Transgenic peppermint (Mentha x piperita L.) plants obtained by cocultivation with Agrobacterium tumefaciens
The first transgenic peppermint (Meniha x piperita L. cultivar Black Mitcham) plants have been obtained by Agrobacterium-mediated transformation by cocultivation with morphogenically responsive leaf explants. Basal leaf explants with petioles, from leaves closest to the apex of in-vitro-culture-main...
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Veröffentlicht in: | Plant cell reports 1998-01, Vol.17 (3), p.165-171 |
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description | The first transgenic peppermint (Meniha x piperita L. cultivar Black Mitcham) plants have been obtained by Agrobacterium-mediated transformation by cocultivation with morphogenically responsive leaf explants. Basal leaf explants with petioles, from leaves closest to the apex of in-vitro-culture-maintained shoots (5 cm), exhibited optimal shoot organogenetic responsiveness on medium supplemented with thidiazuron (8.4 micromolar). Shoot formation occurred at sites of excision on the leaf blade and petiole either directly from cells of the explant or via a primary callus. Analyses of transient GUS activity data indicated that DNA delivery by microprojectile bombardment was more effective than Agrobacterium infection. However, no transgenic plants were obtained from over 22,000 leaf explants after particle bombardment. Cocultivation of leaf explants with Agrobacterium strain EHA 105 and kanamycin selection produced transgenic plants. Greater transient and stable-glucuronidase (GUS) activities were detected in explants or propagules transformed with the construct where gusA was driven by the pBISN1 promoter rather than a CaMV 35S promoter. Eight plants were subsequently regenerated and verified as transgenic based on detection of the nptII transgene by PCR and Southern blot analyses. The Southern analyses indicated that the plants were derived from eight unique transformation events. All transgenic plants appeared morphologically normal. Analyses of GUS activities in leaves sampled from different portions of these transgenic plants, 10 months after transfer to the greenhouse, indicated that six out of the eight original regenerants were uniformly transformed, i.e., did not exhibit chimeric sectors. |
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Basal leaf explants with petioles, from leaves closest to the apex of in-vitro-culture-maintained shoots (5 cm), exhibited optimal shoot organogenetic responsiveness on medium supplemented with thidiazuron (8.4 micromolar). Shoot formation occurred at sites of excision on the leaf blade and petiole either directly from cells of the explant or via a primary callus. Analyses of transient GUS activity data indicated that DNA delivery by microprojectile bombardment was more effective than Agrobacterium infection. However, no transgenic plants were obtained from over 22,000 leaf explants after particle bombardment. Cocultivation of leaf explants with Agrobacterium strain EHA 105 and kanamycin selection produced transgenic plants. Greater transient and stable-glucuronidase (GUS) activities were detected in explants or propagules transformed with the construct where gusA was driven by the pBISN1 promoter rather than a CaMV 35S promoter. Eight plants were subsequently regenerated and verified as transgenic based on detection of the nptII transgene by PCR and Southern blot analyses. The Southern analyses indicated that the plants were derived from eight unique transformation events. All transgenic plants appeared morphologically normal. Analyses of GUS activities in leaves sampled from different portions of these transgenic plants, 10 months after transfer to the greenhouse, indicated that six out of the eight original regenerants were uniformly transformed, i.e., did not exhibit chimeric sectors.</description><identifier>ISSN: 0721-7714</identifier><identifier>EISSN: 1432-203X</identifier><identifier>DOI: 10.1007/s002990050372</identifier><identifier>PMID: 30736494</identifier><identifier>CODEN: PCRPD8</identifier><language>eng</language><publisher>Berlin: Springer</publisher><subject>Agrobacterium tumefaciens ; Biological and medical sciences ; Biotechnology ; Cultivars ; developmental stages ; explants ; Fundamental and applied biological sciences. Psychology ; gene expression ; gene transfer ; Genetic engineering ; Genetic technics ; genetic transformation ; histochemistry ; in vitro culture ; Leaves ; Mentha piperita ; Methods. Procedures. Technologies ; micropropagation ; plant anatomy ; plant morphology ; Plants ; regenerative ability ; Transgenic animals and transgenic plants ; Transgenic plants</subject><ispartof>Plant cell reports, 1998-01, Vol.17 (3), p.165-171</ispartof><rights>1998 INIST-CNRS</rights><rights>Springer-Verlag Berlin Heidelberg 1998</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c402t-2550cbb9716c5b63c5f4ef82ee921d72b768e7f5709a2deb9dafe96862d40ddd3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2097149$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30736494$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Niu, X</creatorcontrib><creatorcontrib>Lin, K</creatorcontrib><creatorcontrib>Hasegawa, P.M</creatorcontrib><creatorcontrib>Bressan, R.A</creatorcontrib><creatorcontrib>Weller, S.C</creatorcontrib><title>Transgenic peppermint (Mentha x piperita L.) plants obtained by cocultivation with Agrobacterium tumefaciens</title><title>Plant cell reports</title><addtitle>Plant Cell Rep</addtitle><description>The first transgenic peppermint (Meniha x piperita L. cultivar Black Mitcham) plants have been obtained by Agrobacterium-mediated transformation by cocultivation with morphogenically responsive leaf explants. Basal leaf explants with petioles, from leaves closest to the apex of in-vitro-culture-maintained shoots (5 cm), exhibited optimal shoot organogenetic responsiveness on medium supplemented with thidiazuron (8.4 micromolar). Shoot formation occurred at sites of excision on the leaf blade and petiole either directly from cells of the explant or via a primary callus. Analyses of transient GUS activity data indicated that DNA delivery by microprojectile bombardment was more effective than Agrobacterium infection. However, no transgenic plants were obtained from over 22,000 leaf explants after particle bombardment. Cocultivation of leaf explants with Agrobacterium strain EHA 105 and kanamycin selection produced transgenic plants. Greater transient and stable-glucuronidase (GUS) activities were detected in explants or propagules transformed with the construct where gusA was driven by the pBISN1 promoter rather than a CaMV 35S promoter. Eight plants were subsequently regenerated and verified as transgenic based on detection of the nptII transgene by PCR and Southern blot analyses. The Southern analyses indicated that the plants were derived from eight unique transformation events. All transgenic plants appeared morphologically normal. Analyses of GUS activities in leaves sampled from different portions of these transgenic plants, 10 months after transfer to the greenhouse, indicated that six out of the eight original regenerants were uniformly transformed, i.e., did not exhibit chimeric sectors.</description><subject>Agrobacterium tumefaciens</subject><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>Cultivars</subject><subject>developmental stages</subject><subject>explants</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>gene expression</subject><subject>gene transfer</subject><subject>Genetic engineering</subject><subject>Genetic technics</subject><subject>genetic transformation</subject><subject>histochemistry</subject><subject>in vitro culture</subject><subject>Leaves</subject><subject>Mentha piperita</subject><subject>Methods. Procedures. Technologies</subject><subject>micropropagation</subject><subject>plant anatomy</subject><subject>plant morphology</subject><subject>Plants</subject><subject>regenerative ability</subject><subject>Transgenic animals and transgenic plants</subject><subject>Transgenic plants</subject><issn>0721-7714</issn><issn>1432-203X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp90ctrFTEUBvAgir1Wl241iEhdTD15TDJZluILrriwBXdDJnNymzKvJhm1_70p91rQhatA8svhSz5CnjM4ZQD6XQLgxgDUIDR_QDZMCl5xEN8fkg1oziqtmTwiT1K6BiiHWj0mRwK0UNLIDRkuop3SDqfg6ILLgnEMU6YnX3DKV5b-oksoeyFbuj19S5fBTjnRucs2TNjT7pa62a1DDj9sDvNEf4Z8Rc92ce6sy-XeOtK8juitCzilp-SRt0PCZ4f1mFx-eH9x_qnafv34-fxsWzkJPFe8rsF1ndFMubpTwtVeom84ouGs17zTqkHtaw3G8h4701uPRjWK9xL6vhfH5GQ_d4nzzYopt2NIDoeSHuc1tZxzA1rLmhX65r-UqZo3ypgCX_0Dr-c1TuUZbdPIRhoFoqBqj1ycU4ro2yWG0cbblkF7V1f7V13FvzgMXbsR-3v9p58CXh-ATc4OvpTlQrp3HMonybtwL_fM27m1u1jI5TcOTABvmrqkF78BBT2mFQ</recordid><startdate>19980101</startdate><enddate>19980101</enddate><creator>Niu, X</creator><creator>Lin, K</creator><creator>Hasegawa, P.M</creator><creator>Bressan, R.A</creator><creator>Weller, S.C</creator><general>Springer</general><general>Springer Nature B.V</general><scope>FBQ</scope><scope>IQODW</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QL</scope><scope>7T5</scope><scope>7T7</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>RC3</scope><scope>7QO</scope><scope>7X8</scope></search><sort><creationdate>19980101</creationdate><title>Transgenic peppermint (Mentha x piperita L.) plants obtained by cocultivation with Agrobacterium tumefaciens</title><author>Niu, X ; Lin, K ; Hasegawa, P.M ; Bressan, R.A ; Weller, S.C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c402t-2550cbb9716c5b63c5f4ef82ee921d72b768e7f5709a2deb9dafe96862d40ddd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Agrobacterium tumefaciens</topic><topic>Biological and medical sciences</topic><topic>Biotechnology</topic><topic>Cultivars</topic><topic>developmental stages</topic><topic>explants</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>gene expression</topic><topic>gene transfer</topic><topic>Genetic engineering</topic><topic>Genetic technics</topic><topic>genetic transformation</topic><topic>histochemistry</topic><topic>in vitro culture</topic><topic>Leaves</topic><topic>Mentha piperita</topic><topic>Methods. Procedures. Technologies</topic><topic>micropropagation</topic><topic>plant anatomy</topic><topic>plant morphology</topic><topic>Plants</topic><topic>regenerative ability</topic><topic>Transgenic animals and transgenic plants</topic><topic>Transgenic plants</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Niu, X</creatorcontrib><creatorcontrib>Lin, K</creatorcontrib><creatorcontrib>Hasegawa, P.M</creatorcontrib><creatorcontrib>Bressan, R.A</creatorcontrib><creatorcontrib>Weller, S.C</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Immunology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Genetics Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Plant cell reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Niu, X</au><au>Lin, K</au><au>Hasegawa, P.M</au><au>Bressan, R.A</au><au>Weller, S.C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Transgenic peppermint (Mentha x piperita L.) plants obtained by cocultivation with Agrobacterium tumefaciens</atitle><jtitle>Plant cell reports</jtitle><addtitle>Plant Cell Rep</addtitle><date>1998-01-01</date><risdate>1998</risdate><volume>17</volume><issue>3</issue><spage>165</spage><epage>171</epage><pages>165-171</pages><issn>0721-7714</issn><eissn>1432-203X</eissn><coden>PCRPD8</coden><abstract>The first transgenic peppermint (Meniha x piperita L. cultivar Black Mitcham) plants have been obtained by Agrobacterium-mediated transformation by cocultivation with morphogenically responsive leaf explants. Basal leaf explants with petioles, from leaves closest to the apex of in-vitro-culture-maintained shoots (5 cm), exhibited optimal shoot organogenetic responsiveness on medium supplemented with thidiazuron (8.4 micromolar). Shoot formation occurred at sites of excision on the leaf blade and petiole either directly from cells of the explant or via a primary callus. Analyses of transient GUS activity data indicated that DNA delivery by microprojectile bombardment was more effective than Agrobacterium infection. However, no transgenic plants were obtained from over 22,000 leaf explants after particle bombardment. Cocultivation of leaf explants with Agrobacterium strain EHA 105 and kanamycin selection produced transgenic plants. Greater transient and stable-glucuronidase (GUS) activities were detected in explants or propagules transformed with the construct where gusA was driven by the pBISN1 promoter rather than a CaMV 35S promoter. Eight plants were subsequently regenerated and verified as transgenic based on detection of the nptII transgene by PCR and Southern blot analyses. The Southern analyses indicated that the plants were derived from eight unique transformation events. All transgenic plants appeared morphologically normal. Analyses of GUS activities in leaves sampled from different portions of these transgenic plants, 10 months after transfer to the greenhouse, indicated that six out of the eight original regenerants were uniformly transformed, i.e., did not exhibit chimeric sectors.</abstract><cop>Berlin</cop><pub>Springer</pub><pmid>30736494</pmid><doi>10.1007/s002990050372</doi><tpages>7</tpages></addata></record> |
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subjects | Agrobacterium tumefaciens Biological and medical sciences Biotechnology Cultivars developmental stages explants Fundamental and applied biological sciences. Psychology gene expression gene transfer Genetic engineering Genetic technics genetic transformation histochemistry in vitro culture Leaves Mentha piperita Methods. Procedures. Technologies micropropagation plant anatomy plant morphology Plants regenerative ability Transgenic animals and transgenic plants Transgenic plants |
title | Transgenic peppermint (Mentha x piperita L.) plants obtained by cocultivation with Agrobacterium tumefaciens |
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