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Ponencias en congresos:
NifQ and NifO are essential to express nitrogenase activity in the presence of nitrate in Azotobacter vinelandii
Año:2015
Áreas de investigación
  • Biología molecular, celular y genética
Datos
Descripción
In the presence of nitrate, Azotobacter vinelandii is able to assimilate nitrogen by using nitrogenase and nitrate reductase/nitrite reductase pathways simultaneously. Nitrogenase and nitrate reductase are Mo-enzymes containing FeMo-co and Mo-MGD at their active sites, respectively. In order to optimize the use of Mo, a scarce metal in nature, regulation of Mo distribution between both enzymes must be strictly controlled during nitrogen assimilation processes. The nifO and nifQ genes are grouped together with nifB, fdxN and rhdN in one transcriptional unit. It has been shown that nifO and nifQ expression levels change antagonistically depending on the presence of Mo in the medium (Rodriguez-Quinones 1993). In addition, the nifO mutant exhibits a Nif- phenotype in the presence of nitrate, whereas nifO overexpression lowers nitrate reductase activity (Gutierrez, J.C. 1997). The nifQ mutant is unable to fix N2 unless growth medium is supplemented with 1000-fold excess of Mo. Importantly, NifQ has been characterized as the physiological Mo donor to a NifEN/NifH complex during FeMo-co synthesis. (Hernandez, J.A. 2008). We aimed to understand the relationship between NifO and NifQ during expression of nitrogenase activity in presence of nitrate in A. vinelandii. The nifQ mutant was unable to fix N2 in the presence of nitrate, independently of the level of Mo in the medium. In contrast nifQ mutant showed enhanced nitrate reductase activity. Analysis of nitrogenase and nitrate reductase activities demonstrated that the nifQ overexpressing strain exhibited lower nitrogenase activity and higher nitrate reductase activity than wild-type when grown diazotrophically in the presence of nitrate, a phenotype similar to the nifO mutant (Gutierrez, J.C. 1997). An antagonist effect had been observed in the nifO overexpressing strain (Gutierrez, J.C. 1997). Simultaneous overexpression of both nifQ and nifO yielded nitrogenase and nitrate reductase activities similar to wild-type. The phenotype observed in nifQ overexpressing, but not in nifOQ overexpressing strain, points to NifO as candidate to preserve NifQ as Mo donor to nitrogenase when nitrate reductase is present. Transcriptional expression analysis performed by RT-qPCR showed lower expression of nitrogenase structural genes in the nifO mutant. In contrast increased expression of nitrate and nitrite reductase structural genes was observed for both nifO mutant and nifQ overexpression strains. Comparison between NifQ proteins isolated before and after addition of nitrate to the same culture of a nifQ overexpressing strain grown under diazotrophic conditions, showed NifQ cluster content alteration, resulting in decrease of [Mo-3Fe-4S]3+ and increase of [3Fe-4S]+ clusters. This effect of nitrate is consistent with the inability of NifQ to donate Mo for FeMo-co biosynthesis under nitrate reductase derepressing conditions. These results revealed two Mo pathways to nitrogenase: one that can be sorted by a large excess of Mo in the medium, and a second pathway strictly dependent on NifQ and NifO that would be essential to maintain active nitrogenase while assimilating nitrate through the molybdoenzyme nitrate reductase.
Internacional
Si
Nombre congreso
IV Portuguese-Spanish meeting on Nitrogen Fixation, XV Reunión de la Sociedad Española de Fijación de Nitrógeno
Tipo de participación
960
Lugar del congreso
León
Revisores
Si
ISBN o ISSN
0000-0000
DOI
Fecha inicio congreso
16/06/2015
Fecha fin congreso
18/06/2015
Desde la página
1
Hasta la página
141
Título de las actas
IV Portuguese-Spanish meeting on Nitrogen Fixation, XV Reunión de la Sociedad Española de Fijación de Nitrógeno
Esta actividad pertenece a memorias de investigación
Participantes
  • Autor: Emilio Jimenez Vicente (UPM)
  • Autor: Emma Barahona Martin (UPM)
  • Autor: Jarett Wilcoxen (UC Davis)
  • Autor: Mónica Navarro Rodríguez (UPM)
  • Autor: José María Buesa Galiano (UPM)
  • Autor: David Britt (UC Davis)
  • Autor: Luis Manuel Rubio Herrero (UPM)
Grupos de investigación, Departamentos, Centros e Institutos de I+D+i relacionados
  • Creador: Grupo de Investigación: BIOLOGÍA MOLECULAR Y COMPUTACIONAL
  • Centro o Instituto I+D+i: Centro de Biotecnología y Genómica de Plantas, CBGP
  • Departamento: Biotecnología - Biología Vegetal
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