Analysis of the carbapenem gene cluster of Erwinia carotovora: definition of the antibiotic biosynthetic genes and evidence for a novel beta-lactam resistance mechanism

被引:70
作者
McGowan, SJ
Sebaihia, M
OLeary, S
Hardie, KR
Williams, P
Stewart, GSAB
Bycroft, BW
Salmond, GPC
机构
[1] UNIV CAMBRIDGE, DEPT BIOCHEM, CAMBRIDGE CB2 1QW, ENGLAND
[2] UNIV NOTTINGHAM, DEPT PHARMACEUT SCI, NOTTINGHAM NG7 2RD, ENGLAND
[3] UNIV NOTTINGHAM, FAC AGR & FOOD SCI, DEPT APPL BIOCHEM & FOOD SCI, SUTTON LE12 5RD, SURREY, ENGLAND
关键词
D O I
10.1046/j.1365-2958.1997.6001974.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Members of two genera of Gram-negative bacteria, Serratia and Erwinia, produce a beta-lactam antibiotic, 1-carbapen-2-em-3-carboxylic acid. We have reported previously the cloning and sequencing of the genes responsible for production of this carbapenem in Erwinia carotovora. These genes are organized as an operon, carA-H, and are controlled by a LuxR-type transcriptional activator, encoded by the linked carR gene. We report in this paper the genetic dissection of this putative operon to determine the function of each of the genes. We demonstrate by mutational analysis that the products of the first five genes of the operon are involved in the synthesis of the carbapenem molecule. Three of these, carABC, are absolutely required. In addition, we provide evidence for the existence of a novel carbapenem resistance mechanism, encoded by the carF and carG genes. Both products of these overlapping and potentially translationally coupled genes have functional, N-terminal signal peptides. Removal of these genes from the Erwinia chromosome results in a carbapenem-sensitive phenotype. We assume that these novel beta-lactam resistance genes have evolved in concert with the biosynthetic genes to ensure 'self-resistance' in the Erwinia carbapenem producer.
引用
收藏
页码:545 / 556
页数:12
相关论文
共 35 条
[1]   N-(3-OXOHEXANOYL)-L-HOMOSERINE LACTONE REGULATES CARBAPENEM ANTIBIOTIC PRODUCTION IN ERWINIA-CAROTOVORA [J].
BAINTON, NJ ;
STEAD, P ;
CHHABRA, SR ;
BYCROFT, BW ;
SALMOND, GPC ;
STEWART, GSAB ;
WILLIAMS, P .
BIOCHEMICAL JOURNAL, 1992, 288 :997-1004
[2]   THE BIOSYNTHETIC IMPLICATIONS OF ACETATE AND GLUTAMATE INCORPORATION INTO (3R,5R)-CARBAPENAM-3-CARBOXYLIC ACID AND (5R)-CARBAPEN-2-EM-3-CARBOXYLIC ACID BY SERRATIA SP [J].
BYCROFT, BW ;
MASLEN, C ;
BOX, SJ ;
BROWN, A ;
TYLER, JW .
JOURNAL OF ANTIBIOTICS, 1988, 41 (09) :1231-1242
[3]   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
[4]   THE PMTL NIC-CLONING VECTORS .1. IMPROVED PUC POLYLINKER REGIONS TO FACILITATE THE USE OF SONICATED DNA FOR NUCLEOTIDE SEQUENCING [J].
CHAMBERS, SP ;
PRIOR, SE ;
BARSTOW, DA ;
MINTON, NP .
GENE, 1988, 68 (01) :139-149
[5]   CONSTRUCTION AND CHARACTERIZATION OF AMPLIFIABLE MULTICOPY DNA CLONING VEHICLES DERIVED FROM P15A CRYPTIC MINIPLASMID [J].
CHANG, ACY ;
COHEN, SN .
JOURNAL OF BACTERIOLOGY, 1978, 134 (03) :1141-1156
[6]  
Dowson Christopher G., 1994, Trends in Microbiology, V2, P361, DOI 10.1016/0966-842X(94)90612-2
[7]   EVALUATION OF IMIPENEM CILASTATIN AGAINST NOSOCOMIAL INFECTIONS AND MULTIRESISTANT PATHOGENS [J].
GIAMARELLOU, H ;
SFIKAKIS, P ;
VOUTSINAS, D ;
GALANAKIS, N ;
DAIKOS, GK .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1986, 18 :175-179
[8]   A BROAD-HOST-RANGE CLONING VECTOR TRANSPOSABLE TO VARIOUS REPLICONS [J].
GRINTER, NJ .
GENE, 1983, 21 (1-2) :133-143
[9]   STUDIES ON TRANSFORMATION OF ESCHERICHIA-COLI WITH PLASMIDS [J].
HANAHAN, D .
JOURNAL OF MOLECULAR BIOLOGY, 1983, 166 (04) :557-580
[10]   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