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Appl Environ Microbiol. 2002 Aug;68(8):4117-21. doi: 10.1128/AEM.68.8.4117-4121.2002.
2
ClpX, an alternative subunit for the ATP-dependent Clp protease of Escherichia coli. Sequence and in vivo activities.ClpX,大肠杆菌ATP依赖性Clp蛋白酶的一种替代亚基。序列及体内活性。
J Biol Chem. 1993 Oct 25;268(30):22618-26.
3
Global transcriptional analysis of clpP mutations of type 2 Streptococcus pneumoniae and their effects on physiology and virulence.2型肺炎链球菌clpP突变的全转录组分析及其对生理学和毒力的影响。
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Global role for ClpP-containing proteases in stationary-phase adaptation of Escherichia coli.含ClpP蛋白酶在大肠杆菌稳定期适应中的全局作用。
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Regulation of Escherichia coli starvation sigma factor (sigma s) by ClpXP protease.ClpXP蛋白酶对大肠杆菌饥饿σ因子(σs)的调控
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Functional domains of the ClpA and ClpX molecular chaperones identified by limited proteolysis and deletion analysis.通过有限蛋白酶解和缺失分析鉴定的ClpA和ClpX分子伴侣的功能结构域。
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The stroma of higher plant plastids contain ClpP and ClpC, functional homologs of Escherichia coli ClpP and ClpA: an archetypal two-component ATP-dependent protease.高等植物质体的基质含有ClpP和ClpC,它们是大肠杆菌ClpP和ClpA的功能同源物:一种典型的双组分ATP依赖性蛋白酶。
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本文引用的文献

1
Activity of the APC(Cdh1) form of the anaphase-promoting complex persists until S phase and prevents the premature expression of Cdc20p.后期促进复合物的APC(Cdh1)形式的活性持续到S期,并阻止Cdc20p的过早表达。
J Cell Biol. 2001 Jul 9;154(1):85-94. doi: 10.1083/jcb.200102007.
2
ClpB cooperates with DnaK, DnaJ, and GrpE in suppressing protein aggregation. A novel multi-chaperone system from Escherichia coli.ClpB与DnaK、DnaJ和GrpE协同作用以抑制蛋白质聚集。一种来自大肠杆菌的新型多分子伴侣系统。
J Biol Chem. 1999 Oct 1;274(40):28083-6. doi: 10.1074/jbc.274.40.28083.
3
Here's the hook: similar substrate binding sites in the chaperone domains of Clp and Lon.关键在于:Clp和Lon的伴侣结构域中存在相似的底物结合位点。
Proc Natl Acad Sci U S A. 1999 Jul 20;96(15):8318-20. doi: 10.1073/pnas.96.15.8318.
4
New insights into the ATP-dependent Clp protease: Escherichia coli and beyond.对ATP依赖型Clp蛋白酶的新见解:从大肠杆菌到其他生物
Mol Microbiol. 1999 May;32(3):449-58. doi: 10.1046/j.1365-2958.1999.01357.x.
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Structure, assembly and regulation of expression of capsules in Escherichia coli.大肠杆菌中荚膜的结构、组装及表达调控
Mol Microbiol. 1999 Mar;31(5):1307-19. doi: 10.1046/j.1365-2958.1999.01276.x.
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rexB of bacteriophage lambda is an anti-cell death gene.噬菌体λ的rexB是一种抗细胞死亡基因。
Proc Natl Acad Sci U S A. 1998 Dec 22;95(26):15481-6. doi: 10.1073/pnas.95.26.15481.
7
Involvement of waaY, waaQ, and waaP in the modification of Escherichia coli lipopolysaccharide and their role in the formation of a stable outer membrane.waaY、waaQ和waaP在大肠杆菌脂多糖修饰中的作用及其在稳定外膜形成中的作用
J Biol Chem. 1998 Oct 9;273(41):26310-6. doi: 10.1074/jbc.273.41.26310.
8
The ClpXP and ClpAP proteases degrade proteins with carboxy-terminal peptide tails added by the SsrA-tagging system.ClpXP蛋白酶和ClpAP蛋白酶可降解由SsrA标记系统添加了羧基末端肽尾的蛋白质。
Genes Dev. 1998 May 1;12(9):1338-47. doi: 10.1101/gad.12.9.1338.
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Regulatory subunits of energy-dependent proteases.能量依赖性蛋白酶的调节亚基。
Cell. 1997 Nov 14;91(4):435-8. doi: 10.1016/s0092-8674(00)80428-6.
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Proteases and their targets in Escherichia coli.大肠杆菌中的蛋白酶及其作用靶点。
Annu Rev Genet. 1996;30:465-506. doi: 10.1146/annurev.genet.30.1.465.

大肠杆菌clpP和clpB突变体对十二烷基硫酸钠的超敏反应

Sodium dodecyl sulfate hypersensitivity of clpP and clpB mutants of Escherichia coli.

作者信息

Rajagopal Soumitra, Sudarsan Narasimhan, Nickerson Kenneth W

机构信息

School of Biological Sciences, University of Nebraska, Lincoln, Nebraska 68588-0666, USA.

出版信息

Appl Environ Microbiol. 2002 Aug;68(8):4117-21. doi: 10.1128/AEM.68.8.4117-4121.2002.

DOI:10.1128/AEM.68.8.4117-4121.2002
PMID:12147516
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC124035/
Abstract

We studied the hypersensitivity of clpP and clpB mutants of Escherichia coli to sodium dodecyl sulfate (SDS). Both wild-type E. coli MC4100 and lon mutants grew in the presence of 10% SDS, whereas isogenic clpP and clpB single mutants could not grow above 0.5% SDS and clpA and clpX single mutants could not grow above 5.0% SDS. For wild-type E. coli, cellular ClpP levels as determined by Western immunoblot analysis increased ca. sixfold as the levels of added SDS increased from 0 to 2%. Capsular colanic acid, measured as uronic acid, increased ca. sixfold as the levels of added SDS increased from 2 to 10%. Based on these findings, 3 of the 19 previously identified SDS shock proteins (M. Adamowicz, P. M. Kelley, and K. W. Nickerson, J. Bacteriol. 173:229-233, 1991) are tentatively identified as ClpP, ClpX, and ClpB.

摘要

我们研究了大肠杆菌的clpP和clpB突变体对十二烷基硫酸钠(SDS)的超敏反应。野生型大肠杆菌MC4100和lon突变体在10% SDS存在的情况下能够生长,而同源的clpP和clpB单突变体在SDS浓度高于0.5%时无法生长,clpA和clpX单突变体在SDS浓度高于5.0%时无法生长。对于野生型大肠杆菌,通过蛋白质免疫印迹分析测定的细胞ClpP水平,随着添加的SDS水平从0%增加到2%,大约增加了六倍。以糖醛酸衡量的荚膜多糖酸,随着添加的SDS水平从2%增加到10%,大约增加了六倍。基于这些发现,在先前鉴定的19种SDS休克蛋白中(M. Adamowicz、P. M. Kelley和K. W. Nickerson,《细菌学杂志》173:229 - 233,1991),暂时确定其中3种为ClpP、ClpX和ClpB。