作　　者： ; ; ; ; ;

机构地区： 中山大学生命科学学院有害生物控制与资源利用国家重点实验室

出　　处： 《微生物学报》 2004年第3期295-298,共4页

摘　　要： 利用PCR方法从斜纹夜蛾核多角体病毒 (SpltMNPV)基因组中扩增获得了细胞凋亡抑制基因p4 9的完整ORF并将其克隆于pMD1 8 T载体 ,其序列分析结果与文献报道一致。将基因重组于硫氧还蛋白融合表达载体pThioHisC ,在大肠杆菌BL2 1 (DE3)中获得了稳定表达 ,表达的P4 9融合蛋白占菌体总蛋白 30 %左右 ,主要以包涵体形式存在。分离纯化重组表达的SpltMNPVP4 9蛋白作为抗原 ,免疫家兔制备得到效价高于 1∶1 0 0 0 0的抗重组P4 9蛋白多克隆抗体。应用制备的抗体对受SpltMNPV感染的Sl细胞中P4 9蛋白的表达时相进行分析 ,结果显示P4 9蛋白在细胞感染后 3h内便可检测到 。 The apoptotic suppressor p49 gene was amplified by PCR from the genome of Spodoptera litura multicapsid nucleopolyhedrovirus (SpltMNPV) and cloned into the pMD18-T vector. Sequence analysis verified the cloned fragment. The gene was then inserted into thioredoxin fusion expression vector pThioHis C and expressed stably in E.coli BL21(DE3) by induction with IPTG. The expression products were about 30% of the total bacteria proteins and exsisted as inclusion bodies. Specific antibodies with a high titre of over 1:10000 were obtained by immunizing rabbits with the purified fusion protein and was used to determine the time course of P49 expression in SpltMNPV-infected Sl cells. The results showed that P49 expression startups within 3 hours post infection and remains low level during the whole course of infection.

关 键 词： 凋亡抑制 多克隆抗体 表达时相

领　　域： [生物学]