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Insights into [FeFe]-hydrogenase structure, mechanism, and maturation
Authors:Mulder David W  Shepard Eric M  Meuser Jonathan E  Joshi Neelambari  King Paul W  Posewitz Matthew C  Broderick Joan B  Peters John W
Institution:Department of Chemistry and Biochemistry, Astrobiology Biogeocatalysis Research Center, Montana State University, Bozeman, MT 59717, USA.
Abstract:Hydrogenases are metalloenzymes that are key to energy metabolism in a variety of microbial communities. Divided into three classes based on their metal content, the Fe]-, FeFe]-, and NiFe]-hydrogenases are evolutionarily unrelated but share similar nonprotein ligand assemblies at their active site metal centers that are not observed elsewhere in biology. These nonprotein ligands are critical in tuning enzyme reactivity, and their synthesis and incorporation into the active site clusters require a number of specific maturation enzymes. The wealth of structural information on different classes and different states of hydrogenase enzymes, biosynthetic intermediates, and maturation enzymes has contributed significantly to understanding the biochemistry of hydrogen metabolism. This review highlights the unique structural features of hydrogenases and emphasizes the recent biochemical and structural work that has created a clearer picture of the FeFe]-hydrogenase maturation pathway.
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