Characterization of the norB gene, encoding nitric oxide reductase, in the nondenitrifying cyanobacterium Synechocystis sp strain PCC6803

被引:42
作者
Büsch, A [1 ]
Friedrich, B [1 ]
Cramm, R [1 ]
机构
[1] Humboldt Univ, Inst Biol Mikrobiol, D-10115 Berlin, Germany
关键词
D O I
10.1128/AEM.68.2.668-672.2002
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
A norB gene encoding a putative nitric oxide reductase is present in the genome of the nondenitrifying cyanobacterium Synechocystis sp. strain PCC6803. The gene product belongs to the quinol-oxidizing single-subunit class of nitric oxide reductases, discovered recently in the denitrifier Ralstonia eutropha. Heterologous complementation of a nitric oxide reductase-negative mutant of R. eutropha with norB from Synechocystis restored nitric oxide reductase activity. With reduced menadione as the electron donor, an enzymatic activity of 101 mmol of NO per min per mg of protein was obtained with membrane fractions of Synechocystis wild-type cells. Virtually no nitric oxide reductase activity was present in a norB-negative mutant of Synechocystis. Growing cells of this mutant are more sensitive toward NO than wild-type cells, indicating that the presence of a nitric oxide reductase is beneficial for Synechocystis when the cells are exposed to NO. Transcriptional fusions with the chloramphenicol acetyltransferase reporter gene were constructed to monitor norB expression in Synechocystis. Transcription of norB was not enhanced by the addition of the NO-generating agent sodium nitroprusside.
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页码:668 / 672
页数:5
相关论文
共 43 条
[1]   NITRIC-OXIDE GENERATION FROM NITROPRUSSIDE BY VASCULAR TISSUE - EVIDENCE THAT REDUCTION OF THE NITROPRUSSIDE ANION AND CYANIDE LOSS ARE REQUIRED [J].
BATES, JN ;
BAKER, MT ;
GUERRA, R ;
HARRISON, DG .
BIOCHEMICAL PHARMACOLOGY, 1991, 42 :S157-S165
[3]   Two isofunctional nitric oxide reductases in Alcaligenes eutrophus H16 [J].
Cramm, R ;
Siddiqui, RA ;
Friedrich, B .
JOURNAL OF BACTERIOLOGY, 1997, 179 (21) :6769-6777
[4]  
CRAMM R, 1994, J BIOL CHEM, V269, P7349
[5]   Purification and characterization of the single-component nitric oxide reductase from Ralstonia eutropha H16 [J].
Cramm, R ;
Pohlmann, A ;
Friedrich, B .
FEBS LETTERS, 1999, 460 (01) :6-10
[6]   Enzymatic removal of nitric oxide catalyzed by cytochrome c′ in Rhodobacter capsulatus [J].
Cross, R ;
Lloyd, D ;
Poole, RK ;
Moir, JWB .
JOURNAL OF BACTERIOLOGY, 2001, 183 (10) :3050-3054
[7]  
DeBoer APN, 1996, EUR J BIOCHEM, V242, P592, DOI 10.1111/j.1432-1033.1996.0592r.x
[8]   A SET OF CASSETTES AND IMPROVED VECTORS FOR GENETIC AND BIOCHEMICAL-CHARACTERIZATION OF PSEUDOMONAS GENES [J].
DERETIC, V ;
CHANDRASEKHARAPPA, S ;
GILL, JF ;
CHATTERJEE, DK ;
CHAKRABARTY, AM .
GENE, 1987, 57 (01) :61-72
[9]   CLONING AND SEQUENCING OF MUTANT PSBB GENES OF THE CYANOBACTERIUM SYNECHOCYSTIS PCC-6803 [J].
ERMAKOVA, SY ;
ELANSKAYA, IV ;
KALLIES, KU ;
WEIHE, A ;
BORNER, T ;
SHESTAKOV, SV .
PHOTOSYNTHESIS RESEARCH, 1993, 37 (02) :139-146
[10]  
FRANCHE C, 1988, METHOD ENZYMOL, V122, P69