FTSL, AN ESSENTIAL CYTOPLASMIC MEMBRANE-PROTEIN INVOLVED IN CELL-DIVISION IN ESCHERICHIA-COLI

被引:123
作者
GUZMAN, LM
BARONDESS, JJ
BECKWITH, J
机构
[1] HARVARD UNIV,SCH MED,DEPT MICROBIOL & MOLEC GENET,200 LONGWOOD AVE,BOSTON,MA 02115
[2] HARVARD UNIV,SCH MED,PROGRAM CELL & DEV BIOL,BOSTON,MA 02115
关键词
D O I
10.1128/JB.174.23.7717-7728.1992
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We have identified a gene involved in bacterial cell division, located immediately upstream of the ftsI gene in the min 2 region of the Escherichia coli chromosome. This gene, which we named ftsL, was detected through characterization of TnphoA insertions in a plasmid containing this chromosomal region. TnphoA topological analysis and fractionation of alkaline phosphatase fusion proteins indicated that the ftsL gene product is a 13.6-kDa cytoplasmic membrane protein with a cytoplasmic amino terminus, a single membrane-spanning segment, and a periplasmic carboxy terminus. The ftsL gene is essential for cell growth and division. A null mutation in ftsL resulted in inhibition of cell division, formation of long, nonseptate filaments, ultimate cessation of growth, and lysis. Under certain growth conditions, depletion of FtsL or expression of the largest ftsL-phoA fusion produced a variety of cell morphologies, including Y-shaped bacteria, indicating a possible general weakening of the cell wall. The FtsL protein is estimated to be present at about 20 to 40 copies per cell. The periplasmic domain of the protein displays a sequence with features characteristic of leucine zippers, which are involved in protein dimerization.
引用
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页码:7716 / 7728
页数:13
相关论文
共 49 条
[11]   THE FTSQ PROTEIN OF ESCHERICHIA-COLI - MEMBRANE TOPOLOGY, ABUNDANCE, AND CELL-DIVISION PHENOTYPES DUE TO OVERPRODUCTION AND INSERTION MUTATIONS [J].
CARSON, MJ ;
BARONDESS, J ;
BECKWITH, J .
JOURNAL OF BACTERIOLOGY, 1991, 173 (07) :2187-2195
[12]  
CORMACK B, COMMUNICATION
[13]   BACTERIAL-CELL DIVISION [J].
DEBOER, PAJ ;
COOK, WR ;
ROTHFIELD, LI .
ANNUAL REVIEW OF GENETICS, 1990, 24 :249-274
[14]   ROLES OF MINC AND MIND IN THE SITE-SPECIFIC SEPTATION BLOCK MEDIATED BY THE MINCDE SYSTEM OF ESCHERICHIA-COLI [J].
DEBOER, PAJ ;
CROSSLEY, RE ;
ROTHFIELD, LI .
JOURNAL OF BACTERIOLOGY, 1992, 174 (01) :63-70
[15]  
Donachie W.D., 1987, ESCHERICHIA COLI SAL, P1578
[16]   AN AMINO-PROXIMAL DOMAIN REQUIRED FOR THE LOCALIZATION OF FTSQ IN THE CYTOPLASMIC MEMBRANE, AND FOR ITS BIOLOGICAL FUNCTION IN ESCHERICHIA-COLI [J].
DOPAZO, A ;
PALACIOS, P ;
SANCHEZ, M ;
PLA, J ;
VICENTE, M .
MOLECULAR MICROBIOLOGY, 1992, 6 (06) :715-722
[17]   EXPORT AND PROCESSING ANALYSIS OF A FUSION BETWEEN THE EXTRACELLULAR HEAT-STABLE ENTEROTOXIN AND THE PERIPLASMIC B-SUBUNIT OF THE HEAT-LABILE ENTEROTOXIN IN ESCHERICHIA-COLI [J].
GUZMANVERDUZCO, LM ;
KUPERSZTOCH, YM .
MOLECULAR MICROBIOLOGY, 1990, 4 (02) :253-264
[18]   THERMOSENSITIVE MUTANTS OF E COLI AFFECTED IN PROCESSES OF DNA SYNTHESIS AND CELLULAR DIVISION [J].
HIROTA, Y ;
RYTER, A ;
JACOB, F .
COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY, 1968, 33 :677-+
[19]   PEPTIDOGLYCAN SYNTHETIC ENZYME-ACTIVITIES OF HIGHLY PURIFIED PENICILLIN-BINDING PROTEIN-3 IN ESCHERICHIA-COLI - A SEPTUM-FORMING REACTION SEQUENCE [J].
ISHINO, F ;
MATSUHASHI, M .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1981, 101 (03) :905-911
[20]   NEW MUTATIONS FTS-36, LTS-33, AND FTSW CLUSTERED IN THE MRA REGION OF THE ESCHERICHIA-COLI CHROMOSOME INDUCE THERMOSENSITIVE CELL-GROWTH AND DIVISION [J].
ISHINO, F ;
JUNG, HK ;
IKEDA, M ;
DOI, M ;
WACHI, M ;
MATSUHASHI, M .
JOURNAL OF BACTERIOLOGY, 1989, 171 (10) :5523-5530