ArticleJournal, genetic engineering & biotechnology2021
Picloram-induced enhanced callus-mediated regeneration, acclimatization, and genetic clonality assessment of gerbera.
Article in Journal, genetic engineering & biotechnology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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Who cites it
6 citing papers in PubMed.
- In Vitro Regeneration Strategies in Woody Citrus of Northeast India (Plants (Basel, Switzerland) · 2026Article
- Elite genotype selection through antioxidant and antimicrobial activities, in vitro multiplication with3 Biotech · 2025Article
- Cytotoxic activity of callus extract from3 Biotech · 2024Article
- Optimized medium composition in Physalis alkekengi callus culture altered nitric oxide level for inducing antioxidant enzyme activities and secondary metabolites.Scientific reports · 2024Article
- Efficient organogenesis and taxifolin production system from mature zygotic embryos and needles in larch.Forestry research · 2023Article
- Biotechnology of banana (Musa spp.): multi-dimensional progress and prospect of in vitro-mediated system.Applied microbiology and biotechnology · 2022Review
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Authors and funding
2 authors.
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Abstract
backgroundGerbera jamesonii Bolus ex Hooker f. (African daisy) is listed among the top five most important ornamental plants in the global floricultural industry. To satisfy its demand, the floriculture industry relies on reproducible and effective propagation protocol while retaining the genetic uniformity of G. jamesonii. The present study, for the first time, reports the potential of picloram for enhanced induction of organogenic calli from leaves of G. jamesonii and its high-frequency indirect regeneration.
resultsThe fastest induction of calli with maximum fresh and dry weight was recorded in the Murashige and Skoog (MS) semisolid medium supplemented with 1 mg/l picloram. In addition, callus induction was observed in 2,4-dichlorophenoxy acetic acid- and α-napthaleneaceticacid-supplemented media but with delayed response and reduced fresh and dry weight. The proliferated calli were transferred to shoot induction media containing MS salt and 0.5-1 mg/l N
conclusionsThe results of the present study should be of interest for commercial propagation and mutagenesis- as well as genetic transformation-related research.
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