ArnR, a novel transcriptional regulator, represses expression of the narKGHJI operon in Corynebacterium glutamicum

被引:33
作者
Nishimura, Taku [1 ]
Teramoto, Haruhiko [1 ]
Vertes, Alain A. [1 ]
Inui, Masayuki [1 ]
Yukawa, Hideaki [1 ]
机构
[1] Res Inst Technol Earth, Kyoto 6190292, Japan
关键词
D O I
10.1128/JB.01801-07
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The narKGHJI operon that comprises putative nitrate/nitrite transporter (narK) and nitrate reductase (narGHJI) genes is required for the anaerobic growth of Corynebacterium glutamicum with nitrate as a terminal electron acceptor. In this study, we identified a gene, arnR, which encodes a transcriptional regulator that represses the expression of the narKGHJI operon in C glutamicum cells under aerobic conditions. Disruption of arnR induced nitrate reductase activities of C. glutamicum cells and increased narKGHJI mRNA levels under aerobic growth conditions. DNA microarray analyses revealed that besides the narKGHJI operon, the hmp gene, which encodes flavohemoglobin, is negatively regulated by ArnR under aerobic conditions. Promoter-reporter assays indicated that arnR gene expression was positively autoregulated by its gene product, ArnR, under both aerobic and anaerobic conditions. Electrophoretic mobility shift assay experiments showed that purified hexahistidyl-tagged ArnR protein specifically binds to promoter regions of the narKGHJI operon and the hmp and arnR genes. A consensus sequence, TA(A/T)TTAA(A/T)TA, found in the promoter regions of these genes was demonstrated to be involved in the binding of ArnR. Effects on LacZ activity by deletion of the ArnR binding sites within the promoter regions fused to the reporter gene were consistent with the view that the expression of the narKGHJI operon is repressed by the ArnR protein under aerobic conditions, whereas the expression of the arnR gene is autoinduced by ArnR.
引用
收藏
页码:3264 / 3273
页数:10
相关论文
共 49 条
[1]  
[Anonymous], 1989, MOL CLONING LAB MANU
[2]   Transcriptional regulation of the flavohemoglobin gene for aerobic nitric oxide detoxification by the second nitric oxide-responsive regulator of Pseudomonas aeruginosa [J].
Arai, H ;
Hayashi, M ;
Kuroi, A ;
Ishii, M ;
Igarashi, Y .
JOURNAL OF BACTERIOLOGY, 2005, 187 (12) :3960-3968
[3]   Mechanisms for redox control of gene expression [J].
Bauer, CE ;
Elsen, S ;
Bird, TH .
ANNUAL REVIEW OF MICROBIOLOGY, 1999, 53 :495-523
[4]   The yjeB (nsrR) gene of Escherichia coli encodes a nitric oxide-sensitive transcriptional regulator [J].
Bodenmiller, DM ;
Spiro, S .
JOURNAL OF BACTERIOLOGY, 2006, 188 (03) :874-881
[5]   NITRATE REDUCTASES IN ESCHERICHIA-COLI [J].
BONNEFOY, V ;
DEMOSS, JA .
ANTONIE VAN LEEUWENHOEK INTERNATIONAL JOURNAL OF GENERAL AND MOLECULAR MICROBIOLOGY, 1994, 66 (1-3) :47-56
[6]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[7]   The individual and common repertoire of DNA-binding transcriptional regulators of Corynebacterium glutamicum, Corynebacterium efficiens, Corynebacterium diphtheriae and Corynebacterium jeikeium deduced from the complete genome sequences -: art. no. 86 [J].
Brune, I ;
Brinkrolf, K ;
Kalinowski, J ;
Pühler, A ;
Tauch, A .
BMC GENOMICS, 2005, 6 (1)
[8]   The roles of the polytopic membrane proteins NarK, NarU and NirC in Escherichia coli K-12:: two nitrate and three nitrite transporters [J].
Clegg, S ;
Yu, F ;
Griffiths, L ;
Cole, JA .
MOLECULAR MICROBIOLOGY, 2002, 44 (01) :143-155
[9]   ANAEROBIC TRANSCRIPTION ACTIVATION IN BACILLUS-SUBTILIS - IDENTIFICATION OF DISTINCT FNR-DEPENDENT AND FNR-INDEPENDENT REGULATORY MECHANISMS [J].
CRUZRAMOS, H ;
BOURSIER, L ;
MOSZER, I ;
KUNST, F ;
DANCHIN, A ;
GLASER, P .
EMBO JOURNAL, 1995, 14 (23) :5984-5994
[10]   Reconstitution of the [4Fe-4S] cluster in FNR and demonstration of the aerobic-anaerobic transcription switch in vitro [J].
Green, J ;
Bennett, B ;
Jordan, P ;
Ralph, ET ;
Thomson, AJ ;
Guest, JR .
BIOCHEMICAL JOURNAL, 1996, 316 :887-892