甘肃农业科技
甘肅農業科技
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GANSU AGRICULTURAL SCIENCE AND TECHNOLOGY
2013年
8期
18-19,20
,共3页
张菲菲%张金文%高宜峰%姚攀锋
張菲菲%張金文%高宜峰%姚攀鋒
장비비%장금문%고의봉%요반봉
人参果%PVM病毒%克隆%鉴定
人參果%PVM病毒%剋隆%鑒定
인삼과%PVM병독%극륭%감정
Ginseng fruit%PVM virus%Cloning%Identification
通过对武威市凉州区人参果感病植株所表现出来的花叶、皱缩、植株矮小等症状观察,初步判断可能感染了马铃薯M病毒(PVM)。结合分子生物学手段,提取感病人参果叶片总RNA,采用RT-PCR方法扩增到一段长300 bp的基因序列,连接至PMD19-T载体并测序。测序结果同GeneBank中PVM CP基因序列[GI:361071296]同源性达到了98.97%,说明成功克隆到了PVM基因片段,即供试人参果确实感染了PVM病毒。
通過對武威市涼州區人參果感病植株所錶現齣來的花葉、皺縮、植株矮小等癥狀觀察,初步判斷可能感染瞭馬鈴藷M病毒(PVM)。結閤分子生物學手段,提取感病人參果葉片總RNA,採用RT-PCR方法擴增到一段長300 bp的基因序列,連接至PMD19-T載體併測序。測序結果同GeneBank中PVM CP基因序列[GI:361071296]同源性達到瞭98.97%,說明成功剋隆到瞭PVM基因片段,即供試人參果確實感染瞭PVM病毒。
통과대무위시량주구인삼과감병식주소표현출래적화협、추축、식주왜소등증상관찰,초보판단가능감염료마령서M병독(PVM)。결합분자생물학수단,제취감병인삼과협편총RNA,채용RT-PCR방법확증도일단장300 bp적기인서렬,련접지PMD19-T재체병측서。측서결과동GeneBank중PVM CP기인서렬[GI:361071296]동원성체도료98.97%,설명성공극륭도료PVM기인편단,즉공시인삼과학실감염료PVM병독。
The mosaic,wrinkled,small plant and other symptoms of susceptible plants of Liangzhou ginseng fruit were observed,the auditor should make a pre-judgment that may be infected with potato virus M (PVM). Experiments combined with molecular biology methods and extract leaves total RNA of the patient feeling of ginseng fruit,it was amplified by RT-PCR method to a long 300 bp gene sequences and connected to PMD19-T vector and sequenced. The Sequencing results showed that homology reached 98.97%with the GeneBank PVM CP gene sequence [GI:361071296],it can explain gene fragment was cloned into the PVM successful,that the test does ginseng fruit infected with PVM virus.