2012
DOI: 10.1093/aobpla/pls054
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A genetically stable rooting protocol for propagating a threatened medicinal plant--Celastrus paniculatus

Abstract: Nodal segments, obtained from 12 years-old mature plant, were used as explants for in vitro propagation of Celastrus paniculatus, an important medicinal plant of India. Shoot multiplication was achieved by repeated transfer of mother explants and subculturing of in vitro produced shoot clumps on MS medium supplemented with various concentrations of BAP alone or in combination with auxin (IAA or NAA). In vitro raised shoots were rooted under ex vitro condition. Genetic fidelity of the regenerated plants was ass… Show more

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Cited by 29 publications
(12 citation statements)
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“…Celastrus paniculatus (Phulwaria et al 2013) and Morinda coreia (Shekhawat et al 2015a). It was observed that nodal segments with one node died due to the effect of HgCl 2 during surface sterilization but the middle nodes were survived even after HgCl 2 treatment when the nodal explants were used with 2-3 nodes.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…Celastrus paniculatus (Phulwaria et al 2013) and Morinda coreia (Shekhawat et al 2015a). It was observed that nodal segments with one node died due to the effect of HgCl 2 during surface sterilization but the middle nodes were survived even after HgCl 2 treatment when the nodal explants were used with 2-3 nodes.…”
Section: Resultsmentioning
confidence: 99%
“…The maximum number of shoots (8.2 ± 0.17 shoots/culture) were produced when the mother explants were subcultured on fresh medium (Table. 3). Shoot multiplication during repeated transfer may be due to inhibition of apical dominance which stimulates basal dormant meristematic cells to produce young shoots (Phulwaria et al 2013). This approach for shoot multiplication has been used in several plant species (Panwar et al 2012).…”
Section: Multiplication Of Shoots In Culturesmentioning
confidence: 99%
“…Every species require optimum pH which promote maximum shoot formation. Molecular markers, mainly RAPD, have been widely used for testing the genetic fidelity among in vitro regenerated plantlets in a number of plant species (Savita et al 2012;Phulwaria et al 2012) owing to their simplicity, cost-effectiveness and lower DNA requirement for analysis.…”
Section: Discussionmentioning
confidence: 99%
“…may lead to genomic changes in the in vitro raised plantlets (Jain 2001) Thus, analysis of the genetic homogeneity of tissue culture raised plants is a prerequisite for their exploitation on a commercial scale . DNA-based molecular markers are useful tools for analysis of the genetic fidelity of micropropagated plantlets (Phulwaria et al 2012;Yadav et al 2013). Limited number of shoots (3.0) regeneration have been reported earlier from seedling derived explants e.g., node (Rajasubramaniam & Pardha Saradhi 1994) and hypocotyl calli (Rajasubramaniam & Pardha Saradhi 1997) of P. fraternus.…”
Section: Introductionmentioning
confidence: 99%
“…Highest percent of bud break and multiple shoots (4.3 ± 0.5) was obtained in MS medium + BA (1.0 mg/L), and 100 % rooting was achieved in half-strength MS medium supplemented with 0.5 mg/L NAA which was followed by acclimatisation in sterile soil and sand (3:1) giving 70 % survival rate. However, the most elaborated, rapid and successful protocol has been described by Phulwaria et al ( 2013 ).…”
Section: Celastrus Paniculatus Willdmentioning
confidence: 99%