酸酯前体生物合成的研究表明,乙酰乳酸合酶在异丁醇生物合成中起重要作用。与对照相比,乙酰乳酸合酶的过表达导致异丁醇产量的2.8倍。除异丁醇外,酒精特性分析还确认了发酵液中存在1.21 g / L乙醇,1.06 g / L 2-苯基乙醇,以及痕量2-甲基-1-丁醇和3-甲基-1-丁醇的存在。 。在微需氧条件下,经工程改造的枯草芽孢杆菌在摇瓶补料分批发酵中产生的异丁醇含量高达2.62 g / L,比分批发酵的产量高21.3%。

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