Zinc(II) tolerance in Escherichia coli K-12: evidence that the zntA gene (o732) encodes a cation transport ATPase

被引:160
作者
Beard, SJ
Hashim, R
MembrilloHernandez, J
Hughes, MN
Poole, RK
机构
[1] UNIV SHEFFIELD,DEPT MOL BIOL & BIOTECHNOL,SHEFFIELD S10 2TN,S YORKSHIRE,ENGLAND
[2] UNIV LONDON KINGS COLL,DIV LIFE SCI,LONDON W8 7AH,ENGLAND
[3] UNIV LONDON KINGS COLL,DEPT CHEM,LONDON W8 7AH,ENGLAND
关键词
D O I
10.1111/j.1365-2958.1997.mmi518.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
A transposon (Tn 10dCam) insertion mutant of Escherichia coli K-12 was isolated that exhibited hypersensitivity to zinc(II) and cadmium(II) and, to a lesser extent, cobalt(II) and nickel (II). The mutated gene, located between 75.5 and 76.2 min on the chromosome, is named zntA (for Zn(II) transport or tolerance). The metal-sensitive phenotype was complemented by a genomic DNA clone mapping at 3677.90-3684.60 kb on the physical map. Insertion of a kanamycin resistance (Kn(R)) cassette at a SalI site in a subcloned fragment generated a plasmid that partially complemented the zinc(II)-sensitive phenotype. DNA sequence analysis revealed that the Kn(R) cassette was located within the putative promoter region of an ORF (o732 or yhhO) predicted to encode a protein of 732 amino acids, similar to cation transport P-type ATPases in the Cpx-type family. Inverse PCR and sequence analysis revealed that the Tn10dCam element was located within o732 in the genome of the zinc(II)-sensitive mutant. The zntA mutant had elevated amounts of intracellular and cell surface-bound Zn(II), consistent with the view that zntA(+) encodes a zinc(II) efflux protein. Exposure of the zntA mutant to cobalt(II) and cadmium(II) also resulted in elevated levels of intracellular and cell surface-bound metal ions.
引用
收藏
页码:883 / 891
页数:9
相关论文
共 42 条
[1]  
[Anonymous], ESCHERICHIA COLI SAL
[2]  
BEARD SJ, 1995, FEMS MICROBIOL LETT, V131, P205, DOI 10.1016/0378-1097(95)00260-C
[3]  
BEARD SJ, 1992, FEMS MICROBIOL LETT, V96, P207
[4]   A COMPUTER ALGORITHM FOR TESTING POTENTIAL PROKARYOTIC TERMINATORS [J].
BRENDEL, V ;
TRIFONOV, EN .
NUCLEIC ACIDS RESEARCH, 1984, 12 (10) :4411-4427
[5]   PHYSICAL MAP LOCATIONS OF GENES ENCODING COMPONENTS OF THE AEROBIC RESPIRATORY-CHAIN OF ESCHERICHIA-COLI [J].
CALHOUN, MW ;
NEWTON, G ;
GENNIS, RB .
JOURNAL OF BACTERIOLOGY, 1991, 173 (05) :1569-1570
[6]   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
[7]  
COHEN I, 1991, MICROBIOS, V68, P157
[8]   CHARACTERIZATION OF TN10D-CAM - A TRANSPOSITION-DEFECTIVE TN10 SPECIFYING CHLORAMPHENICOL RESISTANCE [J].
ELLIOTT, T ;
ROTH, JR .
MOLECULAR AND GENERAL GENETICS, 1988, 213 (2-3) :332-338
[9]   MOLECULAR-GENETICS OF A CHROMOSOMAL LOCUS INVOLVED IN COPPER TOLERANCE IN ESCHERICHIA-COLI K-12 [J].
FONG, ST ;
CAMAKARIS, J ;
LEE, BTO .
MOLECULAR MICROBIOLOGY, 1995, 15 (06) :1127-1137
[10]   MINI-MU BACTERIOPHAGE WITH PLASMID REPLICONS FOR INVIVO CLONING AND LAC GENE FUSING [J].
GROISMAN, EA ;
CASADABAN, MJ .
JOURNAL OF BACTERIOLOGY, 1986, 168 (01) :357-364