Cell-free H-cluster synthesis and [FeFe] hydrogenase activation: all five CO and CN⁻ ligands derive from tyrosine

PLoS One. 2011;6(5):e20346. doi: 10.1371/journal.pone.0020346. Epub 2011 May 31.

Abstract

[FeFe] hydrogenases are promising catalysts for producing hydrogen as a sustainable fuel and chemical feedstock, and they also serve as paradigms for biomimetic hydrogen-evolving compounds. Hydrogen formation is catalyzed by the H-cluster, a unique iron-based cofactor requiring three carbon monoxide (CO) and two cyanide (CN⁻) ligands as well as a dithiolate bridge. Three accessory proteins (HydE, HydF, and HydG) are presumably responsible for assembling and installing the H-cluster, yet their precise roles and the biosynthetic pathway have yet to be fully defined. In this report, we describe effective cell-free methods for investigating H-cluster synthesis and [FeFe] hydrogenase activation. Combining isotopic labeling with FTIR spectroscopy, we conclusively show that each of the CO and CN⁻ ligands derive respectively from the carboxylate and amino substituents of tyrosine. Such in vitro systems with reconstituted pathways comprise a versatile approach for studying biosynthetic mechanisms, and this work marks a significant step towards an understanding of both the protein-protein interactions and complex reactions required for H-cluster assembly and hydrogenase maturation.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Bacterial Proteins / chemistry
  • Bacterial Proteins / metabolism
  • Carbon Monoxide / chemistry
  • Carbon Monoxide / metabolism*
  • Cyanides / chemistry
  • Cyanides / metabolism*
  • Hydrogen / metabolism*
  • Hydrogenase / chemistry
  • Hydrogenase / metabolism*
  • Iron-Sulfur Proteins / chemistry
  • Iron-Sulfur Proteins / metabolism*
  • Ligands
  • Models, Molecular
  • Molecular Structure
  • Protein Conformation
  • Spectroscopy, Fourier Transform Infrared
  • Tyrosine / chemistry
  • Tyrosine / metabolism*

Substances

  • Bacterial Proteins
  • Cyanides
  • Iron-Sulfur Proteins
  • Ligands
  • Tyrosine
  • Carbon Monoxide
  • Hydrogen
  • Hydrogenase