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Nitrogen Fixation Mutants of the Actinobacterium Frankia Casuarinae CcI3

Frankia is a representative genus of nitrogen-fixing (N(2)-fixing) actinobacteria; however, the molecular mechanisms underlying various phenomena such as the differentiation of a N(2) fixation-specific structure (vesicle) and the regulation of N(2) fixation (nif) genes, have yet to be elucidated in...

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Detalles Bibliográficos
Autores principales: Kucho, Ken-ichi, Tamari, Daiki, Matsuyama, Shintaro, Nabekura, Takeshi, Tisa, Louis S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: the Japanese Society of Microbial Ecology (JSME)/the Japanese Society of Soil Microbiology (JSSM)/the Taiwan Society of Microbial Ecology (TSME)/the Japanese Society of Plant Microbe Interactions (JSPMI) 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5745019/
https://www.ncbi.nlm.nih.gov/pubmed/29151446
http://dx.doi.org/10.1264/jsme2.ME17099
Descripción
Sumario:Frankia is a representative genus of nitrogen-fixing (N(2)-fixing) actinobacteria; however, the molecular mechanisms underlying various phenomena such as the differentiation of a N(2) fixation-specific structure (vesicle) and the regulation of N(2) fixation (nif) genes, have yet to be elucidated in detail. In the present study, we screened hyphal fragments of Frankia casuarinae that were mutagenized by 1-methyl-3-nitro-1-nitrosoguanidine or gamma rays, and isolated 49 candidate N(2) fixation mutants. Twelve of these mutants were selected for further study, and their abilities to grow in NH(3)-deficient (N-) liquid media and their rates of acetylene reduction activities were evaluated. Eleven mutant strains were confirmed to lack the ability to fix N(2). Five mutant strains formed significantly reduced numbers of vesicles, while some failed to form large mature vesicles. These vesicle mutants also exhibited an aberrant hyphal morphology, suggesting a relationship between vesicle differentiation and hyphal branching. Ten mutants showed significant reductions in the expression of nifE, nifH, and nifV genes under N- conditions. The genome sequencing of eight mutants identified 20 to 400 mutations. Although mutant strains N3H4 and N6F4 shared a large number of mutations (108), most were unique to each strain. Mutant strain N7C9 had 3 mutations in the nifD and nifH genes that may result in the inability to fix N(2). The other mutant strains did not have any mutations in any known N(2) fixation-related genes, indicating that they are novel N(2) fixation mutants.