Micropropagation of Ceratopetalum gummiferum, an Important Australian Cut Flower Crop
Ceratopetalum gummiferum Sm. 'Albery's Red' (NSW Christmas Bush), a native to eastern Australia, has become an important commercial plant in both the export and domestic markets. A protocol for in vitro culture was investigated for rapid clonal propagation of selected cultivars. Muras...
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Veröffentlicht in: | In vitro cellular & developmental biology. Plant 2001-03, Vol.37 (2), p.173-177 |
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description | Ceratopetalum gummiferum Sm. 'Albery's Red' (NSW Christmas Bush), a native to eastern Australia, has become an important commercial plant in both the export and domestic markets. A protocol for in vitro culture was investigated for rapid clonal propagation of selected cultivars. Murashige and Skoog medium, supplemented with various concentrations of 6-benzylaminopurine, kinetin, 6(γ,γ-dimethylalrylamino)-purine or zeatin were examined for their effects on multiplication. The most successful treatments were 2.2 γM 6-benzylaminopurine and 11.6 γM kinetin which increased shoot number and explant weight. Although zeatin and 6(γ,γ-dimethylalrylamino)-purine increased shoot length, both failed to increase multiplication rates. However, hyperhydricity was found to be a serious physiological disorder in tissue culture of C. gummiferum 'Albery's Red'. Rooting in vitro was also examined with indole-3-butyric acid and naphthalene acetic acid, the most successful being 4.9 mM indole-3-butyric acid. The development of an in vivo rooting protocol, however, may prove to be essential for the commercial production of this plant. |
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'Albery's Red' (NSW Christmas Bush), a native to eastern Australia, has become an important commercial plant in both the export and domestic markets. A protocol for in vitro culture was investigated for rapid clonal propagation of selected cultivars. Murashige and Skoog medium, supplemented with various concentrations of 6-benzylaminopurine, kinetin, 6(γ,γ-dimethylalrylamino)-purine or zeatin were examined for their effects on multiplication. The most successful treatments were 2.2 γM 6-benzylaminopurine and 11.6 γM kinetin which increased shoot number and explant weight. Although zeatin and 6(γ,γ-dimethylalrylamino)-purine increased shoot length, both failed to increase multiplication rates. However, hyperhydricity was found to be a serious physiological disorder in tissue culture of C. gummiferum 'Albery's Red'. Rooting in vitro was also examined with indole-3-butyric acid and naphthalene acetic acid, the most successful being 4.9 mM indole-3-butyric acid. The development of an in vivo rooting protocol, however, may prove to be essential for the commercial production of this plant.</description><identifier>ISSN: 1054-5476</identifier><identifier>EISSN: 1475-2689</identifier><identifier>DOI: 10.1079/IVP2000110</identifier><language>eng</language><publisher>Wallingford: CABI Publishing</publisher><subject>6(^g,^g-dimethylallylamino)-purine ; 6-benzylaminopurine ; Auxins ; Biological and medical sciences ; Biotechnology ; Callus ; Ceratopetalum gummiferum ; Cytokinins ; Developmental biology ; Eukaryotic cell cultures ; Fundamental and applied biological sciences. Psychology ; In vitro propagation: entire plant regeneration from tissues and cell cultures ; kinetin ; Methods. Procedures. Technologies ; Micropropagation ; Plant cells and fungal cells ; Plant propagation ; Plant tissues ; Plants ; Protocols and Research Reports ; Rooting ; Tissue culture techniques ; zeatin</subject><ispartof>In vitro cellular & developmental biology. Plant, 2001-03, Vol.37 (2), p.173-177</ispartof><rights>Copyright 2001 The Society for In Vitro Biology</rights><rights>2001 INIST-CNRS</rights><rights>Copyright Society for In Vitro Biology Mar/Apr 2001</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/4293439$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/4293439$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>309,310,314,780,784,789,790,803,23930,23931,25140,27924,27925,58017,58250</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=993334$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>ARMSTRONG, Gemma</creatorcontrib><creatorcontrib>JOHNSON, Krystyna</creatorcontrib><title>Micropropagation of Ceratopetalum gummiferum, an Important Australian Cut Flower Crop</title><title>In vitro cellular & developmental biology. Plant</title><description>Ceratopetalum gummiferum Sm. 'Albery's Red' (NSW Christmas Bush), a native to eastern Australia, has become an important commercial plant in both the export and domestic markets. A protocol for in vitro culture was investigated for rapid clonal propagation of selected cultivars. Murashige and Skoog medium, supplemented with various concentrations of 6-benzylaminopurine, kinetin, 6(γ,γ-dimethylalrylamino)-purine or zeatin were examined for their effects on multiplication. The most successful treatments were 2.2 γM 6-benzylaminopurine and 11.6 γM kinetin which increased shoot number and explant weight. Although zeatin and 6(γ,γ-dimethylalrylamino)-purine increased shoot length, both failed to increase multiplication rates. However, hyperhydricity was found to be a serious physiological disorder in tissue culture of C. gummiferum 'Albery's Red'. Rooting in vitro was also examined with indole-3-butyric acid and naphthalene acetic acid, the most successful being 4.9 mM indole-3-butyric acid. The development of an in vivo rooting protocol, however, may prove to be essential for the commercial production of this plant.</description><subject>6(^g,^g-dimethylallylamino)-purine</subject><subject>6-benzylaminopurine</subject><subject>Auxins</subject><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>Callus</subject><subject>Ceratopetalum gummiferum</subject><subject>Cytokinins</subject><subject>Developmental biology</subject><subject>Eukaryotic cell cultures</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>In vitro propagation: entire plant regeneration from tissues and cell cultures</subject><subject>kinetin</subject><subject>Methods. Procedures. Technologies</subject><subject>Micropropagation</subject><subject>Plant cells and fungal cells</subject><subject>Plant propagation</subject><subject>Plant tissues</subject><subject>Plants</subject><subject>Protocols and Research Reports</subject><subject>Rooting</subject><subject>Tissue culture techniques</subject><subject>zeatin</subject><issn>1054-5476</issn><issn>1475-2689</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</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>eNpdz0tLw0AQAOAgCtbqxbOHoODJ6D6T7LEEq4WKHqzXMN3sloQkG_eB-O9dafEgDMww8zHMJMklRvcYFeJh9fFGEEIYo6NkhlnBM5KX4jjWiLOMsyI_Tc6c634NwsUs2by00popBuzAt2ZMjU4rZcGbSXnow5DuwjC0Wtkw3KUwpqthMtbD6NNFcN5C38ZmFXy67M2XsmkVd50nJxp6py4OeZ5slo_v1XO2fn1aVYt11mFBfCa3jaYNcKYZ0Qg3mIEsGilJnpMyx5wwLkWJGGEy11zSfEsLUugGJNVCA6Hz5Ha_Nz7wGZTz9dA6qfoeRmWCq3GJBRMURXj9D3Ym2DHeVmNRUIEo5xHdHBA4Cb22MMrW1ZNtB7DftRCUUhbV1V51zhv7N2VExKGgP6L4dWg</recordid><startdate>20010301</startdate><enddate>20010301</enddate><creator>ARMSTRONG, Gemma</creator><creator>JOHNSON, Krystyna</creator><general>CABI Publishing</general><general>Cambridge University Press</general><general>Springer Nature B.V</general><scope>IQODW</scope><scope>3V.</scope><scope>4T-</scope><scope>4U-</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M2P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>S0X</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>20010301</creationdate><title>Micropropagation of Ceratopetalum gummiferum, an Important Australian Cut Flower Crop</title><author>ARMSTRONG, Gemma ; JOHNSON, Krystyna</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-j192t-cbdf3da54f42f01d14ac7dcc26628615245c980424c6f5c36b3727fdac3f9fa23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>6(^g,^g-dimethylallylamino)-purine</topic><topic>6-benzylaminopurine</topic><topic>Auxins</topic><topic>Biological and medical sciences</topic><topic>Biotechnology</topic><topic>Callus</topic><topic>Ceratopetalum gummiferum</topic><topic>Cytokinins</topic><topic>Developmental biology</topic><topic>Eukaryotic cell cultures</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>In vitro propagation: entire plant regeneration from tissues and cell cultures</topic><topic>kinetin</topic><topic>Methods. Procedures. Technologies</topic><topic>Micropropagation</topic><topic>Plant cells and fungal cells</topic><topic>Plant propagation</topic><topic>Plant tissues</topic><topic>Plants</topic><topic>Protocols and Research Reports</topic><topic>Rooting</topic><topic>Tissue culture techniques</topic><topic>zeatin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>ARMSTRONG, Gemma</creatorcontrib><creatorcontrib>JOHNSON, Krystyna</creatorcontrib><collection>Pascal-Francis</collection><collection>ProQuest Central (Corporate)</collection><collection>Docstoc</collection><collection>University Readers</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>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</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 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>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</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>Science Database</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>SIRS Editorial</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>In vitro cellular & developmental biology. Plant</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>ARMSTRONG, Gemma</au><au>JOHNSON, Krystyna</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Micropropagation of Ceratopetalum gummiferum, an Important Australian Cut Flower Crop</atitle><jtitle>In vitro cellular & developmental biology. Plant</jtitle><date>2001-03-01</date><risdate>2001</risdate><volume>37</volume><issue>2</issue><spage>173</spage><epage>177</epage><pages>173-177</pages><issn>1054-5476</issn><eissn>1475-2689</eissn><abstract>Ceratopetalum gummiferum Sm. 'Albery's Red' (NSW Christmas Bush), a native to eastern Australia, has become an important commercial plant in both the export and domestic markets. A protocol for in vitro culture was investigated for rapid clonal propagation of selected cultivars. Murashige and Skoog medium, supplemented with various concentrations of 6-benzylaminopurine, kinetin, 6(γ,γ-dimethylalrylamino)-purine or zeatin were examined for their effects on multiplication. The most successful treatments were 2.2 γM 6-benzylaminopurine and 11.6 γM kinetin which increased shoot number and explant weight. Although zeatin and 6(γ,γ-dimethylalrylamino)-purine increased shoot length, both failed to increase multiplication rates. However, hyperhydricity was found to be a serious physiological disorder in tissue culture of C. gummiferum 'Albery's Red'. Rooting in vitro was also examined with indole-3-butyric acid and naphthalene acetic acid, the most successful being 4.9 mM indole-3-butyric acid. The development of an in vivo rooting protocol, however, may prove to be essential for the commercial production of this plant.</abstract><cop>Wallingford</cop><pub>CABI Publishing</pub><doi>10.1079/IVP2000110</doi><tpages>5</tpages></addata></record> |
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subjects | 6(^g,^g-dimethylallylamino)-purine 6-benzylaminopurine Auxins Biological and medical sciences Biotechnology Callus Ceratopetalum gummiferum Cytokinins Developmental biology Eukaryotic cell cultures Fundamental and applied biological sciences. Psychology In vitro propagation: entire plant regeneration from tissues and cell cultures kinetin Methods. Procedures. Technologies Micropropagation Plant cells and fungal cells Plant propagation Plant tissues Plants Protocols and Research Reports Rooting Tissue culture techniques zeatin |
title | Micropropagation of Ceratopetalum gummiferum, an Important Australian Cut Flower Crop |
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