• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Mathematical modelling of microbes: metabolism, gene expression and growth.微生物的数学建模:代谢、基因表达和生长。
J R Soc Interface. 2017 Nov;14(136). doi: 10.1098/rsif.2017.0502.
2
Macromolecular crowding: chemistry and physics meet biology (Ascona, Switzerland, 10-14 June 2012).大分子拥挤现象:化学与物理邂逅生物学(瑞士阿斯科纳,2012年6月10日至14日)
Phys Biol. 2013 Aug;10(4):040301. doi: 10.1088/1478-3975/10/4/040301. Epub 2013 Aug 2.
3
A review of methods for the reconstruction and analysis of integrated genome-scale models of metabolism and regulation.重建和分析代谢和调控综合基因组规模模型的方法综述。
Biochem Soc Trans. 2020 Oct 30;48(5):1889-1903. doi: 10.1042/BST20190840.
4
Modelling microbial metabolic rewiring during growth in a complex medium.在复杂培养基中生长期间对微生物代谢重布线进行建模。
BMC Genomics. 2016 Nov 24;17(1):970. doi: 10.1186/s12864-016-3311-0.
5
Genome-scale modelling of microbial metabolism with temporal and spatial resolution.具有时间和空间分辨率的微生物代谢基因组规模建模。
Biochem Soc Trans. 2015 Dec;43(6):1164-71. doi: 10.1042/BST20150146.
6
SysBioMed report: advancing systems biology for medical applications.系统生物医学报告:推动系统生物学在医学应用中的发展。
IET Syst Biol. 2009 May;3(3):131-6. doi: 10.1049/iet-syb.2009.0005.
7
An insight to flux-balance analysis for biochemical networks.通量平衡分析在生化网络中的应用研究
Biotechnol Genet Eng Rev. 2020 Apr;36(1):32-55. doi: 10.1080/02648725.2020.1847440. Epub 2020 Dec 9.
8
An ensemble of mathematical models showing diauxic growth behaviour.一组展示双相生长行为的数学模型。
BMC Syst Biol. 2018 Sep 21;12(1):82. doi: 10.1186/s12918-018-0604-8.
9
A survey on methods for modeling and analyzing integrated biological networks.关于建模和分析综合生物网络的方法的调查。
IEEE/ACM Trans Comput Biol Bioinform. 2011 Jul-Aug;8(4):943-58. doi: 10.1109/TCBB.2010.117.
10
Searching for principles of microbial physiology.探寻微生物生理学原理。
FEMS Microbiol Rev. 2020 Nov 24;44(6):821-844. doi: 10.1093/femsre/fuaa034.

引用本文的文献

1
Bioactive exometabolites drive maintenance competition in simple bacterial communities.生物活性外代谢产物驱动简单细菌群落中的维持竞争。
mSystems. 2024 Apr 16;9(4):e0006424. doi: 10.1128/msystems.00064-24. Epub 2024 Mar 12.
2
Predictions of rhizosphere microbiome dynamics with a genome-informed and trait-based energy budget model.基于基因组信息和基于特征的能量预算模型预测根际微生物组动态。
Nat Microbiol. 2024 Feb;9(2):421-433. doi: 10.1038/s41564-023-01582-w. Epub 2024 Feb 5.
3
A coarse-grained resource allocation model of carbon and nitrogen metabolism in unicellular microbes.单细胞微生物中碳氮代谢的粗粒度资源分配模型
J R Soc Interface. 2023 Sep;20(206):20230206. doi: 10.1098/rsif.2023.0206. Epub 2023 Sep 27.
4
Resource allocation accounts for the large variability of rate-yield phenotypes across bacterial strains.资源分配解释了细菌菌株中速率-产量表型的巨大可变性。
Elife. 2023 May 31;12:e79815. doi: 10.7554/eLife.79815.
5
Understanding and application of Bacillus nitrogen regulation: A synthetic biology perspective.理解和应用芽孢杆菌氮调控:合成生物学视角。
J Adv Res. 2023 Jul;49:1-14. doi: 10.1016/j.jare.2022.09.003. Epub 2022 Sep 12.
6
Complex and unexpected outcomes of antibiotic therapy against a polymicrobial infection.对抗混合感染的抗生素治疗的复杂和意外结果。
ISME J. 2022 Sep;16(9):2065-2075. doi: 10.1038/s41396-022-01252-5. Epub 2022 May 21.
7
Elementary vectors and autocatalytic sets for resource allocation in next-generation models of cellular growth.用于细胞生长下一代模型中资源分配的基本向量和自催化集。
PLoS Comput Biol. 2022 Feb 1;18(2):e1009843. doi: 10.1371/journal.pcbi.1009843. eCollection 2022 Feb.
8
Dimensionless parameter predicts bacterial prodrug success.无量纲参数预测细菌前药的成功。
Mol Syst Biol. 2022 Jan;18(1):e10495. doi: 10.15252/msb.202110495.
9
Genome-Scale Reconstruction of Microbial Dynamic Phenotype: Successes and Challenges.微生物动态表型的基因组规模重建:成就与挑战
Microorganisms. 2021 Nov 14;9(11):2352. doi: 10.3390/microorganisms9112352.
10
The effect of natural selection on the propagation of protein expression noise to bacterial growth.自然选择对蛋白质表达噪声传播到细菌生长的影响。
PLoS Comput Biol. 2021 Jul 19;17(7):e1009208. doi: 10.1371/journal.pcbi.1009208. eCollection 2021 Jul.

本文引用的文献

1
Invariance of Initiation Mass and Predictability of Cell Size in Escherichia coli.大肠杆菌中起始质量的不变性和细胞大小的可预测性。
Curr Biol. 2017 May 8;27(9):1278-1287. doi: 10.1016/j.cub.2017.03.022. Epub 2017 Apr 13.
2
Constraint-based stoichiometric modelling from single organisms to microbial communities.从单一生物体到微生物群落的基于约束的化学计量学建模。
J R Soc Interface. 2016 Nov;13(124). doi: 10.1098/rsif.2016.0627.
3
Resource Reallocation in Bacteria by Reengineering the Gene Expression Machinery.通过重新设计基因表达机制在细菌中进行资源再分配。
Trends Microbiol. 2017 Jun;25(6):480-493. doi: 10.1016/j.tim.2016.12.009. Epub 2017 Jan 16.
4
Rethinking cell growth models.重新思考细胞生长模型。
FEMS Yeast Res. 2016 Nov;16(7). doi: 10.1093/femsyr/fow081. Epub 2016 Sep 19.
5
Constrained Allocation Flux Balance Analysis.约束分配通量平衡分析
PLoS Comput Biol. 2016 Jun 29;12(6):e1004913. doi: 10.1371/journal.pcbi.1004913. eCollection 2016 Jun.
6
Global Rebalancing of Cellular Resources by Pleiotropic Point Mutations Illustrates a Multi-scale Mechanism of Adaptive Evolution.细胞资源的全局再平衡由多效点突变阐明了适应性进化的多尺度机制。
Cell Syst. 2016 Apr 27;2(4):260-71. doi: 10.1016/j.cels.2016.04.003.
7
Necessary and sufficient conditions for protocell growth.原始细胞生长的充分必要条件。
J Math Biol. 2016 Dec;73(6-7):1627-1664. doi: 10.1007/s00285-016-0998-0. Epub 2016 Apr 18.
8
Dynamical Allocation of Cellular Resources as an Optimal Control Problem: Novel Insights into Microbial Growth Strategies.作为最优控制问题的细胞资源动态分配:对微生物生长策略的新见解
PLoS Comput Biol. 2016 Mar 9;12(3):e1004802. doi: 10.1371/journal.pcbi.1004802. eCollection 2016 Mar.
9
The post-transcriptional regulatory system CSR controls the balance of metabolic pools in upper glycolysis of Escherichia coli.转录后调控系统CSR控制大肠杆菌上糖酵解中代谢池的平衡。
Mol Microbiol. 2016 May;100(4):686-700. doi: 10.1111/mmi.13343. Epub 2016 Feb 26.
10
Single-cell characterization of metabolic switching in the sugar phosphotransferase system of Escherichia coli.大肠杆菌糖磷酸转移酶系统中代谢转换的单细胞表征
Mol Microbiol. 2016 May;100(3):472-85. doi: 10.1111/mmi.13329. Epub 2016 Feb 19.

微生物的数学建模:代谢、基因表达和生长。

Mathematical modelling of microbes: metabolism, gene expression and growth.

机构信息

University Grenoble-Alpes, Inria, Grenoble, France

University Côte d'Azur, Inria, INRA, CNRS, UPMC University Paris 06, BIOCORE team, Sophia-Antipolis, France.

出版信息

J R Soc Interface. 2017 Nov;14(136). doi: 10.1098/rsif.2017.0502.

DOI:10.1098/rsif.2017.0502
PMID:29187637
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5721159/
Abstract

The growth of microorganisms involves the conversion of nutrients in the environment into biomass, mostly proteins and other macromolecules. This conversion is accomplished by networks of biochemical reactions cutting across cellular functions, such as metabolism, gene expression, transport and signalling. Mathematical modelling is a powerful tool for gaining an understanding of the functioning of this large and complex system and the role played by individual constituents and mechanisms. This requires models of microbial growth that provide an integrated view of the reaction networks and bridge the scale from individual reactions to the growth of a population. In this review, we derive a general framework for the kinetic modelling of microbial growth from basic hypotheses about the underlying reaction systems. Moreover, we show that several families of approximate models presented in the literature, notably flux balance models and coarse-grained whole-cell models, can be derived with the help of additional simplifying hypotheses. This perspective clearly brings out how apparently quite different modelling approaches are related on a deeper level, and suggests directions for further research.

摘要

微生物的生长包括将环境中的营养物质转化为生物量,主要是蛋白质和其他大分子。这种转化是通过跨越细胞功能的生化反应网络来实现的,例如代谢、基因表达、运输和信号传递。数学建模是理解这个庞大而复杂系统的功能以及个体成分和机制所起作用的有力工具。这需要微生物生长模型提供对反应网络的综合视图,并在从单个反应到种群生长的尺度上进行衔接。在这篇综述中,我们从关于基础反应系统的基本假设出发,推导出微生物生长的动力学建模的一般框架。此外,我们还表明,文献中提出的几种近似模型家族,特别是通量平衡模型和粗粒度全细胞模型,可以在其他简化假设的帮助下推导出来。这种观点清楚地表明,表面上截然不同的建模方法在更深层次上是相关的,并为进一步的研究提出了方向。