Macreadie I G, Azad A A
CSIRO, Division of Biomolecular Engineering, Parkville, Australia.
Virology. 1991 Oct;184(2):773-6. doi: 10.1016/0042-6822(91)90450-p.
As part of our efforts to produce native molecules of the host protective antigen (VP2) of infectious bursal disease virus (IBDV) in microorganisms, we have restored nucleotide sequences encoding the VP2 N-terminus which were not present in the original clone. In addition to this process, we produced constructs that contained +5, +4, -1, and -2 frameshifts that still allowed expression of the IBDV polyprotein, VP2 and VP3. The size of translation products and examination of the nucleotide sequence lead us to speculate that both +1 frameshifting and internal initiation events lead to the synthesis of IBDV proteins in Escherichia coli.
作为我们在微生物中生产传染性法氏囊病病毒(IBDV)宿主保护性抗原(VP2)天然分子的努力的一部分,我们恢复了原始克隆中不存在的编码VP2 N端的核苷酸序列。除了这个过程,我们还构建了包含+5、+4、-1和-2移码的构建体,这些构建体仍然允许IBDV多聚蛋白、VP2和VP3的表达。翻译产物的大小和核苷酸序列的检查使我们推测,+1移码和内部起始事件都导致了大肠杆菌中IBDV蛋白的合成。