Periplasmic sulphide dehydrogenase (Sud) from Wolinella succinogenes: isolation, nucleotide sequence of the sud gene and its expression in Escherichia coli.

Wolinella succinogenes contains a periplasmic sulphide dehydrogenase when grown with formate and polysulphide as catabolic substrates. The isolated enzyme catalyzes the reduction of dimethylnaphthoquinone with sulphide at high values of both apparent Km and turnover number. The active enzyme consists of two identical subunits (14 kDa) and amounts to approximately 1% of the soluble cell protein. Prosthetic groups such as flavin, haem or molybdenum are missing. The corresponding gene (sud) encodes a signal peptide together with the mature subunit that consists of 129 amino acid residues including one single cysteine. The sud gene is expressed from a plasmid in Escherichia coli. The resulting enzyme catalyzes sulphide oxidation with dimethylnaphthoquinone and is located in the periplasm of E. coli.