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        <identifier>oai:az.repo.nii.ac.jp:00004857</identifier>
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          <dc:title>パーティクルガンを用いた単子葉植物ホテイアオイへの遺伝子直接導入法の開発 : ホテイアオイの無菌化と外来遺伝子の一過性の発現</dc:title>
          <dc:title xml:lang="en">Development of the direct gene transfer method to monocotyledon water hyacinth using particle gun : Sterilization of water hyacinth and transient expression of foreign gene</dc:title>
          <jpcoar:creator>
            <jpcoar:creatorName>其木, 茂則</jpcoar:creatorName>
            <jpcoar:creatorName xml:lang="ja-Kana">ソノキ, シゲノリ</jpcoar:creatorName>
          </jpcoar:creator>
          <jpcoar:creator>
            <jpcoar:creatorName>佐俣, 哲郎</jpcoar:creatorName>
            <jpcoar:creatorName xml:lang="ja-Kana">サマタ, テツオ</jpcoar:creatorName>
          </jpcoar:creator>
          <jpcoar:creator>
            <jpcoar:creatorName>堂ヶ崎, 知格</jpcoar:creatorName>
            <jpcoar:creatorName xml:lang="ja-Kana">ドウガサキ, チカク</jpcoar:creatorName>
          </jpcoar:creator>
          <jpcoar:creator>
            <jpcoar:creatorName>久松, 伸</jpcoar:creatorName>
            <jpcoar:creatorName xml:lang="ja-Kana">ヒサマツ, シン</jpcoar:creatorName>
          </jpcoar:creator>
          <jpcoar:creator>
            <jpcoar:creatorName xml:lang="en">Sonoki, Shigenori</jpcoar:creatorName>
          </jpcoar:creator>
          <jpcoar:creator>
            <jpcoar:creatorName xml:lang="en">Samata, Tetuo</jpcoar:creatorName>
          </jpcoar:creator>
          <jpcoar:creator>
            <jpcoar:creatorName xml:lang="en">Dougasaki, Chikaku</jpcoar:creatorName>
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          <jpcoar:creator>
            <jpcoar:creatorName xml:lang="en">Hisamatsu, Shin</jpcoar:creatorName>
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          <datacite:description descriptionType="Abstract">ホテイアオイを用いた水圏のファイトレメディエーション技術を開発するために,ホテイアオイの無菌化とホテイアオイで有効なプロモータの検討を行った。その結果,ホテイアオイの種子を滅菌し,外皮の一部を削除することで無菌化と発芽を行うことができた。また,高等植物において外来遺伝子を発現させるためによく使用されるCaMV35Sプロモータは,ホテイアオイでも利用できることがわかった。</datacite:description>
          <datacite:description descriptionType="Other">To develop phytoremediation technology for hydrosphere, we decided to utilize water hyacinth. In this study, sterilization of water hyacinth as base technique for transgenic plant and search of a promoter to foreign-gene expression were performed. For sterilization of water hyacinth, the seed was a good material. However, even if the sterilized seed planted on the culture medium, budding was not observed. Then, when the seed which deleted a part of outer cover was planted, budding was observed. Furthermore, CaMV35S promoter, general promoter for higher plant, can use also for water hyacinth.</datacite:description>
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          <datacite:description descriptionType="Other">FEATURE ARTICLES</datacite:description>
          <dc:publisher>麻布大学</dc:publisher>
          <dc:publisher>Azabu University</dc:publisher>
          <datacite:date dateType="Issued">2006-03-31</datacite:date>
          <dc:language>jpn</dc:language>
          <dc:type rdf:resource="http://purl.org/coar/resource_type/c_6501">departmental bulletin paper</dc:type>
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          <jpcoar:identifier identifierType="URI">https://az.repo.nii.ac.jp/records/4857</jpcoar:identifier>
          <jpcoar:sourceIdentifier identifierType="ISSN">1346-5880</jpcoar:sourceIdentifier>
          <jpcoar:sourceIdentifier identifierType="NCID">AA11561468</jpcoar:sourceIdentifier>
          <jpcoar:sourceTitle>麻布大学雑誌</jpcoar:sourceTitle>
          <jpcoar:sourceTitle xml:lang="en">Journal of Azabu University</jpcoar:sourceTitle>
          <jpcoar:volume>11/12</jpcoar:volume>
          <jpcoar:pageStart>192</jpcoar:pageStart>
          <jpcoar:pageEnd>195</jpcoar:pageEnd>
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            <datacite:date dateType="Available">2005-01-01</datacite:date>
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