Literature DB >> 28726330

Synthetic Analogues of Nitrogenase Metallocofactors: Challenges and Developments.

Nathaniel S Sickerman1, Kazuki Tanifuji1, Yilin Hu1, Markus W Ribbe1,2.   

Abstract

Nitrogenase is the only known biological system capable of reducing N2 to NH3 , which is a critical component of bioavailable nitrogen fixation. Since the discovery of discrete iron-sulfur metalloclusters within the nitrogenase MoFe protein, synthetic inorganic chemists have sought to reproduce the structural features of these clusters in order to understand how they facilitate the binding, activation and hydrogenation of N2 . Through the decades following the initial identification of these clusters, significant progress has been made to synthetically replicate certain compositional and functional aspects of the biogenic clusters. Although much work remains to generate synthetic iron-sulfur clusters that can reduce N2 to NH3 , the insights borne from past and recent developments are discussed in this concept article.
© 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  M-cluster; P-cluster; biomimetic synthesis; cofactors; nitrogenase

Mesh:

Substances:

Year:  2017        PMID: 28726330     DOI: 10.1002/chem.201702496

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  4 in total

1.  Reactions of [Fe6C(CO)14(S)]2-: Cluster Growth, Redox, Sulfiding.

Authors:  Liang Liu; Toby J Woods; Thomas B Rauchfuss
Journal:  Eur J Inorg Chem       Date:  2020-09-04       Impact factor: 2.524

Review 2.  The Spectroscopy of Nitrogenases.

Authors:  Casey Van Stappen; Laure Decamps; George E Cutsail; Ragnar Bjornsson; Justin T Henthorn; James A Birrell; Serena DeBeer
Journal:  Chem Rev       Date:  2020-04-02       Impact factor: 60.622

3.  Reconstruction of Nitrogenase Predecessors Suggests Origin from Maturase-Like Proteins.

Authors:  Amanda K Garcia; Bryan Kolaczkowski; Betül Kaçar
Journal:  Genome Biol Evol       Date:  2022-03-02       Impact factor: 3.416

4.  α-Lys424 Participates in Insertion of FeMoco to MoFe Protein and Maintains Nitrogenase Activity in Klebsiella oxytoca M5al.

Authors:  Lina Song; Pengxi Liu; Wei Jiang; Qingjuan Guo; Chunxi Zhang; Abdul Basit; Ying Li; Jilun Li
Journal:  Front Microbiol       Date:  2019-04-16       Impact factor: 5.640

  4 in total

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