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VAMP721a and VAMP721d are important for pectin dynamics and release of bacteria in soybean nodules.
Gavrin, Aleksandr; Chiasson, David; Ovchinnikova, Evgenia; Kaiser, Brent N; Bisseling, Ton; Fedorova, Elena E.
Afiliación
  • Gavrin A; Laboratory of Molecular Biology, Department of Plant Sciences, Graduate School Experimental Plant Sciences, Wageningen University, 6708 PB, Wageningen, the Netherlands.
  • Chiasson D; School of Agriculture Food and Wine, The University of Adelaide, Adelaide, SA, 5050, Australia.
  • Ovchinnikova E; School of Agriculture Food and Wine, The University of Adelaide, Adelaide, SA, 5050, Australia.
  • Kaiser BN; School of Agriculture Food and Wine, The University of Adelaide, Adelaide, SA, 5050, Australia.
  • Bisseling T; Laboratory of Molecular Biology, Department of Plant Sciences, Graduate School Experimental Plant Sciences, Wageningen University, 6708 PB, Wageningen, the Netherlands.
  • Fedorova EE; Laboratory of Molecular Biology, Department of Plant Sciences, Graduate School Experimental Plant Sciences, Wageningen University, 6708 PB, Wageningen, the Netherlands.
New Phytol ; 210(3): 1011-21, 2016 May.
Article en En | MEDLINE | ID: mdl-26790563
ABSTRACT
In root nodules rhizobia enter host cells via infection threads. The release of bacteria to a host cell is possible from cell wall-free regions of the infection thread. We hypothesized that the VAMP721d and VAMP721e exocytotic pathway, identified before in Medicago truncatula, has a role in the local modification of cell wall during the release of rhizobia. To clarify the role of VAMP721d and VAMP721e we used Glycine max, a plant with a determinate type of nodule. The localization of the main polysaccharide compounds of primary cell walls was analysed in control vs nodules with partially silenced GmVAMP721d. The silencing of GmVAMP721d blocked the release of rhizobia. Instead of rhizobia-containing membrane compartments - symbiosomes - the infected cells contained big clusters of bacteria embedded in a matrix of methyl-esterified and de-methyl-esterified pectin. These clusters were surrounded by a membrane. We found that GmVAMP721d-positive vesicles were not transporting methyl-esterified pectin. We hypothesized that they may deliver the enzymes involved in pectin turnover. Subsequently, we found that GmVAMP721d is partly co-localized with pectate lyase. Therefore, the biological role of VAMP721d may be explained by its action in delivering pectin-modifying enzymes to the site of release.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Proteínas de Plantas / Rhizobium / Glycine max / Pectinas / Nódulos de las Raíces de las Plantas Idioma: En Revista: New Phytol Asunto de la revista: BOTANICA Año: 2016 Tipo del documento: Article País de afiliación: Países Bajos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Proteínas de Plantas / Rhizobium / Glycine max / Pectinas / Nódulos de las Raíces de las Plantas Idioma: En Revista: New Phytol Asunto de la revista: BOTANICA Año: 2016 Tipo del documento: Article País de afiliación: Países Bajos