增强甲酸耐受性的适应性进化的大褐藻及其在3-羟基丙酸生产中的应用。

IF 3.7 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Applied and Environmental Microbiology Pub Date : 2025-09-17 Epub Date: 2025-08-13 DOI:10.1128/aem.02560-24
Xuhua Mo, Yan Zhao, Lin Zhu, Changtai Zhang, Zhe Liu, Zengxin Ma, Kai Bao, Song Yang
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引用次数: 0

摘要

一种利用甲酸的天然细菌Methylorubrum extorquens AM1对甲酸的耐受能力有限。在这项研究中,我们采用了适应性实验室进化(ALE)策略,开发了一种衍生自M.敲诈勒索AM1的进化菌株FT3,具有增强的甲酸耐受性。当用含有90 mM甲酸酯和30 mM甲醇的碳源混合培养时,FT3菌株的光密度(OD600)比亲本菌株高5.3倍。在13c标记碳源的实验中,FT3菌株可以有效地利用甲醇和甲酸酯。此外,通过DNA重测序、转录组分析和ale启发的基因操作实验,研究了FT3菌株甲酸耐受性增强的机制。FT3菌株被鉴定为超突变体,其增强的甲酸耐受性归因于甲酸转运增加,甲醇氧化途径改善,甲酸氧化和同化途径增强。此外,基因过表达实验表明,META1_0287*、META1_3027、META1_3028、META1_3029、META1_1261、META1_1418和META1_2965基因参与了甲酸耐受性。值得注意的是,甲酸的添加显著改善了FT3菌株中NADH和NADPH的生成。此外,以FT3菌株为底盘,通过补料分批发酵,3-羟基丙酸(3-HP)的产量提高到2.47 g/L。该研究为进一步将进化的M.敲诈菌株作为甲醇和甲酸酯在还原性化学品生产中协同利用的有效平台进行工程设计提供了重要的基础。重要性:在本研究中,我们利用ALE策略成功获得了一株衍生自m.o resquens AM1的进化菌株FT3,该菌株具有高的甲酸耐受性。FT3菌株被鉴定为一个超突变体,其增强的甲酸耐受性归因于甲酸转运增加,甲醇氧化途径改善,甲酸氧化和同化途径增强。通过转录组分析和ale启发的基因操作实验,我们确定了几个有助于FT3菌株对甲酸耐受性的基因。还原当量水平的提高和对3-HP的耐受性的提高使FT3成为3-HP生产的合适底盘,通过补料分批发酵实现了2.47 g/L的产量提高。该研究为进一步将进化的M.敲诈菌株作为甲醇和甲酸酯在还原性化学品生产中协同利用的有效平台进行工程设计提供了重要的基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Adaptively evolved Methylorubrum extorquens with enhanced formate tolerance and its application in 3-hydroxypropionic acid production.

Methylorubrum extorquens AM1, a native formate-utilizing bacterium, has exhibited limited capacity to tolerate formate. In this study, we employed an adaptive laboratory evolution (ALE) strategy to develop an evolved strain FT3 derived from M. extorquens AM1, with enhanced formate tolerance. When cultivated with a mixture of carbon sources containing 90 mM formate and 30 mM methanol, the FT3 strain exhibited 5.3 times higher optical density (OD600) compared to the parental strain. FT3 strain was shown to efficiently utilize both methanol and formate in experiments using 13C-labeled carbon sources. Furthermore, the mechanism underlying the enhanced formate tolerance in FT3 strain was investigated through a combination of DNA re-sequencing, transcriptome analysis, and ALE-inspired gene manipulation experiments. The FT3 strain was identified as a hypermutant, and its enhanced formate tolerance was attributed to increased formate transport, an improved methanol oxidation pathway, and enhanced formate oxidation and assimilation pathways. In addition, gene overexpression experiments indicated the involvement of genes META1_0287*, META1_3027, META1_3028, META1_3029, META1_1261, META1_1418, and META1_2965 in formate tolerance. Notably, the addition of formate resulted in a significant improvement in the generation of NADH and NADPH in the FT3 strain. Moreover, using the FT3 strain as a chassis, an improved 3-hydroxypropionic acid (3-HP) production of 2.47 g/L through fed-batch fermentation was achieved. This study provides an important foundation for further engineering of the evolved M. extorquens strain as an efficient platform for the co-utilization of methanol and formate in the production of reduced chemicals.

Importance: In the present study, we successfully obtained an evolved strain FT3 derived from M. extorquens AM1 with high formate tolerance using the ALE strategy. The FT3 strain was identified as a hypermutant, with its enhanced formate tolerance attributed to increased formate transport, an improved methanol oxidation pathway, and enhanced formate oxidation and assimilation pathways. Through transcriptome analysis and ALE-inspired gene manipulation experiments, we identified several genes that contribute to the FT3 strain's tolerance to formate. The enhanced levels of reducing equivalents and the increased tolerance to 3-HP make FT3 a suitable chassis for 3-HP production, achieving an improved yield of 2.47 g/L through fed-batch fermentation. This study provides an important foundation for further engineering of the evolved M. extorquens strain as an efficient platform for the co-utilization of methanol and formate in the production of reduced chemicals.

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来源期刊
Applied and Environmental Microbiology
Applied and Environmental Microbiology 生物-生物工程与应用微生物
CiteScore
7.70
自引率
2.30%
发文量
730
审稿时长
1.9 months
期刊介绍: Applied and Environmental Microbiology (AEM) publishes papers that make significant contributions to (a) applied microbiology, including biotechnology, protein engineering, bioremediation, and food microbiology, (b) microbial ecology, including environmental, organismic, and genomic microbiology, and (c) interdisciplinary microbiology, including invertebrate microbiology, plant microbiology, aquatic microbiology, and geomicrobiology.
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