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Expression and purification of NifB proteins from aerobic and anaerobic sources.
- 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.
- Subjects :
- Aerobiosis
Anaerobiosis
Bacterial Proteins biosynthesis
Chromatography, Affinity
Histidine
Oligopeptides
Recombinant Fusion Proteins isolation & purification
Azotobacter vinelandii metabolism
Bacterial Proteins isolation & purification
Biochemistry methods
Escherichia coli metabolism
Klebsiella pneumoniae metabolism
Subjects
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