Jongkun Kim 1, Seonhwa Lim 1, Daesung Lee 1, Jeonghyun Chi 2, Youngcheol Ju 2, Geonsik Seo 3 and Heewan Kang 1*
1Graduate School of Biotechnology and Information Technology, Hankyong National University, Ansung 456-749, Korea
2Mushroom Research Institute, Gyonggi Province ARES, 464-870, Korea
3Korea National Agricultural College, Hwasung, Kyonggi 445-893, Korea
Correspondence to kanghw2@hknu.ac.kr
Korean Journal of Mycology (Kor J Mycol) December 31, 2007, 35(2):61-67.
https://doi.org/10.4489/kjm.2007.35.2.061
(Received July 23, 2007)
Published: December 31, 2007.
Copyright © 2007 by The Korean Society of Mycology
Twelve URP primers were used to assess genetic characteristics of oyster mushroom including 59 Pleurotus ostreatus cultivars, two of P. florida cultivars, one P. sajor-caju cultivars, one P. abalonus cultivar and two P. eryngii cultivars registered in Korea. Six URP primers produced PCR polymorphic bands within and between the Pleurotus species. Primer URP2F produced distinct cultivar specific PCR polymorphic bands that profiled to 15 cultivar types. PCR polymorphic bands amplified by URP2F, URP6R, URP4R and URP2R were used for UPGMA cluster analysis. Fifty nine cultivars of Pleurotus ostreatus are genetically clustered into 5 groups, showing genetic similarity over 70% among them and P. abalonus, P. eryngii and P. sajor-caju, were involved in outside groups.
Genetic similarity, Pleurotus cultivars, URP-PCR polymorphism