Carbon chain elongation microorganism stimulates caproate production from ethanol and acetate under applied voltage regulation.

IF 4 2区 生物学 Q2 MICROBIOLOGY
Frontiers in Microbiology Pub Date : 2025-06-18 eCollection Date: 2025-01-01 DOI:10.3389/fmicb.2025.1597990
Jing Li, Xing Luo, He Liu, Xuedong Zhang, Hao Tan, Xiaolong Xiong
{"title":"Carbon chain elongation microorganism stimulates caproate production from ethanol and acetate under applied voltage regulation.","authors":"Jing Li, Xing Luo, He Liu, Xuedong Zhang, Hao Tan, Xiaolong Xiong","doi":"10.3389/fmicb.2025.1597990","DOIUrl":null,"url":null,"abstract":"<p><p>Carbon chain elongation has been an innovative process for the synthesis of medium-chain fatty acids (MCFAs). Among them, caproate is a vital multi-functional one. To enhance the synthesis efficiency of caproate, the growth conditions of carbon chain elongation microorganisms need to optimize to develop an ideal niche, ultimately enhancing the production of caproate. In this study, the microbial enrichment of carbon chain elongation was obtained and the optimal system of carbon chain elongation was constructed. The optimal condition for carbon chain elongation was achieved at a pH of 7.00, an ethanol/acetic acid carbon molar ratio of 4:1, and a voltage of 0.7 V. The result showed that the concentration of caproate in the optimal group increased by 83.09% in comparison to the control group. Subsequently, compared with the initial microbial community structure, the relative abundance of microorganisms changed greatly in the optimal system, including <i>Clostridium_sensu_stricto_12</i>, <i>Christensenellaceae_R-7_group</i>, <i>Anaerofilum</i>, <i>Clostridium_sensu_stricto_7</i>, and <i>Intestinimonas</i>. Additionally, functional prediction analysis revealed that the optimal system enhanced amino acid metabolism (alanine, aspartate, and glutamate), carbon metabolism (CoA biosynthesis), and energy metabolism by 33.66, 30.42, and 17.05%, respectively. Besides, both the fatty acid biosynthesis (FAB) and reverse <i>β</i> oxidation (RBO) pathways were enhanced in optimal system. This study elucidates a novel mechanistic insight into the efficient microbial synthesis of caproate through carbon chain elongation pathways, demonstrating how applied voltage regulation can significantly enhance the bioproduction of MCFAs from simple substrates such as ethanol and acetate. Furthermore, this work presents a sustainable and energy-efficient strategy for caproate production, reducing reliance on fossil-derived precursors.</p>","PeriodicalId":12466,"journal":{"name":"Frontiers in Microbiology","volume":"16 ","pages":"1597990"},"PeriodicalIF":4.0000,"publicationDate":"2025-06-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12213838/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in Microbiology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.3389/fmicb.2025.1597990","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Carbon chain elongation has been an innovative process for the synthesis of medium-chain fatty acids (MCFAs). Among them, caproate is a vital multi-functional one. To enhance the synthesis efficiency of caproate, the growth conditions of carbon chain elongation microorganisms need to optimize to develop an ideal niche, ultimately enhancing the production of caproate. In this study, the microbial enrichment of carbon chain elongation was obtained and the optimal system of carbon chain elongation was constructed. The optimal condition for carbon chain elongation was achieved at a pH of 7.00, an ethanol/acetic acid carbon molar ratio of 4:1, and a voltage of 0.7 V. The result showed that the concentration of caproate in the optimal group increased by 83.09% in comparison to the control group. Subsequently, compared with the initial microbial community structure, the relative abundance of microorganisms changed greatly in the optimal system, including Clostridium_sensu_stricto_12, Christensenellaceae_R-7_group, Anaerofilum, Clostridium_sensu_stricto_7, and Intestinimonas. Additionally, functional prediction analysis revealed that the optimal system enhanced amino acid metabolism (alanine, aspartate, and glutamate), carbon metabolism (CoA biosynthesis), and energy metabolism by 33.66, 30.42, and 17.05%, respectively. Besides, both the fatty acid biosynthesis (FAB) and reverse β oxidation (RBO) pathways were enhanced in optimal system. This study elucidates a novel mechanistic insight into the efficient microbial synthesis of caproate through carbon chain elongation pathways, demonstrating how applied voltage regulation can significantly enhance the bioproduction of MCFAs from simple substrates such as ethanol and acetate. Furthermore, this work presents a sustainable and energy-efficient strategy for caproate production, reducing reliance on fossil-derived precursors.

碳链延伸微生物刺激乙醇和醋酸盐在施加电压调节下生产己酸盐。
碳链延伸法是合成中链脂肪酸的一种创新方法。其中己酸是一种重要的多功能氨基酸。为了提高己酸盐的合成效率,需要对碳链延伸微生物的生长条件进行优化,形成理想的生态位,最终提高己酸盐的产量。本研究获得了微生物对碳链延伸的富集,并构建了最佳的碳链延伸体系。碳链延伸的最佳条件为pH为7.00,乙醇/乙酸碳摩尔比为4:1,电压为0.7 V。结果表明:与对照组相比,优化组己酸盐浓度提高了83.09%。随后,与初始微生物群落结构相比,最优系统中微生物的相对丰度发生了较大的变化,包括Clostridium_sensu_stricto_12、Christensenellaceae_R-7_group、厌氧膜、Clostridium_sensu_stricto_7和ntestinimonas。此外,功能预测分析显示,优化后的氨基酸代谢(丙氨酸、天冬氨酸和谷氨酸)、碳代谢(CoA生物合成)和能量代谢分别提高了33.66%、30.42%和17.05%。此外,优化后的脂肪酸生物合成(FAB)和β逆向氧化(RBO)途径均得到增强。这项研究阐明了通过碳链延伸途径高效微生物合成己酸盐的新机制,展示了施加电压调节如何显著提高从简单底物(如乙醇和醋酸酯)生产MCFAs的生物产量。此外,这项工作为己酸生产提出了可持续和节能的战略,减少了对化石衍生前体的依赖。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
7.70
自引率
9.60%
发文量
4837
审稿时长
14 weeks
期刊介绍: Frontiers in Microbiology is a leading journal in its field, publishing rigorously peer-reviewed research across the entire spectrum of microbiology. Field Chief Editor Martin G. Klotz at Washington State University is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信