Literature DB >> 34292546

Expression, Isolation, and Characterization of Vanadium Nitrogenase from Azotobacter vinelandii.

Katharina Parison1, Jakob Gies-Elterlein1, Christian Trncik1, Oliver Einsle2.   

Abstract

Nitrogenases are the sole enzymes known to mediate biological nitrogen fixation, an essential process for sustaining life on earth. Among the three known variants, molybdenum nitrogenase is the best-studied to date. Recent work on the alternative vanadium nitrogenase provided important insights into the mechanism of nitrogen fixation since this enzyme differs from its molybdenum counterpart in some important aspects. Here, we present a protocol to obtain unmodified vanadium nitrogenase in high yield and purity from the paradigmatic diazotroph Azotobacter vinelandii, including procedures for cell cultivation, purification, and protein characterization.
© 2021. Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  Alternative nitrogenase; Anoxic protein biochemistry; Azotobacter vinelandii; Biological nitrogen fixation; Fe protein; Nitrogen fixation; Protein expression; Protein isolation; Protein purification; VFe protein; Vanadium; Vanadium nitrogenase

Mesh:

Substances:

Year:  2021        PMID: 34292546     DOI: 10.1007/978-1-0716-1605-5_6

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  75 in total

1.  Structural Basis of Biological Nitrogen Fixation.

Authors:  James B. Howard; Douglas C. Rees
Journal:  Chem Rev       Date:  1996-11-07       Impact factor: 60.622

2.  Reduction of dinitrogen.

Authors:  Richard R Schrock
Journal:  Proc Natl Acad Sci U S A       Date:  2006-11-06       Impact factor: 11.205

3.  Nucleotide sequences and mutational analysis of the structural genes for nitrogenase 2 of Azotobacter vinelandii.

Authors:  R D Joerger; T M Loveless; R N Pau; L A Mitchenall; B H Simon; P E Bishop
Journal:  J Bacteriol       Date:  1990-06       Impact factor: 3.490

4.  Complete nucleotide sequence of the Azotobacter vinelandii nitrogenase structural gene cluster.

Authors:  K E Brigle; W E Newton; D R Dean
Journal:  Gene       Date:  1985       Impact factor: 3.688

5.  The nitrogenase system from Azotobacter: two-enzyme requirement for N2 reduction, ATP-dependent H2 evolution, and ATP hydrolysis.

Authors:  W A Bulen; J R LeComte
Journal:  Proc Natl Acad Sci U S A       Date:  1966-09       Impact factor: 11.205

6.  Purification of a second alternative nitrogenase from a nifHDK deletion strain of Azotobacter vinelandii.

Authors:  J R Chisnell; R Premakumar; P E Bishop
Journal:  J Bacteriol       Date:  1988-01       Impact factor: 3.490

7.  Distribution of Nitrogen-Fixation Genes in Prokaryotes Containing Alternative Nitrogenases.

Authors:  Maame A Addo; Patricia C Dos Santos
Journal:  Chembiochem       Date:  2020-04-16       Impact factor: 3.164

8.  Nucleotide sequence and mutational analysis of the structural genes (anfHDGK) for the second alternative nitrogenase from Azotobacter vinelandii.

Authors:  R D Joerger; M R Jacobson; R Premakumar; E D Wolfinger; P E Bishop
Journal:  J Bacteriol       Date:  1989-02       Impact factor: 3.490

9.  Evidence for an alternative nitrogen fixation system in Azotobacter vinelandii.

Authors:  P E Bishop; D M Jarlenski; D R Hetherington
Journal:  Proc Natl Acad Sci U S A       Date:  1980-12       Impact factor: 11.205

10.  Distribution of nitrogen fixation and nitrogenase-like sequences amongst microbial genomes.

Authors:  Patricia C Dos Santos; Zhong Fang; Steven W Mason; João C Setubal; Ray Dixon
Journal:  BMC Genomics       Date:  2012-05-03       Impact factor: 3.969

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