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Coregulation of lux Genes and Riboflavin Genes in Bioluminescent Bacteria of Photobacterium phosphoreum

机译:荧光发光细菌生物发光细菌中lux基因和核黄素基因的调控

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Investigation of the expression of the riboflavin (rib) genes, which are found immediately downstream of luxG in the lux operon in Photobacterium phosphoreum, provides more information relevant to the evolution of bioluminescence, as well as to the regulation of supply of flavin substrate for bacterial bioluminescence reactions. In order to answer the question of whether or not the transcriptions of lux and rib genes are integrated, a transcriptional termination assay was performed with P. phosphoreum DNA, containing the possible stem-loop structures, located in the intergenic region of luxF and luxE (Ω_A), of luxG and ribE (Ω_B), and downstream of ribA (Ω_c). The expression of the CAT (Chloram-phenicol Acetyl Transferase) reporter gene was remarkably decreased upon the insertion of the stem-loop structure (Ω_C) into the strong lux promoter and the reporter gene. However, the insertion of the structure (Ω_B) into the intergenic region of the lux and the rib genes caused no significant change in expression from the CAT gene. In addition, the single stranded DNA in the same region was protected by the P. phosphoreum mRNA from the S1 nuclease protection assay. These results suggest that lux genes and rib genes are part of the same operon in P. phosphoreum.
机译:核黄素(rib)基因表达的研究,发现在荧光细菌的荧光操纵子的lux操纵子中luxG的下游,提供了与生物发光的演变有关的更多信息,以及与细菌黄素底物供应的调控有关的信息。生物发光反应。为了回答lux和rib基因的转录是否整合的问题,我们对位于luxF和luxE的基因间区域中的含有潜在茎环结构的P.phosphoum DNA进行了转录终止分析( Ω_A),luxG和ribE(Ω_B),以及ribA(Ω_c)的下游。 CAT(Chloram-phenicol乙酰基转移酶)报告基因的表达显着降低了茎环结构(Ω_C)插入强lux启动子和报告基因。但是,将结构(Ω_B)插入lux和rib基因的基因间区域不会引起CAT基因表达的明显变化。此外,来自S1核酸酶保护试验的磷青霉菌mRNA可以保护同一区域的单链DNA。这些结果表明,lux基因和rib基因是磷青霉中同一操纵子的一部分。

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