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在酿酒酵母中生产辛酸:新前体供应工程策略和内在限制的研究。

Production of octanoic acid in Saccharomyces cerevisiae: Investigation of new precursor supply engineering strategies and intrinsic limitations.

机构信息

Department of Biological Sciences, Institute of Molecular Biosciences, Goethe University Frankfurt, Frankfurt am Main, Germany.

出版信息

Biotechnol Bioeng. 2021 Aug;118(8):3046-3057. doi: 10.1002/bit.27814. Epub 2021 May 18.

Abstract

The eight-carbon fatty acid octanoic acid (OA) is an important platform chemical and precursor of many industrially relevant products. Its microbial biosynthesis is regarded as a promising alternative to current unsustainable production methods. In Saccharomyces cerevisiae, the production of OA had been previously achieved by rational engineering of the fatty acid synthase. For the supply of the precursor molecule acetyl-CoA and of the redox cofactor NADPH, the native pyruvate dehydrogenase bypass had been harnessed, or the cells had been additionally provided with a pathway involving a heterologous ATP-citrate lyase. Here, we redirected the flux of glucose towards the oxidative branch of the pentose phosphate pathway and overexpressed a heterologous phosphoketolase/phosphotransacetylase shunt to improve the supply of NADPH and acetyl-CoA in a strain background with abolished OA degradation. We show that these modifications lead to an increased yield of OA during the consumption of glucose by more than 60% compared to the parental strain. Furthermore, we investigated different genetic engineering targets to identify potential factors that limit the OA production in yeast. Toxicity assays performed with the engineered strains suggest that the inhibitory effects of OA on cell growth likely impose an upper limit to attainable OA yields.

摘要

八碳脂肪酸辛酸(OA)是一种重要的平台化学品,也是许多工业相关产品的前体。其微生物生物合成被认为是一种有前途的替代当前不可持续生产方法的方法。在酿酒酵母中,OA 的生产以前通过脂肪酸合酶的合理工程来实现。为了提供前体分子乙酰辅酶 A 和氧化还原辅酶 NADPH,利用了天然的丙酮酸脱氢酶旁路,或者向细胞中提供了一种涉及异源 ATP-柠檬酸裂合酶的途径。在这里,我们将葡萄糖通量重新定向到戊糖磷酸途径的氧化分支,并过表达了一种异源磷酸酮醇酶/磷酸转乙酰酶支路,以在消除 OA 降解的菌株背景下改善 NADPH 和乙酰辅酶 A 的供应。我们表明,与亲本菌株相比,这些修饰可使葡萄糖消耗过程中的 OA 产量增加超过 60%。此外,我们研究了不同的基因工程靶点,以确定限制酵母中 OA 生产的潜在因素。对工程菌株进行的毒性测定表明,OA 对细胞生长的抑制作用可能对可达到的 OA 产量施加了上限。

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