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PMID: 4218230 Published · ppublish English Journal Article

Activation of inactive nitrogenase by acid-treated component I.

Journal of bacteriology ·Vol. 120 ·No. 2 ·1974-11-00 ·Pages 697-701

Nagatani HH, Shah VK, Brill WJ

Abstract

When Azotobacter vinelandii was derepressed for nitrogenase synthesis in a N-free medium containing tungstate instead of molybdate, an inactive component I was synthesized. Although this inactive component I could be activated in vivo upon addition of molybdate to the medium, it could not be activated in vitro when molybdate was added to the extracts. Activation occurred, however, when an acid-treated component I was added to extracts of cells derepressed in medium containing tungstate. Acid treatment completely abolished component I activity. Mutant strains UW45 and UW10 were unable to fix N(2). Both strains synthesized normal levels of component II but produced inactive component I. Acid-treated component I activated inactive component I in extracts of mutant strain UW45 but not mutant strain UW10. This activating factor could be obtained from N(2)-fixing Klebsiella pneumoniae, Clostridium pasteurianum, and Rhodospirillum rubrum.

MeSH Terms
Azotobacter/enzymology,immunology Bacterial Proteins/pharmacology Clostridium Culture Media Enzyme Activation/drug effects Indicators and Reagents Klebsiella Klebsiella pneumoniae Molybdenum/metabolism Mutation Nitrogen Fixation Nitrogenase/metabolism Rhodospirillum rubrum Tungsten/metabolism
Chemicals
Bacterial Proteins Culture Media Indicators and Reagents Molybdenum Nitrogenase Tungsten
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Nagatani H H
Shah V K
Brill W J
References (25)
25 references, click to expand
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Article Info
Journal
Journal of bacteriology
Abbr.
J Bacteriol
ISSN
0021-9193
Published
1974-11-00
Pages
697-701
Language
English
Region
United States
NLM ID
2985120R
PMCID
PMC245829
Subset
IM
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