Root culturing of Faidherbia=Acacia albida as a source of explants for shoot regeneration
Identifieur interne : 000E83 ( Istex/Corpus ); précédent : 000E82; suivant : 000E84Root culturing of Faidherbia=Acacia albida as a source of explants for shoot regeneration
Auteurs : J. Ahée ; E. DuhouxSource :
- Plant Cell, Tissue and Organ Culture [ 0167-6857 ] ; 1994-02-01.
Abstract
Abstract: Root culture ofFaidherbia=Acacia albida (Del.) A. Chev. can be maintained over several months by successively subculturing excised roots in modified Bonner and Devirian medium, which was found to be the best of the three media compositions tested. Adding auxins had an inhibiting effect on root growth characteristics. Mesoinositol at 0.05 mM slightly enhanced the overall elongation rate, and sucrose at 59 mM significantly increased root elongation. The effect of sucrose could not be replaced by glucose. Subcultured roots showed progressively less elongation in successive transfers. Shoots were regenerated in vitro from root segments beginning with the first passage on 1/5 strength MS medium. The large variability in the root elongation rate indicates that this technique provides an effective way to select clones with good potential for tap root growth.
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DOI: 10.1007/BF00037723
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ISTEX:89F5358D7F044B3406680E5712E28F0DFB1860E8Le document en format XML
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Duhoux</name><affiliation><mods:affiliation>Université Paris VII et Biotechnologie (des Symbioses Forestiéres Tropicales (ORSTOM/CIRAD-Forêt), 45 Bis Avenue de la Belle Gabrielle, 94736, Nogent-sur-Marne, France</mods:affiliation></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">ISTEX</idno><idno type="RBID">ISTEX:89F5358D7F044B3406680E5712E28F0DFB1860E8</idno><date when="1994" year="1994">1994</date><idno type="doi">10.1007/BF00037723</idno><idno type="url">https://api.istex.fr/document/89F5358D7F044B3406680E5712E28F0DFB1860E8/fulltext/pdf</idno><idno type="wicri:Area/Istex/Corpus">000E83</idno></publicationStmt><sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">Root culturing of Faidherbia=Acacia albida as a source of explants for shoot regeneration</title><author><name sortKey="Ahee, J" sort="Ahee, J" uniqKey="Ahee J" first="J." last="Ahée">J. Ahée</name><affiliation><mods:affiliation>Biotechnologie des Symbioses Forestières Tropicales (ORSTOM/CIRAD-Forêt), 45 Bis Avenue de la Belle Gabrielle, 94736, Nogent-sur-Marne, France</mods:affiliation></affiliation></author><author><name sortKey="Duhoux, E" sort="Duhoux, E" uniqKey="Duhoux E" first="E." last="Duhoux">E. Duhoux</name><affiliation><mods:affiliation>Université Paris VII et Biotechnologie (des Symbioses Forestiéres Tropicales (ORSTOM/CIRAD-Forêt), 45 Bis Avenue de la Belle Gabrielle, 94736, Nogent-sur-Marne, France</mods:affiliation></affiliation></author></analytic><monogr></monogr><series><title level="j">Plant Cell, Tissue and Organ Culture</title><title level="j" type="sub">An International Journal on Biotechnology of Higher Plants</title><title level="j" type="abbrev">Plant Cell Tiss Organ Cult</title><idno type="ISSN">0167-6857</idno><idno type="eISSN">1573-5044</idno><imprint><publisher>Kluwer Academic Publishers</publisher><pubPlace>Dordrecht</pubPlace><date type="published" when="1994-02-01">1994-02-01</date><biblScope unit="volume">36</biblScope><biblScope unit="issue">2</biblScope><biblScope unit="page" from="219">219</biblScope><biblScope unit="page" to="225">225</biblScope></imprint><idno type="ISSN">0167-6857</idno></series><idno type="istex">89F5358D7F044B3406680E5712E28F0DFB1860E8</idno><idno type="DOI">10.1007/BF00037723</idno><idno type="ArticleID">BF00037723</idno><idno type="ArticleID">Art12</idno></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0167-6857</idno></seriesStmt></fileDesc><profileDesc><textClass></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Abstract: Root culture ofFaidherbia=Acacia albida (Del.) A. Chev. can be maintained over several months by successively subculturing excised roots in modified Bonner and Devirian medium, which was found to be the best of the three media compositions tested. Adding auxins had an inhibiting effect on root growth characteristics. Mesoinositol at 0.05 mM slightly enhanced the overall elongation rate, and sucrose at 59 mM significantly increased root elongation. The effect of sucrose could not be replaced by glucose. Subcultured roots showed progressively less elongation in successive transfers. Shoots were regenerated in vitro from root segments beginning with the first passage on 1/5 strength MS medium. The large variability in the root elongation rate indicates that this technique provides an effective way to select clones with good potential for tap root growth.</div></front></TEI><istex><corpusName>springer</corpusName><author><json:item><name>J. Ahée</name><affiliations><json:string>Biotechnologie des Symbioses Forestières Tropicales (ORSTOM/CIRAD-Forêt), 45 Bis Avenue de la Belle Gabrielle, 94736, Nogent-sur-Marne, France</json:string></affiliations></json:item><json:item><name>E. Duhoux</name><affiliations><json:string>Université Paris VII et Biotechnologie (des Symbioses Forestiéres Tropicales (ORSTOM/CIRAD-Forêt), 45 Bis Avenue de la Belle Gabrielle, 94736, Nogent-sur-Marne, France</json:string></affiliations></json:item></author><articleId><json:string>BF00037723</json:string><json:string>Art12</json:string></articleId><language><json:string>eng</json:string></language><originalGenre><json:string>OriginalPaper</json:string></originalGenre><abstract>Abstract: Root culture ofFaidherbia=Acacia albida (Del.) A. Chev. can be maintained over several months by successively subculturing excised roots in modified Bonner and Devirian medium, which was found to be the best of the three media compositions tested. Adding auxins had an inhibiting effect on root growth characteristics. Mesoinositol at 0.05 mM slightly enhanced the overall elongation rate, and sucrose at 59 mM significantly increased root elongation. The effect of sucrose could not be replaced by glucose. Subcultured roots showed progressively less elongation in successive transfers. Shoots were regenerated in vitro from root segments beginning with the first passage on 1/5 strength MS medium. The large variability in the root elongation rate indicates that this technique provides an effective way to select clones with good potential for tap root growth.</abstract><qualityIndicators><score>4.339</score><pdfVersion>1.3</pdfVersion><pdfPageSize>540 x 735 pts</pdfPageSize><refBibsNative>false</refBibsNative><keywordCount>0</keywordCount><abstractCharCount>873</abstractCharCount><pdfWordCount>2779</pdfWordCount><pdfCharCount>16768</pdfCharCount><pdfPageCount>7</pdfPageCount><abstractWordCount>130</abstractWordCount></qualityIndicators><title>Root culturing of Faidherbia=Acacia albida as a source of explants for shoot regeneration</title><genre><json:string>research-article</json:string></genre><host><volume>36</volume><pages><last>225</last><first>219</first></pages><issn><json:string>0167-6857</json:string></issn><issue>2</issue><subject><json:item><value>Plant Sciences</value></json:item><json:item><value>Plant Physiology</value></json:item></subject><journalId><json:string>11240</json:string></journalId><genre><json:string>journal</json:string></genre><language><json:string>unknown</json:string></language><eissn><json:string>1573-5044</json:string></eissn><title>Plant Cell, Tissue and Organ Culture</title><publicationDate>1994</publicationDate><copyrightDate>1994</copyrightDate></host><publicationDate>1994</publicationDate><copyrightDate>1994</copyrightDate><doi><json:string>10.1007/BF00037723</json:string></doi><id>89F5358D7F044B3406680E5712E28F0DFB1860E8</id><score>0.22236216</score><fulltext><json:item><original>true</original><mimetype>application/pdf</mimetype><extension>pdf</extension><uri>https://api.istex.fr/document/89F5358D7F044B3406680E5712E28F0DFB1860E8/fulltext/pdf</uri></json:item><json:item><original>false</original><mimetype>application/zip</mimetype><extension>zip</extension><uri>https://api.istex.fr/document/89F5358D7F044B3406680E5712E28F0DFB1860E8/fulltext/zip</uri></json:item><istex:fulltextTEI uri="https://api.istex.fr/document/89F5358D7F044B3406680E5712E28F0DFB1860E8/fulltext/tei"><teiHeader><fileDesc><titleStmt><title level="a" type="main" xml:lang="en">Root culturing of Faidherbia=Acacia albida as a source of explants for shoot regeneration</title><respStmt><resp>Références bibliographiques récupérées via GROBID</resp><name resp="ISTEX-API">ISTEX-API (INIST-CNRS)</name></respStmt></titleStmt><publicationStmt><authority>ISTEX</authority><publisher>Kluwer Academic Publishers</publisher><pubPlace>Dordrecht</pubPlace><availability><p>Kluwer Academic Publishers, 1994</p></availability><date>1993-04-16</date></publicationStmt><notesStmt><note>Original Research Paper</note></notesStmt><sourceDesc><biblStruct type="inbook"><analytic><title level="a" type="main" xml:lang="en">Root culturing of Faidherbia=Acacia albida as a source of explants for shoot regeneration</title><author xml:id="author-1"><persName><forename type="first">J.</forename><surname>Ahée</surname></persName><affiliation>Biotechnologie des Symbioses Forestières Tropicales (ORSTOM/CIRAD-Forêt), 45 Bis Avenue de la Belle Gabrielle, 94736, Nogent-sur-Marne, France</affiliation></author><author xml:id="author-2"><persName><forename type="first">E.</forename><surname>Duhoux</surname></persName><affiliation>Université Paris VII et Biotechnologie (des Symbioses Forestiéres Tropicales (ORSTOM/CIRAD-Forêt), 45 Bis Avenue de la Belle Gabrielle, 94736, Nogent-sur-Marne, France</affiliation></author></analytic><monogr><title level="j">Plant Cell, Tissue and Organ Culture</title><title level="j" type="sub">An International Journal on Biotechnology of Higher Plants</title><title level="j" type="abbrev">Plant Cell Tiss Organ Cult</title><idno type="journal-ID">11240</idno><idno type="pISSN">0167-6857</idno><idno type="eISSN">1573-5044</idno><idno type="issue-article-count">20</idno><idno type="volume-issue-count">3</idno><imprint><publisher>Kluwer Academic Publishers</publisher><pubPlace>Dordrecht</pubPlace><date type="published" when="1994-02-01"></date><biblScope unit="volume">36</biblScope><biblScope unit="issue">2</biblScope><biblScope unit="page" from="219">219</biblScope><biblScope unit="page" to="225">225</biblScope></imprint></monogr><idno type="istex">89F5358D7F044B3406680E5712E28F0DFB1860E8</idno><idno type="DOI">10.1007/BF00037723</idno><idno type="ArticleID">BF00037723</idno><idno type="ArticleID">Art12</idno></biblStruct></sourceDesc></fileDesc><profileDesc><creation><date>1993-04-16</date></creation><langUsage><language ident="en">en</language></langUsage><abstract xml:lang="en"><p>Abstract: Root culture ofFaidherbia=Acacia albida (Del.) A. Chev. can be maintained over several months by successively subculturing excised roots in modified Bonner and Devirian medium, which was found to be the best of the three media compositions tested. Adding auxins had an inhibiting effect on root growth characteristics. Mesoinositol at 0.05 mM slightly enhanced the overall elongation rate, and sucrose at 59 mM significantly increased root elongation. The effect of sucrose could not be replaced by glucose. Subcultured roots showed progressively less elongation in successive transfers. Shoots were regenerated in vitro from root segments beginning with the first passage on 1/5 strength MS medium. The large variability in the root elongation rate indicates that this technique provides an effective way to select clones with good potential for tap root growth.</p></abstract><textClass><keywords scheme="Journal Subject"><list><head>Life Sciences</head><item><term>Plant Sciences</term></item><item><term>Plant Physiology</term></item></list></keywords></textClass></profileDesc><revisionDesc><change when="1993-04-16">Created</change><change when="1994-02-01">Published</change><change xml:id="refBibs-istex" who="#ISTEX-API" when="2016-09-22">References added</change></revisionDesc></teiHeader></istex:fulltextTEI><json:item><original>false</original><mimetype>text/plain</mimetype><extension>txt</extension><uri>https://api.istex.fr/document/89F5358D7F044B3406680E5712E28F0DFB1860E8/fulltext/txt</uri></json:item></fulltext><metadata><istex:metadataXml wicri:clean="Springer, Publisher found" wicri:toSee="no header"><istex:xmlDeclaration>version="1.0" 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explants for shoot regeneration</ArticleTitle><ArticleCategory>Original Research Paper</ArticleCategory><ArticleFirstPage>219</ArticleFirstPage><ArticleLastPage>225</ArticleLastPage><ArticleHistory><RegistrationDate><Year>2004</Year><Month>4</Month><Day>24</Day></RegistrationDate><Received><Year>1993</Year><Month>4</Month><Day>16</Day></Received><Accepted><Year>1993</Year><Month>10</Month><Day>16</Day></Accepted></ArticleHistory><ArticleCopyright><CopyrightHolderName>Kluwer Academic Publishers</CopyrightHolderName><CopyrightYear>1994</CopyrightYear></ArticleCopyright><ArticleGrants Type="Regular"><MetadataGrant Grant="OpenAccess"></MetadataGrant><AbstractGrant Grant="OpenAccess"></AbstractGrant><BodyPDFGrant Grant="Restricted"></BodyPDFGrant><BodyHTMLGrant Grant="Restricted"></BodyHTMLGrant><BibliographyGrant Grant="Restricted"></BibliographyGrant><ESMGrant 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Bis Avenue de la Belle Gabrielle</Street><Postcode>94736</Postcode><City>Nogent-sur-Marne</City><Country>France</Country></OrgAddress></Affiliation></AuthorGroup><Abstract ID="Abs1" Language="En"><Heading>Abstract</Heading><Para>Root culture of<Emphasis Type="Italic">Faidherbia=Acacia albida</Emphasis> (Del.) A. Chev. can be maintained over several months by successively subculturing excised roots in modified Bonner and Devirian medium, which was found to be the best of the three media compositions tested. Adding auxins had an inhibiting effect on root growth characteristics. Mesoinositol at 0.05 mM slightly enhanced the overall elongation rate, and sucrose at 59 mM significantly increased root elongation. The effect of sucrose could not be replaced by glucose. Subcultured roots showed progressively less elongation in successive transfers. Shoots were regenerated in vitro from root segments beginning with the first passage on 1/5 strength MS medium.</Para><Para>The large variability in the root elongation rate indicates that this technique provides an effective way to select clones with good potential for tap root growth.</Para></Abstract><KeywordGroup Language="En"><Heading>Key words</Heading><Keyword><Emphasis Type="Italic">Acacia albida</Emphasis></Keyword><Keyword>intraspecific variation</Keyword><Keyword>in vitro</Keyword><Keyword>root</Keyword></KeywordGroup></ArticleHeader><NoBody></NoBody></Article></Issue></Volume></Journal></Publisher></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Root culturing of Faidherbia=Acacia albida as a source of explants for shoot regeneration</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Root culturing ofFaidherbia=Acacia albida as a source of explants for shoot regeneration</title></titleInfo><name type="personal"><namePart type="given">J.</namePart><namePart type="family">Ahée</namePart><affiliation>Biotechnologie des Symbioses Forestières Tropicales (ORSTOM/CIRAD-Forêt), 45 Bis Avenue de la Belle Gabrielle, 94736, Nogent-sur-Marne, France</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">E.</namePart><namePart type="family">Duhoux</namePart><affiliation>Université Paris VII et Biotechnologie (des Symbioses Forestiéres Tropicales (ORSTOM/CIRAD-Forêt), 45 Bis Avenue de la Belle Gabrielle, 94736, Nogent-sur-Marne, France</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="research-article" displayLabel="OriginalPaper"></genre><originInfo><publisher>Kluwer Academic Publishers</publisher><place><placeTerm type="text">Dordrecht</placeTerm></place><dateCreated encoding="w3cdtf">1993-04-16</dateCreated><dateIssued encoding="w3cdtf">1994-02-01</dateIssued><copyrightDate encoding="w3cdtf">1994</copyrightDate></originInfo><language><languageTerm type="code" authority="rfc3066">en</languageTerm><languageTerm type="code" authority="iso639-2b">eng</languageTerm></language><physicalDescription><internetMediaType>text/html</internetMediaType></physicalDescription><abstract lang="en">Abstract: Root culture ofFaidherbia=Acacia albida (Del.) A. Chev. can be maintained over several months by successively subculturing excised roots in modified Bonner and Devirian medium, which was found to be the best of the three media compositions tested. Adding auxins had an inhibiting effect on root growth characteristics. Mesoinositol at 0.05 mM slightly enhanced the overall elongation rate, and sucrose at 59 mM significantly increased root elongation. The effect of sucrose could not be replaced by glucose. Subcultured roots showed progressively less elongation in successive transfers. Shoots were regenerated in vitro from root segments beginning with the first passage on 1/5 strength MS medium. 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