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dc.contributor.author
Corregido, María Cecilia  
dc.contributor.author
Asención Diez, Matías Damián  
dc.contributor.author
Iglesias, Alberto Alvaro  
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Piattoni, Claudia Vanesa  
dc.date.available
2020-11-22T20:57:31Z  
dc.date.issued
2019-03  
dc.identifier.citation
Corregido, María Cecilia; Asención Diez, Matías Damián; Iglesias, Alberto Alvaro; Piattoni, Claudia Vanesa; New pieces to the carbon metabolism puzzle of Nitrosomonas europaea: Kinetic characterization of glyceraldehyde-3 phosphate and succinate semialdehyde dehydrogenases; Elsevier France-editions Scientifiques Medicales Elsevier; Biochimie; 158; 3-2019; 238-245  
dc.identifier.issn
0300-9084  
dc.identifier.uri
http://hdl.handle.net/11336/118752  
dc.description.abstract
Nitrosomonas europaea is a chemolithotroph that obtains energy through the oxidation of ammonia to hydroxylamine while assimilates atmospheric CO 2 to cover the cell carbon demands for growth. This microorganism plays a relevant role in the nitrogen biogeochemical cycle on Earth but its carbon metabolism remains poorly characterized. Based on sequence homology, we identified two genes (cbbG and gabD) coding for redox enzymes in N. europaea. Cloning and expression of the genes in Escherichia coli, allowed the production of recombinant enzymes purified to determine their biochemical properties. The protein CbbG is a glyceraldehyde-3-phosphate (Ga3P) dehydrogenase (Ga3PDHase) catalyzing the reversible oxidation of Ga3P to 1,3-bis-phospho-glycerate (1,3bisPGA), using specifically NAD + /NADH as cofactor. CbbG showed ∼6-fold higher K m value for 1,3bisPGA but ∼5-fold higher k cat for the oxidation of Ga3P. The protein GabD irreversibly oxidizes Ga3P to 3Pglycerate using NAD + or NADP + , thus resembling a non-phosphorylating Ga3PDHase. However, the enzyme showed ∼6-fold higher K m value and three orders of magnitude higher catalytic efficiency with succinate semialdehyde (SSA) and NADP + . Indeed, the GabD protein identity corresponds to an SSA dehydrogenase (SSADHase). CbbG seems to be the only Ga3PDHase present in N. europaea; which would be involved in reducing triose-P during autotrophic carbon fixation. Otherwise, in cells grown under conditions deprived of ammonia and oxygen, the enzyme could catalyze the glycolytic step of Ga3P oxidation producing NADH. As an SSADHase, GabD would physiologically act producing succinate and preferentially NADPH over NADH; thus being part of an alternative pathway of the tricarboxylic acid cycle converting α-ketoglutarate to succinate. The properties determined for these enzymes contribute to better identify metabolic steps in CO 2 assimilation, glycolysis and the tricarboxylic acid cycle in N. europaea. Results are discussed in the framework of metabolic pathways that launch biosynthetic intermediates relevant in the microorganism to develop and fulfill its role in nature.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Elsevier France-editions Scientifiques Medicales Elsevier  
dc.rights
info:eu-repo/semantics/restrictedAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
ALDEHYDE DEHYDROGENASE  
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CHEMOLITHOTROPH  
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GLYCOLYSIS  
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NITRIFIER BACTERIA  
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REDOX  
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SUCCINATE SEMIALDEHYDE  
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TRIOSE-PHOSPHATE  
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Bioquímica y Biología Molecular  
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Ciencias Biológicas  
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CIENCIAS NATURALES Y EXACTAS  
dc.title
New pieces to the carbon metabolism puzzle of Nitrosomonas europaea: Kinetic characterization of glyceraldehyde-3 phosphate and succinate semialdehyde dehydrogenases  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2020-11-20T19:59:30Z  
dc.journal.volume
158  
dc.journal.pagination
238-245  
dc.journal.pais
Francia  
dc.description.fil
Fil: Corregido, María Cecilia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Agrobiotecnología del Litoral. Universidad Nacional del Litoral. Instituto de Agrobiotecnología del Litoral; Argentina  
dc.description.fil
Fil: Asención Diez, Matías Damián. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Agrobiotecnología del Litoral. Universidad Nacional del Litoral. Instituto de Agrobiotecnología del Litoral; Argentina  
dc.description.fil
Fil: Iglesias, Alberto Alvaro. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Agrobiotecnología del Litoral. Universidad Nacional del Litoral. Instituto de Agrobiotecnología del Litoral; Argentina  
dc.description.fil
Fil: Piattoni, Claudia Vanesa. Instituto Pasteur de Montevideo; Uruguay  
dc.journal.title
Biochimie  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.biochi.2019.01.013