Cloning and expression of cadD, a new cadmium resistance gene of Staphylococcus aureus

被引:58
作者
Crupper, SS
Worrell, V
Stewart, GC
Iandolo, JJ [1 ]
机构
[1] Univ Oklahoma, Hlth Sci Ctr, Dept Microbiol & Immunol, Oklahoma City, OK 73190 USA
[2] Emporia State Univ, Div Biol Sci, Emporia, KS 66801 USA
[3] Kansas State Univ, Coll Vet Med, Dept Diagnost Med Pathobiol, Manhattan, KS 66506 USA
关键词
D O I
10.1128/JB.181.13.4071-4075.1999
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
A cadmium resistance gene, designated cadD, has been identified in and cloned from the Staphylococcus aureus plasmid pRW001, The gene is part of a two-component operon which contains the resistance gene cadD and an inactive regulatory gene, cadX*. A high degree of sequence similarity was observed between cadD and the cadB-like gene from S. lugnunensis, but no significant similarity was found with either cadA or cadB from the S, aureus plasmids pI258 and pII147. The positive regulatory gene cadX* is identical to cadX from pLUG10 over a stretch of 78 codons beginning at the N terminus, but it is truncated at this point and inactive. Sequence analysis showed that the cadmium resistance operon resides on a 3,972-bp element that is flanked by direct repeats of IS257, The expression of cadD in S, aureus and Bacillus subtilis resulted in low-level resistance to cadmium; in contrast, cadA and cadB from S, aureus induced higher level resistance. However, when the truncated version of cadX contained in pRW001 is complemented in trans with cadX from plasmid pLUG10, resistance increased approximately 10-fold suggesting that the cadmium resistance operons from pRW001 and pLUG10 are evolutionarily related. Moreover, the truncated version of cadX contained in pRW001 is nonfunctional and may have been generated by deletion during recombination to acquire the cadmium resistance element.
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页码:4071 / 4075
页数:5
相关论文
共 29 条
[1]   BASIC LOCAL ALIGNMENT SEARCH TOOL [J].
ALTSCHUL, SF ;
GISH, W ;
MILLER, W ;
MYERS, EW ;
LIPMAN, DJ .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 215 (03) :403-410
[2]   REQUIREMENTS FOR TRANSFORMATION IN BACILLUS SUBTILIS [J].
ANAGNOSTOPOULOS, C ;
SPIZIZEN, J .
JOURNAL OF BACTERIOLOGY, 1961, 81 (05) :741-&
[3]  
[Anonymous], [No title captured]
[5]   Nucleic acid sequence and affiliation of pLUG10, a novel cadmium resistance plasmid from Staphylococcus lugdunensis [J].
Chaouni, LBA ;
Etienne, J ;
Greenland, T ;
Vandenesch, F .
PLASMID, 1996, 36 (01) :1-8
[6]   CADC, THE TRANSCRIPTIONAL REGULATORY PROTEIN OF THE CADMIUM RESISTANCE SYSTEM OF STAPHYLOCOCCUS-AUREUS PLASMID PI258 [J].
ENDO, G ;
SILVER, S .
JOURNAL OF BACTERIOLOGY, 1995, 177 (15) :4437-4441
[7]   IDENTIFICATION OF PROTEIN CODING REGIONS BY DATABASE SIMILARITY SEARCH [J].
GISH, W ;
STATES, DJ .
NATURE GENETICS, 1993, 3 (03) :266-272
[8]  
IANDOLO JJ, 1989, ANNU REV MICROBIOL, V43, P375, DOI 10.1146/annurev.micro.43.1.375
[9]   CLONING AND EXPRESSION OF THE EXFOLIATIVE TOXIN-B GENE FROM STAPHYLOCOCCUS-AUREUS [J].
JACKSON, MP ;
IANDOLO, JJ .
JOURNAL OF BACTERIOLOGY, 1986, 166 (02) :574-580
[10]   HIGH-FREQUENCY TRANSFORMATION OF STAPHYLOCOCCUS-AUREUS BY ELECTROPORATION [J].
KRAEMER, GR ;
IANDOLO, JJ .
CURRENT MICROBIOLOGY, 1990, 21 (06) :373-376