2019
DOI: 10.1007/s42535-019-00069-6
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High frequency in vitro plantlet regeneration in Solanum trilobatum L., an important ethno-medicinal plant and confirmation of genetic fidelity of R1 plantlets by using ISSR and RAPD markers

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Cited by 19 publications
(4 citation statements)
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“…2 b) and a maximum of 3.75 ± 0.12 roots per shoot with 5.22 ± 0.32 cm root length was induced on the medium (Table 3 ). Earlier researchers established the beneficial effect of reducing the concentration of MS basal medium on in vitro rooting in Quercus sobur L., Solanum trilobatum and Wrightia tomentosa 47 49 . Half strength MS basal medium suited the best for in vitro rooting in regenerated T. coccinea shootlet s .…”
Section: Resultsmentioning
confidence: 99%
“…2 b) and a maximum of 3.75 ± 0.12 roots per shoot with 5.22 ± 0.32 cm root length was induced on the medium (Table 3 ). Earlier researchers established the beneficial effect of reducing the concentration of MS basal medium on in vitro rooting in Quercus sobur L., Solanum trilobatum and Wrightia tomentosa 47 49 . Half strength MS basal medium suited the best for in vitro rooting in regenerated T. coccinea shootlet s .…”
Section: Resultsmentioning
confidence: 99%
“…Kumlay and Ercisli, (2015) also observed the highest number of shoots per explant in S. tuberosum in combination with BAP+GA3. In Solanum trilobatum, Sreenu et al (2019) found the highest mean number of shoots differentiated de novo augmented with TDZ+NAA. Similarly, Ya-Long Qin et al (2017) observed the maximum regeneration frequency at 0.5 mg/L BA+1.0 mg/L 2,4-D from S. torvum leaf and stem segments derived callus, as it was observed by Ghan Singh et al (2022a) showing the synergistic effect of both auxin+cytokinin combinations.…”
Section: ) Regeneration From Leaf Derived Callusmentioning
confidence: 89%
“…These results, as per SCoT, ISSR, and RAPD analyses, suggest that there is apparent variation within the species Corynandra chelidonii. The SCoT, RAPD, and ISSR markers were demonstrated to be not only effective techniques to screen genetic differences but also quick, very consistent, cost-effective and one can investigate the whole genome of the plant randomly (Jogam et al 2020;Pendli et al 2019;Rohela et al 2020). The use of more than one molecular marker to detect the genetic dissimilarity is always useful for better results because every molecular marker has its benefits and drawbacks.…”
Section: Relative Differentiation and Estimate Of Gene Flowmentioning
confidence: 99%