IN INOCULANTS Nodulaid - 17th International Nitrogen Fixation ...
IN INOCULANTS Nodulaid - 17th International Nitrogen Fixation ...
IN INOCULANTS Nodulaid - 17th International Nitrogen Fixation ...
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17 th <strong>International</strong> Congress on <strong>Nitrogen</strong> <strong>Fixation</strong><br />
Fremantle, Western Australia<br />
27 November – 1 December 2011<br />
Session Details: Wednesday 30 November 2011<br />
Plenary Session 5<br />
0900 - 1030<br />
Authors: Erik Limpens 1 , Sergey Ivanov 1 , Evgenia Ovchinnikova 1,2 , Alexey Borisov 2 , Rik op den<br />
Camp 1 , Stephane de Mita 3 , René Geurts 1 , Elena Fedorova 1,4 , Ton Bisseling 1<br />
1 Laboratory of Molecular Biology, Wageningen University, The Netherlands.<br />
2 All-Russia Research Institute for Agricultural Microbiology, Laboratory of Genetics of<br />
Plant-Microbe Interactions, St. Petersburg, Russia.<br />
3 Plant Diversity and Adaptation, Institute for Research and Development, Montpellier,<br />
France.<br />
4 Timiryazev Institute of Plant Physiology RAS, Moscow, Russia.<br />
Presentation Title: Formation of a symbiotic interface in rhizobial and mycorrhizal symbioses<br />
Presentation Time: 0930 – 1000<br />
In both the rhizobium-legume symbiosis and the arbuscular mycorrhizal symbiosis the microbes are hosted<br />
intracellularly in a novel, specialized membrane compartment that forms a symbiotic interface. The formation of<br />
this interface is at the heart of symbiosis. In the case of rhizobia they are accommodated as novel nitrogen-fixing<br />
organelles, called symbiosomes, inside infected cells of the root nodule. Arbuscular mycorrhizal (AM) fungi form<br />
highly branched hyphal structures, called arbuscules, in infected root cortical cells. In both cases the microbial<br />
symbiont is surrounded by a plant derived membrane that has a special plasma membrane identity and where<br />
generally a structured plant cell wall is lacking. It has recently become clear that the signaling molecules and<br />
signaling pathway that trigger these different symbioses are strikingly similar. We show that this signaling<br />
pathway also controls the formation of the symbiotic interfaces in both symbioses. The observed plasma<br />
membrane identity of both interface membranes indicates a major role for exocytotic vesicle traffic. By studying<br />
plasma membrane (PM) SNARE proteins we show that knock-down of specific PM SNARE members blocks the<br />
release of the bacteria from cell wall bound infection threads and/or subsequent symbiosome development.<br />
Furthermore, two specific SNARE proteins required for symbiosome formation are also essential for arbuscule<br />
formation by AM fungi. These results suggest that in evolution the ability to produce Nod factors gave rhizobia<br />
the ability to use the ancient AM machinery to recruit a specific exocytotic pathway for the establishment of a<br />
symbiotic interface.<br />
65<br />
2011