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大肠杆菌敲除株的代谢通量分析:来自 Keio 文库的经验教训和未来展望。

Metabolic flux analysis of Escherichia coli knockouts: lessons from the Keio collection and future outlook.

机构信息

Department of Chemical and Biomolecular Engineering, Metabolic Engineering and Systems Biology Laboratory, University of Delaware, Newark, DE 19716, USA.

Department of Chemical and Biomolecular Engineering, Metabolic Engineering and Systems Biology Laboratory, University of Delaware, Newark, DE 19716, USA.

出版信息

Curr Opin Biotechnol. 2014 Aug;28:127-33. doi: 10.1016/j.copbio.2014.02.006. Epub 2014 Mar 28.

DOI:10.1016/j.copbio.2014.02.006
PMID:24686285
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5842030/
Abstract

Cellular metabolic and regulatory systems are of fundamental interest to biologists and engineers. Incomplete understanding of these complex systems remains an obstacle to progress in biotechnology and metabolic engineering. An established method for obtaining new information on network structure, regulation and dynamics is to study the cellular system following a perturbation such as a genetic knockout. The Keio collection of all viable Escherichia coli single-gene knockouts is facilitating a systematic investigation of the regulation and metabolism of E. coli. Of all omics measurements available, the metabolic flux profile (the fluxome) provides the most direct and relevant representation of the cellular phenotype. Recent advances in (13)C-metabolic flux analysis are now permitting highly precise and accurate flux measurements for investigating cellular systems and guiding metabolic engineering efforts.

摘要

细胞代谢和调节系统是生物学家和工程师非常感兴趣的基础。对这些复杂系统的不完全了解仍然是生物技术和代谢工程进展的障碍。获得有关网络结构、调节和动力学的新信息的一种既定方法是在受到诸如基因敲除等扰动后研究细胞系统。京都大肠杆菌单基因敲除菌集合正在促进对大肠杆菌的调节和代谢的系统研究。在所有可用的组学测量中,代谢通量谱(通量组)为细胞表型提供了最直接和最相关的表示。(13)C 代谢通量分析的最新进展现在允许进行高度精确和准确的通量测量,以研究细胞系统并指导代谢工程工作。

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本文引用的文献

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Central metabolic responses to the overproduction of fatty acids in Escherichia coli based on 13C-metabolic flux analysis.基于 13C 代谢通量分析的大肠杆菌脂肪酸过度生产的中心代谢响应。
Biotechnol Bioeng. 2014 Mar;111(3):575-85. doi: 10.1002/bit.25124.
2
Publishing 13C metabolic flux analysis studies: a review and future perspectives.发表 13C 代谢通量分析研究:综述与未来展望。
Metab Eng. 2013 Nov;20:42-8. doi: 10.1016/j.ymben.2013.08.005. Epub 2013 Sep 8.
3
COMPLETE-MFA: complementary parallel labeling experiments technique for metabolic flux analysis.COMPLETE-MFA:代谢通量分析互补平行标记实验技术。
Metab Eng. 2013 Nov;20:49-55. doi: 10.1016/j.ymben.2013.08.006. Epub 2013 Sep 8.
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Dynamic metabolic flux analysis--tools for probing transient states of metabolic networks.动态代谢通量分析——探测代谢网络瞬态状态的工具。
Curr Opin Biotechnol. 2013 Dec;24(6):973-8. doi: 10.1016/j.copbio.2013.03.018. Epub 2013 Apr 20.
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13C metabolic flux analysis: optimal design of isotopic labeling experiments.13C 代谢通量分析:最佳同位素标记实验设计。
Curr Opin Biotechnol. 2013 Dec;24(6):1116-21. doi: 10.1016/j.copbio.2013.02.003. Epub 2013 Feb 28.
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Flux-coupled genes and their use in metabolic flux analysis.通量耦联基因及其在代谢通量分析中的应用。
Biotechnol J. 2013 Sep;8(9):1035-42. doi: 10.1002/biot.201200279. Epub 2013 Mar 21.
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Parallel labeling experiments and metabolic flux analysis: Past, present and future methodologies.平行标记实验和代谢通量分析:过去、现在和未来的方法学。
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Tandem mass spectrometry for measuring stable-isotope labeling.串联质谱法测量稳定同位素标记。
Curr Opin Biotechnol. 2013 Feb;24(1):48-53. doi: 10.1016/j.copbio.2012.10.011. Epub 2012 Nov 8.
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Parallel labeling experiments with [1,2-(13)C]glucose and [U-(13)C]glutamine provide new insights into CHO cell metabolism.采用 [1,2-(13)C]葡萄糖和 [U-(13)C]谷氨酰胺进行平行标记实验,为 CHO 细胞代谢研究提供了新的见解。
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Genome Biol. 2012 Jul 5;13(9):R78. doi: 10.1186/gb-2012-13-9-r78.