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增强枯草芽孢杆菌中表面活性剂的产量:硝酸根诱导过量生产的蛋白质组学分析的见解和组合代谢工程策略。

Enhancing surfactin production in Bacillus subtilis: Insights from proteomic analysis of nitrate-induced overproduction and strategies for combinatorial metabolic engineering.

机构信息

Key Laboratory of Systems Bioengineering of the Ministry of Education, Tianjin University, Tianjin, 300350, PR China; Frontier Science Center of the Ministry of Education, Tianjin University, Tianjin 300350, PR China; Center for Chemical Science and Engineering, Tianjin University, 300350, PR China.

Key Laboratory of Systems Bioengineering of the Ministry of Education, Tianjin University, Tianjin, 300350, PR China; Frontier Science Center of the Ministry of Education, Tianjin University, Tianjin 300350, PR China.

出版信息

Bioresour Technol. 2024 Apr;397:130499. doi: 10.1016/j.biortech.2024.130499. Epub 2024 Feb 27.

Abstract

Surfactin biosynthesis in Bacillus subtilis is intricately regulated by environmental conditions. In the present study, addition of nitrate, a nitrogen source, increased the production of surfactin in B. subtilis ATCC 21332, whereas its absence resulted in minimal or no surfactin production. Proteomics revealed the mechanism underlying nitrate-induced surfactin overproduction, identifying three key differential proteins (preprotein translocase subunit SecA, signal recognition particle receptor FtsY, and cell division adenosine triphosphate-binding protein FtsE) relevant to surfactin transport and regulation. Combinatorial metabolic engineering strategies (enhanced nitrate reduction, fatty acid hydroxylation, rational transporter engineering, and feeding) led to a 41.4-fold increase in surfactin production compared with the initial production in the wild-type strain. This study provides insights into the molecular mechanism of nitrate-induced surfactin overproduction and strategies to enhance the performance of surfactin-producing strains.

摘要

在枯草芽孢杆菌中,表面活性剂的生物合成受到环境条件的复杂调节。在本研究中,添加氮源硝酸盐会增加枯草芽孢杆菌 ATCC 21332 中表面活性剂的产量,而缺乏硝酸盐则会导致表面活性剂产量极少或没有。蛋白质组学揭示了硝酸盐诱导表面活性剂过量产生的机制,确定了与表面活性剂运输和调节相关的三个关键差异蛋白(前体蛋白转运亚基 SecA、信号识别颗粒受体 FtsY 和细胞分裂三磷酸腺苷结合蛋白 FtsE)。组合代谢工程策略(增强硝酸盐还原、脂肪酸羟化、合理的转运蛋白工程和补料)使表面活性剂的产量与野生型菌株的初始产量相比增加了 41.4 倍。本研究提供了对硝酸盐诱导表面活性剂过量产生的分子机制的深入了解,并为增强表面活性剂产生菌株的性能提供了策略。

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