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PMID: 1328150 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Synthesis of nitrogenase in mutants of the cyanobacterium Anabaena sp. strain PCC 7120 affected in heterocyst development or metabolism.

Journal of bacteriology ·Vol. 174 ·No. 19 ·1992-10-00 ·Pages 6025-32

Ernst A, Black T, Cai Y, Panoff JM, Tiwari DN, Wolk CP

Abstract

Mutants of Anabaena sp. strain PCC 7120 that are incapable of sustained growth with air as the sole source of nitrogen were generated by using Tn5-derived transposons. Nitrogenase was expressed only in mutants that showed obvious morphological signs of heterocyst differentiation. Even under rigorously anaerobic conditions, nitrogenase was not synthesized in filaments that were unable to develop heterocysts. These results suggest that competence to synthesize nitrogenase requires a process that leads to an early stage of visible heterocyst development and are consistent with the idea that synthesis of nitrogenase is under developmental control (J. Elhai and C. P. Wolk, EMBO J. 9:3379-3388, 1990). We isolated mutants in which differentiation was arrested at an intermediate stage of heterocyst formation, suggesting that differentiation proceeds in stages; those mutants, as well as mutants with aberrant heterocyst envelopes and a mutant with defective respiration, expressed active nitrogenase under anaerobic conditions only. These results support the idea that the heterocyst envelope and heterocyst respiration are required for protection of nitrogenase from inactivation by oxygen. In the presence of air, such mutants contained less nitrogenase than under anaerobic conditions, and the Fe-protein was present in a posttranslationally modified inactive form. We conclude that internal partial oxygen pressure sufficient to inactivate nitrogenase is insufficient to repress synthesis of the enzyme completely. Among mutants with an apparently intact heterocyst envelope and normal respiration, three had virtually undetectable levels of dinitrogenase reductase under all conditions employed. However, three others expressed oxygen-sensitive nitrogenase activity, suggesting that respiration and barrier to diffusion of gases may not suffice for oxygen protection of nitrogenase in these mutants; two of these mutants reduced acetylene to ethylene and ethane.

MeSH Terms
Anabaena/drug effects,physiology Anaerobiosis Blotting, Western DNA Transposable Elements Dinitrogenase Reductase/biosynthesis,immunology Enzyme Stability Gene Expression Regulation, Enzymologic Morphogenesis Mutagenesis, Insertional Nitrogen/metabolism Nitrogenase/biosynthesis,drug effects,genetics Oxygen/pharmacology Oxygen Consumption Phenotype
Chemicals
DNA Transposable Elements Dinitrogenase Reductase Nitrogenase Nitrogen Oxygen
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Ernst A
MSU-DOE Plant Research Laboratory, Michigan State University, East Lansing 48824-1312.
Black T
Cai Y
Panoff J M
Tiwari D N
Wolk C P
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Article Info
Journal
Journal of bacteriology
Abbr.
J Bacteriol
ISSN
0021-9193
Published
1992-10-00
Pages
6025-32
Language
English
Region
United States
NLM ID
2985120R
PMCID
PMC207667
Subset
IM
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