Sugihara J, Baldwin T O
Department of Biochemistry and Biophysics, Texas A&M University, College Station 77843.
Biochemistry. 1988 Apr 19;27(8):2872-80. doi: 10.1021/bi00408a031.
Ten recombinant plasmids have been constructed by deletion of specific regions from the plasmid pTB7 that carries the luxA and luxB genes, encoding the alpha and beta subunits of luciferase from Vibrio harveyi, such that luciferases with normal alpha subunits and variant beta subunits were produced in Escherichia coli cells carrying the recombinant plasmids. The original plasmid, which conferred bioluminescence (upon addition of exogenous aldehyde substrate) on E. coli carrying it, was constructed by insertion of a 4.0-kb HindIII fragment of V. harveyi DNA into the HindIII site of plasmid pBR322 [Baldwin, T.O., Berends, T., Bunch, T. A., Holzman, T. F., Rausch, S. K., Shamansky, L., Treat, M. L., & Ziegler, M. M. (1984) Biochemistry 23, 3663-3667]. Deletion mutants in the 3' region of luxB were divided into three groups: (A) those with deletions in the 3' untranslated region that left the coding sequences intact, (B) those that left the 3' untranslated sequences intact but deleted short stretches of the 3' coding region of the beta subunit, and (C) those for which the 3' deletions extended from the untranslated region into the coding sequences. Analysis of the expression of luciferase from these variant plasmids has demonstrated two points concerning the synthesis of luciferase subunits and the assembly of those subunits into active luciferase in E. coli. First, deletion of DNA sequences 3' to the translational open reading frame of the beta subunit that contain a potential stem and loop structure resulted in dramatic reduction in the level of accumulation of active luciferase in cells carrying the variant plasmids, even though the luxAB coding regions remained intact.
通过从携带luxA和luxB基因的质粒pTB7中缺失特定区域构建了十个重组质粒,luxA和luxB基因编码哈维氏弧菌荧光素酶的α和β亚基,使得在携带重组质粒的大肠杆菌细胞中产生具有正常α亚基和变异β亚基的荧光素酶。原始质粒通过将哈维氏弧菌DNA的4.0 kb HindIII片段插入质粒pBR322的HindIII位点构建而成,该质粒赋予携带它的大肠杆菌生物发光能力(添加外源醛底物后)[鲍德温,T.O.,贝伦兹,T.,邦奇,T.A.,霍尔兹曼,T.F.,劳施,S.K.,沙曼斯基,L.,特里特,M.L.,&齐格勒,M.M.(1984年)《生物化学》23,3663 - 3667]。luxB 3'区域的缺失突变体分为三组:(A)那些在3'非翻译区有缺失但编码序列完整的突变体,(B)那些3'非翻译序列完整但β亚基3'编码区有短片段缺失的突变体,以及(C)那些3'缺失从非翻译区延伸到编码序列的突变体。对这些变异质粒中荧光素酶表达的分析揭示了关于荧光素酶亚基合成以及这些亚基在大肠杆菌中组装成活性荧光素酶的两点情况。首先,β亚基翻译开放阅读框3'端包含潜在茎环结构的DNA序列的缺失导致携带变异质粒的细胞中活性荧光素酶积累水平显著降低,尽管luxAB编码区保持完整。