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在添加氨基酸的化学成分确定的培养基中培养重组大肠杆菌可增加β-胡萝卜素的产量。

Increase in the production of β-carotene in recombinant Escherichia coli cultured in a chemically defined medium supplemented with amino acids.

机构信息

Department of Bioscience and Biotechnology, Konkuk University, 1 Hwayang-dong, Gwangjin-gu, Seoul, South Korea.

出版信息

Biotechnol Lett. 2013 Feb;35(2):265-71. doi: 10.1007/s10529-012-1072-7. Epub 2012 Oct 30.

Abstract

Escherichia coli DH5α strain was selected as the recombinant host, and a chemically defined medium supplemented with amino acids was used instead of a complex medium for the efficient production of β-carotene. In a fed-batch culture using glycerol with a chemically defined medium supplemented with amino acids, the concentration, specific content, and productivity of β-carotene were 2,470 mg/l, 72 mg/g cells, and 77 mg/l h after 32 h, respectively. These values were, respectively, 43, 33, and 26 % higher than those obtained using the complex medium. This is the highest β-carotene production that has been reported among the recombinant cells to date.

摘要

选用大肠杆菌 DH5α 菌株作为重组宿主,用添加氨基酸的化学成分确定的培养基代替复杂培养基,以有效生产β-胡萝卜素。在使用甘油进行补料分批培养、添加氨基酸的化学成分确定的培养基中,β-胡萝卜素的浓度、比含量和产率分别为 32 小时后的 2,470mg/L、72mg/g 细胞和 77mg/L·h,分别比用复杂培养基时高 43%、33%和 26%。这是迄今为止重组细胞中报道的最高的β-胡萝卜素产量。

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