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The identification, characterization, sequencing and mutagenesis of the genes ( hupSL ) encoding the small and large subunits of the H 2 ‐uptake hydrogenase of Azotobacter chroococcum
Author(s) -
Ford C. M.,
Garg N.,
Garg R. P.,
Tibelius K. H.,
Yates M. G.,
Arp D. J.,
Seefeldt L. C.
Publication year - 1990
Publication title -
molecular microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.857
H-Index - 247
eISSN - 1365-2958
pISSN - 0950-382X
DOI - 10.1111/j.1365-2958.1990.tb00672.x
Subject(s) - azotobacter chroococcum , biology , gene , biochemistry , rhodobacter , structural gene , amino acid , homology (biology) , bradyrhizobium japonicum , mutant , hydrogenase , peptide sequence , protein subunit , azotobacteraceae , cysteine , site directed mutagenesis , genetics , bacteria , rhizobiaceae , enzyme , nitrogenase , symbiosis , nitrogen fixation
Summary The structural genes ( hupSL ) of the membrane‐bound NiFe‐containing H 2 ‐uptake hydrogenase (Hup) of Azotobacter chroococcum were identified by oligo‐nucleotide screening and sequenced. The small subunit gene ( hupS ) encodes a signal sequence of 34 amino acids followed by a 310‐amino‐acid, 34 156 D protein containing 12 cysteine residues. The large subunit gene ( hupL ) overlaps hupS by one base and codes for a predicted 601‐amino‐acid, 66433 D protein. There are two regions of strong homology with other Ni hydrogenases: a Cys‐Thr‐Cys‐Cys‐Ser motif near the N ‐terminus of HupS and an Asp‐Pro‐Cys‐Leu‐Ala‐Cys motif near the carboxy‐terminus of HupL. Strong overall homology exists between Azotobacter, Bradyrhizobium japonicum and Rhodobacter capsulatus Hup proteins but less exists between the Azotobacter proteins and hydrogenases from Desulfovibrio strains. Mutagenesis of either hupS or hupL genes of A. chrooooccum yielded Hup − phenotypes but some of these mutants retained a partial H 2 ‐evolving activity. Hybridization experiments at different stages of gene segregation confirmed the multicopy nature of the Azotobacter genome.