Stahl S, MacKay P, Magazin M, Bruce S A, Murray K
Proc Natl Acad Sci U S A. 1982 Mar;79(5):1606-10. doi: 10.1073/pnas.79.5.1606.
Fragments of hepatitis B virus DNA cloned in plasmid pBR322 carrying the gene for the viral core antigen have been placed under the control of the lac promoter of Escherichia coli. Several of the new recombinants direct higher levels of synthesis of the antigen, but the degree of enhancement varies with the different structures of the plasmids and hence the mRNAs produced. The antigen in crude bacterial lysates is a satisfactory diagnostic reagent for antibodies to the core antigen in serum samples.
克隆于携带病毒核心抗原基因的质粒pBR322中的乙肝病毒DNA片段,已置于大肠杆菌乳糖启动子的控制之下。一些新的重组体指导合成更高水平的抗原,但增强程度因质粒的不同结构以及由此产生的信使核糖核酸而异。粗制细菌裂解物中的抗原是血清样本中核心抗原抗体的一种令人满意的诊断试剂。