Mariac C, Trouslot P, Poteaux C, Bezançon G, Renno J F
Laboratoire de Génétique des Plantes, Institut de Recherche pour le Développement (IRD), Niamey, Niger.
Biotechniques. 2000 Jan;28(1):110-3. doi: 10.2144/00281st07.
The technique described here is a fast and simple method of extracting chloroplast DNA (cpDNA). It overcomes the need for differential centrifugation using density gradients. The leaves do not have to be kept in the dark and lyophilized before extraction, but lyophilization is still possible. The chloroplasts are specifically lysed in a cell extract of leaves, using a non-ionic detergent. After isolation by centrifugation, the cpDNA is purified by the combined action of proteolytic enzymes and detergents, followed by the elimination of proteins using a mixture of chloroform and isoamyl alcohol. This method provided good quality restriction profiles for all species analyzed.
这里描述的技术是一种快速且简单的提取叶绿体DNA(cpDNA)的方法。它克服了使用密度梯度进行差速离心的需求。叶片在提取前无需避光保存和冻干,但冻干仍是可行的。使用非离子型去污剂在叶片的细胞提取物中特异性裂解叶绿体。通过离心分离后,cpDNA通过蛋白水解酶和去污剂的联合作用进行纯化,随后用氯仿和异戊醇的混合物去除蛋白质。该方法为所有分析的物种提供了高质量的限制性图谱。