ArticleScientific reports2020
Shoot organogenesis and somatic embryogenesis from leaf and root explants of Scaevola sericea.
Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.
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12 citing papers in PubMed, 57 citations in OpenAlex.
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- The improvement of the in vitro plant regeneration in barley with the epigenetic modifier of histone acetylation, trichostatin A.Journal of applied genetics · 2024Article
- Improvement of Culture Conditions and Plant Growth Regulators for In Vitro Callus Induction and Plant Regeneration inPlants (Basel, Switzerland) · 2023Article
- Efficient Plant Regeneration System from Leaf Explant Cultures ofPlants (Basel, Switzerland) · 2023Article
- Application ofPlants (Basel, Switzerland) · 2022Review
- Use of polylactic acid microvessel to obtain microplantlets of3 Biotech · 2021Article
- Efficient plant regeneration from embryogenic cell suspension cultures of Euonymus alatus.Scientific reports · 2021Article
- Genetic modification of Water spinach (Ipomoea aquatica), a genoprotective perennial leafy green.Physiologia plantarumArticle
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Authors and funding
14 authors at 5 institutions in 1 country.
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No grant is acknowledged in the PubMed record.
Abstract
An efficient regeneration system via shoot organogenesis and somatic embryogenesis from in vitro leaf and root explants was established for Scaevola sericea for the first time. The highest axillary shoot proliferation coefficient (4.8) was obtained on Murashige and Skoog (MS) medium supplemented with 1.0 mg/L 6-benzyladenine (BA) and 0.1 mg/L α-naphthaleneacetic acid (NAA) every 45 days. Young in vitro leaves and roots, which were used as explants, were cultured onto medium supplemented with different plant growth regulators. Our results showed that only cytokinins BA and thidiazuron (TDZ), could induce adventitious shoots and somatic embryos from leaf and root explants. The optimal medium to achieve this was MS medium supplemented with 2.5 mg/L BA and which induced most adventitious shoots (2.7) and somatic embryos (17.3) from leaf explants within 30 days. From root explants, 1.1 adventitious shoots and 7.6 somatic embryos could be induced on MS medium supplemented with 2.5 mg/L TDZ. Histological observation showed that both somatic embryos and adventitious shoots were originated from homogeneous parenchyma and the development of somatic embryos was visible. Maximum rooting percentage (99.0%) was achieved on half-strength MS medium supplemented with 2.5 mg/L NAA. Well-rooted plantlets, which were transplanted into a substrate of pure river sand, displayed a high survival percentage of 91.7% after transplanting for 45 days while the best substrate for plantlet growth was river sand: coral sand (1:1).
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