Follettie M T, Peoples O P, Agoropoulou C, Sinskey A J
Department of Biology, Massachusetts Institute of Technology, Cambridge 02139.
J Bacteriol. 1993 Jul;175(13):4096-103. doi: 10.1128/jb.175.13.4096-4103.1993.
Two promoters required for expression of the ask-asd genes, encoding aspartokinase (AK) and aspartate-semialdehyde dehydrogenase (ASD), in Corynebacterium flavum N13, askP1 and askP2, have been identified by deletion analysis and S1 nuclease mapping. Transcription from askP1 initiates 35 and 38 bp upstream of the ask structural gene. A second promoter, askP2, lies within the ask coding region, upstream of the translation start site of the AK beta subunit and can direct the expression of AK beta and ASD. Western immunoblot analysis and heterologous expression in Escherichia coli demonstrate that two separate polypeptides, a 44.8-kDa alpha subunit and an 18.5-kDa beta subunit, are expressed from the C. flavum N13 ask gene from distinct, in-frame translation initiation sites. A second AK mutation, G345D, which reduces the sensitivity of AK to concerted feedback inhibition by threonine plus lysine, was identified.
通过缺失分析和S1核酸酶作图,已鉴定出黄色棒杆菌N13中编码天冬氨酸激酶(AK)和天冬氨酸-半醛脱氢酶(ASD)的ask-asd基因表达所需的两个启动子,即askP1和askP2。askP1的转录起始于ask结构基因上游35和38 bp处。第二个启动子askP2位于ask编码区内,在AKβ亚基翻译起始位点上游,可指导AKβ和ASD的表达。蛋白质免疫印迹分析和在大肠杆菌中的异源表达表明,从黄色棒杆菌N13的ask基因的不同读框内翻译起始位点表达出两种独立的多肽,一种是44.8 kDa的α亚基,另一种是18.5 kDa的β亚基。还鉴定出第二个AK突变G345D,该突变降低了AK对苏氨酸加赖氨酸协同反馈抑制的敏感性。