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通过降低ATCC 9937发酵过程中的褐变水平高效生产2,5-二酮-D-葡萄糖酸

Efficient Production of 2,5-Diketo-D-gluconic Acid by Reducing Browning Levels During ATCC 9937 Fermentation.

作者信息

Li Guang, Shan Xiaoyu, Zeng Weizhu, Yu Shiqin, Zhang Guoqiang, Chen Jian, Zhou Jingwen

机构信息

Science Center for Future Foods, Jiangnan University, Wuxi, China.

Key Laboratory of Industrial Biotechnology, Ministry of Education and School of Biotechnology, Jiangnan University, Wuxi, China.

出版信息

Front Bioeng Biotechnol. 2022 Jul 8;10:918277. doi: 10.3389/fbioe.2022.918277. eCollection 2022.

Abstract

D-Glucose directly generates 2-keto-L-gulonic acid (2-KLG, precursor of vitamin C) through the 2,5-diketo-D-gluconic acid (2,5-DKG) pathway. 2,5-DKG is the main rate-limiting factor of the reaction, and there are few relevant studies on it. In this study, a more accurate quantitative method of 2,5-DKG was developed and used to screen ATCC9937 as the chassis strain for the production of 2,5-DKG. Combining the metabolite profile analysis and knockout and overexpression of production strain, the non-enzymatic browning of 2,5-DKG was identified as the main factor leading to low yield of the target compound. By optimizing the fermentation process, the fermentation time was reduced to 48 h, and 2,5-DKG production peaked at 50.9 g/L, which was 139.02% higher than in the control group. Effectively eliminating browning and reducing the degradation of 2,5-DKG will help increase the conversion of 2,5-DKG to 2-KLG, and finally, establish a one-step D-glucose to 2-KLG fermentation pathway.

摘要

D-葡萄糖通过2,5-二酮-D-葡萄糖酸(2,5-DKG)途径直接生成2-酮-L-古龙酸(2-KLG,维生素C的前体)。2,5-DKG是该反应的主要限速因子,目前针对它的相关研究较少。在本研究中,开发了一种更精确的2,5-DKG定量方法,并用于筛选ATCC9937作为生产2,5-DKG的底盘菌株。结合代谢物谱分析以及生产菌株的基因敲除和过表达,确定2,5-DKG的非酶褐变是导致目标化合物产量低的主要因素。通过优化发酵工艺,发酵时间缩短至48小时,2,5-DKG产量达到峰值50.9 g/L,比对照组高出139.02%。有效消除褐变并减少2,5-DKG的降解将有助于提高2,5-DKG向2-KLG的转化率,最终建立一条从D-葡萄糖一步发酵生成2-KLG的途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f29/9304662/373c406a4a11/fbioe-10-918277-g001.jpg

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