Vakharia V N, Raina A K, Kingan T G, Kempe T G
Center for Agricultural Biotechnology of Maryland Biotechnology Institute and College of Veterinary Medicine, University of Maryland, College Park 20742, USA.
Insect Biochem Mol Biol. 1995 May;25(5):583-9. doi: 10.1016/0965-1748(94)00097-2.
A synthetic gene of the pheromone biosynthesis activating neuropeptide (PBAN) of corn earworm Helicoverpa zea, with and without a signal sequence of the cuticle protein of Drosophila melanogaster, was cloned behind the polyhedrin promoter of AcMNPV. Two recombinant baculoviruses were constructed and used to infect a number of insect cell lines including Sf9 and 5B1-4. High pheromonotropic activity was consistently obtained from 5B1-4 cell culture that was infected with the recombinant baculovirus vINV-4 containing the signal sequence. The PBAN gene-product was isolated by HPLC and analyzed by electrospray ionization mass spectrometry. Low levels of biological activity obtained from Sf9 cells infected with the recombinant virus vPBAN may be due to lack of proper amidation at the C-terminus of the expressed peptide or rapid proteolytic degradation of the product.
将含有和不含有黑腹果蝇表皮蛋白信号序列的玉米穗虫(Helicoverpa zea)性信息素生物合成激活神经肽(PBAN)的合成基因,克隆到苜蓿银纹夜蛾核型多角体病毒(AcMNPV)的多角体蛋白启动子之后。构建了两种重组杆状病毒,并用于感染包括Sf9和5B1-4在内的多种昆虫细胞系。用含有信号序列的重组杆状病毒vINV-4感染5B1-4细胞培养物,始终能获得高促性信息素活性。通过高效液相色谱法分离PBAN基因产物,并用电喷雾电离质谱法进行分析。用重组病毒vPBAN感染Sf9细胞获得的低水平生物活性,可能是由于表达的肽在C末端缺乏适当的酰胺化,或者产物被快速蛋白水解降解所致。