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通过优化全局代谢途径提高重组酿酒酵母的d-乳酸产量。

Enhanced d-lactic acid production by recombinant Saccharomyces cerevisiae following optimization of the global metabolic pathway.

作者信息

Yamada Ryosuke, Wakita Kazuki, Mitsui Ryosuke, Ogino Hiroyasu

机构信息

Department of Chemical Engineering, Osaka Prefecture University, 1-1 Gakuen-cho, Naka-ku, Sakai, Osaka, 599-8531, Japan.

出版信息

Biotechnol Bioeng. 2017 Sep;114(9):2075-2084. doi: 10.1002/bit.26330. Epub 2017 May 18.

Abstract

Utilization of renewable feedstocks for the production of bio-based chemicals such as d-lactic acid by engineering metabolic pathways in the yeast Saccharomyces cerevisiae has recently become an attractive option. In this study, to realize efficient d-lactic acid production by S. cerevisiae, the expression of 12 glycolysis-related genes and the Leuconostoc mesenteroides d-LDH gene was optimized using a previously developed global metabolic engineering strategy, and repeated batch fermentation was carried out using the resultant strain YPH499/dPdA3-34/DLDH/1-18. Stable d-lactic acid production through 10 repeated batch fermentations was achieved using YPH499/dPdA3-34/DLDH/1-18. The average d-lactic acid production, productivity, and yield with 10 repeated batch fermentations were 60.3 g/L, 2.80 g/L/h, and 0.646, respectively. The present study is the first report of the application of a global metabolic engineering strategy for bio-based chemical production, and it shows the potential for efficient production of such chemicals by global metabolic engineering of the yeast S. cerevisiae. Biotechnol. Bioeng. 2017;114: 2075-2084. © 2017 Wiley Periodicals, Inc.

摘要

通过对酿酒酵母代谢途径进行工程改造,利用可再生原料生产生物基化学品(如d-乳酸),最近已成为一种有吸引力的选择。在本研究中,为了实现酿酒酵母高效生产d-乳酸,使用先前开发的全局代谢工程策略优化了12个糖酵解相关基因和肠系膜明串珠菌d-LDH基因的表达,并使用所得菌株YPH499/dPdA3-34/DLDH/1-18进行了重复分批发酵。使用YPH499/dPdA3-34/DLDH/1-18通过10次重复分批发酵实现了稳定的d-乳酸生产。10次重复分批发酵的平均d-乳酸产量、生产率和产率分别为60.3 g/L、2.80 g/L/h和0.646。本研究是关于全局代谢工程策略应用于生物基化学品生产的首次报道,它展示了通过对酿酒酵母进行全局代谢工程高效生产此类化学品的潜力。《生物技术与生物工程》2017年;114:2075 - 2084。© 2017威利期刊公司

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