重组大肠杆菌BL21中葡萄糖和木糖协同合成肌醇的研究。

IF 2 4区 生物学 Q3 BIOCHEMICAL RESEARCH METHODS
Min Wu, Bing Fu, Fuyao Guan, Chuyang Yan, Peize Wang, Haoju Wang, Xin Xu, Lei Zhang, Ping Yu
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引用次数: 0

摘要

肌醇是一种具有重要生理功能的活性糖醇。本研究构建了一株能同时利用葡萄糖和木糖生产肌醇的工程菌株,并对其发酵性能进行了测定。首先,删除ptsG基因,使大肠杆菌BL21能够同时利用葡萄糖和木糖作为混合碳源。在敲除ptsG后,引入Galp和glk基因促进葡萄糖吸收。其次,引入酿酒酵母SC288的ino1基因,过表达suhB基因,在大肠杆菌BL21中构建肌醇的完整生物合成途径;最终,以20 g/L葡萄糖和木糖以3:2的比例作为混合碳源,在50 mL/250 mL培养体系中,总糖消耗速度最快,肌醇产量为0.63 g/L。当发酵体系扩大到1 L摇瓶时,肌醇产率为0.69 g/L。本研究有助于以混合糖为碳源生产肌醇。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synergistic utilization of glucose and xylose for the myo-inositol biosynthesis in recombinant Escherichia coli BL21.

Myo-inositol is an active sugar alcohol which has important physiological functions. In this study, an engineered strain that could simultaneously utilize glucose and xylose to produce myo-inositol was constructed, and its fermentation performance was determined. Firstly, the ptsG gene was deleted to make E. coli BL21 capable of utilizing glucose and xylose simultaneously as mixed carbon source. Galp and glk genes were introduced to promote the glucose absorption after ptsG knockout. Secondly, the ino1 gene from Saccharomyces cerevisiae SC288 was introduced and the suhB gene was overexpressed to construct the complete biosynthetic pathway of myo-inositol in E. coli BL21. Ultimately, when 20 g/L glucose and xylose with a ratio of 3:2 were used as the mixed carbon source, the consumption rate of the total sugar was the fastest, and the yield of myo-inositol was 0.63 g/L in 50 mL/250 mL culture system. When the fermentation system was expanded to 1 L shake flask, the yield of myo-inositol was 0.69 g/L. This study contributes to the production of myo-inositol with mixed sugar as the carbon source.

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来源期刊
Preparative Biochemistry & Biotechnology
Preparative Biochemistry & Biotechnology 工程技术-生化研究方法
CiteScore
4.90
自引率
3.40%
发文量
98
审稿时长
2 months
期刊介绍: Preparative Biochemistry & Biotechnology is an international forum for rapid dissemination of high quality research results dealing with all aspects of preparative techniques in biochemistry, biotechnology and other life science disciplines.
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