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大肠杆菌对长链脂肪酸的蛋白质组水平响应以及脂肪酸诱导型启动子在蛋白质生产中的应用。

Proteome-level responses of Escherichia coli to long-chain fatty acids and use of fatty acid inducible promoter in protein production.

作者信息

Han Mee-Jung, Lee Jeong Wook, Lee Sang Yup, Yoo Jong Shin

机构信息

Metabolic and Biomolecular Engineering National Research Laboratory, Department of Chemical & Biomolecular Engineering (BK21 Program), Yuseong-gu, Daejeon 305-701, South Korea.

出版信息

J Biomed Biotechnol. 2008;2008:735101. doi: 10.1155/2008/735101.

DOI:10.1155/2008/735101
PMID:18317523
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2218904/
Abstract

In Escherichia coli, a long-chain acyl-CoA is a regulatory signal that modulates gene expression through its binding to a transcription factor FadR. In this study, comparative proteomic analysis of E. coli in the presence of glucose and oleic acid was performed to understand cell physiology in response to oleic acid. Among total of 52 proteins showing altered expression levels with oleic acid presence, 9 proteins including AldA, Cdd, FadA, FadB, FadL, MalE, RbsB, Udp, and YccU were newly synthesized. Among the genes that were induced by oleic acid, the promoter of the aldA gene was used for the production of a green fluorescent protein (GFP). Analysis of fluorescence intensities and confocal microscopic images revealed that soluble GFP was highly expressed under the control of the aldA promoter. These results suggest that proteomics is playing an important role not only in biological research but also in various biotechnological applications.

摘要

在大肠杆菌中,长链酰基辅酶A是一种调节信号,它通过与转录因子FadR结合来调节基因表达。在本研究中,对存在葡萄糖和油酸情况下的大肠杆菌进行了比较蛋白质组学分析,以了解细胞对油酸的生理反应。在因油酸存在而表达水平发生改变的总共52种蛋白质中,包括AldA、Cdd、FadA、FadB、FadL、MalE、RbsB、Udp和YccU在内的9种蛋白质是新合成的。在由油酸诱导的基因中,aldA基因的启动子被用于生产绿色荧光蛋白(GFP)。荧光强度分析和共聚焦显微镜图像显示,可溶性GFP在aldA启动子的控制下高度表达。这些结果表明,蛋白质组学不仅在生物学研究中,而且在各种生物技术应用中都发挥着重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e76/2218904/7b244b3dba47/JBB2008-735101.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e76/2218904/bf695ccfb4ec/JBB2008-735101.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e76/2218904/7c790948d0a6/JBB2008-735101.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e76/2218904/0cc531d29536/JBB2008-735101.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e76/2218904/881737a8d55a/JBB2008-735101.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e76/2218904/6a16d690daac/JBB2008-735101.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e76/2218904/7b244b3dba47/JBB2008-735101.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e76/2218904/bf695ccfb4ec/JBB2008-735101.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e76/2218904/7c790948d0a6/JBB2008-735101.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e76/2218904/0cc531d29536/JBB2008-735101.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e76/2218904/881737a8d55a/JBB2008-735101.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e76/2218904/6a16d690daac/JBB2008-735101.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e76/2218904/7b244b3dba47/JBB2008-735101.006.jpg

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本文引用的文献

1
The Escherichia coli proteome: past, present, and future prospects.大肠杆菌蛋白质组:过去、现在及未来展望
Microbiol Mol Biol Rev. 2006 Jun;70(2):362-439. doi: 10.1128/MMBR.00036-05.
2
The proteome of Mannheimia succiniciproducens, a capnophilic rumen bacterium.嗜二氧化碳瘤胃菌——产琥珀酸曼氏杆菌的蛋白质组
Proteomics. 2006 Jun;6(12):3550-66. doi: 10.1002/pmic.200500837.
3
Enhanced proteome profiling by inhibiting proteolysis with small heat shock proteins.通过小分子热休克蛋白抑制蛋白水解来增强蛋白质组分析
蛋白质表达的异质性导致模型大肠杆菌群体中的代谢变异性。
Proc Natl Acad Sci U S A. 2013 Aug 20;110(34):14006-11. doi: 10.1073/pnas.1222569110. Epub 2013 Aug 1.
4
Membrane stresses induced by overproduction of free fatty acids in Escherichia coli.大肠杆菌中游离脂肪酸过度产生引起的膜应力。
Appl Environ Microbiol. 2011 Nov;77(22):8114-28. doi: 10.1128/AEM.05421-11. Epub 2011 Sep 23.
J Proteome Res. 2005 Nov-Dec;4(6):2429-34. doi: 10.1021/pr050259m.
4
Identification and characterization of a new enoyl coenzyme A hydratase involved in biosynthesis of medium-chain-length polyhydroxyalkanoates in recombinant Escherichia coli.重组大肠杆菌中参与中链长度聚羟基脂肪酸酯生物合成的一种新型烯酰辅酶A水合酶的鉴定与表征
J Bacteriol. 2003 Sep;185(18):5391-7. doi: 10.1128/JB.185.18.5391-5397.2003.
5
Escherichia coli FadR positively regulates transcription of the fabB fatty acid biosynthetic gene.大肠杆菌FadR正向调控脂肪酸生物合成基因fabB的转录。
J Bacteriol. 2001 Oct;183(20):5982-90. doi: 10.1128/JB.183.20.5982-5990.2001.
6
Constitutive expression of protective antigen gene of Bacillus anthracis in Escherichia coli.炭疽芽孢杆菌保护性抗原基因在大肠杆菌中的组成型表达。
Biochem Biophys Res Commun. 2001 May 4;283(2):308-15. doi: 10.1006/bbrc.2001.4777.
7
Proteome analysis of metabolically engineered Escherichia coli producing Poly(3-hydroxybutyrate).对生产聚(3-羟基丁酸酯)的代谢工程改造大肠杆菌进行蛋白质组分析。
J Bacteriol. 2001 Jan;183(1):301-8. doi: 10.1128/JB.183.1.301-308.2001.
8
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9
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Prog Lipid Res. 1999 Mar;38(2):129-97. doi: 10.1016/s0163-7827(98)00022-8.
10
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Appl Environ Microbiol. 1999 Jul;65(7):3027-32. doi: 10.1128/AEM.65.7.3027-3032.1999.