期刊文献+
共找到2篇文章
< 1 >
每页显示 20 50 100
Analysis of the Germplasm Resources and Genetic Relationships Among Hybrid Cymbidium Cultivars and Native Species with RAPD Markers 被引量:8
1
作者 LI Dong-mei YE Qing-sheng zhu gen-fa 《Agricultural Sciences in China》 CAS CSCD 2007年第8期922-929,共8页
The random amplified polymorphic DNA (RAPD) marker was assessed to detect the genetic relationships among 48 hybrid Cymbidium cultivars from Japan, Korea, China, and USA, and 2 species of native Cymbidium. Twenty pr... The random amplified polymorphic DNA (RAPD) marker was assessed to detect the genetic relationships among 48 hybrid Cymbidium cultivars from Japan, Korea, China, and USA, and 2 species of native Cymbidium. Twenty primers were screened from 100 random decamer primers, and a total of 258 DNA bands were amplified, 253 of which (98.1%) were polymorphic. The average number of polymorphic DNA bands amplified by each primer was 12.6. All cultivars were distinguishable when a number of primers were considered. Genetic similarities among the cultivars and species were estimated based on the amount of band sharing ranging from 0.364-0.817 with an average of 0.581. According to the data, a dendrogram of genetic relationship, which was constructed using the UPGMA method, showed that all the tested cultivars and native species were classified into five cluster groups with the similarity coefficient of 0.592. It revealed that the genetic relationships among tested accessions were to some extent related with their origin, flower colour, branch type, and genealogy. It further indicated that the RAPD technique is a useful tool for studying the genetic relationships among hybrid Cymbidium cultivars. 展开更多
关键词 CYMBIDIUM genetic relationship RAPD markers cluster analysis
下载PDF
紫花山奈的组培快繁研究 被引量:2
2
作者 吴满良 李冬梅 +1 位作者 朱根发 刘小飞 《广东农业科学》 CAS 2018年第7期29-33,173,共6页
以紫花山柰无菌苗的芽基部为外植体,对芽基部进行继代增殖、丛生芽诱导以及生根培养基的筛选,建立了紫花山柰无菌苗芽基部的组培快繁体系。结果表明:紫花山柰无菌苗芽基部继代增殖比较合适的培养基为MS+6-BA 8~12 mg/L+NAA 0~0.1 mg/L+... 以紫花山柰无菌苗的芽基部为外植体,对芽基部进行继代增殖、丛生芽诱导以及生根培养基的筛选,建立了紫花山柰无菌苗芽基部的组培快繁体系。结果表明:紫花山柰无菌苗芽基部继代增殖比较合适的培养基为MS+6-BA 8~12 mg/L+NAA 0~0.1 mg/L+椰汁10%+白砂糖30 g/L+卡拉胶粉10 g/L,最佳继代增殖培养基为MS+6-BA 8 mg/L+NAA 0.1 mg/L+椰汁10%+白砂糖30 g/L+卡拉胶粉10 g/L;丛生芽诱导较合适的培养基为MS+6-BA 3~5 mg/L+NAA 0.05~0.1 mg/L+椰汁10%+白砂糖30 g/L+卡拉胶粉10 g/L,最佳的丛生芽诱导培养基为MS+6-BA 3 mg/L+NAA 0.05 mg/L+椰汁10%+白砂糖30 g/L+卡拉胶粉10 g/L;生根较佳的培养基为MS+NAA0.1 mg/L+香蕉泥10~15%+活性炭0.5~1.0 g/L+白砂糖30 g/L+卡拉胶粉9.5 g/L。 展开更多
关键词 紫花山奈 组织培养 芽基部 增殖 芽诱导 生根
下载PDF
上一页 1 下一页 到第
使用帮助 返回顶部