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首页> 外文期刊>FEMS Microbiology Letters >Development of a gene knockout system for Ralstonia eutropha H16 based on the broad-host-range vector expressing a mobile group II intron
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Development of a gene knockout system for Ralstonia eutropha H16 based on the broad-host-range vector expressing a mobile group II intron

机译:基于表达宿主II型内含子的广泛宿主载体开发富营养小球藻H16基因敲除系统

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摘要

Ralstonia eutropha H16 is a Gram-negative lithoautotrophic bacterium and is one of the best biopolymer-producing bacteria. It can grow to high cell densities either under lithoautotrophic or under heterotrophic conditions, which makes it suitable for a number of biotechnological applications. Also, R. eutropha H16 can degrade various aromatic compounds for environmental applications. The mobile group II intron can be used for the rapid and specific disruption of various bacterial genes by insertion into any desired target genes. Here, we applied the mobile group II intron to R. eutropha H16 and developed a markerless gene knockout system for R. eutropha: RalsTron. As a demonstration of the system, the phaC1 gene encoding polyhydroxyalkanoate synthase was successfully knocked out in R. eutropha H16. Furthermore, this knockout system would be useful for knocking out genes in other bacteria as well because it is based on a broad-host-range vector and the mobile group II intron that minimally depends on the bacterial hosts.
机译:Ralstonia eutropha H16是革兰氏阴性的自养细菌,是产生生物聚合物的最佳细菌之一。它可以在自养营养或异养营养条件下生长至高细胞密度,这使其适用于许多生物技术应用。而且,富营养罗汉果H16可以降解各种芳香族化合物,用于环境应用。通过插入任何所需的靶基因,可移动的II组内含子可用于各种细菌基因的快速和特异性破坏。在这里,我们将可移动的II组内含子应用于富营养R. eutropha H16,并开发了富营养R. eutropha的无标记基因敲除系统:RalsTron。作为该系统的演示,成功地在富营养R. eutropha H16中敲除了编码聚羟基链烷酸合酶的phaC1基因。此外,该敲除系统也适用于敲除其他细菌中的基因,因为它基于广泛宿主范围的载体和最小限度依赖细菌宿主的II型可移动内含子。

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