Enzyme catalyzed radical dehydrations of hydroxy acids

BackgroundThe steadily increasing field of radical biochemistry is dominated by the large family of S-adenosylmethionine dependent enzymes, the so-called radical SAM enzymes, of which several new members are discovered every year. Here we report on 2- and 4-hydroxyacyl-CoA dehydratases which apply a very different method of radical generation. In these enzymes ketyl radicals are formed by one-electron reduction or oxidation and are recycled after each turnover without further energy input. Earlier reviews on 2-hydroxyacyl-CoA dehydratases were published in 2004 [J. Kim, M. Hetzel, C.D. Boiangiu, W. Buckel, FEMS Microbiol. Rev. 28 (2004) 455–468. W. Buckel, M. Hetzel, J. Kim, Curr. Opin. Chem. Biol. 8 (2004) 462–467.]Scope of reviewThe review focuses on four types of 2-hydroxyacyl-CoA dehydratases that are involved in the fermentation of amino acids by anaerobic bacteria, especially clostridia. These enzymes require activation by one-electron transfer from an iron–sulfur protein driven by hydrolysis of ATP. The review further describes the proposed mechanism that is highlighted by the identification of the allylic ketyl radical intermediate and the elucidation of the crystal structure of 2-hydroxyisocapryloyl-CoA dehydratase. With 4-hydroxybutyryl-CoA dehydratase the crystal structure, the complete stereochemistry and the function of several conserved residues around the active site could be identified. Finally potential biotechnological applications of the radical dehydratases are presented.General significanceThe action of the activator as an ‘Archerase’ shooting electrons into difficultly reducible acceptors becomes an emerging principle in anaerobic metabolism. The dehydratases may provide useful tools in biotechnology. This article is part of a Special Issue entitled: Radical SAM enzymes and Radical Enzymology.

► 2- and 4-Hydroxyacyl-CoA contain non-acidic beta-hydrogens.
► ATP-dependent reduction generates the ketyl radical in 2-hydroxyacyl-CoA.
► Deprotonation and oxidation generates the ketyl radical of 4-hydroxybutyryl-CoA.
► 2- and 4-Hydroxyacyl-CoA dehydratases contain aconitase-like [4Fe-4S] clusters.
► 2-Hydroxyisocaproyl-CoA dehydratase comprises in addition an [4Fe-5S] cluster.