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논문 기본 정보

자료유형
학술저널
저자정보
Eom, Seung-Hee (Plant Molecular Biology & Microbial Biotechnology Laboratory, Division of Applied Plant Sciences, College of Agriculture and Life Sciences, Kangwon National University) Kim, Kwon-Jong (Plant Molecular Biology & Microbial Biotechnology Laboratory, Division of Applied Plant Sciences, College of Agriculture and Life Sciences, Kangwon National University) Jung, Hee-Sun (Plant Molecular Biology & Microbial Biotechnology Laboratory, Division of Applied Plant Sciences, College of Agriculture and Life Sciences, Kangwon National University) Lee, Sang-Pyo (Plant Molecular Biology & Microbial Biotechnology Laboratory, Division of Applied Plant Sciences, College of Agriculture and Life Sciences, Kangwon National University) Lee, Youn-Su (Plant Molecular Biology & Microbial Biotechnology Laboratory, Division of Applied Plant Sciences, College of Agriculture and Life Sciences, Kangwon National University)
저널정보
한국균학회 Mycobiology Mycobiology 제32권 제3호
발행연도
2004.1
수록면
123 - 127 (5page)

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Sweet persimmons have been increasingly cultivated in the southern part of Korea. However, anthracnose disease caused by Colletotrichum species is one of the major hindrances in cultivation and productions. In this study, we used polymerase chain reaction(PCR) to detect Colletotrichum species with the AFLP(amplified fragment length polymorphism) method. In AFLP, we used E3(5'-GACTGCGTACCAATTCTA-3') and M1(5'-GATGAGTCCTGAGTAACAG-3') primer combination and, as a result, 262 bp segment was observed in Colletotrichum species only. Specific PCR primers were designed from the sequence data and used to detect the presence of the fungus in genomic DNA isolated from symptomless sweet persimmon plants. Based on sequence data for specific segments, Co.B1(5'-GAGAGAGTAGAATTGCGCTG-3') and Co.B2(5'-CTACCATTCTTCTA GGTGGG-3') were designed to detect Colletotrichum species. The 220 bp segment was observed in Colletotrichum species only, but not in other fungal and bacterial isolates.

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