Clostridium autoethanogenum alters cofactor synthesis, redox metabolism, and lysine-acetylation in response to elevated H2:CO feedstock ratios for enhancing carbon capture efficiency

IF 6.1 1区 工程技术 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Megan E. Davin, R. Adam Thompson, Richard J. Giannone, Lucas W. Mendelson, Dana L. Carper, Madhavi Z. Martin, Michael E. Martin, Nancy L. Engle, Timothy J. Tschaplinski, Steven D. Brown, Robert L. Hettich
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引用次数: 0

Abstract

Background

Clostridium autoethanogenum is an acetogenic bacterium that autotrophically converts carbon monoxide (CO) and carbon dioxide (CO2) gases into bioproducts and fuels via the Wood–Ljungdahl pathway (WLP). To facilitate overall carbon capture efficiency, the reaction stoichiometry requires supplementation of hydrogen at an increased ratio of H2:CO to maximize CO2 utilization; however, the molecular details and thus the ability to understand the mechanism of this supplementation are largely unknown.

Results

In order to elucidate the microbial physiology and fermentation where at least 75% of the carbon in ethanol comes from CO2, we established controlled chemostats that facilitated a novel and high (11:1) H2:CO uptake ratio. We compared and contrasted proteomic and metabolomics profiles to replicate continuous stirred tank reactors (CSTRs) at the same growth rate from a lower (5:1) H2:CO condition where ~ 50% of the carbon in ethanol is derived from CO2. Our hypothesis was that major changes would be observed in the hydrogenases and/or redox-related proteins and the WLP to compensate for the elevated hydrogen feed gas. Our analyses did reveal protein abundance differences between the two conditions largely related to reduction–oxidation (redox) pathways and cofactor biosynthesis, but the changes were more minor than we would have expected. While the Wood–Ljungdahl pathway proteins remained consistent across the conditions, other post-translational regulatory processes, such as lysine-acetylation, were observed and appeared to be more important for fine-tuning this carbon metabolism pathway. Metabolomic analyses showed that the increase in H2:CO ratio drives the organism to higher carbon dioxide utilization resulting in lower carbon storages and accumulated fatty acid metabolite levels.

Conclusions

This research delves into the intricate dynamics of carbon fixation in C. autoethanogenum, examining the influence of highly elevated H2:CO ratios on metabolic processes and product outcomes. The study underscores the significance of optimizing gas feed composition for enhanced industrial efficiency, shedding light on potential mechanisms, such as post-translational modifications (PTMs), to fine-tune enzymatic activities and improve desired product yields.

自乙烷梭菌改变辅助因子合成、氧化还原代谢和赖氨酸-乙酰化,以应对 H2:CO 原料比的升高,从而提高碳捕获效率
背景自乙烷梭菌是一种产乙酸细菌,可通过伍德-荣格达尔途径(WLP)将一氧化碳(CO)和二氧化碳(CO2)气体自养转化为生物产品和燃料。为了提高整体碳捕获效率,反应的化学计量学要求以 H2:CO 的更高比例补充氢气,以最大限度地利用 CO2;然而,分子细节以及了解这种补充机制的能力在很大程度上是未知的。结果为了阐明乙醇中至少 75% 的碳来自 CO2 的微生物生理学和发酵,我们建立了受控恒温器,以促进新颖的高(11:1)H2:CO 吸收比。我们比较并对比了蛋白质组学和代谢组学图谱,以及在相同生长速率下,从较低(5:1)H2:CO 条件下复制的连续搅拌罐反应器(CSTR)的图谱,在该条件下,乙醇中约 50% 的碳来自二氧化碳。我们的假设是,氢化酶和/或氧化还原相关蛋白以及 WLP 会发生重大变化,以补偿氢气原料的升高。我们的分析确实发现了两种条件下蛋白质丰度的差异,主要与还原氧化(氧化还原)途径和辅助因子生物合成有关,但变化比我们预期的要小。虽然伍德-荣格达尔途径蛋白在不同条件下保持一致,但也观察到其他翻译后调控过程,如赖氨酸-乙酰化,而且似乎对微调这一碳代谢途径更为重要。代谢组学分析表明,H2:CO 比率的增加会促使生物体提高二氧化碳利用率,从而降低碳储存量和累积的脂肪酸代谢物水平。 结论 这项研究深入探讨了 C. autoethanogenum 碳固定的复杂动态,考察了高度升高的 H2:CO 比率对代谢过程和产物结果的影响。该研究强调了优化气体原料成分以提高工业效率的重要性,揭示了翻译后修饰 (PTM) 等潜在机制,以微调酶活性并提高所需的产品产量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Biotechnology for Biofuels
Biotechnology for Biofuels 工程技术-生物工程与应用微生物
自引率
0.00%
发文量
0
审稿时长
2.7 months
期刊介绍: Biotechnology for Biofuels is an open access peer-reviewed journal featuring high-quality studies describing technological and operational advances in the production of biofuels, chemicals and other bioproducts. The journal emphasizes understanding and advancing the application of biotechnology and synergistic operations to improve plants and biological conversion systems for the biological production of these products from biomass, intermediates derived from biomass, or CO2, as well as upstream or downstream operations that are integral to biological conversion of biomass. Biotechnology for Biofuels focuses on the following areas: • Development of terrestrial plant feedstocks • Development of algal feedstocks • Biomass pretreatment, fractionation and extraction for biological conversion • Enzyme engineering, production and analysis • Bacterial genetics, physiology and metabolic engineering • Fungal/yeast genetics, physiology and metabolic engineering • Fermentation, biocatalytic conversion and reaction dynamics • Biological production of chemicals and bioproducts from biomass • Anaerobic digestion, biohydrogen and bioelectricity • Bioprocess integration, techno-economic analysis, modelling and policy • Life cycle assessment and environmental impact analysis
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