1979
DOI: 10.1071/bt9790103
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Some Conditions Governing Zoospore Production in Axenic Cultures of Phytophthora cinnamomi Rands

Abstract: A method for the production of zoospores from the plant pathogen Phytophthora cinnamomi is described. The use of siliconized cellulose pads as a hyphal support, which in turn allows shake- grown mycelia to be used, results in the production of zoospores in concentrations of 107-108/litre. It allows one person to produce the equivalent of 1-10 mg of zoospore protein per batch, which is sufficient for a variety of biochemical studies.

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Cited by 75 publications
(35 citation statements)
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“…The medium for all count data of antheridial types contained 10 % cleared V8-juice, 0n01 % CaCO $ , 0n002 % β-sitosterol, 2 % Difco bacteriological agar (V8A), and was prepared as described by Byrt & Grant (1979). From the set of 72 isolates, seven which formed paragynous antheridia and two which formed only amphigynous antheridia were paired individually with the Cape Hope A1 isolate on V8A in Petri dishes and replicated four times.…”
Section: Development and Behaviour Of Paragynous Antheridiamentioning
confidence: 99%
“…The medium for all count data of antheridial types contained 10 % cleared V8-juice, 0n01 % CaCO $ , 0n002 % β-sitosterol, 2 % Difco bacteriological agar (V8A), and was prepared as described by Byrt & Grant (1979). From the set of 72 isolates, seven which formed paragynous antheridia and two which formed only amphigynous antheridia were paired individually with the Cape Hope A1 isolate on V8A in Petri dishes and replicated four times.…”
Section: Development and Behaviour Of Paragynous Antheridiamentioning
confidence: 99%
“…Hyphae of P. cinnamomi (DAR 522646;ATCC 200982) were cut from the growing edge of a nutrient agar culture, transferred to liquid nutrient medium (Chen and Zentmyer, 1970;Byrt and Grant, 1979), and left to grow for 2 days at 25°C. Sporangial production was initiated by washing the mycelium four times over a 4-h period with nutrient-poor mineral salts solution at 22°C .…”
Section: Culture Of Sporangiamentioning
confidence: 99%
“…For experiment 1, mycelial discs (6 mm diameter) of Phytophthora cinnamomi bearing sporangia, produced using the axenic method of Byrt & Grant (1979), were placed in 3 cm diam Petri dishes containing 5 ml sterile distilled water. The dishes were chilled for 30 min at 4 °C for synchronized zoospore release and zoospore density was determined to be 10-20 zoospores μl −1…”
Section: Inoculum and Inoculationmentioning
confidence: 99%