AZIDE-RESISTANT MUTANTS OF ESCHERICHIA-COLI ALTER THE SECA-PROTEIN, AN AZIDE-SENSITIVE COMPONENT OF THE PROTEIN EXPORT MACHINERY

被引:296
作者
OLIVER, DB
CABELLI, RJ
DOLAN, KM
JAROSIK, GP
机构
[1] Department of Microbiology, State University of New York, Stony Brook
关键词
ATPase inhibitors; protein translocation; sodium azide;
D O I
10.1073/pnas.87.21.8227
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Escherichia coli azi mutants, whose growth is resistant to millimolar concentrations of sodium azide, were among the earliest E. coli mutants isolated. Genetic complementation, mapping, and DNA sequence analysis now show that these mutations are alleles of the secA gene, which is essential for protein export across the E. coli plasma membrane. We have found that sodium azide is an extremely rapid and potent inhibitor of protein export in vivo and that azi mutants are more resistant to such inhibition. Furthermore, SecA-dependent in vitro protein translocation and ATPase activities are inhibited by sodium azide, and SecA protein prepared from an azi mutant strain is more resistant to such inhibition. These studies point to the utility of specific inhibitors of protein export, such as sodium azide, in facilitating the dissection of the function of individual components of the protein export machinery.
引用
收藏
页码:8227 / 8231
页数:5
相关论文
共 36 条
[1]  
BHATNAGAR SK, 1988, J BIOL CHEM, V263, P8953
[2]   GENETIC APPROACHES TO THE ANALYSIS OF MICROBIAL DEVELOPMENT [J].
BOTSTEIN, D ;
MAURER, R .
ANNUAL REVIEW OF GENETICS, 1982, 16 :61-83
[3]   SECA PROTEIN IS REQUIRED FOR SECRETORY PROTEIN TRANSLOCATION INTO ESCHERICHIA-COLI MEMBRANE-VESICLES [J].
CABELLI, RJ ;
CHEN, LL ;
TAI, PC ;
OLIVER, DB .
CELL, 1988, 55 (04) :683-692
[4]   ATP IS ESSENTIAL FOR PROTEIN TRANSLOCATION INTO ESCHERICHIA-COLI MEMBRANE-VESICLES [J].
CHEN, LL ;
TAI, PC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (13) :4384-4388
[5]  
CHIN DT, 1988, J BIOL CHEM, V263, P11718
[6]   70K HEAT-SHOCK RELATED PROTEINS STIMULATE PROTEIN TRANSLOCATION INTO MICROSOMES [J].
CHIRICO, WJ ;
WATERS, MG ;
BLOBEL, G .
NATURE, 1988, 332 (6167) :805-810
[7]   PROOMPA IS STABILIZED FOR MEMBRANE TRANSLOCATION BY EITHER PURIFIED ESCHERICHIA-COLI TRIGGER FACTOR OR CANINE SIGNAL RECOGNITION PARTICLE [J].
CROOKE, E ;
GUTHRIE, B ;
LECKER, S ;
LILL, R ;
WICKNER, W .
CELL, 1988, 54 (07) :1003-1011
[8]   SPECIFIC RECOGNITION OF THE LEADER REGION OF PRECURSOR PROTEINS IS REQUIRED FOR THE ACTIVATION OF TRANSLOCATION ATPASE OF ESCHERICHIA-COLI [J].
CUNNINGHAM, K ;
WICKNER, W .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (22) :8630-8634
[9]   SECA PROTEIN, A PERIPHERAL PROTEIN OF THE ESCHERICHIA-COLI PLASMA-MEMBRANE, IS ESSENTIAL FOR THE FUNCTIONAL BINDING AND TRANSLOCATION OF PROOMPA [J].
CUNNINGHAM, K ;
LILL, R ;
CROOKE, E ;
RICE, M ;
MOORE, K ;
WICKNER, W ;
OLIVER, D .
EMBO JOURNAL, 1989, 8 (03) :955-959
[10]   A SUBFAMILY OF STRESS PROTEINS FACILITATES TRANSLOCATION OF SECRETORY AND MITOCHONDRIAL PRECURSOR POLYPEPTIDES [J].
DESHAIES, RJ ;
KOCH, BD ;
WERNERWASHBURNE, M ;
CRAIG, EA ;
SCHEKMAN, R .
NATURE, 1988, 332 (6167) :800-805