COMMON CIS-ACTING REGION RESPONSIBLE FOR TRANSCRIPTIONAL REGULATION OF BRADYRHIZOBIUM-JAPONICUM HYDROGENASE BY NICKEL, OXYGEN, AND HYDROGEN

被引:43
作者
KIM, H [1 ]
YU, CB [1 ]
MAIER, RJ [1 ]
机构
[1] JOHNS HOPKINS UNIV,DEPT BIOL,BALTIMORE,MD 21218
关键词
D O I
10.1128/jb.173.13.3993-3999.1991
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Bradyrhizobium japonicum expresses hydrogenase in microaerophilic free-living conditions in the presence of nickel. Plasmid-borne hup-lacZ transcriptional fusion constructs were used to study the regulation of the hydrogenase gene. The hydrogenase gene was transcriptionally induced under microaerobic conditions (0.1 to 3.0% partial pressure O2). The hydrogenase gene was not transcribed or was poorly transcribed in strictly anaerobic conditions or conditions above 3.0% O2. Hydrogen gas at levels as low as 0.1% partial pressure induced hydrogenase transcription, and a high level of transcription was maintained up to at least 10% H-2 concentration. No transcription was observed in the absence of H-2. Hydrogenase was regulated by H-2, O2, and Ni when the 5'-upstream sequence was pared down to include base number -168. However, when the upstream sequence was pared down to base number -118, the regulatory response to O2, H-2, and Ni levels was negated. Thus, a common cis-acting regulatory region localized within 50 bp is critical for the regulation of hydrogenase by hydrogen, oxygen, and nickel. As a control, the B. japonicum hemA gene which codes for delta-aminolevulinic acid synthase was also fused to the promoterless lacZ gene, and its regulation was tested in the presence of various concentrations of O2 and H-2. hemA-lacZ transcription was not dependent on levels of Ni, O2, or H-2. Two different hup-lacZ fusions were tested in a Hup- background, strain JH47; these hup-lacZ constructs in JH47 demonstrated dependency on nickel, O2, and H-2, indicating that the hydrogenase protein itself is not a sensor for regulation by O2, H-2, or nickel.
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页码:3993 / 3999
页数:7
相关论文
共 37 条
[1]  
APPLEBY CA, 1985, NITROGEN FIXATION CO, P41
[2]   PHYSIOLOGICAL CHARACTERIZATION OF HYDROGEN BACTERIUM AQUASPIRILLUM-AUTOTROPHICUM [J].
ARAGNO, M ;
SCHLEGEL, HG .
ARCHIVES OF MICROBIOLOGY, 1978, 116 (03) :221-229
[4]  
Ausubel FM., 1995, MOL REPROD DEV, V3rd edn, DOI DOI 10.1002/MRD.1080010210
[5]   RELATION BETWEEN GLUTAMINE-SYNTHETASE AND NITROGENASE ACTIVITIES IN SYMBIOTIC ASSOCIATION BETWEEN RHIZOBIUM-JAPONICUM AND GLYCINE-MAX [J].
BISHOP, PE ;
GUEVARA, JG ;
ENGELKE, JA ;
EVANS, HJ .
PLANT PHYSIOLOGY, 1976, 57 (04) :542-546
[6]   REGULATION BY MOLECULAR-OXYGEN AND ORGANIC SUBSTRATES OF HYDROGENASE SYNTHESIS IN ALCALIGENES-EUTROPHUS [J].
CANGELOSI, GA ;
WHEELIS, ML .
JOURNAL OF BACTERIOLOGY, 1984, 159 (01) :138-144
[7]   REGULATION OF 2 NICKEL-REQUIRING (INDUCIBLE AND CONSTITUTIVE) HYDROGENASES AND THEIR COUPLING TO NITROGENASE IN METHYLOSINUS-TRICHOSPORIUM OB3B [J].
CHEN, YP ;
YOCH, DC .
JOURNAL OF BACTERIOLOGY, 1987, 169 (10) :4778-4783
[8]   PLASMIDS RELATED TO THE BROAD HOST RANGE VECTOR, PRK290, USEFUL FOR GENE CLONING AND FOR MONITORING GENE-EXPRESSION [J].
DITTA, G ;
SCHMIDHAUSER, T ;
YAKOBSON, E ;
LU, P ;
LIANG, XW ;
FINLAY, DR ;
GUINEY, D ;
HELINSKI, DR .
PLASMID, 1985, 13 (02) :149-153
[9]  
DOYLE CM, 1987, J BACTERIOL, V170, P3217
[10]   A SIMPLE PLANT NUTRIENT SOLUTION PURIFICATION METHOD FOR EFFECTIVE REMOVAL OF TRACE-METALS USING CONTROLLED PORE GLASS-8-HYDROXYQUINOLINE CHELATION COLUMN CHROMATOGRAPHY [J].
ESKEW, DL ;
WELCH, RM ;
CARY, EE .
PLANT PHYSIOLOGY, 1984, 76 (01) :103-105