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Expression of translesion DNA polymerase genes from Deinococcus grandis in Escherichia coli

https://repo.qst.go.jp/records/72957
https://repo.qst.go.jp/records/72957
6e21dd2f-499e-4fab-96a6-a1b3b1ddd171
Item type 会議発表用資料 / Presentation(1)
公開日 2018-09-26
タイトル
タイトル Expression of translesion DNA polymerase genes from Deinococcus grandis in Escherichia coli
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_c94f
資源タイプ conference object
アクセス権
アクセス権 metadata only access
アクセス権URI http://purl.org/coar/access_right/c_14cb
著者 Sanzen, Toshihiko

× Sanzen, Toshihiko

WEKO 718870

Sanzen, Toshihiko

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佐藤, 勝也

× 佐藤, 勝也

WEKO 718871

佐藤, 勝也

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Narumi, Issay

× Narumi, Issay

WEKO 718872

Narumi, Issay

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佐藤 勝也

× 佐藤 勝也

WEKO 718873

en 佐藤 勝也

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内容記述タイプ Abstract
内容記述 While Deinococcus radiodurans, the type species of the genus Deinococcus, does not possess any genes involved in translesion DNA synthesis, the draft genome sequencing of Deinococcus grandis KS0485 revealed that this bacterium possesses two lexA-imuB-dnaE2 gene clusters, which will be involved in translesion DNA synthesis. In this study, we expressed deinococcal dnaE2 and imuB genes in Escherichia coli to further delineate the function of these genes. The dnaE2 and imuB genes were cloned in pET-based vector and p15A-base vector, respectively, and introduced in E. coli BL21(DE3) cells. Mutant frequency was measured by colony formation assay based on rifampicin resistance. As a result, when both the dnaE2 and imuB genes were expressed in E. coli under IPTG induction, the mutant frequency was increased, confirming that the functionality of dnaE2 and imuB as mutagenesis genes. However, when dnaE2 or imuB gene was separately expressed in E. coli, no increase in mutant frequency was observed. These results suggest that both gene products are necessary to operate mutagenesis.
会議概要(会議名, 開催地, 会期, 主催者等)
内容記述タイプ Other
内容記述 第12回極限環境生物国際会議(Extremophiles2018)出席
発表年月日
日付 2018-09-19
日付タイプ Issued
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