Jones I M, Brownlee G G
Gene. 1985;35(3):333-42. doi: 10.1016/0378-1119(85)90012-5.
Two influenza gene products of similar size and codon usage have been expressed in Escherichia coli under control of the phage lambda pR promoter. The influenza N protein (NP) was expressed in its entirety after fusion to a short (12 amino acid) segment of the lambda cro gene product and constituted about 1-2% of total soluble cell protein after induction. By contrast, constructions using the full length neuraminidase (NA) gene failed to give rise to detectable amounts of NA antigen after fusion to either the 12 amino acid Cro peptide or after fusion to bacterial beta-galactosidase (beta gal). Rather, expression of NA antigenic determinants was only achieved after deletion of coding sequences at the 3' end of the beta gal-NA fusion construct such that the encoded protein precipitated within the cell.
两种大小和密码子使用情况相似的流感病毒基因产物已在噬菌体λ pR启动子的控制下在大肠杆菌中表达。流感病毒N蛋白(NP)在与λ cro基因产物的短片段(12个氨基酸)融合后完整表达,诱导后占总可溶性细胞蛋白的约1-2%。相比之下,使用全长神经氨酸酶(NA)基因构建体,在与12个氨基酸的Cro肽融合后或与细菌β-半乳糖苷酶(β-gal)融合后,均未能产生可检测量的NA抗原。相反,只有在删除β-gal-NA融合构建体3'端的编码序列后,NA抗原决定簇才得以表达,使得编码的蛋白质在细胞内沉淀。