1991
DOI: 10.1094/phyto-81-1395
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Characterization of Anastomosis Groups of BinucleateRhizoctoniaSpecies Using Restriction Analysis of an Amplified Ribosomal RNA Gene

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Cited by 212 publications
(107 citation statements)
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“…It has been reported that RFLP analysis of rDNA is a useful technique for identification of some fungi (Cubeta et al, 1991;Chen, 1992;Ward and Akrofi, 1994;Erland, 1995), and that RAPD analysis is also useful for identification of fungi (Bentley et al, 1995;Theodore et al, 1995) and for investigation of the correlation of genetic variation with pathotype (Nicholson and Rezanoor, 1994). Nakada et al (1994) have reported that analysis of RFLPs of total DNA using arbitrarily chosen genomic clones as probe revealed clear differences among the most common plant pathogenic fungi, Bipolaris and Curvularia species, on gramineous plants.…”
Section: Discussionmentioning
confidence: 99%
“…It has been reported that RFLP analysis of rDNA is a useful technique for identification of some fungi (Cubeta et al, 1991;Chen, 1992;Ward and Akrofi, 1994;Erland, 1995), and that RAPD analysis is also useful for identification of fungi (Bentley et al, 1995;Theodore et al, 1995) and for investigation of the correlation of genetic variation with pathotype (Nicholson and Rezanoor, 1994). Nakada et al (1994) have reported that analysis of RFLPs of total DNA using arbitrarily chosen genomic clones as probe revealed clear differences among the most common plant pathogenic fungi, Bipolaris and Curvularia species, on gramineous plants.…”
Section: Discussionmentioning
confidence: 99%
“…After a new centrifugation of 15 min at the same speed, the pellet was washed in cold ethanol 70%, centrifuged again for 2 min, and dried. It was finally resuspended in 200 µL of ddH 2 O. PCR amplification was performed with primers ITS1F and ITS4 (White et al, 1990;Gardes and Bruns, 1993) for the ITS region, while LR0R and LR5 (Vilgalys and Hester, 1990;Cubeta et al, 1991) were used to amplify the 28S rDNA region. PCR reactions were performed under a program consisting of a hot start at 95 °C for 5 min, followed by 35 cycles at 94 °C, 54 °C, and 72 °C (45, 30, and 45 s, respectively) and a final 72 °C step for 10 min.…”
Section: Methodsmentioning
confidence: 99%
“…The polymerase chain reaction (PCR) targeting ITS1-5.8S-ITS2 region of the rDNA was carried out using primers ITS1 and ITS4 (White et al 1990). The large ribosomal subunit (28S rDNA) was amplified using the primers pair LR0R-LR5 (Vilgalys & Hester 1990, Cubeta et al 1991. PCR amplifications were performed as described by Zitouni-Haouar et al (2015).…”
Section: Morphological Studiesmentioning
confidence: 99%