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Characterization of two genes (hupD and hupE) required for hydrogenase activity in Azotobacter chroococcum.
- Source :
-
FEMS microbiology letters [FEMS Microbiol Lett] 1992 Sep 01; Vol. 75 (1), pp. 93-101. - Publication Year :
- 1992
-
Abstract
- In Azotobacter chroococcum the hydrogenase structural genes (hupSL) cover about 2.8 kb of a 15-kb region associated with hydrogen-uptake (Hup) activity. Two other genes in this region, hupD and hupE, were located 8.9 kb downstream of hupL and were shown to be essential for hydrogenase activity by insertion mutagenesis. A fragment of DNA beginning 3.4 kb downstream of hupL was able to complement the hupE mutant, supporting earlier evidence for a promoter downstream of hupSL. Hybridization experiments showed that hupD and hupE share some similarity with a region of Alcaligenes eutrophus DNA which is apparently involved in the formation of catalytically active hydrogenase. The hupD gene encodes a 379-amino acid, 41.4-kDa polypeptide while hupE codes for a 341-amino acid, 36.1-kDa product. The predicted amino acid sequences of the hupD and hupE genes are homologous to the Escherichia coli hypD and hypE gene products, respectively. A polar mutation in hupD had no effect on beta-galactosidase activity in a strain also carrying a hupL-lacZ fusion, indicating that hupD and hupE are probably not involved in regulating hydrogenase structural gene expression.
- Subjects :
- Amino Acid Sequence
Azotobacter enzymology
Bacterial Proteins metabolism
Base Sequence
DNA, Bacterial
Gene Expression Regulation, Bacterial
Genetic Complementation Test
Hydrogenase metabolism
Membrane Proteins metabolism
Molecular Sequence Data
Mutagenesis, Site-Directed
Nucleic Acid Hybridization
Restriction Mapping
Sequence Homology, Nucleic Acid
Azotobacter genetics
Bacterial Proteins genetics
Genes, Bacterial
Hydrogenase genetics
Membrane Proteins genetics
Subjects
Details
- Language :
- English
- ISSN :
- 0378-1097
- Volume :
- 75
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- FEMS microbiology letters
- Publication Type :
- Academic Journal
- Accession number :
- 1526470
- Full Text :
- https://doi.org/10.1016/0378-1097(92)90462-w