4.4 Article Proceedings Paper

The discovery of Mo(III) in FeMoco: reuniting enzyme and model chemistry

Journal

JOURNAL OF BIOLOGICAL INORGANIC CHEMISTRY
Volume 20, Issue 2, Pages 447-460

Publisher

SPRINGER
DOI: 10.1007/s00775-014-1230-6

Keywords

Nitrogenase; FeMoco; Molybdenum; Model compounds; Catalysis

Funding

  1. Max Planck Society
  2. European Research Council under the European Union [615414]
  3. Icelandic Research Fund [141218051]
  4. European Research Council (ERC) [615414] Funding Source: European Research Council (ERC)

Ask authors/readers for more resources

Biological nitrogen fixation is enabled by molybdenum-dependent nitrogenase enzymes, which effect the reduction of dinitrogen to ammonia using an Fe7MoS9C active site, referred to as the iron molybdenum cofactor or FeMoco. In this mini-review, we summarize the current understanding of the molecular and electronic structure of FeMoco. The advances in our understanding of the active site structure are placed in context with the parallel evolution of synthetic model studies. The recent discovery of Mo(III) in the FeMoco active site is highlighted with an emphasis placed on the important role that model studies have played in this finding. In addition, the reactivities of synthetic models are discussed in terms of their relevance to the enzymatic system.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.4
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available