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In vitro multiplication of cashew (Anacardium occidentale L.) using shoot node explants of glasshouse-raised plants
Using glasshouse-raised plants (1 month, 1 year and 5 years old), factors affecting shoot development from shoot nodes of two Brazilian and one Tanzanian elite selections of cashew (Anacardium occidentale L.) were assessed. Sprouting of buds decreased strongly with increasing age of mother plants. S...
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Published in: | Plant cell reports 1999-02, Vol.18 (6), p.456-461 |
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description | Using glasshouse-raised plants (1 month, 1 year and 5 years old), factors affecting shoot development from shoot nodes of two Brazilian and one Tanzanian elite selections of cashew (Anacardium occidentale L.) were assessed. Sprouting of buds decreased strongly with increasing age of mother plants. Solidified media, mainly when purified agar was used, gave better results than liquid medium. Murashige and Skoog salts containing 1/2-strength macroelements were the most suitable for bud sprouting and shoot elongation. Vitamins and sucrose concentration did not have a significant effect but by replacing 20 g/l sucrose with glucose or maltose all estimated parameters were improved. Gibberellins supported bud sprouting and shoot elongation but blocked rooting. Shoots developed in the presence of cytokinins were short and produced axillary branches. Activated charcoal, cultivation of explants in darkness for the first 7 days and superoptimal temperature (35 degrees C) decreased bud sprouting and supported shoot elongation. Microshoots rooted in vitro at a frequency of 42% when cultured for 5 days with 100 micromolar indole-3-butyric acid. Over 40% of rooted microshoots survived weaning. |
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Sprouting of buds decreased strongly with increasing age of mother plants. Solidified media, mainly when purified agar was used, gave better results than liquid medium. Murashige and Skoog salts containing 1/2-strength macroelements were the most suitable for bud sprouting and shoot elongation. Vitamins and sucrose concentration did not have a significant effect but by replacing 20 g/l sucrose with glucose or maltose all estimated parameters were improved. Gibberellins supported bud sprouting and shoot elongation but blocked rooting. Shoots developed in the presence of cytokinins were short and produced axillary branches. Activated charcoal, cultivation of explants in darkness for the first 7 days and superoptimal temperature (35 degrees C) decreased bud sprouting and supported shoot elongation. Microshoots rooted in vitro at a frequency of 42% when cultured for 5 days with 100 micromolar indole-3-butyric acid. Over 40% of rooted microshoots survived weaning.</description><identifier>ISSN: 0721-7714</identifier><identifier>EISSN: 1432-203X</identifier><identifier>DOI: 10.1007/s002990050603</identifier><identifier>CODEN: PCRPD8</identifier><language>eng</language><publisher>Berlin: Springer</publisher><subject>Activated charcoal ; age ; air temperature ; Anacardium occidentale ; Biological and medical sciences ; Biotechnology ; buds ; Charcoal ; cultivars ; culture media ; cytokinins ; dark ; Eukaryotic cell cultures ; explants ; Fundamental and applied biological sciences. Psychology ; gibberellins ; glucose ; growth ; In vitro propagation: entire plant regeneration from tissues and cell cultures ; indole butyric acid ; maltose ; Methods. Procedures. Technologies ; micropropagation ; Plant cells and fungal cells ; plant development ; rooting ; shoots ; sprouting ; sucrose ; tissue culture ; Vitamins</subject><ispartof>Plant cell reports, 1999-02, Vol.18 (6), p.456-461</ispartof><rights>1999 INIST-CNRS</rights><rights>Springer-Verlag Berlin Heidelberg 1999</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c346t-6eb4495bfeecb6ffed86d6619916a2b333874d7a61456fff06acc9805a8801d93</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=1696405$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Boggetti, B</creatorcontrib><creatorcontrib>Jasik, J</creatorcontrib><creatorcontrib>Mantell, S</creatorcontrib><title>In vitro multiplication of cashew (Anacardium occidentale L.) using shoot node explants of glasshouse-raised plants</title><title>Plant cell reports</title><description>Using glasshouse-raised plants (1 month, 1 year and 5 years old), factors affecting shoot development from shoot nodes of two Brazilian and one Tanzanian elite selections of cashew (Anacardium occidentale L.) were assessed. Sprouting of buds decreased strongly with increasing age of mother plants. Solidified media, mainly when purified agar was used, gave better results than liquid medium. Murashige and Skoog salts containing 1/2-strength macroelements were the most suitable for bud sprouting and shoot elongation. Vitamins and sucrose concentration did not have a significant effect but by replacing 20 g/l sucrose with glucose or maltose all estimated parameters were improved. Gibberellins supported bud sprouting and shoot elongation but blocked rooting. Shoots developed in the presence of cytokinins were short and produced axillary branches. Activated charcoal, cultivation of explants in darkness for the first 7 days and superoptimal temperature (35 degrees C) decreased bud sprouting and supported shoot elongation. Microshoots rooted in vitro at a frequency of 42% when cultured for 5 days with 100 micromolar indole-3-butyric acid. Over 40% of rooted microshoots survived weaning.</description><subject>Activated charcoal</subject><subject>age</subject><subject>air temperature</subject><subject>Anacardium occidentale</subject><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>buds</subject><subject>Charcoal</subject><subject>cultivars</subject><subject>culture media</subject><subject>cytokinins</subject><subject>dark</subject><subject>Eukaryotic cell cultures</subject><subject>explants</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>gibberellins</subject><subject>glucose</subject><subject>growth</subject><subject>In vitro propagation: entire plant regeneration from tissues and cell cultures</subject><subject>indole butyric acid</subject><subject>maltose</subject><subject>Methods. Procedures. Technologies</subject><subject>micropropagation</subject><subject>Plant cells and fungal cells</subject><subject>plant development</subject><subject>rooting</subject><subject>shoots</subject><subject>sprouting</subject><subject>sucrose</subject><subject>tissue culture</subject><subject>Vitamins</subject><issn>0721-7714</issn><issn>1432-203X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><recordid>eNpdkMFrFDEUxoMouLYePRtERA9TXyaZTHIsRdvCQg-14G14m0m2KbPJmjej9b83ZQvSnt7h9_s-Ph5j7wScCID-KwG01gJ0oEG-YCuhZNu0IH--ZCvoW9H0vVCv2RuiO4AKe71idJn47ziXzHfLNMf9FB3OMSeeA3dIt_4P_3ya0GEZ47Lj2bk4-jTj5Pn65AtfKKYtp9ucZ57y6Lm_30-YZnrIbyekihbyTcFIfuQHdsxeBZzIv328R-zm-7cfZxfN-ur88ux03Tip9Nxov1HKdpvgvdvoEPxo9Ki1sFZobDdSStOrsUctVFdxAI3OWQMdGgNitPKIfTr07kv-tXiah10k56c6wtdVg-g7K4TRVfzwTLzLS0l122CMMp3UUlWpOUiuZKLiw7AvcYfl7yBgePj_8OT_1f_4WIrkcAoFk4v0P6StVtBV7f1BC5gH3Jaq3Fy3IGTtElKClv8AMsSOnA</recordid><startdate>19990201</startdate><enddate>19990201</enddate><creator>Boggetti, B</creator><creator>Jasik, J</creator><creator>Mantell, S</creator><general>Springer</general><general>Springer Nature B.V</general><scope>FBQ</scope><scope>IQODW</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></search><sort><creationdate>19990201</creationdate><title>In vitro multiplication of cashew (Anacardium occidentale L.) using shoot node explants of glasshouse-raised plants</title><author>Boggetti, B ; Jasik, J ; Mantell, S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c346t-6eb4495bfeecb6ffed86d6619916a2b333874d7a61456fff06acc9805a8801d93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Activated charcoal</topic><topic>age</topic><topic>air temperature</topic><topic>Anacardium occidentale</topic><topic>Biological and medical sciences</topic><topic>Biotechnology</topic><topic>buds</topic><topic>Charcoal</topic><topic>cultivars</topic><topic>culture media</topic><topic>cytokinins</topic><topic>dark</topic><topic>Eukaryotic cell cultures</topic><topic>explants</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>gibberellins</topic><topic>glucose</topic><topic>growth</topic><topic>In vitro propagation: entire plant regeneration from tissues and cell cultures</topic><topic>indole butyric acid</topic><topic>maltose</topic><topic>Methods. Procedures. Technologies</topic><topic>micropropagation</topic><topic>Plant cells and fungal cells</topic><topic>plant development</topic><topic>rooting</topic><topic>shoots</topic><topic>sprouting</topic><topic>sucrose</topic><topic>tissue culture</topic><topic>Vitamins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Boggetti, B</creatorcontrib><creatorcontrib>Jasik, J</creatorcontrib><creatorcontrib>Mantell, S</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</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>ProQuest Health and Medical</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>ProQuest Agriculture & Environmental Science Database</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</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 (Proquest) (PQ_SDU_P3)</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>ProQuest Biological Science Journals</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><jtitle>Plant cell reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Boggetti, B</au><au>Jasik, J</au><au>Mantell, S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In vitro multiplication of cashew (Anacardium occidentale L.) using shoot node explants of glasshouse-raised plants</atitle><jtitle>Plant cell reports</jtitle><date>1999-02-01</date><risdate>1999</risdate><volume>18</volume><issue>6</issue><spage>456</spage><epage>461</epage><pages>456-461</pages><issn>0721-7714</issn><eissn>1432-203X</eissn><coden>PCRPD8</coden><abstract>Using glasshouse-raised plants (1 month, 1 year and 5 years old), factors affecting shoot development from shoot nodes of two Brazilian and one Tanzanian elite selections of cashew (Anacardium occidentale L.) were assessed. Sprouting of buds decreased strongly with increasing age of mother plants. Solidified media, mainly when purified agar was used, gave better results than liquid medium. Murashige and Skoog salts containing 1/2-strength macroelements were the most suitable for bud sprouting and shoot elongation. Vitamins and sucrose concentration did not have a significant effect but by replacing 20 g/l sucrose with glucose or maltose all estimated parameters were improved. Gibberellins supported bud sprouting and shoot elongation but blocked rooting. Shoots developed in the presence of cytokinins were short and produced axillary branches. Activated charcoal, cultivation of explants in darkness for the first 7 days and superoptimal temperature (35 degrees C) decreased bud sprouting and supported shoot elongation. Microshoots rooted in vitro at a frequency of 42% when cultured for 5 days with 100 micromolar indole-3-butyric acid. Over 40% of rooted microshoots survived weaning.</abstract><cop>Berlin</cop><pub>Springer</pub><doi>10.1007/s002990050603</doi><tpages>6</tpages></addata></record> |
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subjects | Activated charcoal age air temperature Anacardium occidentale Biological and medical sciences Biotechnology buds Charcoal cultivars culture media cytokinins dark Eukaryotic cell cultures explants Fundamental and applied biological sciences. Psychology gibberellins glucose growth In vitro propagation: entire plant regeneration from tissues and cell cultures indole butyric acid maltose Methods. Procedures. Technologies micropropagation Plant cells and fungal cells plant development rooting shoots sprouting sucrose tissue culture Vitamins |
title | In vitro multiplication of cashew (Anacardium occidentale L.) using shoot node explants of glasshouse-raised plants |
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