华北农学报
華北農學報
화북농학보
ACTA AGRICULTURAE BOREALI-SINICA
2014年
2期
127-132
,共6页
容万韬%王金成%刘鹏%林宇%郭京泽%黄国明%孙建华
容萬韜%王金成%劉鵬%林宇%郭京澤%黃國明%孫建華
용만도%왕금성%류붕%림우%곽경택%황국명%손건화
蛋白酶K%裂解%冻融%管内切虫%DNA提取
蛋白酶K%裂解%凍融%管內切蟲%DNA提取
단백매K%렬해%동융%관내절충%DNA제취
Proteinase K%Lysis%Freeze-thaw%Nematode-cutting in tube%DNA extraction
为探寻一种高效、稳定、廉价的单条线虫DNA提取方法,以6种植物寄生线虫作为试验材料,比较了4种方法,即直接裂解法、冻融裂解法、切割裂解法、切割冻融裂解法对单条线虫DNA的提取效果。结果表明,对线虫进行管内切割的切割冻融裂解法与切割裂解法高效、稳定,冻融裂解法效果较差,直接裂解法效果最差。对线虫进行管内切割的切割冻融裂解法和切割裂解法可高效、稳定地获得高质量的单条线虫总DNA,满足下一步的PCR扩增需求。
為探尋一種高效、穩定、廉價的單條線蟲DNA提取方法,以6種植物寄生線蟲作為試驗材料,比較瞭4種方法,即直接裂解法、凍融裂解法、切割裂解法、切割凍融裂解法對單條線蟲DNA的提取效果。結果錶明,對線蟲進行管內切割的切割凍融裂解法與切割裂解法高效、穩定,凍融裂解法效果較差,直接裂解法效果最差。對線蟲進行管內切割的切割凍融裂解法和切割裂解法可高效、穩定地穫得高質量的單條線蟲總DNA,滿足下一步的PCR擴增需求。
위탐심일충고효、은정、렴개적단조선충DNA제취방법,이6충식물기생선충작위시험재료,비교료4충방법,즉직접렬해법、동융렬해법、절할렬해법、절할동융렬해법대단조선충DNA적제취효과。결과표명,대선충진행관내절할적절할동융렬해법여절할렬해법고효、은정,동융렬해법효과교차,직접렬해법효과최차。대선충진행관내절할적절할동융렬해법화절할렬해법가고효、은정지획득고질량적단조선충총DNA,만족하일보적PCR확증수구。
To explore an efficient,stable,low-cost DNA extraction method from single nematode for the support of molecular identification of nematodes,using six species of plant-parasitic nematodes as experimental materials, four DNA extraction methods,namely,direct lysis method,freeze-thaw lysis method,cutting lysis method,freeze-thaw cutting lysis method were designed and compared in order to check their efficiency of DNA extraction from single nematode. The results showed that cutting lysis method and freeze-thaw cutting lysis method were the most efficient and stable methods for DNA extraction of single nematode,then the freeze-thaw lysis method,and the direct lysis method was the worst one. Total DNA with high-quality from a single nematode could be gained efficiently and stab-ly through two methods,namely,cutting lysis method and freeze-thaw cutting lysis method. And the extracted DNA meeted requirement of the following PCR amplification.