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自养乙醇梭菌会改变辅因子合成、氧化还原代谢和赖氨酸乙酰化,以响应提高的H₂:CO原料比,从而提高碳捕获效率。

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

作者信息

Davin Megan E, Thompson R Adam, Giannone Richard J, Mendelson Lucas W, Carper Dana L, Martin Madhavi Z, Martin Michael E, Engle Nancy L, Tschaplinski Timothy J, Brown Steven D, Hettich Robert L

机构信息

Bredesen Center for Interdisciplinary Research, Graduate School of Genome Science and Technology, University of Tennessee, Knoxville, TN, USA.

Oak Ridge National Laboratory, Oak Ridge, TN, 37831, USA.

出版信息

Biotechnol Biofuels Bioprod. 2024 Sep 3;17(1):119. doi: 10.1186/s13068-024-02554-w.

DOI:10.1186/s13068-024-02554-w
PMID:39227857
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11370222/
Abstract

BACKGROUND

Clostridium autoethanogenum is an acetogenic bacterium that autotrophically converts carbon monoxide (CO) and carbon dioxide (CO) 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 H:CO to maximize CO 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 CO, we established controlled chemostats that facilitated a novel and high (11:1) H: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) H:CO condition where ~ 50% of the carbon in ethanol is derived from CO. 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 H: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 H: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.

摘要

背景

自养乙醇梭菌是一种产乙酸细菌,它通过伍德-Ljungdahl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,反应化学计量需要以增加的H:CO比例补充氢气,以最大限度地利用CO;然而,这种补充机制的分子细节以及理解该机制的能力在很大程度上尚不清楚。

结果

为了阐明微生物生理学和发酵过程,其中乙醇中至少75%的碳来自CO,我们建立了可控的恒化器,其促进了新颖且高(11:1)的H:CO摄取比例。我们比较并对比了蛋白质组学和代谢组学图谱,以在相同生长速率下复制来自较低(5:1)H:CO条件的连续搅拌罐反应器(CSTR),在该条件下乙醇中约50%的碳来自CO。我们的假设是,在氢化酶和/或氧化还原相关蛋白以及WLP中会观察到主要变化,以补偿氢气进料气体的增加。我们的分析确实揭示了两种条件之间的蛋白质丰度差异,主要与氧化还原途径和辅因子生物合成有关,但变化比我们预期的要小。虽然伍德-Ljungdahl途径蛋白在不同条件下保持一致,但观察到了其他翻译后调控过程,如赖氨酸乙酰化,并且似乎对微调这种碳代谢途径更为重要。代谢组学分析表明,H:CO比例的增加促使生物体提高二氧化碳利用率,导致碳储存和积累的脂肪酸代谢物水平降低。

结论

本研究深入探讨了自养乙醇梭菌中碳固定的复杂动态,研究了高度升高的H:CO比例对代谢过程和产物结果的影响。该研究强调了优化气体进料组成以提高工业效率的重要性,揭示了潜在机制,如翻译后修饰(PTM),以微调酶活性并提高所需产物产量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bef3/11370222/576b251ed9ca/13068_2024_2554_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bef3/11370222/2ab12341ddfd/13068_2024_2554_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bef3/11370222/1207727e646f/13068_2024_2554_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bef3/11370222/97ad5afcd320/13068_2024_2554_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bef3/11370222/576b251ed9ca/13068_2024_2554_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bef3/11370222/2ab12341ddfd/13068_2024_2554_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bef3/11370222/1207727e646f/13068_2024_2554_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bef3/11370222/97ad5afcd320/13068_2024_2554_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bef3/11370222/576b251ed9ca/13068_2024_2554_Fig4_HTML.jpg

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