特内拉
紫菜
生物
限制性片段长度多态性
植物
内转录区
鲁比斯科
质体
限制性酶
聚合酶链反应
基因
遗传学
核糖体RNA
藻类
叶绿体
农林复合经营
棕榈油
作者
Kyosuke Niwa,Atsushi Kobiyama
标识
DOI:10.1111/j.1440-1835.2009.00549.x
摘要
SUMMARY To discriminate between cultivated Porphyra species ( Porphyra yezoensi s and Porphyra tenera ) and closely related wild Porphyra species, we developed a polymerase chain reaction‐restriction fragment length polymorphism (PCR‐RFLP) analysis of the rbc L gene using five restriction enzymes. Although our previous PCR‐RFLP analyses of internal transcribed spacer (ITS) rDNA and plastid RuBisCO spacer regions could not always discriminate wild P. yezoensis , wild P. tenera , and closely related wild species, the PCR‐RFLP profiles of the rbc L gene were useful in discriminating samples collected from natural habitats. Therefore, PCR‐RFLP analysis of the rbc L gene will help in the simple identification of a large number of samples, not only for the establishment of reliable cultures as breeding material, but also for the taxonomic investigations of species that are closely related to cultivated Porphyra .
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