A NEW ESCHERICHIA-COLI HEAT-SHOCK GENE, HTRC, WHOSE PRODUCT IS ESSENTIAL FOR VIABILITY ONLY AT HIGH-TEMPERATURES

被引:49
作者
RAINA, S
GEORGOPOULOS, C
机构
[1] Dept. Cell./Viral/Mol. Biology, University of Utah Med. Center, Salt Lake City
关键词
D O I
10.1128/jb.172.6.3417-3426.1990
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We identified and characterized a new Escherichia coli gene, htrC. Inactivation of the htrC gene results in the inability to form colonies at 42°C. An identical bacterial phenotype is found whether the htrC gene is inactivated either to Tn5 insertions or by a deletion spanning the entire gene. The htrC gene has been localized at 90 min, immediately downstream of the rpoC gene, and has been previously sequenced. It codes for a basic polypeptide with an M(r) of 21,130. The htrC gene is under heat shock regulation, since it is transcribed actively only in bacteria possessing functional σ32. Inactivation of htrC results in (i) bacterial filamentation at intermediate temperatures, (ii) cell lysis at temperatures above 42°C, (iii) overproduction of σ32-dependent heat shock proteins at all temperatures, (iv) overproduction of a few additional polypeptides, (v) underproduction of many polypeptides, and (vi) an overall defect in cellular proteolysis as judged by the reduced rate of puromycyl polypeptide degradation. In addition, the presence of an htrC mutation eliminates the UV sensitivity normally exhibited by lon mutant bacteria.
引用
收藏
页码:3417 / 3426
页数:10
相关论文
共 39 条
[1]   THE HEAT-SHOCK-REGULATED GRPE GENE OF ESCHERICHIA-COLI IS REQUIRED FOR BACTERIAL-GROWTH AT ALL TEMPERATURES BUT IS DISPENSABLE IN CERTAIN MUTANT BACKGROUNDS [J].
ANG, D ;
GEORGOPOULOS, C .
JOURNAL OF BACTERIOLOGY, 1989, 171 (05) :2748-2755
[2]   CELL-SHAPE AND DIVISION IN ESCHERICHIA-COLI - EXPERIMENTS WITH SHAPE AND DIVISION MUTANTS [J].
BEGG, KJ ;
DONACHIE, WD .
JOURNAL OF BACTERIOLOGY, 1985, 163 (02) :615-622
[3]  
BERG DE, 1983, GENETICS, V105, P813
[4]   A PSC101-DERIVED PLASMID WHICH SHOWS NO SEQUENCE HOMOLOGY TO OTHER COMMONLY USED CLONING VECTORS [J].
CHURCHWARD, G ;
BELIN, D ;
NAGAMINE, Y .
GENE, 1984, 31 (1-3) :165-171
[5]  
Colman A., 1984, TRANSCRIPTION TRANSL, P49
[6]   CONSENSUS SEQUENCE FOR ESCHERICHIA-COLI HEAT-SHOCK GENE PROMOTERS [J].
COWING, DW ;
BARDWELL, JCA ;
CRAIG, EA ;
WOOLFORD, C ;
HENDRIX, RW ;
GROSS, CA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (09) :2679-2683
[7]   IDENTIFICATION OF THE SIGMA-E SUBUNIT OF ESCHERICHIA-COLI RNA-POLYMERASE - A 2ND ALTERNATE SIGMA-FACTOR INVOLVED IN HIGH-TEMPERATURE GENE-EXPRESSION [J].
ERICKSON, JW ;
GROSS, CA .
GENES & DEVELOPMENT, 1989, 3 (09) :1462-1471
[8]   THE GROES AND GROEL HEAT-SHOCK GENE-PRODUCTS OF ESCHERICHIA-COLI ARE ESSENTIAL FOR BACTERIAL-GROWTH AT ALL TEMPERATURES [J].
FAYET, O ;
ZIEGELHOFFER, T ;
GEORGOPOULOS, C .
JOURNAL OF BACTERIOLOGY, 1989, 171 (03) :1379-1385
[9]   INTERPOSON MUTAGENESIS OF SOIL AND WATER BACTERIA - A FAMILY OF DNA FRAGMENTS DESIGNED FOR INVITRO INSERTIONAL MUTAGENESIS OF GRAM-NEGATIVE BACTERIA [J].
FELLAY, R ;
FREY, J ;
KRISCH, H .
GENE, 1987, 52 (2-3) :147-154
[10]   INTERACTIONS OF BACTERIOPHAGE AND HOST MACROMOLECULES IN THE GROWTH OF BACTERIOPHAGE-LAMBDA [J].
FRIEDMAN, DI ;
OLSON, ER ;
GEORGOPOULOS, C ;
TILLY, K ;
HERSKOWITZ, I ;
BANUETT, F .
MICROBIOLOGICAL REVIEWS, 1984, 48 (04) :299-325