Transcriptional regulation of the proton-translocating ATPase (atpIBEFHAGDC) operon of Escherichia coli: Control by cell growth rate

被引:58
作者
Kasimoglu, E
Park, SJ
Malek, J
Tseng, CP
Gunsalus, RP
机构
[1] UNIV CALIF LOS ANGELES,DEPT MICROBIOL & MOL GENET,LOS ANGELES,CA 90095
[2] UNIV CALIF LOS ANGELES,INST MOL BIOL,LOS ANGELES,CA 90095
关键词
D O I
10.1128/jb.178.19.5563-5567.1996
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The F0F1 proton-translocating ATPase complex of Escherichia coli, encoded by the atplBEFHAGDC operon, catalyzes the synthesis of ATP from ADP and P-i during aerobic and anaerobic growth when respiratory substrates are present, It can also catalyze the reverse reaction to hydrolyze ATP during nonrespiratory conditions (i.e., during fermentation of simple sugars) in order to maintain a electrochemical proton gradient across the cytoplasmic membrane, To examine how the atp genes are expressed under different conditions of cell culture, atpI-lacZ operon fusions were constructed and analyzed in single copy on the bacterial chromosome or on low-copy-number plasmids, Expression varied over a relatively narrow range (about threefold) regardless of the complexity of the cell growth medium, the availability of different electron accepters or carbon compounds, or the pH of the culture medium, In contrast to prior proposals, atp operon expression was shown to occur from a single promoter located immediately before atpI rather than from within it. The results of continuous-culture experiments suggest that the cell growth rate rather than the type of carbon compound used for growth is the major variable in controlling ntp gene expression, Together, these studies establish that synthesis of the F0F1 ATPase is not greatly varied by modulating atp operon transcription.
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页码:5563 / 5567
页数:5
相关论文
共 37 条
[11]   PCNB IS REQUIRED FOR THE RAPID DEGRADATION OF RNAI, THE ANTISENSE RNA THAT CONTROLS THE COPY NUMBER OF COLE1-RELATED PLASMIDS [J].
HE, L ;
SODERBOM, F ;
WAGNER, EGH ;
BINNIE, U ;
BINNS, N ;
MASTERS, M .
MOLECULAR MICROBIOLOGY, 1993, 9 (06) :1131-1142
[12]   ADAPTATION OF ESCHERICHIA-COLI TO REDOX ENVIRONMENTS BY GENE-EXPRESSION [J].
IUCHI, S ;
LIN, ECC .
MOLECULAR MICROBIOLOGY, 1993, 9 (01) :9-15
[13]   INVIVO 5' TERMINUS AND LENGTH OF THE MESSENGER-RNA FOR THE PROTON-TRANSLOCATING ATPASE (UNC) OPERON OF ESCHERICHIA-COLI [J].
JONES, HM ;
BRAJKOVICH, CM ;
GUNSALUS, RP .
JOURNAL OF BACTERIOLOGY, 1983, 155 (03) :1279-1287
[14]   NUCLEOTIDE-SEQUENCE OF THE GENES FOR FO COMPONENTS OF THE PROTON-TRANSLOCATING ATPASE FROM ESCHERICHIA-COLI - PREDICTION OF THE PRIMARY STRUCTURE OF FO SUBUNITS [J].
KANAZAWA, H ;
MABUCHI, K ;
KAYANO, T ;
NOUMI, T ;
SEKIYA, T ;
FUTAI, M .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1981, 103 (02) :613-620
[15]  
KANAZAWA H, 1983, BIOCHEM BIOPH RES CO, V107, P568
[16]  
LAPILATO J, 1986, MOL GEN GENET, V205, P285
[17]  
Maniatis T., 1982, MOL CLONING
[18]   DIFFERENTIAL GENE-EXPRESSION FROM THE ESCHERICHIA-COLI ATP OPERON MEDIATED BY SEGMENTAL DIFFERENCES IN MESSENGER-RNA STABILITY [J].
MCCARTHY, JEG ;
GERSTEL, B ;
SURIN, B ;
WIEDEMANN, U ;
ZIEMKE, P .
MOLECULAR MICROBIOLOGY, 1991, 5 (10) :2447-2458
[19]   EXPRESSION OF THE UNC GENES IN ESCHERICHIA-COLI [J].
MCCARTHY, JEG .
JOURNAL OF BIOENERGETICS AND BIOMEMBRANES, 1988, 20 (01) :19-39
[20]   A NEW PAIR OF M13 VECTORS FOR SELECTING EITHER DNA STRAND OF DOUBLE-DIGEST RESTRICTION FRAGMENTS [J].
MESSING, J ;
VIEIRA, J .
GENE, 1982, 19 (03) :269-276