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ANALYSIS OF THE 1ST 2 GENES OF THE CS1 FIMBRIAL OPERON IN HUMAN ENTEROTOXIGENIC ESCHERICHIA-COLI OF SEROTYPE 0139-H28
被引:15
作者:
JORDI, BJAM
VANVLIET, AHM
WILLSHAW, GA
VANDERZEIJST, BAM
GAASTRA, W
机构:
[1] STATE UNIV UTRECHT,FAC VET MED,INST INFECT DIS & IMMUNOL,DEPT BACTERIOL,YALELAAN 1,POB 80165,3508 TD UTRECHT,NETHERLANDS
[2] CENT PUBL HLTH LAB,DIV ENTER PATHOGENS,LONDON NW9 5HT,ENGLAND
关键词:
ESCHERICHIA-COLI;
ENTEROTOXIGENIC;
CS1;
FIMBRIAE;
STRUCTURAL GENE;
NUCLEOTIDE SEQUENCE;
PROMOTER REGION;
D O I:
10.1111/j.1574-6968.1991.tb04673.x
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
An oligonucleotide, derived from the N-terminal amino acid sequence of the CS1 fimbrial subunit protein was used to identify the subunit gene on recombinant plasmid pDEP23 containing the structural genes of the Cs1 fimbrial operon. The nucleotide sequence of the subunit gene (cosA), encoding a protein of 171 amino acids, was determined. Flanking it upstream, a gene (csoB) encoding a protein of 238 amino acids was found. The CsoB and CsoA proteins are homologous to the CfaA and CfaB proteins in the CFA/I fimbrial operon. For all the CS1 producing strains investigated the structural genes are located on plasmids. Like CFA/I fimbriae, CS1 fimbriae are only expressed in the presence of a positive regulator, CfaD for CFA/I and Rns for CS1, respectively. The promoter region upstream of the csoB gene was cloned in front of the promoterless alkaline phosphatase (phoA) gene of the promoter-probe vector pCB267. PhoA activity was enhanced approximately two-fold by the introduction of compatible plasmids containing either rns of cfaD.
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页码:265 / 270
页数:6
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