摘要
:以含传染性支气管炎病毒 ( ZJ971毒株 ) S1基因的质粒 PBS为模板 ,根据其序列设计引物进行PCR扩增 ,得到 1.7kb左右的 S1基因产物 ;用 Xbal I和 Bam HI酶切纯化 ,并在 T4 DNA连接酶的作用下 ,定向克隆到植物表达载体 PBI12 1中 ,PCR及酶切鉴定表明 。
WT5”BZ]The S1 gene of avian infectious bronchitis virus (ZJ971 strain) was amplified by polymerase chain reaction with special primers containing XbalI and BamHI. The purified PCR product was digested by the restricted enzyme XbalI and BamHI. The digested and purified S1 gene of infectious bronchitis virus was cloned into plant expression vector pBI121. The result shows that pBI121 with S1 gene was successfully transferred into Agrobacterium tume faciens (Aotumefaciens) with methods of PCR and restricted enzymes. [WT5”HZ]
出处
《浙江大学学报(农业与生命科学版)》
CAS
CSCD
北大核心
2001年第3期293-296,共4页
Journal of Zhejiang University:Agriculture and Life Sciences
基金
国家自然科学基金资助项目!(30 0 70 5 70 )