Multiple adventitious shoot formation in Spanish Red Cedar ( Cedreto odorata L.) cultured in vitro using juvenile and mature tissues: an improved micropropagation protocol for a highly valuable tropical tree species
Cedrela odorata L. is a valuable tropical tree widely appreciated for its wood. This species confronts serious problems due to both overexploitation of its natural populations and its susceptibility to the Meliaceae borer Hypsipyla grandella, which destroys the apical meristems and produces structur...
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creator | Peña-Ramírez, Yuri Jorge Juárez-Gómez, Juan Gómez-López, Lucero Jerónimo-Pérez, José L. García-Sheseña, Israel González-Rodríguez, José A. Robert, Manuel L. |
description | Cedrela odorata L. is a valuable tropical tree widely appreciated for its wood. This species confronts serious problems due to both overexploitation of its natural populations and its susceptibility to the Meliaceae borer Hypsipyla grandella, which destroys the apical meristems and produces structural deformations. The rapid introduction of new varieties through clonal forestry has been demonstrated to be the most effective way to improve the production of perennial plantation species. In this work, we report both a protocol for the rejuvenation of elite mature trees of C. odorata and the optimization of an in vitro culture system to scale up micropropagation. Several media formulations and the use of temporary immersion culture in bioreactors were evaluated. The addition of 20% coconut water to TY17 medium increased the number of adventitious shoots from hypocotyl segments to an average number of 4.68 shoots per expiant. To replace coconut water and to define the culture medium, several cytokinins were tested at various concentrations; however, none of them produced the effect of coconut water. Rejuvenation of elite mature individuals was investigated by ex vitro grafting of mature tree twigs onto 3-mo-old juvenile trees. Although the grafting had a positive effect on the micropropagation of mature material, the multiplication rate of 1.5 new shoots per expiant did not compare to the organogenic capacity of younger materials. Shoot and root elongation as well as acclimatization to ex vitro conditions were carried out in a temporary immersion culture of juvenile material using BioMINT® bioreactors. A 3.5-fold increase in shoot elongation and a 4-fold increase in root elongation were achieved compared to material cultured on semisolid media. Furthermore, this culture system allowed for 98% effectiveness in the soil adaptation of the in vitro grown plants. The scaled-up multiplication capacity over a period of 6 mo calculated for the system is above 16,000 plants per mother plant with young materials but is only 125 with mature materials. |
doi_str_mv | 10.1007/s11627-010-9280-0 |
format | Article |
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This species confronts serious problems due to both overexploitation of its natural populations and its susceptibility to the Meliaceae borer Hypsipyla grandella, which destroys the apical meristems and produces structural deformations. The rapid introduction of new varieties through clonal forestry has been demonstrated to be the most effective way to improve the production of perennial plantation species. In this work, we report both a protocol for the rejuvenation of elite mature trees of C. odorata and the optimization of an in vitro culture system to scale up micropropagation. Several media formulations and the use of temporary immersion culture in bioreactors were evaluated. The addition of 20% coconut water to TY17 medium increased the number of adventitious shoots from hypocotyl segments to an average number of 4.68 shoots per expiant. To replace coconut water and to define the culture medium, several cytokinins were tested at various concentrations; however, none of them produced the effect of coconut water. Rejuvenation of elite mature individuals was investigated by ex vitro grafting of mature tree twigs onto 3-mo-old juvenile trees. Although the grafting had a positive effect on the micropropagation of mature material, the multiplication rate of 1.5 new shoots per expiant did not compare to the organogenic capacity of younger materials. Shoot and root elongation as well as acclimatization to ex vitro conditions were carried out in a temporary immersion culture of juvenile material using BioMINT® bioreactors. A 3.5-fold increase in shoot elongation and a 4-fold increase in root elongation were achieved compared to material cultured on semisolid media. Furthermore, this culture system allowed for 98% effectiveness in the soil adaptation of the in vitro grown plants. The scaled-up multiplication capacity over a period of 6 mo calculated for the system is above 16,000 plants per mother plant with young materials but is only 125 with mature materials.</description><identifier>ISSN: 1054-5476</identifier><identifier>EISSN: 1475-2689</identifier><identifier>DOI: 10.1007/s11627-010-9280-0</identifier><language>eng</language><publisher>New York: Springer</publisher><subject>Acclimatization ; Adventitious shoots ; Biomedical and Life Sciences ; Bioreactors ; Cell Biology ; Coconuts ; Cytokinins ; Developmental Biology ; Graftage ; Hypocotyls ; Life Sciences ; Micropropagation ; Natural populations ; Overexploitation ; Plant Breeding/Biotechnology ; Plant Genetics and Genomics ; Plant Sciences ; Plant species ; Plants ; Rejuvenation ; Shoots ; Timber industry ; Trees</subject><ispartof>In vitro cellular & developmental biology. Plant, 2010-04, Vol.46 (2), p.149-160</ispartof><rights>2010 Society for In Vitro Biology</rights><rights>The Society for In Vitro Biology 2010</rights><rights>Copyright Society for In Vitro Biology Apr 2010</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c337t-83f168f15496d31359bfadf78f79157a4cb87f8c94cb97262f03c9979d53d1103</citedby><cites>FETCH-LOGICAL-c337t-83f168f15496d31359bfadf78f79157a4cb87f8c94cb97262f03c9979d53d1103</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/40663782$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/40663782$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,776,780,799,27903,27904,41467,42536,51297,57995,58228</link.rule.ids></links><search><creatorcontrib>Peña-Ramírez, Yuri Jorge</creatorcontrib><creatorcontrib>Juárez-Gómez, Juan</creatorcontrib><creatorcontrib>Gómez-López, Lucero</creatorcontrib><creatorcontrib>Jerónimo-Pérez, José L.</creatorcontrib><creatorcontrib>García-Sheseña, Israel</creatorcontrib><creatorcontrib>González-Rodríguez, José A.</creatorcontrib><creatorcontrib>Robert, Manuel L.</creatorcontrib><title>Multiple adventitious shoot formation in Spanish Red Cedar ( Cedreto odorata L.) cultured in vitro using juvenile and mature tissues: an improved micropropagation protocol for a highly valuable tropical tree species</title><title>In vitro cellular & developmental biology. Plant</title><addtitle>In Vitro Cell.Dev.Biol.-Plant</addtitle><description>Cedrela odorata L. is a valuable tropical tree widely appreciated for its wood. This species confronts serious problems due to both overexploitation of its natural populations and its susceptibility to the Meliaceae borer Hypsipyla grandella, which destroys the apical meristems and produces structural deformations. The rapid introduction of new varieties through clonal forestry has been demonstrated to be the most effective way to improve the production of perennial plantation species. In this work, we report both a protocol for the rejuvenation of elite mature trees of C. odorata and the optimization of an in vitro culture system to scale up micropropagation. Several media formulations and the use of temporary immersion culture in bioreactors were evaluated. The addition of 20% coconut water to TY17 medium increased the number of adventitious shoots from hypocotyl segments to an average number of 4.68 shoots per expiant. To replace coconut water and to define the culture medium, several cytokinins were tested at various concentrations; however, none of them produced the effect of coconut water. Rejuvenation of elite mature individuals was investigated by ex vitro grafting of mature tree twigs onto 3-mo-old juvenile trees. Although the grafting had a positive effect on the micropropagation of mature material, the multiplication rate of 1.5 new shoots per expiant did not compare to the organogenic capacity of younger materials. Shoot and root elongation as well as acclimatization to ex vitro conditions were carried out in a temporary immersion culture of juvenile material using BioMINT® bioreactors. A 3.5-fold increase in shoot elongation and a 4-fold increase in root elongation were achieved compared to material cultured on semisolid media. Furthermore, this culture system allowed for 98% effectiveness in the soil adaptation of the in vitro grown plants. The scaled-up multiplication capacity over a period of 6 mo calculated for the system is above 16,000 plants per mother plant with young materials but is only 125 with mature materials.</description><subject>Acclimatization</subject><subject>Adventitious shoots</subject><subject>Biomedical and Life Sciences</subject><subject>Bioreactors</subject><subject>Cell Biology</subject><subject>Coconuts</subject><subject>Cytokinins</subject><subject>Developmental Biology</subject><subject>Graftage</subject><subject>Hypocotyls</subject><subject>Life Sciences</subject><subject>Micropropagation</subject><subject>Natural populations</subject><subject>Overexploitation</subject><subject>Plant Breeding/Biotechnology</subject><subject>Plant Genetics and Genomics</subject><subject>Plant Sciences</subject><subject>Plant species</subject><subject>Plants</subject><subject>Rejuvenation</subject><subject>Shoots</subject><subject>Timber industry</subject><subject>Trees</subject><issn>1054-5476</issn><issn>1475-2689</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</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>eNp9Uctu1DAUjRCVKC0fwALpihUs0vqR2DE7NCoUaSokHmvLE9szHmXiYDsj9Uv5HW4URHes7tHVedyrU1WvKbmhhMjbTKlgsiaU1Ip1pCbPqkvayLZmolPPEZO2qdtGihfVy5yPhCCTysvq98M8lDANDow9u7GEEuKcIR9iLOBjOhlcjBBG-D6ZMeQDfHMWNs6aBO-WmVyJEG1MphjY3ryHHg3nhCTUnENJEeYcxj0cZ_QPS9BoAW2RAyXkPLv8AXcQTlOKZ9SdQp8i4sns13DEJfZxWO4BA4ewPwyPcDbDbHbohxFT6M2AwDnIk-uDy9fVhTdDdq_-zqvq56e7H5v7evv185fNx23dcy5L3XFPRedp2yhhOeWt2nljvey8VLSVpul3nfRdrxAoyQTzhPdKSWVbbikl_Kp6u_rikb_wlaKPcU4jRmpBkNgywpBEVxI-lnNyXk8pnEx61JTopT691qexFL3Upxdjtmoycse9S0_G_xO9WUXHXGL6l9IQIbjsGP8DU7qruA</recordid><startdate>20100401</startdate><enddate>20100401</enddate><creator>Peña-Ramírez, Yuri Jorge</creator><creator>Juárez-Gómez, Juan</creator><creator>Gómez-López, Lucero</creator><creator>Jerónimo-Pérez, José L.</creator><creator>García-Sheseña, Israel</creator><creator>González-Rodríguez, José A.</creator><creator>Robert, Manuel L.</creator><general>Springer</general><general>Springer-Verlag</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</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>AEUYN</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></search><sort><creationdate>20100401</creationdate><title>Multiple adventitious shoot formation in Spanish Red Cedar ( Cedreto odorata L.) cultured in vitro using juvenile and mature tissues: an improved micropropagation protocol for a highly valuable tropical tree species</title><author>Peña-Ramírez, Yuri Jorge ; Juárez-Gómez, Juan ; Gómez-López, Lucero ; Jerónimo-Pérez, José L. ; García-Sheseña, Israel ; González-Rodríguez, José A. ; Robert, Manuel L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c337t-83f168f15496d31359bfadf78f79157a4cb87f8c94cb97262f03c9979d53d1103</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Acclimatization</topic><topic>Adventitious shoots</topic><topic>Biomedical and Life Sciences</topic><topic>Bioreactors</topic><topic>Cell Biology</topic><topic>Coconuts</topic><topic>Cytokinins</topic><topic>Developmental Biology</topic><topic>Graftage</topic><topic>Hypocotyls</topic><topic>Life Sciences</topic><topic>Micropropagation</topic><topic>Natural populations</topic><topic>Overexploitation</topic><topic>Plant Breeding/Biotechnology</topic><topic>Plant Genetics and Genomics</topic><topic>Plant Sciences</topic><topic>Plant species</topic><topic>Plants</topic><topic>Rejuvenation</topic><topic>Shoots</topic><topic>Timber industry</topic><topic>Trees</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Peña-Ramírez, Yuri Jorge</creatorcontrib><creatorcontrib>Juárez-Gómez, Juan</creatorcontrib><creatorcontrib>Gómez-López, Lucero</creatorcontrib><creatorcontrib>Jerónimo-Pérez, José L.</creatorcontrib><creatorcontrib>García-Sheseña, Israel</creatorcontrib><creatorcontrib>González-Rodríguez, José A.</creatorcontrib><creatorcontrib>Robert, Manuel L.</creatorcontrib><collection>CrossRef</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 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>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><jtitle>In vitro cellular & developmental biology. Plant</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Peña-Ramírez, Yuri Jorge</au><au>Juárez-Gómez, Juan</au><au>Gómez-López, Lucero</au><au>Jerónimo-Pérez, José L.</au><au>García-Sheseña, Israel</au><au>González-Rodríguez, José A.</au><au>Robert, Manuel L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Multiple adventitious shoot formation in Spanish Red Cedar ( Cedreto odorata L.) cultured in vitro using juvenile and mature tissues: an improved micropropagation protocol for a highly valuable tropical tree species</atitle><jtitle>In vitro cellular & developmental biology. Plant</jtitle><stitle>In Vitro Cell.Dev.Biol.-Plant</stitle><date>2010-04-01</date><risdate>2010</risdate><volume>46</volume><issue>2</issue><spage>149</spage><epage>160</epage><pages>149-160</pages><issn>1054-5476</issn><eissn>1475-2689</eissn><abstract>Cedrela odorata L. is a valuable tropical tree widely appreciated for its wood. This species confronts serious problems due to both overexploitation of its natural populations and its susceptibility to the Meliaceae borer Hypsipyla grandella, which destroys the apical meristems and produces structural deformations. The rapid introduction of new varieties through clonal forestry has been demonstrated to be the most effective way to improve the production of perennial plantation species. In this work, we report both a protocol for the rejuvenation of elite mature trees of C. odorata and the optimization of an in vitro culture system to scale up micropropagation. Several media formulations and the use of temporary immersion culture in bioreactors were evaluated. The addition of 20% coconut water to TY17 medium increased the number of adventitious shoots from hypocotyl segments to an average number of 4.68 shoots per expiant. To replace coconut water and to define the culture medium, several cytokinins were tested at various concentrations; however, none of them produced the effect of coconut water. Rejuvenation of elite mature individuals was investigated by ex vitro grafting of mature tree twigs onto 3-mo-old juvenile trees. Although the grafting had a positive effect on the micropropagation of mature material, the multiplication rate of 1.5 new shoots per expiant did not compare to the organogenic capacity of younger materials. Shoot and root elongation as well as acclimatization to ex vitro conditions were carried out in a temporary immersion culture of juvenile material using BioMINT® bioreactors. A 3.5-fold increase in shoot elongation and a 4-fold increase in root elongation were achieved compared to material cultured on semisolid media. Furthermore, this culture system allowed for 98% effectiveness in the soil adaptation of the in vitro grown plants. The scaled-up multiplication capacity over a period of 6 mo calculated for the system is above 16,000 plants per mother plant with young materials but is only 125 with mature materials.</abstract><cop>New York</cop><pub>Springer</pub><doi>10.1007/s11627-010-9280-0</doi><tpages>12</tpages></addata></record> |
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subjects | Acclimatization Adventitious shoots Biomedical and Life Sciences Bioreactors Cell Biology Coconuts Cytokinins Developmental Biology Graftage Hypocotyls Life Sciences Micropropagation Natural populations Overexploitation Plant Breeding/Biotechnology Plant Genetics and Genomics Plant Sciences Plant species Plants Rejuvenation Shoots Timber industry Trees |
title | Multiple adventitious shoot formation in Spanish Red Cedar ( Cedreto odorata L.) cultured in vitro using juvenile and mature tissues: an improved micropropagation protocol for a highly valuable tropical tree species |
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