In vitro micropropagation of Dracaena sanderiana Sander ex Mast: An important indoor ornamental plant
Identifieur interne : 001435 ( Main/Exploration ); précédent : 001434; suivant : 001436In vitro micropropagation of Dracaena sanderiana Sander ex Mast: An important indoor ornamental plant
Auteurs : Junaid Aslam [Inde] ; Abdul Mujib [Inde] ; Maheshwar Prasad Sharma [Inde]Source :
- Saudi Journal of Biological Sciences [ 1319-562X ] ; 2012.
Abstract
A protocol has been developed for
Url:
DOI: 10.1016/j.sjbs.2012.11.005
PubMed: 23961221
PubMed Central: 3730903
Affiliations:
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micropropagation of <italic>Dracaena sanderiana</italic>
Sander ex Mast: An important indoor ornamental plant</title>
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<affiliation wicri:level="1"><nlm:aff id="aff2">Department of Biotechnology, Jamia Hamdard (Hamdard University), New Delhi 110 062, India</nlm:aff>
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<author><name sortKey="Sharma, Maheshwar Prasad" sort="Sharma, Maheshwar Prasad" uniqKey="Sharma M" first="Maheshwar Prasad" last="Sharma">Maheshwar Prasad Sharma</name>
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<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 wicri:level="1"><nlm:aff id="aff1">Cellular Differentiation and Molecular Genetics Section, Department of Botany, Hamdard University, New Delhi 110 062, India</nlm:aff>
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<country xml:lang="fr">Inde</country>
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<series><title level="j">Saudi Journal of Biological Sciences</title>
<idno type="ISSN">1319-562X</idno>
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<imprint><date when="2012">2012</date>
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<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>
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<name sortKey="Aslam, Junaid" sort="Aslam, Junaid" uniqKey="Aslam J" first="Junaid" last="Aslam">Junaid Aslam</name>
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<name sortKey="Sharma, Maheshwar Prasad" sort="Sharma, Maheshwar Prasad" uniqKey="Sharma M" first="Maheshwar Prasad" last="Sharma">Maheshwar Prasad Sharma</name>
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