Trimethylammonia-lyases of Shewanella oneidensis and Their Role in Anaerobic Respiration
Yulia V. Bertsova, Marina V. SerebryakovaiD, Olga S. Godovanets, Victor A. Anashkin, Alexander A. BaykoviD, Alexander V. BogacheviD
Abstract
The facultatively anaerobic bacterium Shewanella oneidensis MR-1 contains in its genome two operons, so_3056-3058 and so_3299-3301, each including genes for putative periplasmic flavocytochrome c and ammonia-lyase of aromatic amino acids. To determine their role in anaerobic respiration, we produced the encoded ammonia-lyases SO_3057 and SO_3299 in Escherichia coli and determined their substrate specificities. SO_3057 was found to cleave trimethylammonium group from ergothioneine to yield thiourocanic acid, whereas SO_3299 catalyzed a similar conversion of N({pi})-methyl histidine betaine to yield N({pi})-methyl urocanate. The catalytic efficiencies (kcat/Km values) were (3-4) x 106 M-1 s-1, and the pH optima of activity were between 8 and 9. Ergothioneine induced SO_3057 synthesis in anaerobic S. oneidensis cells and their growth, and thiourocanate stimulated respiration as an alternative terminal electron acceptor. The predicted 3D structures of the genetically coupled flavocytochromes c (SO_3056/58 and SO_3300/3301) are consistent with their use of thiourocanate and N({pi})-methyl urocanate, respectively, as electron acceptors. We therefore conclude that the periplasmic lyases encoded by the so_3057 and so_3299 genes contribute to anaerobic respiration in S. oneidensis by producing terminal electron acceptors for the genetically coupled flavocytochromes c.
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