CLPB IS THE ESCHERICHIA-COLI HEAT-SHOCK PROTEIN F84.1

被引:294
作者
SQUIRES, CL [1 ]
PEDERSEN, S [1 ]
ROSS, BM [1 ]
SQUIRES, C [1 ]
机构
[1] UNIV COPENHAGEN,INST MICROBIOL,DK-1353 COPENHAGEN,DENMARK
关键词
D O I
10.1128/JB.173.14.4254-4262.1991
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
ClpB is thought to be involved in proteolysis because of its sequence similarity to the ClpA subunit of the ClpA-ClpP protease. It has recently been shown that ClpP is a heat shock protein. Here we show that ClpB is the Escherichia coli heat shock protein F84.1. The F84.1 protein was overproduced in strains containing the clpB gene on a plasmid and was absent from two-dimensional gels from a clpB null mutation. Besides possessing a slower growth rate at 44-degrees-C, the null mutant strain had a higher rate of death at 50-degrees-C. We used reverse transcription of in vivo mRNA to show that the clpB gene was expressed from a sigma-32-specific promoter consensus sequence at both 37 and 42-degrees-C. We noted that the clpB+ gene also caused the appearance of a second protein spot, F68.5, on two-dimensional gels. This spot was approximately 147 amino acids smaller than F84.1 and most probably is the result of a second translational start on the clpB mRNA. F68.5 can be observed on many published two-dimensional gels of heat-induced E. coli proteins, but the original catalog of 17 heat shock proteins did not include this spot.
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页码:4254 / 4262
页数:9
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