2005
DOI: 10.1017/s0953756204001820
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Ampelomyces mycoparasites from apple powdery mildew identified as a distinct group based on single-stranded conformation polymorphism analysis of the rDNA ITS region

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Cited by 45 publications
(53 citation statements)
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“…DNAs of KTP-05 and KMP-01 were extracted from conidia using a Qiagen DNeasy plant mini kit (Qiagen, Hilden, Germany), and ribosomal DNA internal transcribed spacer (ITS) sequences were amplified by polymerase chain reaction (PCR), using the ITS1F (Gardes & Bruns 1993) and ITS4 fungalspecific primers (White et al 1990). PCR was carried out with an iCycler (Bio-Rad, Hercules, USA) according to the protocols of Szentiványi et al (2005). The nucleotide sequences of both isolates were deposited at the DNA Data Bank of Japan (DDBJ) under the accession numbers AB808656 for KTP-05 and AB808657 for KMP-01.…”
Section: Methodsmentioning
confidence: 99%
“…DNAs of KTP-05 and KMP-01 were extracted from conidia using a Qiagen DNeasy plant mini kit (Qiagen, Hilden, Germany), and ribosomal DNA internal transcribed spacer (ITS) sequences were amplified by polymerase chain reaction (PCR), using the ITS1F (Gardes & Bruns 1993) and ITS4 fungalspecific primers (White et al 1990). PCR was carried out with an iCycler (Bio-Rad, Hercules, USA) according to the protocols of Szentiványi et al (2005). The nucleotide sequences of both isolates were deposited at the DNA Data Bank of Japan (DDBJ) under the accession numbers AB808656 for KTP-05 and AB808657 for KMP-01.…”
Section: Methodsmentioning
confidence: 99%
“…The rDNA ITS region was amplified using the ITS1F/ITS4 fungal-specific primer pair as described in Szentiványi et al (60). PCR products were purified using a PCR-M Clean Up System (Viogene) and sequenced using a BigDye Terminator v3.1 Cycle Sequencing Kit (Applied Biosystems, Foster City, CA), according to the instructions of the manufacturer.…”
Section: Methodsmentioning
confidence: 99%
“…Polymerase chain reaction (PCR) was carried out in an iCycler (Bio-Rad, Hercules, CA, USA) using the ITS1F and ITS4 fungal-specific primers designed by Gardes and Bruns (1993) and White et al (1990), respectively. PCR was performed according to the protocols described by Szentiványi et al (2005): 5 min denaturation at 95°C and 35 cycles, consisting of a 30 s denaturation at 95°C, annealing at 52°C, and extension at 72°C, were followed by a final extension cycle of 5 min at 71°C. The nucleotide sequence of the amplified region was determined using the BigDye Terminator Cycle Sequencing Ready Reaction Kit from Applied Biosystems (Tokyo, Japan) on an ABI Prism 3130 Genetic Analyzer (Applied Biosystems) in the Pharmaceutical Research and Technology Institute, Kinki University, Japan.…”
Section: Sequencing Of the Rdna Its Regionmentioning
confidence: 99%