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  1. 原著論文

Expression of Ascorbate Peroxidase Derived from Cyanidioschyzon merolae in Mammalian Cells

https://repo.qst.go.jp/records/80155
https://repo.qst.go.jp/records/80155
0795419b-377f-40ff-b229-4338145a1de1
名前 / ファイル ライセンス アクション
75808c811c7089c9a2ccd3f2660d6987.pdf Hitomi.S.2020.In.Vivo.34.2437-2441.AscorbatePeroxidase.pdf (1.1 MB)
Item type 学術雑誌論文 / Journal Article(1)
公開日 2020-06-08
タイトル
タイトル Expression of Ascorbate Peroxidase Derived from Cyanidioschyzon merolae in Mammalian Cells
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_6501
資源タイプ journal article
著者 Hitomi, Suzuro

× Hitomi, Suzuro

WEKO 888987

Hitomi, Suzuro

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Kokabu, Shoichiro

× Kokabu, Shoichiro

WEKO 888988

Kokabu, Shoichiro

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Ken-ichiro, Matsumoto

× Ken-ichiro, Matsumoto

WEKO 888989

Ken-ichiro, Matsumoto

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Shoji, Yoshimi

× Shoji, Yoshimi

WEKO 888990

Shoji, Yoshimi

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Ujihara, Izumi

× Ujihara, Izumi

WEKO 888991

Ujihara, Izumi

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Ono, Kentaro

× Ono, Kentaro

WEKO 888992

Ono, Kentaro

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Matsumoto, Kenichiro

× Matsumoto, Kenichiro

WEKO 888993

en Matsumoto, Kenichiro

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Shoji, Yoshimi

× Shoji, Yoshimi

WEKO 888994

en Shoji, Yoshimi

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抄録
内容記述タイプ Abstract
内容記述 Background: Ascorbate peroxidase (APX) derived from Cyanidioschyzon merolae, a primitive red alga living in high temperature and acidic environments, has a greater anti-oxidative capacity than similar peroxidases occurring in other plants. In the present study, we examined the ability of Cyanidioschyzon merolae-derived APX (cAPX) to increase anti-oxidative capacity when expressed in mammalian cells. Materials and Methods: The cAPX gene was introduced into the mouse fibroblast-like cell line C3H10T1/2. Production of reactive oxygen species (ROS) and/or cell viability was assessed after heat, H2O2 and acid stimulation. Results: Heat and H2O2 stimulation caused ROS production. cAPX-expressing cells were more tolerant to oxidative stress induced by heat, H2O2 and acid stimulations than control cells lacking cAPX. Conclusion: Introduction of cAPX increases anti-oxidative capacity in mammalian cells.
書誌情報 in vivo

巻 34, 号 5, p. 2437-2441, 発行日 2020-09
ISSN
収録物識別子タイプ ISSN
収録物識別子 0258-851X
DOI
識別子タイプ DOI
関連識別子 10.21873/invivo.12058
関連サイト
識別子タイプ URI
関連識別子 http://iv.iiarjournals.org/content/34/5/2437.full
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