EVIDENCE THAT A NOVEL TETRACYCLINE RESISTANCE GENE FOUND ON 2 BACTEROIDES TRANSPOSONS ENCODES AN NADP-REQUIRING OXIDOREDUCTASE

被引:129
作者
SPEER, BS [1 ]
BEDZYK, L [1 ]
SALYERS, AA [1 ]
机构
[1] UNIV ILLINOIS,DEPT MICROBIOL,URBANA,IL 61801
关键词
D O I
10.1128/jb.173.1.176-183.1991
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Two transposons, Tn4351 and Tn4400, which were originally isolated from the obligate anaerobe Bacteroides fragilis, carry a tetracycline resistance (Tc(r)) gene that confers resistance only on aerobically grown Escherichia coli. This aerobic Tc(r) gene, designated tetX, has been shown previously to act by chemically modifying tetracycline in a reaction that appears to require oxygen. We have now obtained the DNA sequence of tetX and 0.6 kb of its upstream region from Tn4400. Analysis of the DNA sequence of tetX revealed that this gene encoded a 43.7-kDa protein. The deduced amino acid sequence of the amino terminus of the protein had homology with a number of enzymes, all of which had in common a requirement for NAD(P). In an earlier study, we had observed the disrupted cells, could not carry out the alteration of tetracycline. We have now shown that if NADPH (1 mM) is added to the disrupted cell preparation, alteration of tetracycline occurs. Thus, TetX appears to be an NADP-requiring oxidoreductase. Tn4400 conferred a fivefold-lower level of tetracycline resistance than Tn4351. This finding appears to be due to a lower level of expression of the tetX on Tn4400, because of the activity of a tetX-lacZ fusion from Tn4400 was 10-fold lower than that of the same fusion from Tn4351. A comparison of the sequence of the tetX region on Tn4351 with that on Tn4400 showed that the only difference between the upstream regions of the two transposons was a 4-base change 350 bp upstream of the start of the tetX coding region. The 4-base change difference creates a good consensus -35 region on Tn4351 that is not present on Tn4400 and could be creating an extra promoter.
引用
收藏
页码:176 / 183
页数:8
相关论文
共 25 条
[1]   SELECTION OF LAC GENE FUSIONS INVIVO - OMPR-LACZ FUSIONS THAT DEFINE A FUNCTIONAL DOMAIN OF THE OMPR GENE-PRODUCT [J].
BERMAN, ML ;
JACKSON, DE .
JOURNAL OF BACTERIOLOGY, 1984, 159 (02) :750-756
[2]   REINSTATEMENT OF SPECIES RANK FOR BACTEROIDES-FRAGILIS, BACTEROIDES-OVATUS, BACTEROIDES-DISTASONIS, BACTEROIDES-THETAIOTAOMICRON, AND BACTEROIDES-VULGATUS - DESIGNATION OF NEOTYPE STRAINS FOR BACTEROIDES-FRAGILIS (VEILLON AND ZUBER) CASTELLANI AND CHALMERS AND BACTEROIDES-THETAIOTAOMICRON (DISTASO) CASTELLANI AND CHALMERS [J].
CATO, EP ;
JOHNSON, JL .
INTERNATIONAL JOURNAL OF SYSTEMATIC BACTERIOLOGY, 1976, 26 (02) :230-237
[3]   ACINETOBACTER CYCLOHEXANONE MONOOXYGENASE - GENE CLONING AND SEQUENCE DETERMINATION [J].
CHEN, YCJ ;
PEOPLES, OP ;
WALSH, CT .
JOURNAL OF BACTERIOLOGY, 1988, 170 (02) :781-789
[4]   A COMPREHENSIVE SET OF SEQUENCE-ANALYSIS PROGRAMS FOR THE VAX [J].
DEVEREUX, J ;
HAEBERLI, P ;
SMITHIES, O .
NUCLEIC ACIDS RESEARCH, 1984, 12 (01) :387-395
[5]  
GREER S, 1984, FLAVINS FLAVOPROTEIN, P125
[6]   EXPRESSION IN ESCHERICHIA-COLI OF CRYPTIC TETRACYCLINE RESISTANCE GENES FROM BACTEROIDES R-PLASMIDS [J].
GUINEY, DG ;
HASEGAWA, P ;
DAVIS, CE .
PLASMID, 1984, 11 (03) :248-252
[7]   COMPILATION AND ANALYSIS OF ESCHERICHIA-COLI PROMOTER DNA-SEQUENCES [J].
HAWLEY, DK ;
MCCLURE, WR .
NUCLEIC ACIDS RESEARCH, 1983, 11 (08) :2237-2255
[8]   NUCLEOTIDE-SEQUENCE OF THE TN10 ENCODED TETRACYCLINE RESISTANCE GENE [J].
HILLEN, W ;
SCHOLLMEIER, K .
NUCLEIC ACIDS RESEARCH, 1983, 11 (02) :525-539
[9]  
HOSHINO T, 1985, GENE, V37, P131
[10]   IDENTIFICATION AND ANALYSIS OF GENES FOR TETRACYCLINE RESISTANCE AND REPLICATION FUNCTIONS IN THE BROAD-HOST-RANGE PLASMID PLS1 [J].
LACKS, SA ;
LOPEZ, P ;
GREENBERG, B ;
ESPINOSA, M .
JOURNAL OF MOLECULAR BIOLOGY, 1986, 192 (04) :753-765