Suppr超能文献

大肠杆菌menaquinone-8 途径的代谢工程改造作为维生素 K 生产的微生物平台。

Metabolic engineering of menaquinone-8 pathway of Escherichia coli as a microbial platform for vitamin K production.

机构信息

Department of Molecular Science and Technology, Ajou University, Woncheon-dong, Yeongtong-gu, Suwon 443-749, South Korea.

出版信息

Biotechnol Bioeng. 2011 Aug;108(8):1997-2002. doi: 10.1002/bit.23142. Epub 2011 Apr 5.

Abstract

Menaquinone-8 (MK-8, vitamin K) is composed of a non-polar side chain and a polar head group. Escherichia coli was chosen and metabolically engineered as a microbial platform for production of MK-8. MK-8 content in E. coli was significantly enhanced by modulating two precursor pools, which supply a non-polar side chain and a polar head group, and further increased by blocking formation of the competitor ubiquinone-8 (Q-8). Overexpression of E. coli IspA, DXR, or IDI increased MK-8 content up to twofold. A similar positive effect was also observed when E. coli MenA, MenB, MenC, MenD, MenE, MenF, or UbiE was overexpressed. The Q-8-deficient ubiCA mutant enhanced MK-8 content by 30% compared to wild-type E. coli. When MenA or MenD was overexpressed, MK-8 content was enhanced fivefold compared with wild-type E. coli.

摘要

甲萘醌-8(MK-8,维生素 K)由非极性侧链和极性头部基团组成。选择大肠杆菌并对其进行代谢工程改造,作为生产 MK-8 的微生物平台。通过调节供应非极性侧链和极性头部基团的两个前体池,显著提高了大肠杆菌中的 MK-8 含量,并通过阻断竞争物质泛醌-8(Q-8)的形成进一步提高了含量。大肠杆菌 IspA、DXR 或 IDI 的过表达使 MK-8 含量增加了一倍。当大肠杆菌 MenA、MenB、MenC、MenD、MenE、MenF 或 UbiE 过表达时,也观察到类似的积极效果。与野生型大肠杆菌相比,缺乏 Q-8 的 ubiCA 突变体使 MK-8 含量提高了 30%。当过表达 MenA 或 MenD 时,MK-8 含量比野生型大肠杆菌提高了五倍。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验