The membrane-bound H+-ATPase complex is essential for growth of Lactococcus lactis

被引:76
作者
Koebmann, BJ
Nilsson, D
Kuipers, OP
Jensen, PR
机构
[1] Tech Univ Denmark, Dept Microbiol, DK-2800 Lyngby, Denmark
[2] Chr Hansen AS, Dept Physiol, DK-2970 Horsholm, Denmark
[3] NIZO Food Res, Microbial Ingredients Sect, NL-6710 BA Ede, Netherlands
关键词
D O I
10.1128/JB.182.17.4738-4743.2000
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The eight genes which encode the (F1F0) H+-ATPase in Lactococcus lactis subsp, cremoris MG1363 were cloned and sequenced. The genes were organized in an operon with the gene order atpEBFNAGDC; i.e., the order of atpE and atpB is reversed with respect to the more typical bacterial organization. The deduced amino acid sequences of the corresponding H+-ATPase subunits showed significant homology with the subunits from other organisms. Results of Northern blot analysis showed a transcript at approximately 7 kb, which corresponds to the size of the atp operon, The transcription initiation site was mapped by primer extension and coincided with a standard promoter sequence. In order to analyze the importance of the H+-ATPase for L, lactis physiology, a mutant strain was constructed in which the original atp promoter on the chromosome was replaced with an inducible nisin promoter. When grown on GM17 plates the resulting strain was completely dependent on the presence of nisin for growth. These data demonstrate that the H+-ATPase is essential for growth oft. lactis under these conditions.
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页码:4738 / 4743
页数:6
相关论文
共 43 条
[1]   STRUCTURE AT 2.8-ANGSTROM RESOLUTION OF F1-ATPASE FROM BOVINE HEART-MITOCHONDRIA [J].
ABRAHAMS, JP ;
LESLIE, AGW ;
LUTTER, R ;
WALKER, JE .
NATURE, 1994, 370 (6491) :621-628
[2]   ALTERED EXPRESSION OF THE H+ ATPASE IN STREPTOCOCCUS-FAECALIS MEMBRANES [J].
ABRAMS, A ;
JENSEN, C .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1984, 122 (01) :151-157
[3]   GENETIC AND MOLECULAR ANALYSIS OF THE RPOD GENE FROM LACTOCOCCUS-LACTIS [J].
ARAYA, T ;
ISHIBASHI, N ;
SHIMAMURA, S ;
TANAKA, K ;
TAKAHASHI, H .
BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 1993, 57 (01) :88-92
[4]   ACID TOLERANCE, PROTON PERMEABILITIES, AND MEMBRANE ATPASES OF ORAL STREPTOCOCCI [J].
BENDER, GR ;
SUTTON, SVW ;
MARQUIS, RE .
INFECTION AND IMMUNITY, 1986, 53 (02) :331-338
[5]   SYNTHETIC CURVED DNA-SEQUENCES CAN ACT AS TRANSCRIPTIONAL ACTIVATORS IN ESCHERICHIA-COLI [J].
BRACCO, L ;
KOTLARZ, D ;
KOLB, A ;
DIEKMANN, S ;
BUC, H .
EMBO JOURNAL, 1989, 8 (13) :4289-4296
[6]   ENERGY RECYCLING BY LACTATE EFFLUX IN GROWING AND NONGROWING CELLS OF STREPTOCOCCUS-CREMORIS [J].
BRINK, BT ;
OTTO, R ;
HANSEN, UP ;
KONINGS, WN .
JOURNAL OF BACTERIOLOGY, 1985, 162 (01) :383-390
[7]  
BRUSILOW WSA, 1989, J BIOL CHEM, V264, P1528
[8]   ANALYSIS OF GENE-CONTROL SIGNALS BY DNA-FUSION AND CLONING IN ESCHERICHIA-COLI [J].
CASADABAN, MJ ;
COHEN, SN .
JOURNAL OF MOLECULAR BIOLOGY, 1980, 138 (02) :179-207
[9]   GENE ORGANIZATION, PRIMARY STRUCTURE AND RNA PROCESSING ANALYSIS OF A RIBOSOMAL-RNA OPERON IN LACTOCOCCUS-LACTIS [J].
CHIARUTTINI, C ;
MILET, M .
JOURNAL OF MOLECULAR BIOLOGY, 1993, 230 (01) :57-76
[10]   THE ORGANIZATION AND SEQUENCE OF THE GENES FOR ATP SYNTHASE SUBUNITS IN THE CYANOBACTERIUM SYNECHOCOCCUS-6301 - SUPPORT FOR AN ENDOSYMBIOTIC ORIGIN OF CHLOROPLASTS [J].
COZENS, AL ;
WALKER, JE .
JOURNAL OF MOLECULAR BIOLOGY, 1987, 194 (03) :359-383