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1.
Appl Environ Microbiol ; 73(16): 5075-82, 2007 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-17557843

RESUMEN

Application of glyphosate (N-[phosphonomethyl] glycine) to Bradyrhizobium sp. (Lupinus)-nodulated lupin plants caused modifications in the protein pattern of bacteroids. The most significant change was the presence of a 44-kDa polypeptide in bacteroids from plants treated with the higher doses of glyphosate employed (5 and 10 mM). The polypeptide has been characterized by the amino acid sequencing of its N terminus and the isolation and nucleic acid sequencing of its encoding gene. It is putatively encoded by a single gene, and the protein has been identified as a putative porin. Protein modeling revealed the existence of several domains sharing similarity to different porins, such as a transmembrane beta-barrel. The protein has been designated BLpp, for Bradyrhizobium sp. (Lupinus) putative porin, and would be the first porin described in Bradyrhizobium sp. (Lupinus). In addition, a putative conserved domain of porins has been identified which consists of 87 amino acids, located in the BLpp sequence 30 amino acids downstream of the N-terminal region. In bacteroids, mRNA of the BLpp gene shows a basal constitutive expression that increases under glyphosate treatment, and the expression of the gene is seemingly regulated at the transcriptional level. By contrast, in free-living bacteria glyphosate treatment leads to an inhibition of BLpp mRNA accumulation, indicating a different effect of glyphosate on BLpp gene expression in bacteroids and free-living bacteria. The possible role of BLpp in a metabolite interchange between Bradyrhizobium and lupin is discussed.


Asunto(s)
Proteínas Bacterianas/metabolismo , Bradyrhizobium/efectos de los fármacos , Glicina/análogos & derivados , Porinas/metabolismo , Secuencia de Aminoácidos , Proteínas Bacterianas/química , Proteínas Bacterianas/genética , Northern Blotting , Southern Blotting , Bradyrhizobium/genética , Bradyrhizobium/metabolismo , Electroforesis en Gel de Poliacrilamida , Fabaceae/microbiología , Regulación Bacteriana de la Expresión Génica/efectos de los fármacos , Glicina/farmacología , Modelos Moleculares , Datos de Secuencia Molecular , Peso Molecular , Filogenia , Porinas/química , Porinas/genética , Estructura Secundaria de Proteína , ARN Mensajero/genética , ARN Mensajero/metabolismo , Análisis de Secuencia de Proteína , Glifosato
2.
Mol Plant Microbe Interact ; 18(5): 405-13, 2005 May.
Artículo en Inglés | MEDLINE | ID: mdl-15915639

RESUMEN

Phytohormones are involved in the organogenesis of legume root nodules. The source of the auxin indole-3-acetic acid (IAA) in nodules has not been clearly determined. We studied the enzyme aldehyde oxidase (AO; EC 1.2.3.1), that catalyzes the last step of IAA biosynthesis in plants, in the nodules of Lupinus albus and Medicago truncatula. Primordia and young lupin nodules and mature M. truncatula nodules showed AO activity bands after native polyacrylamide gel electrophoresis. Gel activity analyses using indole-3-aldehyde as substrate indicated that the nodules of white lupin and M. truncatula have the capability to synthesize IAA via the indole-3-pyruvic acid pathway. Immunolocalization and in situ hybridization experiments revealed that AO is preferentially expressed in the meristematic and the invasion zones in Medicago nodules and in the lateral meristematic zone of Lupinus nodules. High IAA immunolabeling was also detected in the meristematic and invasion zones. Low expression levels and no AO activity were detected in lupin Fix- nodules that displayed restricted growth and early senescence. We propose that local synthesis of IAA in the root nodule meristem and modulation of AO expression and activity are involved in regulation of nodule development.


Asunto(s)
Aldehído Oxidasa/metabolismo , Lupinus/enzimología , Medicago truncatula/enzimología , Micorrizas/fisiología , Raíces de Plantas/enzimología , Ácido Abscísico/biosíntesis , Expresión Génica , Ácidos Indolacéticos/metabolismo , Isoenzimas , Lupinus/microbiología , Medicago truncatula/microbiología
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