4.7 Review

Insights into [FeFe]-Hydrogenase Structure, Mechanism, and Maturation

Journal

STRUCTURE
Volume 19, Issue 8, Pages 1038-1052

Publisher

CELL PRESS
DOI: 10.1016/j.str.2011.06.008

Keywords

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Funding

  1. NASA Astrobiology Institute [NNA08CN85A]
  2. Air Force Office of Scientific Research
  3. Chemical Sciences, Geosciences and Biosciences Division, Office of Basic Energy Sciences, Office of Science, U.S. Department of Energy [DE-FG02-10ER16194, DE-AC36-08GO28308]
  4. U.S. Department of Energy, Office of Biological and Environmental Research
  5. U.S. National Institutes of Health, National Center for Research Resources
  6. U.S. National Institute of General Medical Sciences
  7. NASA [NNA08CN85A, 103836] Funding Source: Federal RePORTER

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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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