Identification of Wild and Cultivated Gastrodia elata Bl. by SSR Molecular Marker
[Objective] Wild and cultivated Gastrodia elata B1. were identified by SSR molecular marker. [ Method ] Distinctive primers were synthesized to the PCR amplification of the genomic DNA. [ Result ] The number of bands amplified was two in generative propagated individuals which was heterozygote and one in wild and clone propagated individuals which were homozygote. [ Conclusion ] SSR could effectively dis-tinguish heterozygote and homozygote, which would provide effective pathway for the identification and protection of Gastrodia elata B1, germ-plasm-resources and select breeding.
国家科技期刊平台
NSTL
万方数据
维普
