1988
DOI: 10.1111/j.1469-8137.1988.tb03698.x
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Early events of vesicular–arbuscular mycorrhiza formation on Ri T‐DNA transformed roots

Abstract: .\n tn vitro system using Ri T-DN.A transformed roots and the vesiculat-arbuscular mycorrhizal fungus Gigaspora margarita Becker & Hall has been developed to study the initial events of mycorrhiza formation. Sucrose, sodium and phosphorus were found to be critical components of the n-iedium used to establish the dual culture. L'sing a single spore as inoculum it vvas consistently possible to obtain colonization of a preselected point on the root and to time the colonization process (within . S days), .'\hundan… Show more

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Cited by 735 publications
(496 citation statements)
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“…After 35±45 days, fresh roots were harvested for immunolocalisation studies and the remaining tissue was frozen in liquid N 2 and stored at ±80°C for RNA and protein isolation. Glomus intraradices was cultured with carrot hairy roots in two-compartment Petri-plates (St-Arnaud et al, 1996) and spores were prepared from these plates according to Be  card and Fortin (1988). Inoculation of plants with Glomus intraradices spores was carried out according to Harrison and Dixon (1993).…”
Section: Methodsmentioning
confidence: 99%
“…After 35±45 days, fresh roots were harvested for immunolocalisation studies and the remaining tissue was frozen in liquid N 2 and stored at ±80°C for RNA and protein isolation. Glomus intraradices was cultured with carrot hairy roots in two-compartment Petri-plates (St-Arnaud et al, 1996) and spores were prepared from these plates according to Be  card and Fortin (1988). Inoculation of plants with Glomus intraradices spores was carried out according to Harrison and Dixon (1993).…”
Section: Methodsmentioning
confidence: 99%
“…Rhizophagus irregularis (DAOM 197198), recently reassigned from Glomus intraradices Schenck and Smith (Krüger et al 2012), was produced in monoaxenic cultures maintained on Agrobacterium rhizogenes-transformed chicory roots (Bécard and Fortin 1988) in twocompartment Petri plates, as described in Pérez-Tienda et al (2011). Plates were incubated in the dark at 24 °C until the fungal compartment, which contained a solid M medium without sucrose (M-C medium), was profusely colonized by the fungus (approximately 6 weeks).…”
Section: Biological Materialsmentioning
confidence: 99%
“…Germination was induced under sterile conditions in 0.6% agar/water. Seedlings were transferred to minimal medium (Bécard and Fortin 1988) without sucrose and grown for 10 days in a growth chamber (16 h daylight at 21°C/8 h night at 18°C). Agrobacterium rhizogenes transformed roots from M. truncatula wild-type and the three mutants, dmi1-1 ), dmi2-2 (Endre et al 2002), dmi3-1 Mitra et al 2004) of M. truncatula Gaertn.…”
Section: Plant Materialsmentioning
confidence: 99%
“…cv. Jemalong (kindly provided by M. Chabaud and D. Barker, LIPM, Toulouse, France) were grown in sterile conditions in minimal medium at 25°C in the dark (Bécard and Fortin 1988). Arabidopsis thaliana seeds were sterilized with 1 min wash in 70% ethanol followed by 20 min wash in 10% commercial bleach and rinsed three times for 10 min with sterile distilled water.…”
Section: Plant Materialsmentioning
confidence: 99%