Function of periplasmic hydrogenases in the sulfate-reducing bacterium Desulfovibrio vulgaris Hildenborough

被引:68
作者
Caffrey, Sean A.
Park, Hyung-Soo
Voordouw, Johanna K.
He, Zhili
Zhou, Jizhong
Voordouw, Gerrit
机构
[1] Univ Calgary, Dept Biol Sci, Calgary, AB T2N 1N4, Canada
[2] Univ Oklahoma, Inst Environm Genom, Norman, OK 73019 USA
[3] Univ Oklahoma, Dept Bot & Microbiol, Norman, OK 73019 USA
关键词
D O I
10.1128/JB.00747-07
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The sulfate-reducing bacterium Desutfovibrio vulgaris Hildenborough possesses four periplasmic hydrogenases to facilitate the oxidation of molecular hydrogen. These include an [Fe] hydrogenase, an [NiFeSe] hydrogenase, and two [NiFe] hydrogenases encoded by the hyd, hys, hyn1, and hyn2 genes, respectively. In order to understand their cellular functions, we have compared the growth rates of existing (hyd and hyn1) and newly constructed (hys and hyn-1 hyd) mutants to those of the wild type in defined media in which lactate or hydrogen at either 5 or 50% (vol/vol) was used as the sole electron donor for sulfate reduction. Only strains missing the [Fe] hydrogenase were significantly affected during growth with lactate or with 50% (vol/vol) hydrogen as the sole electron donor. When the cells were grown at low (5% [vol/vol]) hydrogen concentrations, those missing the [NiFeSe] hydrogenase suffered the greatest impairment. The growth rate data correlated strongly with gene expression results obtained from microarray hybridizations and real-time PCR using mRNA extracted from cells grown under the three conditions. Expression of the hys genes followed the order 5% hydrogen > 50% hydrogen > lactate, whereas expression of the hyd genes followed the reverse order. These results suggest that growth with lactate and 50% hydrogen is associated with high intracellular hydrogen concentrations, which are best captured by the higher activity, lower affinity [Fe] hydrogenase. In contrast, growth with 5% hydrogen is associated with a low intracellular hydrogen concentration, requiring the lower activity, higher affinity [NiFeSe] hydrogenase.
引用
收藏
页码:6159 / 6167
页数:9
相关论文
共 38 条
[1]   MINI-TN10 TRANSPOSON DERIVATIVES FOR INSERTION MUTAGENESIS AND GENE DELIVERY INTO THE CHROMOSOME OF GRAM-NEGATIVE BACTERIA [J].
ALEXEYEV, MF ;
SHOKOLENKO, IN .
GENE, 1995, 160 (01) :59-62
[2]  
Bender Kelly S, 2006, Biotechnol Genet Eng Rev, V23, P157
[3]   Global analysis of heat shock response in Desulfovibrio vulgaris Hildenborough [J].
Chhabra, SR ;
He, Q ;
Huang, KH ;
Gaucher, SP ;
Alm, EJ ;
He, Z ;
Hadi, MZ ;
Hazen, TC ;
Wall, JD ;
Zhou, J ;
Arkin, AP ;
Singh, AK .
JOURNAL OF BACTERIOLOGY, 2006, 188 (05) :1817-1828
[4]   Deletion of the hmc operon of Desulfovibrio vulgaris subsp vulgaris Hildenborough hampers hydrogen metabolism and low-redox-potential niche establishment [J].
Dolla, A ;
Pohorelic, BKJ ;
Voordouw, JK ;
Voordouw, G .
ARCHIVES OF MICROBIOLOGY, 2000, 174 (03) :143-151
[5]   Gene Expression Omnibus: NCBI gene expression and hybridization array data repository [J].
Edgar, R ;
Domrachev, M ;
Lash, AE .
NUCLEIC ACIDS RESEARCH, 2002, 30 (01) :207-210
[6]   Transcriptional profiling of Helicobacter pylori Fur- and iron-regulated gene expression [J].
Ernst, FD ;
Bereswill, S ;
Waidner, B ;
Stoof, J ;
Mäder, U ;
Kusters, JG ;
Kuipers, EJ ;
Kist, M ;
van Vliet, AHM ;
Homuth, G .
MICROBIOLOGY-SGM, 2005, 151 :533-546
[7]   THE 3 CLASSES OF HYDROGENASES FROM SULFATE-REDUCING BACTERIA OF THE GENUS DESULFOVIBRIO [J].
FAUQUE, G ;
PECK, HD ;
MOURA, JJG ;
HUYNH, BH ;
BERLIER, Y ;
DERVARTANIAN, DV ;
TEIXEIRA, M ;
PRZYBYLA, AE ;
LESPINAT, PA ;
MOURA, I ;
LEGALL, J .
FEMS MICROBIOLOGY LETTERS, 1988, 54 (04) :299-344
[8]   A new function of the Desulfovibrio vulgaris Hildenborough [Fe] hydrogenase in the protection against oxidative stress [J].
Fournier, M ;
Dermoun, Z ;
Durand, MC ;
Dolla, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (03) :1787-1793
[9]  
Frey M, 2002, CHEMBIOCHEM, V3, P153, DOI 10.1002/1439-7633(20020301)3:2/3<153::AID-CBIC153>3.0.CO
[10]  
2-B