混合碳源下pH对凝固芽孢杆菌乳酸发酵影响的系统生物学分析

IF 3.6 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Zhihao Liu, Yonghong Wang
{"title":"混合碳源下pH对凝固芽孢杆菌乳酸发酵影响的系统生物学分析","authors":"Zhihao Liu,&nbsp;Yonghong Wang","doi":"10.1002/bit.70001","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>Environmental pH plays a crucial role in microbial metabolism. Microorganisms adapt their metabolic strategies in response to different pH conditions, which must be carefully controlled in industrial production processes to achieve desired outcomes. However, the dynamic impact of pH on hierarchical utilization of mixed carbon sources remains poorly understood. In this study, we observed that <i>Bacillus coagulans</i> exhibited distinct carbon source consumption rates and lactate yields at different pH levels under mixed carbon sources. We employed dynamic simulation methods using an enzyme-constrained genome-scale metabolic model, combined with transcriptomic and metabolomic data, to investigate the metabolic differences at pH 5.5, 6.0, and 6.5 conditions. The results revealed the significant flux differences in the glycolysis pathway across the tested pH conditions. Predictions also indicated that pH changes altered energy demands. Integrating omics data further revealed that under pH 5.5 conditions, a higher proportion of carbon was allocated to the phosphoketolase pathway, which provides high ATP yield. This strategy helps meet the energy demand of energy-consuming reactions that could maintain intracellular pH stability under acid stress, such as the reactions in amino acid metabolism. Consequently, we observed increased acetate production and decreased lactate production. Additionally, different pH conditions triggered a global response involving multiple metabolic pathways.</p>\n </div>","PeriodicalId":9168,"journal":{"name":"Biotechnology and Bioengineering","volume":"122 9","pages":"2559-2573"},"PeriodicalIF":3.6000,"publicationDate":"2025-06-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Systems Biology Analysis of the Effect of pH on Lactate Fermentation in Bacillus coagulans Under Mixed Carbon Sources\",\"authors\":\"Zhihao Liu,&nbsp;Yonghong Wang\",\"doi\":\"10.1002/bit.70001\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n <p>Environmental pH plays a crucial role in microbial metabolism. Microorganisms adapt their metabolic strategies in response to different pH conditions, which must be carefully controlled in industrial production processes to achieve desired outcomes. However, the dynamic impact of pH on hierarchical utilization of mixed carbon sources remains poorly understood. In this study, we observed that <i>Bacillus coagulans</i> exhibited distinct carbon source consumption rates and lactate yields at different pH levels under mixed carbon sources. We employed dynamic simulation methods using an enzyme-constrained genome-scale metabolic model, combined with transcriptomic and metabolomic data, to investigate the metabolic differences at pH 5.5, 6.0, and 6.5 conditions. The results revealed the significant flux differences in the glycolysis pathway across the tested pH conditions. Predictions also indicated that pH changes altered energy demands. Integrating omics data further revealed that under pH 5.5 conditions, a higher proportion of carbon was allocated to the phosphoketolase pathway, which provides high ATP yield. This strategy helps meet the energy demand of energy-consuming reactions that could maintain intracellular pH stability under acid stress, such as the reactions in amino acid metabolism. Consequently, we observed increased acetate production and decreased lactate production. Additionally, different pH conditions triggered a global response involving multiple metabolic pathways.</p>\\n </div>\",\"PeriodicalId\":9168,\"journal\":{\"name\":\"Biotechnology and Bioengineering\",\"volume\":\"122 9\",\"pages\":\"2559-2573\"},\"PeriodicalIF\":3.6000,\"publicationDate\":\"2025-06-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Biotechnology and Bioengineering\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://analyticalsciencejournals.onlinelibrary.wiley.com/doi/10.1002/bit.70001\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"BIOTECHNOLOGY & APPLIED MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biotechnology and Bioengineering","FirstCategoryId":"5","ListUrlMain":"https://analyticalsciencejournals.onlinelibrary.wiley.com/doi/10.1002/bit.70001","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

环境pH值在微生物代谢中起着至关重要的作用。微生物根据不同的pH值条件调整其代谢策略,在工业生产过程中必须仔细控制以达到预期的结果。然而,pH对混合碳源分级利用的动态影响尚不清楚。在本研究中,我们观察到在混合碳源下,不同pH水平下凝结芽孢杆菌的碳源消耗速率和乳酸产量是不同的。我们采用动态模拟方法,利用酶约束的基因组尺度代谢模型,结合转录组学和代谢组学数据,研究pH 5.5、6.0和6.5条件下的代谢差异。结果显示糖酵解途径在不同的pH条件下存在显著的通量差异。预测还表明,pH值的变化会改变能量需求。整合组学数据进一步揭示,在pH 5.5条件下,更高比例的碳分配给磷酸酮醇酶途径,从而提供高ATP产量。这种策略有助于满足酸胁迫下维持细胞内pH稳定的耗能反应的能量需求,如氨基酸代谢反应。因此,我们观察到醋酸盐产量增加,乳酸盐产量减少。此外,不同的pH条件引发了涉及多种代谢途径的全球反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Systems Biology Analysis of the Effect of pH on Lactate Fermentation in Bacillus coagulans Under Mixed Carbon Sources

Systems Biology Analysis of the Effect of pH on Lactate Fermentation in Bacillus coagulans Under Mixed Carbon Sources

Systems Biology Analysis of the Effect of pH on Lactate Fermentation in Bacillus coagulans Under Mixed Carbon Sources

Systems Biology Analysis of the Effect of pH on Lactate Fermentation in Bacillus coagulans Under Mixed Carbon Sources

Environmental pH plays a crucial role in microbial metabolism. Microorganisms adapt their metabolic strategies in response to different pH conditions, which must be carefully controlled in industrial production processes to achieve desired outcomes. However, the dynamic impact of pH on hierarchical utilization of mixed carbon sources remains poorly understood. In this study, we observed that Bacillus coagulans exhibited distinct carbon source consumption rates and lactate yields at different pH levels under mixed carbon sources. We employed dynamic simulation methods using an enzyme-constrained genome-scale metabolic model, combined with transcriptomic and metabolomic data, to investigate the metabolic differences at pH 5.5, 6.0, and 6.5 conditions. The results revealed the significant flux differences in the glycolysis pathway across the tested pH conditions. Predictions also indicated that pH changes altered energy demands. Integrating omics data further revealed that under pH 5.5 conditions, a higher proportion of carbon was allocated to the phosphoketolase pathway, which provides high ATP yield. This strategy helps meet the energy demand of energy-consuming reactions that could maintain intracellular pH stability under acid stress, such as the reactions in amino acid metabolism. Consequently, we observed increased acetate production and decreased lactate production. Additionally, different pH conditions triggered a global response involving multiple metabolic pathways.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Biotechnology and Bioengineering
Biotechnology and Bioengineering 工程技术-生物工程与应用微生物
CiteScore
7.90
自引率
5.30%
发文量
280
审稿时长
2.1 months
期刊介绍: Biotechnology & Bioengineering publishes Perspectives, Articles, Reviews, Mini-Reviews, and Communications to the Editor that embrace all aspects of biotechnology. These include: -Enzyme systems and their applications, including enzyme reactors, purification, and applied aspects of protein engineering -Animal-cell biotechnology, including media development -Applied aspects of cellular physiology, metabolism, and energetics -Biocatalysis and applied enzymology, including enzyme reactors, protein engineering, and nanobiotechnology -Biothermodynamics -Biofuels, including biomass and renewable resource engineering -Biomaterials, including delivery systems and materials for tissue engineering -Bioprocess engineering, including kinetics and modeling of biological systems, transport phenomena in bioreactors, bioreactor design, monitoring, and control -Biosensors and instrumentation -Computational and systems biology, including bioinformatics and genomic/proteomic studies -Environmental biotechnology, including biofilms, algal systems, and bioremediation -Metabolic and cellular engineering -Plant-cell biotechnology -Spectroscopic and other analytical techniques for biotechnological applications -Synthetic biology -Tissue engineering, stem-cell bioengineering, regenerative medicine, gene therapy and delivery systems The editors will consider papers for publication based on novelty, their immediate or future impact on biotechnological processes, and their contribution to the advancement of biochemical engineering science. Submission of papers dealing with routine aspects of bioprocessing, description of established equipment, and routine applications of established methodologies (e.g., control strategies, modeling, experimental methods) is discouraged. Theoretical papers will be judged based on the novelty of the approach and their potential impact, or on their novel capability to predict and elucidate experimental observations.
×
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