Characterization of two genes (hupD and hupE) required for hydrogenase activity in Azotobacter chroococcum

• Published in: FEMS microbiology letters Vol. 96; no. 1; pp. 93 - 102
• Main Authors: Du, L, Stejskal, F, Tibelius, K.H
• Format: Journal Article
• Language: English
• Published: 01.09.1992
• Subjects: amino acid sequences; Azotobacter chroococcum; comparisons; embl/m92282; enzyme activity; ferredoxin hydrogenase; genbank/m92282; genes; genetic complementation; genetic regulation; molecular sequence data; mutants; nitrogen-fixing bacteria; nucleotide sequences
• ISSN: 0378-1097; 1574-6968
• DOI: 10.1111/j.1574-6968.1992.tb05399.x

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.