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Expression and purification of NifB proteins from aerobic and anaerobic sources.

Authors :
Echavarri-Erasun C
Arragain S
Scandurra AA
Rubio LM
Source :
Methods in molecular biology (Clifton, N.J.) [Methods Mol Biol] 2014; Vol. 1122, pp. 19-31.
Publication Year :
2014

Abstract

NifB is the key protein in the biosynthesis of nitrogenase iron-molybdenum cofactor. Due to its extreme sensitivity to O2 and inherent protein instability, NifB proteins must be purified under strict anaerobic conditions by using affinity chromatography methods. We describe here the methods for NifB purification from cells of the strict aerobic nitrogen-fixing bacterium Azotobacter vinelandii, the facultative anaerobic nitrogen-fixing bacterium Klebsiella pneumoniae, and the facultative anaerobic non-nitrogen fixing bacterium Escherichia coli recombinantly expressing a nifB gene of thermophilic origin.

Details

Language :
English
ISSN :
1940-6029
Volume :
1122
Database :
MEDLINE
Journal :
Methods in molecular biology (Clifton, N.J.)
Publication Type :
Academic Journal
Accession number :
24639251
Full Text :
https://doi.org/10.1007/978-1-62703-794-5_3