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嗜热新兴工业主力菌对高渗透压的响应:谷氨酸合成与输出增强

Enhanced Glutamate Synthesis and Export by the Thermotolerant Emerging Industrial Workhorse in Response to High Osmolarity.

作者信息

Frank Christine, Hoffmann Tamara, Zelder Oskar, Felle Max F, Bremer Erhard

机构信息

Laboratory for Microbiology, Department of Biology, Philipps-University Marburg, Marburg, Germany.

Center for Synthetic Microbiology (SYNMIKRO), Philipps-University Marburg, Marburg, Germany.

出版信息

Front Microbiol. 2021 Apr 8;12:640980. doi: 10.3389/fmicb.2021.640980. eCollection 2021.

Abstract

The thermotolerant methylotroph MGA3 was originally isolated from freshwater marsh soil. Due to its ability to use methanol as sole carbon and energy source, is increasingly explored as a cell factory for the production of amino acids, fine chemicals, and proteins of biotechnological interest. During high cell density fermentation in industrial settings with the membrane-permeable methanol as the feed, the excretion of low molecular weight products synthesized from it will increase the osmotic pressure of the medium. This in turn will impair cell growth and productivity of the overall biotechnological production process. With this in mind, we have analyzed the core of the physiological adjustment process of MGA3 to sustained high osmolarity surroundings. Through growth assays, we found that MGA3 possesses only a restricted ability to cope with sustained osmotic stress. This finding is consistent with the ecophysiological conditions in the habitat from which it was originally isolated. None of the externally provided compatible solutes and proline-containing peptides affording osmostress protection for were able to stimulate growth of MGA3 at high salinity. MGA3 synthesized the moderately effective compatible solute L-glutamate in a pattern such that the cellular pool increased concomitantly with increases in the external osmolarity. Counterintuitively, a large portion of the newly synthesized L-glutamate was excreted. The expression of the genes ( and ) for two L-glutamate synthases were upregulated in response to high salinity along with that of the regulatory gene. Such a regulatory pattern of the system(s) for L-glutamate synthesis in Bacilli is new. Our findings might thus be generally relevant to understand the production of the osmostress protectant L-glutamate by those Bacilli that exclusively rely on this compatible solute for their physiological adjustment to high osmolarity surroundings.

摘要

耐热甲基营养菌MGA3最初是从淡水沼泽土壤中分离出来的。由于其能够将甲醇作为唯一的碳源和能源,它越来越多地被开发为用于生产氨基酸、精细化学品和具有生物技术意义的蛋白质的细胞工厂。在工业环境中以膜可渗透的甲醇为进料进行高细胞密度发酵时,由甲醇合成的低分子量产物的排泄会增加培养基的渗透压。这反过来又会损害细胞生长和整个生物技术生产过程的生产力。考虑到这一点,我们分析了MGA3对持续高渗透压环境的生理调节过程的核心。通过生长试验,我们发现MGA3应对持续渗透胁迫的能力有限。这一发现与它最初分离的栖息地的生态生理条件一致。外部提供的任何一种为其提供渗透胁迫保护的相容性溶质和含脯氨酸的肽都不能在高盐度下刺激MGA3的生长。MGA3以一种细胞内池随着外部渗透压的增加而相应增加的模式合成中等效力的相容性溶质L-谷氨酸。与直觉相反的是,新合成的L-谷氨酸有很大一部分被排泄出去。两种L-谷氨酸合酶的基因(和)的表达以及调控基因的表达在高盐度下均上调。芽孢杆菌中L-谷氨酸合成系统的这种调控模式是新的。因此,我们的发现可能普遍适用于理解那些完全依赖这种相容性溶质来对高渗透压环境进行生理调节的芽孢杆菌对渗透胁迫保护剂L-谷氨酸的产生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82f8/8060640/b7a1c3ecccec/fmicb-12-640980-g001.jpg

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