2002
DOI: 10.1007/s00572-002-0174-9
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Increased spore production by Glomus intraradices in the split-plate monoxenic culture system by repeated harvest, gel replacement, and resupply of glucose to the mycorrhiza

Abstract: Monoxenic culture of Glomus intraradices Schenck and Smith with Ri T-DNA transformed roots in two-compartment Petri dishes is a very useful technique for physiological studies and the production of clean fungal tissues. Experiments were conducted to increase the efficiency of this method for the production of arbuscular mycorrhizal fungus spores. Approximately 20,000 spores could be harvested every 2 months from the distal (fungus only) compartment of a 9-cm-diameter divided Petri dish. The method requires rep… Show more

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Cited by 44 publications
(27 citation statements)
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“…The co-cultivation of G. intraradices spores with carrot hairy root was used in present study, because of their comfort of propagation and better adaption in culture than normal root. This result is supported by Douds (2002) and Gadkar et al (2006), where transformed Daucus carota DC1 and DC2 hairy roots respectively have been successfully used to initiate monoxenic culture of AM fungi through root organ culture. In our study 3-7 days Co-Cultivation with transformed carrot root and G. intraradices spores, the hyphal growth was moves towards host root.…”
Section: Discussionsupporting
confidence: 51%
“…The co-cultivation of G. intraradices spores with carrot hairy root was used in present study, because of their comfort of propagation and better adaption in culture than normal root. This result is supported by Douds (2002) and Gadkar et al (2006), where transformed Daucus carota DC1 and DC2 hairy roots respectively have been successfully used to initiate monoxenic culture of AM fungi through root organ culture. In our study 3-7 days Co-Cultivation with transformed carrot root and G. intraradices spores, the hyphal growth was moves towards host root.…”
Section: Discussionsupporting
confidence: 51%
“…After 15 weeks, the fungal compartment of all plates from each isolate was removed and pooled for extraction of hyphae and spores (26). This compartment was refilled with medium to allow the growth of more fungal material for a second extraction (27).…”
Section: Methodsmentioning
confidence: 99%
“…However, no significant effects on the d. wt of the FERM were found, probably because the variability in the amount of FERM was larger than any fungal growth during the 3-and 6-d treatment. Douds (2002) reported that spore production in the fungal compartment can be increased by replenishing carbohydrates in the root compartment. This is consistent with several reports that AM fungal growth and mycorrhizal colonization are affected by altered light conditions that change the C availability for the fungus (Hayman, 1974;Son & Smith, 1988;Smith & Gianinazzi-Pearson, 1990).…”
mentioning
confidence: 99%