Chromosome-determined zinc-responsible operon czr in Staphylococcus aureus strain 912

被引:69
作者
Kuroda, M
Hayashi, H
Ohta, T [1 ]
机构
[1] Univ Tsukuba, Coll Med Technol, Ibaraki, Osaka 3058577, Japan
[2] Univ Tsukuba, Inst Basic Med Sci, Dept Microbiol, Ibaraki, Osaka 3058577, Japan
关键词
Staphylococcus aureus; zinc transporter; zinc-responsible gene czr; stress-inducible genes;
D O I
10.1111/j.1348-0421.1999.tb02382.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
A novel operon, czrAB (zinc-responsible genes), was identified in the chromosome of Staphylococcus aureus. The operon consists of two genes, czrA and czrB. The czrA gene, coding for an 11.5 kDa protein, was homologous to cadC, arsR of S. aureus plasmid pI258 and smtB of Synechococcus PCC7942. The czrB, coding for a 36 kDa membrane spanning protein, was homologous to the czcD gene, cobalt, zinc and the cadmium-resistant factor of Bacillus subtilis and Alcaligenes eutrophus. In the presence of zinc (0.1-10 mM), the transcription of czrAB was enhanced in a concentration-dependent manner. Other heavy metals, such as cobalt, copper, manganese and nickel showed no effect on czrAB expression. The disruptant of the czrB gene became sensitive to zinc ion (MIC, 2 mM; MBC, 10 mM), and the complementation with the plasmid recovered the resistance to zinc at the same concentration as a parental strain (MIC, 5 mM; MBC, 20 mM). The disruptant accumulated intracellular zinc up to 0.4 mg per g dry weight of the organism, while that of the parental strain was 0.25 mg per g dry weight. The findings indicated that the novel operon czrAB should play a role in the transportation of zinc across the cell membrane to maintain the proper intracellular concentration.
引用
收藏
页码:115 / 125
页数:11
相关论文
共 45 条
[1]  
BAIROCH A, 1993, NUCLEIC ACIDS RES, V21, P2513
[2]   Zinc(II) tolerance in Escherichia coli K-12: evidence that the zntA gene (o732) encodes a cation transport ATPase [J].
Beard, SJ ;
Hashim, R ;
MembrilloHernandez, J ;
Hughes, MN ;
Poole, RK .
MOLECULAR MICROBIOLOGY, 1997, 25 (05) :883-891
[3]   The complete genome sequence of Escherichia coli K-12 [J].
Blattner, FR ;
Plunkett, G ;
Bloch, CA ;
Perna, NT ;
Burland, V ;
Riley, M ;
ColladoVides, J ;
Glasner, JD ;
Rode, CK ;
Mayhew, GF ;
Gregor, J ;
Davis, NW ;
Kirkpatrick, HA ;
Goeden, MA ;
Rose, DJ ;
Mau, B ;
Shao, Y .
SCIENCE, 1997, 277 (5331) :1453-+
[4]   HIGH-EFFICIENCY TRANSFORMATION OF BACTERIAL-CELLS BY ELECTROPORATION [J].
CALVIN, NM ;
HANAWALT, PC .
JOURNAL OF BACTERIOLOGY, 1988, 170 (06) :2796-2801
[5]   GLOBAL REGULATION OF GENE-EXPRESSION IN ESCHERICHIA-COLI [J].
CHUANG, SE ;
DANIELS, DL ;
BLATTNER, FR .
JOURNAL OF BACTERIOLOGY, 1993, 175 (07) :2026-2036
[6]   Characterization of the primary sigma factor of Staphylococcus aureus [J].
Deora, R ;
Misra, TK .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (36) :21828-21834
[7]   IMPROVED DETECTION OF HELIX-TURN-HELIX DNA-BINDING MOTIFS IN PROTEIN SEQUENCES [J].
DODD, IB ;
EGAN, JB .
NUCLEIC ACIDS RESEARCH, 1990, 18 (17) :5019-5026
[8]   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
[9]   METALLOREGULATION OF THE CYANOBACTERIAL SMT LOCUS - IDENTIFICATION OF SMTB BINDING-SITES AND DIRECT INTERACTION WITH METALS [J].
ERBE, JL ;
TAYLOR, KB ;
HALL, LM .
NUCLEIC ACIDS RESEARCH, 1995, 23 (13) :2472-2478
[10]  
HASIMOTOGOTOH T, 1993, GENE, V137, P211