Analysis of genes involved in arsenic resistance in Corynebacterium glutamicum ATCC 13032

被引:115
作者
Ordóñez, E [1 ]
Letek, M [1 ]
Valbuena, N [1 ]
Gil, JA [1 ]
Mateos, LM [1 ]
机构
[1] Univ Leon, Dept Ecol Genet & Microbiol, Area Microbiol, Fac Biol, E-24071 Leon, Spain
关键词
D O I
10.1128/AEM.71.10.6206-6215.2005
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Corynebacterium glutamicum is able to grow in media containing up to 12 mM arsenite and 500 mM arsenate and is one of the most arsenic-resistant microorganisms described to date. Two operons (ars1 and ars2) involved in arsenate and arsenite resistance have been identified in the complete genome sequence of Corynebacterium glutamicum. The operons ars1 and ars2 are located some distance from each other in the bacterial chromosome, but they are both composed of genes encoding a regulatory protein (arsR), an arsenite permease (arsB), and an arsenate reductase (arsC); operon ars1 contains an additional arsenate reductase gene (arsCl') located immediately downstream from arsC1 Additional arsenite permease and arsenate reductase genes (arsB3 and arsC4) scattered on the chromosome were also identified. The involvement of ars operons in arsenic resistance in C. glutamicurn was confirmed by gene disruption experiments of the three arsenite permease genes present in its genome. Wild-type and arsB3 insertional mutant C. glutamicum strains were able to grow with up to 12 mM arsenite, whereas arsB1 and arsB2 C. glutamicum insertional mutants were resistant to 4 mM and 9 mM arsenite, respectively. The double arsB1-arsB2 insertional mutant was resistant to only 0.4 mM arsenite and 10 mM arsenate. Gene amplification assays of operons ars1 and ars2 in C. glutamicum revealed that the recombinant strains containing the ars1 operon were resistant to up to 60 mM arsenite, this being one of the highest levels of bacterial resistance to arsenite so far described, whereas recombinant strains containing operon ars2 were resistant to only 20 mM arsenite. Northern blot and reverse transcription-PCR analysis confirmed the presence of transcripts for all the ars genes, the expression of arsB3 and arsC4 being constitutive, and the expression of arsR1, arsB1, arsC1, arsC1', arsR2, arsB2, and arsC2 being inducible by arsenite.
引用
收藏
页码:6206 / 6215
页数:10
相关论文
共 63 条
[1]  
ABDRASHITOVA S A, 1986, Mikrobiologiya, V55, P212
[2]   Improved vectors for transcriptional/translational signal screening in corynebacteria using the melC operon from Streptomyces glaucescens as reporter [J].
Adham, SAI ;
Rodríguez, S ;
Ramos, A ;
Santamaría, RI ;
Gil, JA .
ARCHIVES OF MICROBIOLOGY, 2003, 180 (01) :53-59
[3]   PEDIGREES OF SOME MUTANT STRAINS OF ESCHERICHIA-COLI K-12 [J].
BACHMANN, BJ .
BACTERIOLOGICAL REVIEWS, 1972, 36 (04) :525-557
[4]   Bacillus subtilis arsenate reductase is structurally and functionally similar to low molecular weight protein tyrosine phosphatases [J].
Bennett, MS ;
Guan, Z ;
Laurberg, M ;
Su, XD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (24) :13577-13582
[5]   ROLE OF CYSTEINYL RESIDUES IN METALLOACTIVATION OF THE OXYANION-TRANSLOCATING ARSA ATPASE [J].
BHATTACHARJEE, H ;
LI, JX ;
KSENZENKO, MY ;
ROSEN, BP .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (19) :11245-11250
[6]   PLASMID CLONING VECTORS FOR THE CONJUGAL TRANSFER OF DNA FROM ESCHERICHIA-COLI TO STREPTOMYCES SPP [J].
BIERMAN, M ;
LOGAN, R ;
OBRIEN, K ;
SENO, ET ;
RAO, RN ;
SCHONER, BE .
GENE, 1992, 116 (01) :43-49
[7]  
Bobrowicz P, 1997, YEAST, V13, P819, DOI 10.1002/(SICI)1097-0061(199707)13:9<819::AID-YEA142>3.0.CO
[8]  
2-Y
[9]   ARSENIC EFFLUX GOVERNED BY THE ARSENIC RESISTANCE DETERMINANT OF STAPHYLOCOCCUS-AUREUS PLASMID PI258 [J].
BROER, S ;
JI, GY ;
BROER, A ;
SILVER, S .
JOURNAL OF BACTERIOLOGY, 1993, 175 (11) :3480-3485
[10]   Independent regulation of the divergent Escherichia coli nrfA and acsP1 promoters by a nucleoprotein assembly at a shared regulatory region [J].
Browning, DF ;
Beatty, CM ;
Wolfe, AJ ;
Cole, JA ;
Busby, SJW .
MOLECULAR MICROBIOLOGY, 2002, 43 (03) :687-701