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  1. 080 繊維学部
  2. 0802 紀要・刊行物
  3. 08030 先端繊維技術科学に関する研究報告
  4. Vol. 10

15-2-14 :細胞壁合成・修飾・分解機構の研究

http://hdl.handle.net/10091/13635
http://hdl.handle.net/10091/13635
686ce37c-d642-4857-8cdb-b77a2b6b486b
名前 / ファイル ライセンス アクション
AFSTT10-214.pdf AFSTT10-214.pdf (666.1 kB)
Item type 研究報告書 / Research Paper(1)
公開日 2012-02-23
タイトル
言語 ja
タイトル 15-2-14 :細胞壁合成・修飾・分解機構の研究
言語
言語 jpn
資源タイプ
資源 http://purl.org/coar/resource_type/c_18ws
タイプ research report
その他(別言語等)のタイトル
その他のタイトル バイオファイバー生合成機構の解明
著者 関口, 順一

× 関口, 順一

WEKO 43930

関口, 順一

Search repository
山本, 博規

× 山本, 博規

WEKO 43931

山本, 博規

Search repository
信州大学研究者総覧へのリンク
氏名 山本, 博規
URL http://soar-rd.shinshu-u.ac.jp/profile/ja.uhDNjekV.html
出版者
出版者 信州大学繊維学部
引用
内容記述タイプ Other
内容記述 先進ファイバー工学研究教育拠点研究成果報告書 10: 60-60(2004)
書誌情報 先進ファイバー工学研究教育拠点研究成果報告書

巻 10, p. 60-60, 発行日 2004-03-31
抄録
内容記述タイプ Abstract
内容記述 Modification of peptidoglycan is important in various bacteria. Especially Bacillus subtilis produces spore under the starvation conditions. We investigated the modification of spore peptidoglycan called cortex with the use of the polysaccharide deacetylase gene (pdaA) of Bacillus subtilis. PdaA-deficient spore did not lead to germination and this mutant completely lacked muramic-delta-lactam which is essential to germination. In-vitro experiments indicated that PdaA did not catalyze deacetylation reaction when the native polysaccharide was used as a substrate, but catalyzed deacetylation when the amidase-digested polysaccharide was used as a substrate. These results indicate PdaA plays a key role in cortex biosynthesis. On the other hand, cell surface targeting of peptidoglycan hydrolases was investigated by the immuno-fluorescence microscopy with 3xFLAG tagged protein, and localization of three proteins was identified.
資源タイプ(コンテンツの種類)
内容記述タイプ Other
内容記述 Article
書誌レコードID
収録物識別子タイプ NCID
収録物識別子 AA1200368X
出版タイプ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
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