Marraccini P, Cassier-Chauvat C, Bulteau S, Chavez S, Chauvat F
Service de Biochemie et Génétique Moléculaire, CEA Saclay, Gif Sur Yvette, France.
Mol Microbiol. 1994 Jun;12(6):1005-12. doi: 10.1111/j.1365-2958.1994.tb01088.x.
A library of Synechocystis PCC6803 (S.6803) DNA cloned in front of the promoterless cat reporter gene of the plasmid pFF11 was used to transform S.6803 to high light-dependent resistance to chloramphenicol. In five clones harbouring a stably replicating pFF11-derived plasmid, this phenotype occurred independently of the photosystem II electron transport and resulted from the correlated increase of CAT activity level and cat mRNA accumulation. The five promoter inserts contained no Escherichia coli sigma 70 promoter element, in agreement with their lack of activity in this organism, but shared two conserved motifs. Two secondary mutations, which restored light-regulated promoter activity to an inactive mutant of the smallest insert, mapped within one of the common motifs, emphasizing the probable involvement of this element in photoregulation.
利用克隆在质粒pFF11无启动子氯霉素乙酰转移酶(cat)报告基因前的集胞藻PCC6803(S.6803)DNA文库,将S.6803转化为对氯霉素的高光依赖性抗性。在五个含有稳定复制的源自pFF11质粒的克隆中,这种表型独立于光系统II电子传递而出现,并且是由CAT活性水平和cat mRNA积累的相关性增加所导致的。这五个启动子插入片段不包含大肠杆菌σ70启动子元件,这与它们在该生物体中缺乏活性一致,但共享两个保守基序。两个二次突变将光调节启动子活性恢复到最小插入片段的无活性突变体,这两个突变位于其中一个共同基序内,强调了该元件可能参与光调节。