首页> 外文期刊>Journal of Microbiological Methods >The glpD gene is a novel reporter gene for E. coli that is superior to established reporter genes like lacZ and gusA
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The glpD gene is a novel reporter gene for E. coli that is superior to established reporter genes like lacZ and gusA

机译:glpD基因是一种新的大肠杆菌报告基因,优于已建立的报告基因,如lacZ和gusA

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摘要

Reporter genes facilitate the characterization of promoter activities, transcript stabilities, translational efficiencies, or intracellular localization. Various reporter genes for Escherichia coli have been established, however, most of them have drawbacks like transcript instability or the inability to be used in genetic selections. Therefore, the glpD gene encoding glycerol-3-phosphate dehydrogenase was introduced as a novel reporter gene for E. coli. The enzymatic assay was optimized; and it was verified that growth on glycerol strictly depends on the presence of GlpD. The 5'-UTRs of three E. coli genes were chosen and cloned upstream of the new reporter gene glpD as well as the established reporter genes lacZ and gusA. Protein and transcript levels were quantified and translational efficiencies were calculated. The lacZ transcript was very unstable and its level highly depended on its translation, compromising its use as a reporter. The results obtained with gusA and glpD were similar, however, only glpD can be used for genetic selections. Therefore, glpD was found to be a superior novel reporter gene compared to the established reporter genes lacZ and gusA. (C) 2016 Elsevier B.V. All rights reserved.
机译:报告基因促进了启动子活性,转录本稳定性,翻译效率或细胞内定位的表征。已经建立了大肠杆菌的多种报道基因,但是,它们中的大多数具有诸如转录本不稳定或不能用于遗传选择的缺点。因此,引入编码3-磷酸甘油脱氢酶的glpD基因作为大肠杆菌的新报道基因。优化了酶促分析;并证实甘油的生长完全取决于GlpD的存在。选择了三个大肠杆菌基因的5'-UTR,并将其克隆到新的报告基因glpD以及已建立的报告基因lacZ和gusA的上游。定量蛋白质和转录本水平并计算翻译效率。 lacZ转录本非常不稳定,其水平高度依赖于其翻译,从而损害了其作为报道基因的用途。用gusA和glpD获得的结果相似,但是只有glpD可以用于遗传选择。因此,与已建立的报道基因lacZ和gusA相比,发现glpD是更好的新颖报道基因。 (C)2016 Elsevier B.V.保留所有权利。

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