Department of Microbiology and Immunology, Virginia Commonwealth University Medical Center, P.O. Box 980678, Richmond, VA 23298-0678, USA.
Curr Microbiol. 2012 Dec;65(6):770-5. doi: 10.1007/s00284-012-0228-y. Epub 2012 Sep 18.
While much is known about the transcriptional regulation of the 12 gene alginate biosynthesis operon from the algD promoter in Pseudomonas aeruginosa, there has been little investigation into the possibility of other transcription starts within this operon, especially those genes dealing with the epimerization and acetylation of the alginate polymer. In this study, we utilized quantitative reverse transcription polymerase chain reaction, a β-galactosidase reporter assay and sequence scanning to identify two putative promoters within the alginate biosynthesis operon upstream of the alginate epimerase gene algG and the alginate acetylation gene algI. These data support the possibility of differential regulation within the operon to alter polymer structure under varying environmental conditions.
虽然人们对铜绿假单胞菌 algD 启动子控制的 12 基因海藻酸盐生物合成操纵子的转录调控有了很多了解,但对于该操纵子内其他转录起始的可能性,特别是与海藻酸盐聚合物的差向异构化和乙酰化有关的基因,研究甚少。在这项研究中,我们利用定量逆转录聚合酶链反应、β-半乳糖苷酶报告基因检测和序列扫描,在海藻酸盐差向异构酶基因 algG 和海藻酸盐乙酰化基因 algI 上游的海藻酸盐生物合成操纵子中鉴定出两个可能的启动子。这些数据支持在不同环境条件下通过改变聚合物结构进行操纵子内差异调控的可能性。