The general secretion pathway of Erwinia carotovora subsp carotovora: Analysis of the membrane topology of OutC and OutF

被引:52
作者
Thomas, JD
Reeves, PJ
Salmond, GPC
机构
[1] UNIV CAMBRIDGE,DEPT BIOCHEM,CAMBRIDGE CB2 1QW,ENGLAND
[2] UNIV WARWICK,DEPT BIOL SCI,COVENTRY CV4 7AL,W MIDLANDS,ENGLAND
来源
MICROBIOLOGY-UK | 1997年 / 143卷
关键词
Erwinia carotovora; out proteins; membrane topology; secretion; beta-lactamase;
D O I
10.1099/00221287-143-3-713
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The out gene cluster of Erwinia carotovora subsp, carotovora (Ecc) encodes the proteins of the type II or general secretory pathway (GSP) apparatus which is required for secretion of pectinase and cellulase. In this study, fusions between Ecc out genes and the topology probe blaM were constructed. The ability of Out protein domains to export BlaM across the cytoplasmic membrane in both Escherichia coli and the cognate host was utilized to confirm the computer-predicted cytoplasmic membrane topology of OutC and OutF. When outC was fused to blaM, the resulting phenotype suggested that the majority of OutC is targeted to the periplasm, typical of a type II bitopic conformation in the cytoplasmic membrane. In contrast, for the outF gene product, three transmembrane regions were identified which connect a large N-terminal cytoplasmic domain, a smaller periplasmic domain, and a large cytoplasmic loop. Fusions between blaM and outD and outE were used to further substantiate the locations of these gene products in the outer membrane and the cytoplasm respectively. The data derived suggest that a number of the Out apparatus components possess domains in the cytoplasm and/or the periplasm with potential for protein-protein interactions which facilitate the secretion of periplasmic enzyme intermediates across the outer membrane to the external milieu.
引用
收藏
页码:713 / 720
页数:8
相关论文
共 24 条
[1]   Membrane topology of three Xcp proteins involved in exoprotein transport by Pseudomonas aeruginosa [J].
Bleves, S ;
Lazdunski, A ;
Filloux, A .
JOURNAL OF BACTERIOLOGY, 1996, 178 (14) :4297-4300
[2]   BETA-LACTAMASE AS A PROBE OF MEMBRANE-PROTEIN ASSEMBLY AND PROTEIN EXPORT [J].
BROOMESMITH, JK ;
TADAYYON, M ;
ZHANG, Y .
MOLECULAR MICROBIOLOGY, 1990, 4 (10) :1637-1644
[3]   ANALYSIS OF LAMBDA-RECEPTOR AND BETA-LACTAMASE SYNTHESIS AND EXPORT USING CLONED GENES IN A MINI-CELL SYSTEM [J].
CLEMENT, J ;
PERRIN, D ;
HEDGPETH, J .
MOLECULAR AND GENERAL GENETICS, 1982, 185 (02) :302-310
[4]  
DENFERT C, 1989, J BIOL CHEM, V264, P17462
[5]   USE OF A BETA-LACTAMASE FUSION VECTOR TO INVESTIGATE THE ORGANIZATION OF PENICILLIN-BINDING PROTEIN 1B IN THE CYTOPLASMIC MEMBRANE OF ESCHERICHIA-COLI [J].
EDELMAN, A ;
BOWLER, L ;
BROOMESMITH, JK ;
SPRATT, BG .
MOLECULAR MICROBIOLOGY, 1987, 1 (01) :101-106
[6]  
Gibson T.J., 1984, THESIS CAMBRIDGE U E
[7]   STUDIES ON TRANSFORMATION OF ESCHERICHIA-COLI WITH PLASMIDS [J].
HANAHAN, D .
JOURNAL OF MOLECULAR BIOLOGY, 1983, 166 (04) :557-580
[8]   Insertion of an outer membrane protein in Escherichia coli requires a chaperone-like protein [J].
Hardie, KR ;
Lory, S ;
Pugsley, AP .
EMBO JOURNAL, 1996, 15 (05) :978-988
[9]   SUBCELLULAR LOCATION OF XPSD, A PROTEIN REQUIRED FOR EXTRACELLULAR PROTEIN SECRETION BY XANTHOMONAS-CAMPESTRIS PV CAMPESTRIS [J].
HU, NT ;
HUNG, MN ;
LIAO, CT ;
LI, MH .
MICROBIOLOGY-UK, 1995, 141 :1395-1406
[10]   SEQUENCE ELEMENTS DETERMINING AMPC PROMOTER STRENGTH IN ESCHERICHIA-COLI [J].
JAURIN, B ;
GRUNDSTROM, T ;
NORMARK, S .
EMBO JOURNAL, 1982, 1 (07) :875-881