Serveur d'exploration sur l'oranger

Attention, ce site est en cours de développement !
Attention, site généré par des moyens informatiques à partir de corpus bruts.
Les informations ne sont donc pas validées.

In vitro micropropagation of Dracaena sanderiana Sander ex Mast: An important indoor ornamental plant

Identifieur interne : 000D47 ( Pmc/Corpus ); précédent : 000D46; suivant : 000D48

In vitro micropropagation of Dracaena sanderiana Sander ex Mast: An important indoor ornamental plant

Auteurs : Junaid Aslam ; Abdul Mujib ; Maheshwar Prasad Sharma

Source :

RBID : PMC:3730903

Abstract

A protocol has been developed for in vitro plant regeneration from a nodal explant of Dracaena sanderiana Sander ex Mast. Nodal explant showed high callus induction potentiality on MS medium supplemented with 6.78 μM 2,4-dichlorophenoxyacetic acid (2,4-D) followed by 46.5 μM chlorophenoxy acetic acid (CPA). The highest frequency of shoot regeneration (85%) and number of shoots per explant (5.6) were obtained on medium supplemented with 7.84 μM N6-benzylaminopurine (BA). Rooting was high on MS solid compared to liquid medium when added with 7.38 μM indole-3-butyric acid (IBA). Fifty percent of the roots were also directly rooted as microcuttings on soil rite, sand and peat mixture (1:1:1). In vitro and ex vitro raised plantlets were used for acclimatization. More than 90% of the plantlets was successfully acclimatized and established in plastic pots. Ex vitro transferred plantlets were normal without any phenotypic aberrations.


Url:
DOI: 10.1016/j.sjbs.2012.11.005
PubMed: 23961221
PubMed Central: 3730903

Links to Exploration step

PMC:3730903

Le document en format XML

<record>
<TEI>
<teiHeader>
<fileDesc>
<titleStmt>
<title xml:lang="en">
<italic>In vitro</italic>
micropropagation of
<italic>Dracaena sanderiana</italic>
Sander ex Mast: An important indoor ornamental plant</title>
<author>
<name sortKey="Aslam, Junaid" sort="Aslam, Junaid" uniqKey="Aslam J" first="Junaid" last="Aslam">Junaid Aslam</name>
<affiliation>
<nlm:aff id="aff1">Cellular Differentiation and Molecular Genetics Section, Department of Botany, Hamdard University, New Delhi 110 062, India</nlm:aff>
</affiliation>
<affiliation>
<nlm:aff id="aff2">Department of Biotechnology, Jamia Hamdard (Hamdard University), New Delhi 110 062, India</nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Mujib, Abdul" sort="Mujib, Abdul" uniqKey="Mujib A" first="Abdul" last="Mujib">Abdul Mujib</name>
<affiliation>
<nlm:aff id="aff1">Cellular Differentiation and Molecular Genetics Section, Department of Botany, Hamdard University, New Delhi 110 062, India</nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Sharma, Maheshwar Prasad" sort="Sharma, Maheshwar Prasad" uniqKey="Sharma M" first="Maheshwar Prasad" last="Sharma">Maheshwar Prasad Sharma</name>
<affiliation>
<nlm:aff id="aff1">Cellular Differentiation and Molecular Genetics Section, Department of Botany, Hamdard University, New Delhi 110 062, India</nlm:aff>
</affiliation>
</author>
</titleStmt>
<publicationStmt>
<idno type="wicri:source">PMC</idno>
<idno type="pmid">23961221</idno>
<idno type="pmc">3730903</idno>
<idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3730903</idno>
<idno type="RBID">PMC:3730903</idno>
<idno type="doi">10.1016/j.sjbs.2012.11.005</idno>
<date when="2012">2012</date>
<idno type="wicri:Area/Pmc/Corpus">000D47</idno>
</publicationStmt>
<sourceDesc>
<biblStruct>
<analytic>
<title xml:lang="en" level="a" type="main">
<italic>In vitro</italic>
micropropagation of
<italic>Dracaena sanderiana</italic>
Sander ex Mast: An important indoor ornamental plant</title>
<author>
<name sortKey="Aslam, Junaid" sort="Aslam, Junaid" uniqKey="Aslam J" first="Junaid" last="Aslam">Junaid Aslam</name>
<affiliation>
<nlm:aff id="aff1">Cellular Differentiation and Molecular Genetics Section, Department of Botany, Hamdard University, New Delhi 110 062, India</nlm:aff>
</affiliation>
<affiliation>
<nlm:aff id="aff2">Department of Biotechnology, Jamia Hamdard (Hamdard University), New Delhi 110 062, India</nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Mujib, Abdul" sort="Mujib, Abdul" uniqKey="Mujib A" first="Abdul" last="Mujib">Abdul Mujib</name>
<affiliation>
<nlm:aff id="aff1">Cellular Differentiation and Molecular Genetics Section, Department of Botany, Hamdard University, New Delhi 110 062, India</nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Sharma, Maheshwar Prasad" sort="Sharma, Maheshwar Prasad" uniqKey="Sharma M" first="Maheshwar Prasad" last="Sharma">Maheshwar Prasad Sharma</name>
<affiliation>
<nlm:aff id="aff1">Cellular Differentiation and Molecular Genetics Section, Department of Botany, Hamdard University, New Delhi 110 062, India</nlm:aff>
</affiliation>
</author>
</analytic>
<series>
<title level="j">Saudi Journal of Biological Sciences</title>
<idno type="ISSN">1319-562X</idno>
<idno type="eISSN">2213-7106</idno>
<imprint>
<date when="2012">2012</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc>
<textClass></textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">
<p>A protocol has been developed for
<italic>in vitro</italic>
plant regeneration from a nodal explant of
<italic>Dracaena sanderiana</italic>
Sander ex Mast. Nodal explant showed high callus induction potentiality on MS medium supplemented with 6.78 μM 2,4-dichlorophenoxyacetic acid (2,4-D) followed by 46.5 μM chlorophenoxy acetic acid (CPA). The highest frequency of shoot regeneration (85%) and number of shoots per explant (5.6) were obtained on medium supplemented with 7.84 μM N
<sup>6</sup>
-benzylaminopurine (BA). Rooting was high on MS solid compared to liquid medium when added with 7.38 μM indole-3-butyric acid (IBA). Fifty percent of the roots were also directly rooted as microcuttings on soil rite, sand and peat mixture (1:1:1).
<italic>In vitro</italic>
and
<italic>ex vitro</italic>
raised plantlets were used for acclimatization. More than 90% of the plantlets was successfully acclimatized and established in plastic pots.
<italic>Ex vitro</italic>
transferred plantlets were normal without any phenotypic aberrations.</p>
</div>
</front>
</TEI>
<pmc article-type="research-article">
<pmc-comment>The publisher of this article does not allow downloading of the full text in XML form.</pmc-comment>
<front>
<journal-meta>
<journal-id journal-id-type="nlm-ta">Saudi J Biol Sci</journal-id>
<journal-title-group>
<journal-title>Saudi Journal of Biological Sciences</journal-title>
</journal-title-group>
<issn pub-type="ppub">1319-562X</issn>
<issn pub-type="epub">2213-7106</issn>
</journal-meta>
<article-meta>
<article-id pub-id-type="pmid">23961221</article-id>
<article-id pub-id-type="pmc">3730903</article-id>
<article-id pub-id-type="publisher-id">SJBS200</article-id>
<article-id pub-id-type="doi">10.1016/j.sjbs.2012.11.005</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Original Article</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>
<italic>In vitro</italic>
micropropagation of
<italic>Dracaena sanderiana</italic>
Sander ex Mast: An important indoor ornamental plant</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Aslam</surname>
<given-names>Junaid</given-names>
</name>
<xref rid="aff1" ref-type="aff">a</xref>
<xref rid="aff2" ref-type="aff">b</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Mujib</surname>
<given-names>Abdul</given-names>
</name>
<email>amujib3@yahoo.co.in</email>
<xref rid="aff1" ref-type="aff">a</xref>
<xref rid="cor1" ref-type="corresp"></xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Sharma</surname>
<given-names>Maheshwar Prasad</given-names>
</name>
<xref rid="aff1" ref-type="aff">a</xref>
</contrib>
</contrib-group>
<aff id="aff1">
<label>a</label>
Cellular Differentiation and Molecular Genetics Section, Department of Botany, Hamdard University, New Delhi 110 062, India</aff>
<aff id="aff2">
<label>b</label>
Department of Biotechnology, Jamia Hamdard (Hamdard University), New Delhi 110 062, India</aff>
<author-notes>
<corresp id="cor1">
<label></label>
Corresponding author. Tel.: +9109868112120; fax: +911126059683.
<email>amujib3@yahoo.co.in</email>
</corresp>
</author-notes>
<pub-date pub-type="pmc-release">
<day>17</day>
<month>11</month>
<year>2012</year>
</pub-date>
<pmc-comment> PMC Release delay is 0 months and 0 days and was based on .</pmc-comment>
<pub-date pub-type="epub">
<day>17</day>
<month>11</month>
<year>2012</year>
</pub-date>
<pub-date pub-type="ppub">
<month>1</month>
<year>2013</year>
</pub-date>
<volume>20</volume>
<issue>1</issue>
<fpage>63</fpage>
<lpage>68</lpage>
<history>
<date date-type="received">
<day>1</day>
<month>8</month>
<year>2012</year>
</date>
<date date-type="rev-recd">
<day>4</day>
<month>11</month>
<year>2012</year>
</date>
<date date-type="accepted">
<day>6</day>
<month>11</month>
<year>2012</year>
</date>
</history>
<permissions>
<copyright-statement>© 2013 King Saud University. Production and Hosting by Elsevier B.V. All rights reserved.</copyright-statement>
<copyright-year>2012</copyright-year>
<copyright-holder></copyright-holder>
</permissions>
<abstract>
<p>A protocol has been developed for
<italic>in vitro</italic>
plant regeneration from a nodal explant of
<italic>Dracaena sanderiana</italic>
Sander ex Mast. Nodal explant showed high callus induction potentiality on MS medium supplemented with 6.78 μM 2,4-dichlorophenoxyacetic acid (2,4-D) followed by 46.5 μM chlorophenoxy acetic acid (CPA). The highest frequency of shoot regeneration (85%) and number of shoots per explant (5.6) were obtained on medium supplemented with 7.84 μM N
<sup>6</sup>
-benzylaminopurine (BA). Rooting was high on MS solid compared to liquid medium when added with 7.38 μM indole-3-butyric acid (IBA). Fifty percent of the roots were also directly rooted as microcuttings on soil rite, sand and peat mixture (1:1:1).
<italic>In vitro</italic>
and
<italic>ex vitro</italic>
raised plantlets were used for acclimatization. More than 90% of the plantlets was successfully acclimatized and established in plastic pots.
<italic>Ex vitro</italic>
transferred plantlets were normal without any phenotypic aberrations.</p>
</abstract>
<kwd-group>
<title>Keywords</title>
<kwd>
<italic>In vitro rooting</italic>
</kwd>
<kwd>
<italic>Dracaena sanderiana</italic>
</kwd>
<kwd>Indoor ornamental</kwd>
<kwd>Plant regeneration</kwd>
<kwd>Shoot multiplication</kwd>
</kwd-group>
</article-meta>
</front>
</pmc>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Wicri/Bois/explor/OrangerV1/Data/Pmc/Corpus
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000D47 | SxmlIndent | more

Ou

HfdSelect -h $EXPLOR_AREA/Data/Pmc/Corpus/biblio.hfd -nk 000D47 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Wicri/Bois
   |area=    OrangerV1
   |flux=    Pmc
   |étape=   Corpus
   |type=    RBID
   |clé=     PMC:3730903
   |texte=   In vitro micropropagation of Dracaena sanderiana Sander ex Mast: An important indoor ornamental plant
}}

Pour générer des pages wiki

HfdIndexSelect -h $EXPLOR_AREA/Data/Pmc/Corpus/RBID.i   -Sk "pubmed:23961221" \
       | HfdSelect -Kh $EXPLOR_AREA/Data/Pmc/Corpus/biblio.hfd   \
       | NlmPubMed2Wicri -a OrangerV1 

Wicri

This area was generated with Dilib version V0.6.25.
Data generation: Sat Dec 3 17:11:04 2016. Site generation: Wed Mar 6 18:18:32 2024