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琼脂固体培养基培养蜜环菌菌索总DNA的提取

DNA Extraction from Rhizomorph of Armillaria mellea Cultured by Solid Agar Medium

  • 摘要: 野外采集的蜜环菌Armillaria mellea(Vahl.ex Fr.)Quel在提取DNA前需要分离获得纯化的菌丝体。常规液体培养获得菌丝团的方法感杂率较高,采集固体培养基表面cellophane膜上形成的菌丝则难以获得足量的DNA提取材料。蜜环菌细胞内含有大量多醣类物质,也使得蜜环菌高质量DNA的提取存在一定的困难。本研究通过改进试验,提供一个直接从琼脂固体培养基培养的蜜环菌菌索中提取高质量DNA的方法。其中样品的预先冻融处理方法可以促使蜜环菌菌索与琼脂分离;而在裂解提取缓冲液裂解材料细胞后加入1.25 mol/L KAc溶液,则有利于除去蜜环菌细胞内的多醣类物质以及残留的少量琼脂。通过琼脂糖电泳、紫外分光光度计对DNA浓度及OD值的测定、ISSR引物的PCR扩增以及酶切产物的PCR扩增等方法的检测,结果均表明该方法提取的DNA质量较好,符合进一步进行分子生物学研究的要求。

     

    Abstract: To obtain pure mycelia before DNA extraction,Armillaria mellea(Vahl.ex Fr.)Quel collected from the field need to be isolated.Traditional liquid culture purifying method has the disadvantage of low efficiency.Although pure mycelia can be collected from cellophane film on solid medium,it is difficult to obtain sufficient materials for DNA extraction.We therefore put forward a modified method that is extracting DNA from rhizomorph of A.mellea cultured by solid agar medium.The results show that agar around the rhizomorph materials can be mostly removed when samples were pretreated via freezing-melting.DNA extraction buffer mixed with KAc solution(1.25 mol/L) can effectively eliminate agar and other polysaccharid residuals.The quality of extracted DNA was then tested by a series of measures,including ultraviolet absorption test,agarose gel electrophoresis,amplification by using ISSR primers and digestion by restriction endonuclease Mse I.The results confirmed that the quality of extracted DNA using this modified method is very high,and proven to be suitable for further molecular analysis.

     

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