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Influence of genotype and gelling agents on in vitro regeneration by organogenesis in sunflower
Fourteen recombinant inbred lines of sunflower (Helianthus annuus L.) and their parents (PAC-2 and RHA-266) were tested for their organogenesis ability. Seeds were surface sterilized and germinated on hormone free half strength MS basal medium containing 10 g l(-1) sucrose solidified with five diffe...
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Published in: | Plant cell, tissue and organ culture tissue and organ culture, 1999, Vol.59 (1), p.65-69 |
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creator | Flores Berrios, E Gentzbittel, L Serieys, H Alibert, G Sarrafi, A |
description | Fourteen recombinant inbred lines of sunflower (Helianthus annuus L.) and their parents (PAC-2 and RHA-266) were tested for their organogenesis ability. Seeds were surface sterilized and germinated on hormone free half strength MS basal medium containing 10 g l(-1) sucrose solidified with five different gelling agents: Phytagar (Gibco laboratoires) 3 g l(-1), Phytagel (Sigma) 3 g l(-1), Agarose (Sigma) 5 g l(-1), Arcagel (Sigma) 4 g l(-1) and Agar-Agar (Fisher France) 7 g l(-1). Cotyledons from 2-day-old seedlings were split in half and the four explants of each seed were cultived in 55 mm diameter petri dishes containing 10 ml of MS medium supplemented with 50 micromolar KNO(3), 1 micromolar myo-inositol, 5 micromolar casein hydrolysate, 4.4 micromolar of BA and 5.4 micromolar of NAA solidified with the same gelling agents. The experimental design was a randomized complete block with 3 replications. A replicate for each genotype consisted of ten petri dishes containing four explants. The statistical analysis showed significant differences among genotypes and gelling agents. Of the fourteen recombinant inbred lines tested C93' presented the highest values for all regeneration traits in the five different media and it was better than the best parent. Agarose and Agar-Agar were more better than other gelling agents for shoot induction. |
doi_str_mv | 10.1023/A:1006433607812 |
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Seeds were surface sterilized and germinated on hormone free half strength MS basal medium containing 10 g l(-1) sucrose solidified with five different gelling agents: Phytagar (Gibco laboratoires) 3 g l(-1), Phytagel (Sigma) 3 g l(-1), Agarose (Sigma) 5 g l(-1), Arcagel (Sigma) 4 g l(-1) and Agar-Agar (Fisher France) 7 g l(-1). Cotyledons from 2-day-old seedlings were split in half and the four explants of each seed were cultived in 55 mm diameter petri dishes containing 10 ml of MS medium supplemented with 50 micromolar KNO(3), 1 micromolar myo-inositol, 5 micromolar casein hydrolysate, 4.4 micromolar of BA and 5.4 micromolar of NAA solidified with the same gelling agents. The experimental design was a randomized complete block with 3 replications. A replicate for each genotype consisted of ten petri dishes containing four explants. The statistical analysis showed significant differences among genotypes and gelling agents. Of the fourteen recombinant inbred lines tested C93' presented the highest values for all regeneration traits in the five different media and it was better than the best parent. Agarose and Agar-Agar were more better than other gelling agents for shoot induction.</description><identifier>ISSN: 0167-6857</identifier><identifier>EISSN: 1573-5044</identifier><identifier>DOI: 10.1023/A:1006433607812</identifier><identifier>CODEN: PTCEDJ</identifier><language>eng</language><publisher>Dordrecht: Springer</publisher><subject>benzyladenine ; Biological and medical sciences ; Biotechnology ; culture media ; dose response ; Eukaryotic cell cultures ; Fundamental and applied biological sciences. Psychology ; gels ; genetic variation ; genotype ; Helianthus annuus ; in vitro culture ; In vitro propagation: entire plant regeneration from tissues and cell cultures ; inbred lines ; Methods. Procedures. Technologies ; naphthaleneacetic acid ; organogenesis ; Plant cells and fungal cells ; regenerative ability</subject><ispartof>Plant cell, tissue and organ culture, 1999, Vol.59 (1), p.65-69</ispartof><rights>2000 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c252t-9e1a0883f4e2056e834b860a56d3884a82de688f45ae4d9cd1509567f114b3c83</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1426493$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Flores Berrios, E</creatorcontrib><creatorcontrib>Gentzbittel, L</creatorcontrib><creatorcontrib>Serieys, H</creatorcontrib><creatorcontrib>Alibert, G</creatorcontrib><creatorcontrib>Sarrafi, A</creatorcontrib><title>Influence of genotype and gelling agents on in vitro regeneration by organogenesis in sunflower</title><title>Plant cell, tissue and organ culture</title><description>Fourteen recombinant inbred lines of sunflower (Helianthus annuus L.) and their parents (PAC-2 and RHA-266) were tested for their organogenesis ability. Seeds were surface sterilized and germinated on hormone free half strength MS basal medium containing 10 g l(-1) sucrose solidified with five different gelling agents: Phytagar (Gibco laboratoires) 3 g l(-1), Phytagel (Sigma) 3 g l(-1), Agarose (Sigma) 5 g l(-1), Arcagel (Sigma) 4 g l(-1) and Agar-Agar (Fisher France) 7 g l(-1). Cotyledons from 2-day-old seedlings were split in half and the four explants of each seed were cultived in 55 mm diameter petri dishes containing 10 ml of MS medium supplemented with 50 micromolar KNO(3), 1 micromolar myo-inositol, 5 micromolar casein hydrolysate, 4.4 micromolar of BA and 5.4 micromolar of NAA solidified with the same gelling agents. The experimental design was a randomized complete block with 3 replications. A replicate for each genotype consisted of ten petri dishes containing four explants. The statistical analysis showed significant differences among genotypes and gelling agents. Of the fourteen recombinant inbred lines tested C93' presented the highest values for all regeneration traits in the five different media and it was better than the best parent. Agarose and Agar-Agar were more better than other gelling agents for shoot induction.</description><subject>benzyladenine</subject><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>culture media</subject><subject>dose response</subject><subject>Eukaryotic cell cultures</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>gels</subject><subject>genetic variation</subject><subject>genotype</subject><subject>Helianthus annuus</subject><subject>in vitro culture</subject><subject>In vitro propagation: entire plant regeneration from tissues and cell cultures</subject><subject>inbred lines</subject><subject>Methods. Procedures. Technologies</subject><subject>naphthaleneacetic acid</subject><subject>organogenesis</subject><subject>Plant cells and fungal cells</subject><subject>regenerative ability</subject><issn>0167-6857</issn><issn>1573-5044</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><recordid>eNotkEtLAzEUhYMoWKtrl2bhdvTmORl3pfgoFFxo18PtTDJExqQkU6X_3pS6OpyPj7M4hNwyeGDAxePiiQFoKYSG2jB-RmZM1aJSIOU5mQHTdaWNqi_JVc5fUFQh2Yy0q-DGvQ2dpdHRwYY4HXaWYuhLGUcfBoqFTpnGQH2gP35KkSZbmE04-UK3BxrTgCEeWfb5qOV9mY2_Nl2TC4djtjf_OSebl-fP5Vu1fn9dLRfrquOKT1VjGYIxwknLQWlrhNwaDah0L4yRaHhvtTFOKrSyb7qeKWiUrh1jcis6I-bk_rS7w9zh6BKGzud2l_w3pkPLJNeyEUW7O2kOY4tDKsrmgwMTwJvyltDiD73QYCw</recordid><startdate>1999</startdate><enddate>1999</enddate><creator>Flores Berrios, E</creator><creator>Gentzbittel, L</creator><creator>Serieys, H</creator><creator>Alibert, G</creator><creator>Sarrafi, A</creator><general>Springer</general><scope>FBQ</scope><scope>IQODW</scope></search><sort><creationdate>1999</creationdate><title>Influence of genotype and gelling agents on in vitro regeneration by organogenesis in sunflower</title><author>Flores Berrios, E ; Gentzbittel, L ; Serieys, H ; Alibert, G ; Sarrafi, A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c252t-9e1a0883f4e2056e834b860a56d3884a82de688f45ae4d9cd1509567f114b3c83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>benzyladenine</topic><topic>Biological and medical sciences</topic><topic>Biotechnology</topic><topic>culture media</topic><topic>dose response</topic><topic>Eukaryotic cell cultures</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>gels</topic><topic>genetic variation</topic><topic>genotype</topic><topic>Helianthus annuus</topic><topic>in vitro culture</topic><topic>In vitro propagation: entire plant regeneration from tissues and cell cultures</topic><topic>inbred lines</topic><topic>Methods. Procedures. Technologies</topic><topic>naphthaleneacetic acid</topic><topic>organogenesis</topic><topic>Plant cells and fungal cells</topic><topic>regenerative ability</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Flores Berrios, E</creatorcontrib><creatorcontrib>Gentzbittel, L</creatorcontrib><creatorcontrib>Serieys, H</creatorcontrib><creatorcontrib>Alibert, G</creatorcontrib><creatorcontrib>Sarrafi, A</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><jtitle>Plant cell, tissue and organ culture</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Flores Berrios, E</au><au>Gentzbittel, L</au><au>Serieys, H</au><au>Alibert, G</au><au>Sarrafi, A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Influence of genotype and gelling agents on in vitro regeneration by organogenesis in sunflower</atitle><jtitle>Plant cell, tissue and organ culture</jtitle><date>1999</date><risdate>1999</risdate><volume>59</volume><issue>1</issue><spage>65</spage><epage>69</epage><pages>65-69</pages><issn>0167-6857</issn><eissn>1573-5044</eissn><coden>PTCEDJ</coden><abstract>Fourteen recombinant inbred lines of sunflower (Helianthus annuus L.) and their parents (PAC-2 and RHA-266) were tested for their organogenesis ability. Seeds were surface sterilized and germinated on hormone free half strength MS basal medium containing 10 g l(-1) sucrose solidified with five different gelling agents: Phytagar (Gibco laboratoires) 3 g l(-1), Phytagel (Sigma) 3 g l(-1), Agarose (Sigma) 5 g l(-1), Arcagel (Sigma) 4 g l(-1) and Agar-Agar (Fisher France) 7 g l(-1). Cotyledons from 2-day-old seedlings were split in half and the four explants of each seed were cultived in 55 mm diameter petri dishes containing 10 ml of MS medium supplemented with 50 micromolar KNO(3), 1 micromolar myo-inositol, 5 micromolar casein hydrolysate, 4.4 micromolar of BA and 5.4 micromolar of NAA solidified with the same gelling agents. The experimental design was a randomized complete block with 3 replications. A replicate for each genotype consisted of ten petri dishes containing four explants. The statistical analysis showed significant differences among genotypes and gelling agents. Of the fourteen recombinant inbred lines tested C93' presented the highest values for all regeneration traits in the five different media and it was better than the best parent. Agarose and Agar-Agar were more better than other gelling agents for shoot induction.</abstract><cop>Dordrecht</cop><pub>Springer</pub><doi>10.1023/A:1006433607812</doi><tpages>5</tpages></addata></record> |
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subjects | benzyladenine Biological and medical sciences Biotechnology culture media dose response Eukaryotic cell cultures Fundamental and applied biological sciences. Psychology gels genetic variation genotype Helianthus annuus in vitro culture In vitro propagation: entire plant regeneration from tissues and cell cultures inbred lines Methods. Procedures. Technologies naphthaleneacetic acid organogenesis Plant cells and fungal cells regenerative ability |
title | Influence of genotype and gelling agents on in vitro regeneration by organogenesis in sunflower |
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