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.
引用
收藏
页码:3993 / 3999
页数:7
相关论文
共 37 条
[31]   CONTENT AND LOCALIZATION OF FMN, FE-S CLUSTERS AND NICKEL IN THE NAD-LINKED HYDROGENASE OF NOCARDIA-OPACA 1B [J].
SCHNEIDER, K ;
CAMMACK, R ;
SCHLEGEL, HG .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1984, 142 (01) :75-84
[32]   REGULATION OF HYDROGENASE BIOSYNTHESIS BY NICKEL IN BRADYRHIZOBIUM-JAPONICUM [J].
STULTS, LW ;
SRAY, WA ;
MAIER, RJ .
ARCHIVES OF MICROBIOLOGY, 1986, 146 (03) :280-283
[33]   AEROBIC PURIFICATION OF HYDROGENASE FROM RHIZOBIUM-JAPONICUM BY AFFINITY-CHROMATOGRAPHY [J].
STULTS, LW ;
MOSHIRI, F ;
MAIER, RJ .
JOURNAL OF BACTERIOLOGY, 1986, 166 (03) :795-800
[34]   NICKEL IS A COMPONENT OF HYDROGENASE IN RHIZOBIUM-JAPONICUM [J].
STULTS, LW ;
OHARA, EB ;
MAIER, RJ .
JOURNAL OF BACTERIOLOGY, 1984, 159 (01) :153-158
[35]   LACK OF CARBON SUBSTRATE REPRESSION OF UPTAKE HYDROGENASE ACTIVITY IN BRADYRHIZOBIUM-JAPONICUM SR [J].
VANBERKUM, P ;
MAIER, RJ .
JOURNAL OF BACTERIOLOGY, 1988, 170 (04) :1962-1964
[36]   EXPRESSION OF UPTAKE HYDROGENASE AND HYDROGEN OXIDATION DURING HETEROTROPHIC GROWTH OF BRADYRHIZOBIUM-JAPONICUM [J].
VANBERKUM, P .
JOURNAL OF BACTERIOLOGY, 1987, 169 (10) :4565-4569
[37]  
Wang R. T., 1980, METHOD ENZYMOL, V69, P409