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首页> 外文期刊>Applied Microbiology and Biotechnology >I-SceI endonuclease: A new tool for DNA repair studies and genetic manipulations in streptomycetes
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I-SceI endonuclease: A new tool for DNA repair studies and genetic manipulations in streptomycetes

机译:I-SceI核酸内切酶:链霉菌中DNA修复研究和基因操作的新工具

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摘要

Actinomycetes are Gram-positive bacteria with a complex life cycle. They produce many pharmaceutically relevant secondary metabolites, including antibiotics and anticancer drugs. However, there is a limited number of biotechnological applications available as opposed to genetic model organisms like Bacillus subtilis or Escherichia coli. We report here a system for the functional expression of a synthetic gene encoding the I-SceI homing endonuclease in several streptomycetes. Using the synthetic sce(a) gene, we were able to create controlled genomic DNA double-strand breaks. A mutagenesis system, based on the homing endonuclease I-SceI, has been developed to construct targeted, non-polar, unmarked gene mutations in Streptomyces sp. Tü6071. In addition, we have shown that homologous recombination is a major pathway in streptomycetes to repair an I-SceI-generated DNA double-strand break. This novel I-SceI-based tool will be useful in fundamental studies on the repair mechanism of DNA double-strand breaks and for a variety of biotechnological applications.
机译:放线菌是具有复杂生命周期的革兰氏阳性细菌。它们产生许多与药物有关的次级代谢产物,包括抗生素和抗癌药。然而,与诸如枯草芽孢杆菌或大肠杆菌的遗传模型生物相反,可利用的生物技术应用数量有限。我们在这里报告的系统编码的几个链霉菌中的I-SceI归巢核酸内切酶的合成基因的功能表达。使用合成的sce(a)基因,我们能够创建受控的基因组DNA双链断裂。已经开发了一种基于归巢内切核酸酶I-SceI的诱变系统,可在链霉菌属物种中构建靶向,非极性,未标记的基因突变。 Tü6071。此外,我们已经表明,同源重组是链霉菌修复I-SceI生成的DNA双链断裂的主要途径。这种新颖的基于I-SceI的工具将可用于DNA双链断裂修复机制的基础研究以及各种生物技术应用。

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