ISOLATION AND CHARACTERIZATION OF KIKA, A REGION ON INCN GROUP PLASMIDS THAT DETERMINES KILLING OF KLEBSIELLA-OXYTOCA

被引:11
作者
HENGEN, PN
DENICOURT, D
IYER, VN
机构
[1] CARLETON UNIV,DEPT BIOL,OTTAWA K1S 5B6,ONTARIO,CANADA
[2] CARLETON UNIV,INST BIOCHEM,OTTAWA K1S 5B6,ONTARIO,CANADA
关键词
D O I
10.1128/JB.174.9.3070-3077.1992
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Transfer of the IncN group plasmid pCU1 from Escherichia coli to Klebsiella oxytoca by conjugation kills a large proportion (90 to 95%) of the recipients of plasmid DNA, whereas transfer to E. coli or even to the closely related Enterobacter aerogenes does not. Two regions, kikA and kikB, have been identified on pCU1 that contribute to the Kik (killing in klebsiellas) phenotype. We have localized the kikA region to 500 bp by deletion analysis and show by DNA-DNA hybridization that kikA is highly conserved among the plasmids of incompatibility group N. The expression in K. oxytoca of kikA under the control of the strong inducible E. coli tac promoter results in loss of cell viability. The nucleotide sequence showed two overlapping open reading frames (ORFs) within the kikA region. The first ORF codes for a putative polypeptide of 104 amino acids (ORF104). The second ORF codes for a 70-amino-acid polypeptide (ORF70). The properties of the putative protein encoded by ORF104 and gene fusions of kikA to alkaline phosphatase by using TnphoA suggest that killing may involve an association with the bacterial membrane; however, we could not rule out the possibility that ORF70 plays a role in the Kik phenotype.
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页码:3070 / 3077
页数:8
相关论文
共 55 条
[1]  
AKIMOTO S, 1986, FEMS MICROBIOL LETT, V33, P241
[2]   RESTORATION OF MUTABILITY IN NON-MUTABLE ESCHERICHIA-COLI CARRYING DIFFERENT PLASMIDS [J].
BABUDRI, N ;
MONTIBRAGADIN, C .
MOLECULAR & GENERAL GENETICS, 1977, 155 (03) :287-290
[3]   PEDIGREES OF SOME MUTANT STRAINS OF ESCHERICHIA-COLI K-12 [J].
BACHMANN, BJ .
BACTERIOLOGICAL REVIEWS, 1972, 36 (04) :525-557
[4]   THE NIF PROMOTERS OF KLEBSIELLA-PNEUMONIAE HAVE A CHARACTERISTIC PRIMARY STRUCTURE [J].
BEYNON, J ;
CANNON, M ;
BUCHANANWOLLASTON, V ;
CANNON, F .
CELL, 1983, 34 (02) :665-671
[5]  
BIRNBOIM HC, 1979, NUCLEIC ACIDS RES, V7, P1513
[6]   CONSTRUCTION AND CHARACTERIZATION OF NEW CLONING VEHICLES .2. MULTIPURPOSE CLONING SYSTEM [J].
BOLIVAR, F ;
RODRIGUEZ, RL ;
GREENE, PJ ;
BETLACH, MC ;
HEYNEKER, HL ;
BOYER, HW ;
CROSA, JH ;
FALKOW, S .
GENE, 1977, 2 (02) :95-113
[7]   KILLING OF ESCHERICHIA-COLI-CELLS MODULATED BY COMPONENTS OF THE STABILITY SYSTEM PARD OF PLASMID R1 [J].
BRAVO, A ;
ORTEGA, S ;
DETORRONTEGUI, G ;
DIAZ, R .
MOLECULAR & GENERAL GENETICS, 1988, 215 (01) :146-151
[8]   A PHYSICAL AND GENETIC-MAP OF THE INCN PLASMID R46 [J].
BROWN, AMC ;
WILLETTS, NS .
PLASMID, 1981, 5 (02) :188-201
[9]   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
[10]   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