| Literature DB >> 6993623 |
S S Hom, H Hennecke, K T Shanmugam.
Abstract
The rate of biosynthesis of nitrogenase polypeptides in Klebsiella pneumoniae was determined in a medium containing NaNO3 or NaNO2. Nitrogenase biosynthesis was completely repressed by NO3- in a mutant strain, strain SK-25, that is derepressed for nitrogenase biosynthesis in the presence of NH4+. Chlorate-resistant mutants, derived from strain SK-25, that are defective in NO3- respiration produced nitrogenase in the presence of NO3-. Strain SK-56), a chlorate-resistant derivative capable of NO3- respiration, produced no nitrogenase in the presence of NO3- or NO2-. Klebsiella pneumoniae respired under anaerobic conditions utilizing either NO3- or NO2- as terminal electron acceptor. A mechanism for the control of nitrogenase biosynthesis is discussed involving the redox control of anaerobic enzyme systems.Entities:
Mesh:
Substances:
Year: 1980 PMID: 6993623 DOI: 10.1099/00221287-117-1-169
Source DB: PubMed Journal: J Gen Microbiol ISSN: 0022-1287