The catabolic nature of fermentative substrates influences proteomic rewiring in Escherichia coli under anoxic growth.

IF 4.9 2区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Microbial Cell Factories Pub Date : 2025-03-25 DOI:10.1186/s12934-025-02658-4
Huda Momin, Deepti Appukuttan, K V Venkatesh
{"title":"The catabolic nature of fermentative substrates influences proteomic rewiring in Escherichia coli under anoxic growth.","authors":"Huda Momin, Deepti Appukuttan, K V Venkatesh","doi":"10.1186/s12934-025-02658-4","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>During anaerobic batch fermentation of substrates by Escherichia coli, there is a decline in cell proliferation rates and a huge demand is placed on cellular proteome to cater to its catabolic and anabolic needs under anoxic growth. Considering cell growth rates as a physiological parameter, previous studies have established a direct relationship between E. coli growth rate and cellular ribosomal content for fast-proliferating cells. In this study, we integrated experimental findings with a systemic coarse-grained proteome allocation model, to characterize the physiological outcomes at slow growth rate during anaerobic fermentative catabolism of different glycolytic and non-glycolytic substrates.</p><p><strong>Results: </strong>The anaerobic catabolism of substrates favored high ribosomal abundances at lower growth rates. Interestingly, a modification of the previously discussed \"growth law\", the ratio of active to inactive ribosomal proteome was found to be linearly related to the growth rate for cells proliferating at slow to moderate regime (growth rate < 0.8 h<sup>- 1</sup>). Also, under nutrient- and oxygen-limiting growth conditions, the proteome proportion allocated for ribosomal activity was reduced, and the resources were channelized towards metabolic activities to overcome the limitations imposed during uptake and metabolizing substrate. The energy-intensive uptake mechanism or lower substrate affinity, expended more catabolic proteome, which reduced its availability to other cellular functions.</p><p><strong>Conclusions: </strong>Thus, the nature of catabolic substrates imposed either uptake limitation or metabolic limitation coupled with ribosomal limitation (arising due to anoxic and nutritional stress), which resulted in higher proteome expenditure leading to sub-optimal growth phenotype. This study can form the basis for analyzing E. coli's ability to optimize metabolic efficiency under different environmental conditions- including stress responses. It can be further extended to optimizing the industrial anaerobic conversions for improving productivity and yield.</p>","PeriodicalId":18582,"journal":{"name":"Microbial Cell Factories","volume":"24 1","pages":"71"},"PeriodicalIF":4.9000,"publicationDate":"2025-03-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11938722/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Microbial Cell Factories","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1186/s12934-025-02658-4","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Background: During anaerobic batch fermentation of substrates by Escherichia coli, there is a decline in cell proliferation rates and a huge demand is placed on cellular proteome to cater to its catabolic and anabolic needs under anoxic growth. Considering cell growth rates as a physiological parameter, previous studies have established a direct relationship between E. coli growth rate and cellular ribosomal content for fast-proliferating cells. In this study, we integrated experimental findings with a systemic coarse-grained proteome allocation model, to characterize the physiological outcomes at slow growth rate during anaerobic fermentative catabolism of different glycolytic and non-glycolytic substrates.

Results: The anaerobic catabolism of substrates favored high ribosomal abundances at lower growth rates. Interestingly, a modification of the previously discussed "growth law", the ratio of active to inactive ribosomal proteome was found to be linearly related to the growth rate for cells proliferating at slow to moderate regime (growth rate < 0.8 h- 1). Also, under nutrient- and oxygen-limiting growth conditions, the proteome proportion allocated for ribosomal activity was reduced, and the resources were channelized towards metabolic activities to overcome the limitations imposed during uptake and metabolizing substrate. The energy-intensive uptake mechanism or lower substrate affinity, expended more catabolic proteome, which reduced its availability to other cellular functions.

Conclusions: Thus, the nature of catabolic substrates imposed either uptake limitation or metabolic limitation coupled with ribosomal limitation (arising due to anoxic and nutritional stress), which resulted in higher proteome expenditure leading to sub-optimal growth phenotype. This study can form the basis for analyzing E. coli's ability to optimize metabolic efficiency under different environmental conditions- including stress responses. It can be further extended to optimizing the industrial anaerobic conversions for improving productivity and yield.

Abstract Image

Abstract Image

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
发酵底物的分解代谢性质影响大肠杆菌在缺氧生长下的蛋白质组重新布线。
背景:在大肠杆菌对底物进行厌氧分批发酵的过程中,细胞增殖率下降,对细胞蛋白质组有巨大的需求,以满足其在缺氧生长下的分解代谢和合成代谢需求。以往的研究将细胞生长速率作为一个生理参数,建立了大肠杆菌生长速率与快速增殖细胞的细胞核糖体含量之间的直接关系。在本研究中,我们将实验结果与系统粗粒度蛋白质组分配模型相结合,以表征不同糖酵解和非糖酵解底物在厌氧发酵分解代谢过程中缓慢生长的生理结果。结果:底物的厌氧分解代谢有利于低生长速率下的高核糖体丰度。有趣的是,对先前讨论的“生长规律”进行了修改,发现在缓慢到中等增殖的细胞中,活性核糖体蛋白质组与非活性核糖体蛋白质组的比例与生长速率呈线性相关(生长速率- 1)。此外,在营养和氧气限制的生长条件下,分配给核糖体活性的蛋白质组比例降低,资源被引导到代谢活动中,以克服在摄取和代谢底物过程中施加的限制。能量密集型摄取机制或较低的底物亲和力,消耗了更多的分解代谢蛋白质组,从而降低了其对其他细胞功能的可用性。因此,分解代谢底物的性质施加了摄取限制或代谢限制,以及核糖体限制(由缺氧和营养应激引起),这导致更高的蛋白质组消耗,导致次优生长表型。本研究可以为分析大肠杆菌在不同环境条件下(包括应激反应)优化代谢效率的能力奠定基础。它可以进一步扩展到优化工业厌氧转化,以提高生产率和产量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Microbial Cell Factories
Microbial Cell Factories 工程技术-生物工程与应用微生物
CiteScore
9.30
自引率
4.70%
发文量
235
审稿时长
2.3 months
期刊介绍: Microbial Cell Factories is an open access peer-reviewed journal that covers any topic related to the development, use and investigation of microbial cells as producers of recombinant proteins and natural products, or as catalyzers of biological transformations of industrial interest. Microbial Cell Factories is the world leading, primary research journal fully focusing on Applied Microbiology. The journal is divided into the following editorial sections: -Metabolic engineering -Synthetic biology -Whole-cell biocatalysis -Microbial regulations -Recombinant protein production/bioprocessing -Production of natural compounds -Systems biology of cell factories -Microbial production processes -Cell-free systems
期刊最新文献
Catalytically active inclusion bodies of Bacillus clausii laccase protein recombinantly produced in E. coli for dye decolorization. Acetyl- and malonyl-CoA availability drive EPA selectivity in polyketide synthase-engineered Yarrowia lipolytica. Establishing Saccharomyces cerevisiae as a host for renewable acrylic acid production. Bioactivities and biosynthesis of monoterpene-based biopesticides: current state and perspectives. Overexpression of msnA reprograms metabolism to enhance recombinant protein secretion across Aspergillus species.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1