In vitro plant regeneration from leaves and internode sections of sweet cherry cultivars (Prunus avium L.)
Regeneration of adventitious shoots from leaves and, for the first time, from internode sections were compared and optimized for five economically important sweet cherry cultivars, i.e. 'Schneiders,' 'Sweetheart', 'Starking Hardy Giant', 'Kordia' and 'Reg...
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| Veröffentlicht in: | Plant cell reports 2005-10, Vol.24 (8), p.468-476 |
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| description | Regeneration of adventitious shoots from leaves and, for the first time, from internode sections were compared and optimized for five economically important sweet cherry cultivars, i.e. 'Schneiders,' 'Sweetheart', 'Starking Hardy Giant', 'Kordia' and 'Regina' (Prunus avium L.). The influence of basal media, carbon source, combination and dosage of phytohormones, ethylene inhibitor such as silver thiosulfate and a 16 h:8 h light:dark photoperiod versus complete darkness were evaluated. Both, DKW/WPM (1:1) and Quoirin/Lepoivre (QL) basal media stimulated organogenesis more than QL/WPM (1:1), Chee and Pool (CP), Murashige Skoog (MS), Driver and Kuniyuki (DKW) or woody plant (WPM) media did. An induction phase in darkness resulted in lower or zero regeneration rates. The best regeneration efficiencies were generally obtained with thidiazuron in combination with indole-3-butyric-acid. The addition of silver thiosulfate resulted in a similar or reduced regeneration efficiency. Significant genotypic variability in adventitious bud formation was evident for both explant sources, leaf and internode section. Adventitious shoots were obtained from 11% of leaf explants and 50% of internode sections indicating that shoot regeneration from internodes was significantly more efficient than from leaves. |
| doi_str_mv | 10.1007/s00299-005-0964-6 |
| format | Article |
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The influence of basal media, carbon source, combination and dosage of phytohormones, ethylene inhibitor such as silver thiosulfate and a 16 h:8 h light:dark photoperiod versus complete darkness were evaluated. Both, DKW/WPM (1:1) and Quoirin/Lepoivre (QL) basal media stimulated organogenesis more than QL/WPM (1:1), Chee and Pool (CP), Murashige Skoog (MS), Driver and Kuniyuki (DKW) or woody plant (WPM) media did. An induction phase in darkness resulted in lower or zero regeneration rates. The best regeneration efficiencies were generally obtained with thidiazuron in combination with indole-3-butyric-acid. The addition of silver thiosulfate resulted in a similar or reduced regeneration efficiency. Significant genotypic variability in adventitious bud formation was evident for both explant sources, leaf and internode section. Adventitious shoots were obtained from 11% of leaf explants and 50% of internode sections indicating that shoot regeneration from internodes was significantly more efficient than from leaves.</description><identifier>ISSN: 0721-7714</identifier><identifier>EISSN: 1432-203X</identifier><identifier>DOI: 10.1007/s00299-005-0964-6</identifier><identifier>PMID: 15948004</identifier><identifier>CODEN: PCRPD8</identifier><language>eng</language><publisher>Berlin: Springer</publisher><subject>adventitious shoots ; benzyladenine ; Biological and medical sciences ; Biotechnology ; Carbon sources ; cherries ; Cultivars ; culture media ; Economic importance ; Eukaryotic cell cultures ; fruit trees ; Fundamental and applied biological sciences. Psychology ; indole acetic acid ; indole butyric acid ; internodes ; Leaves ; Methods. Procedures. Technologies ; micropropagation ; Miscellaneous ; naphthaleneacetic acid ; photoperiod ; Plant cells and fungal cells ; Plant Leaves - growth & development ; Plant Leaves - physiology ; plant regeneration ; Plant Shoots - growth & development ; Plant Shoots - physiology ; Prunus - growth & development ; Prunus - physiology ; Prunus avium ; Regeneration ; rooting ; Shoots ; somatic embryogenesis ; somatic embryos ; thidiazuron ; Woody plants</subject><ispartof>Plant cell reports, 2005-10, Vol.24 (8), p.468-476</ispartof><rights>2006 INIST-CNRS</rights><rights>Springer-Verlag 2005</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c411t-33b3593e0c913971bfe57c65813d152fd398882b429a76ce5503eae596b3f9c03</citedby><cites>FETCH-LOGICAL-c411t-33b3593e0c913971bfe57c65813d152fd398882b429a76ce5503eae596b3f9c03</cites></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=17194946$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15948004$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Matt, A</creatorcontrib><creatorcontrib>Jehle, J.A</creatorcontrib><title>In vitro plant regeneration from leaves and internode sections of sweet cherry cultivars (Prunus avium L.)</title><title>Plant cell reports</title><addtitle>Plant Cell Rep</addtitle><description>Regeneration of adventitious shoots from leaves and, for the first time, from internode sections were compared and optimized for five economically important sweet cherry cultivars, i.e. 'Schneiders,' 'Sweetheart', 'Starking Hardy Giant', 'Kordia' and 'Regina' (Prunus avium L.). The influence of basal media, carbon source, combination and dosage of phytohormones, ethylene inhibitor such as silver thiosulfate and a 16 h:8 h light:dark photoperiod versus complete darkness were evaluated. Both, DKW/WPM (1:1) and Quoirin/Lepoivre (QL) basal media stimulated organogenesis more than QL/WPM (1:1), Chee and Pool (CP), Murashige Skoog (MS), Driver and Kuniyuki (DKW) or woody plant (WPM) media did. An induction phase in darkness resulted in lower or zero regeneration rates. The best regeneration efficiencies were generally obtained with thidiazuron in combination with indole-3-butyric-acid. The addition of silver thiosulfate resulted in a similar or reduced regeneration efficiency. Significant genotypic variability in adventitious bud formation was evident for both explant sources, leaf and internode section. Adventitious shoots were obtained from 11% of leaf explants and 50% of internode sections indicating that shoot regeneration from internodes was significantly more efficient than from leaves.</description><subject>adventitious shoots</subject><subject>benzyladenine</subject><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>Carbon sources</subject><subject>cherries</subject><subject>Cultivars</subject><subject>culture media</subject><subject>Economic importance</subject><subject>Eukaryotic cell cultures</subject><subject>fruit trees</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>indole acetic acid</subject><subject>indole butyric acid</subject><subject>internodes</subject><subject>Leaves</subject><subject>Methods. Procedures. Technologies</subject><subject>micropropagation</subject><subject>Miscellaneous</subject><subject>naphthaleneacetic acid</subject><subject>photoperiod</subject><subject>Plant cells and fungal cells</subject><subject>Plant Leaves - growth & development</subject><subject>Plant Leaves - physiology</subject><subject>plant regeneration</subject><subject>Plant Shoots - growth & development</subject><subject>Plant Shoots - physiology</subject><subject>Prunus - growth & development</subject><subject>Prunus - physiology</subject><subject>Prunus avium</subject><subject>Regeneration</subject><subject>rooting</subject><subject>Shoots</subject><subject>somatic embryogenesis</subject><subject>somatic embryos</subject><subject>thidiazuron</subject><subject>Woody plants</subject><issn>0721-7714</issn><issn>1432-203X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqFkUuLFDEUhYMoTs_oD3CjQRjRRY03lfdSBh8DDQo64C6kUrfGaqqTNqlqmX9vmm4YcOMqi_udEw4fIS8YXDEA_b4AtNY2ALIBq0SjHpEVE7xtWuA_H5MV6JY1WjNxRs5L2QDUo1ZPyRmTVhgAsSKbm0j345wT3U0-zjTjHUbMfh5TpENOWzqh32OhPvZ0jDPmmHqkBcOBKDQNtPxBnGn4hTnf07BM87j3udC33_ISlxrcj8uWrq_ePSNPBj8VfH56L8jtp48_rr8066-fb64_rJsgGJsbzjsuLUcIlnGrWTeg1EFJw3jPZDv03Bpj2k601msVUErg6FFa1fHBBuAX5M2xd5fT7wXL7LZjCTjVfZiW4pRRdX_94n8g0y0ozk0FX_8DbtKSYx3hDGgJxnBZIXaEQk6lZBzcLo9bn-8dA3fQ5Y66XNXlDrqcqpmXp-Kl22L_kDj5qcDlCfAl-GnIPoaxPHCaWWHFoejVkRt8cv4uV-b2ewuMAwOlRN3wFzHvpWA</recordid><startdate>20051001</startdate><enddate>20051001</enddate><creator>Matt, A</creator><creator>Jehle, J.A</creator><general>Springer</general><general>Springer Nature B.V</general><scope>FBQ</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</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>20051001</creationdate><title>In vitro plant regeneration from leaves and internode sections of sweet cherry cultivars (Prunus avium L.)</title><author>Matt, A ; Jehle, J.A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c411t-33b3593e0c913971bfe57c65813d152fd398882b429a76ce5503eae596b3f9c03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>adventitious shoots</topic><topic>benzyladenine</topic><topic>Biological and medical sciences</topic><topic>Biotechnology</topic><topic>Carbon sources</topic><topic>cherries</topic><topic>Cultivars</topic><topic>culture media</topic><topic>Economic importance</topic><topic>Eukaryotic cell cultures</topic><topic>fruit trees</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>indole acetic acid</topic><topic>indole butyric acid</topic><topic>internodes</topic><topic>Leaves</topic><topic>Methods. Procedures. Technologies</topic><topic>micropropagation</topic><topic>Miscellaneous</topic><topic>naphthaleneacetic acid</topic><topic>photoperiod</topic><topic>Plant cells and fungal cells</topic><topic>Plant Leaves - growth & development</topic><topic>Plant Leaves - physiology</topic><topic>plant regeneration</topic><topic>Plant Shoots - growth & development</topic><topic>Plant Shoots - physiology</topic><topic>Prunus - growth & development</topic><topic>Prunus - physiology</topic><topic>Prunus avium</topic><topic>Regeneration</topic><topic>rooting</topic><topic>Shoots</topic><topic>somatic embryogenesis</topic><topic>somatic embryos</topic><topic>thidiazuron</topic><topic>Woody plants</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Matt, A</creatorcontrib><creatorcontrib>Jehle, J.A</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</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)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central</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>Biological Sciences</collection><collection>Agriculture 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>Matt, A</au><au>Jehle, J.A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In vitro plant regeneration from leaves and internode sections of sweet cherry cultivars (Prunus avium L.)</atitle><jtitle>Plant cell reports</jtitle><addtitle>Plant Cell Rep</addtitle><date>2005-10-01</date><risdate>2005</risdate><volume>24</volume><issue>8</issue><spage>468</spage><epage>476</epage><pages>468-476</pages><issn>0721-7714</issn><eissn>1432-203X</eissn><coden>PCRPD8</coden><abstract>Regeneration of adventitious shoots from leaves and, for the first time, from internode sections were compared and optimized for five economically important sweet cherry cultivars, i.e. 'Schneiders,' 'Sweetheart', 'Starking Hardy Giant', 'Kordia' and 'Regina' (Prunus avium L.). The influence of basal media, carbon source, combination and dosage of phytohormones, ethylene inhibitor such as silver thiosulfate and a 16 h:8 h light:dark photoperiod versus complete darkness were evaluated. Both, DKW/WPM (1:1) and Quoirin/Lepoivre (QL) basal media stimulated organogenesis more than QL/WPM (1:1), Chee and Pool (CP), Murashige Skoog (MS), Driver and Kuniyuki (DKW) or woody plant (WPM) media did. An induction phase in darkness resulted in lower or zero regeneration rates. The best regeneration efficiencies were generally obtained with thidiazuron in combination with indole-3-butyric-acid. The addition of silver thiosulfate resulted in a similar or reduced regeneration efficiency. Significant genotypic variability in adventitious bud formation was evident for both explant sources, leaf and internode section. Adventitious shoots were obtained from 11% of leaf explants and 50% of internode sections indicating that shoot regeneration from internodes was significantly more efficient than from leaves.</abstract><cop>Berlin</cop><pub>Springer</pub><pmid>15948004</pmid><doi>10.1007/s00299-005-0964-6</doi><tpages>9</tpages></addata></record> |
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| ispartof | Plant cell reports, 2005-10, Vol.24 (8), p.468-476 |
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| source | MEDLINE; Springer Nature - Complete Springer Journals |
| subjects | adventitious shoots benzyladenine Biological and medical sciences Biotechnology Carbon sources cherries Cultivars culture media Economic importance Eukaryotic cell cultures fruit trees Fundamental and applied biological sciences. Psychology indole acetic acid indole butyric acid internodes Leaves Methods. Procedures. Technologies micropropagation Miscellaneous naphthaleneacetic acid photoperiod Plant cells and fungal cells Plant Leaves - growth & development Plant Leaves - physiology plant regeneration Plant Shoots - growth & development Plant Shoots - physiology Prunus - growth & development Prunus - physiology Prunus avium Regeneration rooting Shoots somatic embryogenesis somatic embryos thidiazuron Woody plants |
| title | In vitro plant regeneration from leaves and internode sections of sweet cherry cultivars (Prunus avium L.) |
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