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1.
Prikl Biokhim Mikrobiol ; 49(3): 229-35, 2013.
Artigo em Russo | MEDLINE | ID: mdl-23882940

RESUMO

The review summarizes the results of studies on the comigration of tubercular bacteria and bean plants to new habitats, which is often accompanied by a decrease in the symbiosis efficiency due to a loss of the diversity of genes responsible for the interaction. This migration may lead to a rise in new symbionts as a result of gene transfers from initial symbionts to local bacteria. It was demonstrated that typically new symbionts lack an ability for N2 fixation but are highly competitive, blocking the inoculation of bean cultures by industrial strains. The design of coadapted systems of recognition and signal interaction of partners is a perspective approach to ensure competitive advantages of efficient rhizobia strains introduced into agrocenoses, together with host plants, over inactive local strains.


Assuntos
Fabaceae/genética , Rhizobium/genética , Nódulos Radiculares de Plantas/genética , Simbiose/genética , Ecossistema , Fixação de Nitrogênio/genética , Fenômenos Fisiológicos Vegetais , Raízes de Plantas , Nódulos Radiculares de Plantas/microbiologia , Nódulos Radiculares de Plantas/fisiologia , Especificidade da Espécie
2.
Mol Plant Microbe Interact ; 13(8): 799-807, 2000 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-10939251

RESUMO

Nod factors (NFs) are rhizobial lipo-chitooligosaccharide signals that trigger root nodule development in legumes. Modifications of NF structures influence their biological activity and affect their degradation by plant chitinases. Nodulation of certain pea cultivars by Rhizobium leguminosarum bv. viciae requires modification of NFs at the reducing end by either an O-acetyl or a fucosyl group. Fucosylated NFs were produced by an in vitro reaction with NodZ fucosyltransferase and purified. Their biological activity on pea was tested by measuring their capacity to stimulate the activity of a hydrolase that cleaves NFs. Nonmodified and fucosylated NFs displayed this activity at nano- to picomolar concentrations, while a sulfated NF from Sinorhizobium meliloti was inactive. In an additional series of experiments, the stability of non-modified and fucosylated NFs in the presence of purified tobacco chitinases was compared. The presence of the fucosyl group affected the degradation rates and the accessibility of specific cleavage sites on the chitooligosaccharide backbone. These results suggest that the fucosyl group in NFs also weakens the interaction of NFs with certain chitinases or chitinase-related proteins in pea roots.


Assuntos
Quitinases/metabolismo , Fucose/metabolismo , Lipopolissacarídeos/metabolismo , Pisum sativum/metabolismo , Rhizobium leguminosarum/metabolismo , Cromatografia Líquida de Alta Pressão , Cinética , Lipopolissacarídeos/isolamento & purificação , Raízes de Plantas/metabolismo , Plantas Tóxicas , Nicotiana/enzimologia
3.
Mol Plant Microbe Interact ; 12(3): 252-8, 1999 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-10065561

RESUMO

We have analyzed the nucleotide sequences of the nodX genes from two strains of Rhizobium leguminosarum bv. viciae able to nodulate Afghan peas (strains A1 and Himalaya) and from two strains of R. leguminosarum bv. trifolii (ANU843 and CSF). The nodX genes of strains A1 and ANU843 were shown to be functional for the induction of nodules on Afghan peas. To analyze the cause of phenotypic differences of strain A1 and strain TOM we have studied the composition of the lipochitin-oligosaccharides (LCOs) produced by strain A1 after induction by the flavonoid naringenin or various pea root exudates. The structural analysis of the LCOs by mass spectrometry revealed that strain A1 synthesizes a family of at least 23 different LCOs. The use of exudates instead of naringenin resulted only in quantitative differences in the ratios of various LCOs produced.


Assuntos
Proteínas de Bactérias/genética , Genes Bacterianos , Rhizobium leguminosarum/genética , Sequência de Aminoácidos , Proteínas de Bactérias/química , Cromatografia Líquida de Alta Pressão , Espectrometria de Massas , Dados de Sequência Molecular , Homologia de Sequência de Aminoácidos , Especificidade da Espécie
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