In vitro plant regeneration of Christmas cactus (Schlumbergera truncata (Haw.) Moran) by indirect morphogenesis
Autor: | Oksana Chornobrov, Svitlana Bilous |
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Jazyk: | angličtina |
Rok vydání: | 2021 |
Předmět: |
040101 forestry
0106 biological sciences biology shoot proliferation Regeneration (biology) fungi explant Morphogenesis food and beverages nutrient medium Forestry 04 agricultural and veterinary sciences SD1-669.5 biology.organism_classification 01 natural sciences microclonal propagation Schlumbergera truncata callus Botany Cactus 0401 agriculture forestry and fisheries christmas cactus 010606 plant biology & botany |
Zdroj: | Folia Forestalia Polonica: Series A-Forestry, Vol 63, Iss 1, Pp 68-73 (2021) |
ISSN: | 2199-5907 |
Popis: | Plants of Schlumbergera truncata (Haw.) Moran were obtained by indirect morphogenesis from the segment section of shoots in vitro, they were multiplied and rooted. Also were determined the effect of the lighting regime, the composition of the nutrient medium on the consistency and frequency of callus formation. The studies were conducted during 2016–2018. The mode of effective sterilization (more than 90%) of S. truncata plant explants using 0.1% HgCl2 for 7–8 min was established. Optimal conditions for the induction of callus formation in stem node segments of S. truncata plants (rate more than 90% and significant growth) were created on MS (Murashige and Skoog 1962) nutrient medium supplemented with 1.0 mg/l BAP (6-benzylaminopurine) and 0.3 mg/l NAA (1-naphthylacetic acid) under conditions of placement on the nutrient medium and doing a significant number of cuts on the explants. The light intensity of 2.0–3.0 klx, obtained by a callus of dense consistency of dark green pigmentation, when using the thermostat condition without illumination, the callus had loose consistency, dark yellow pigmentation. It is established that the influence of the lighting regime and the composition of the nutrient medium on the frequency of callus formation is statistically significant. The largest number of shoots was obtained on the MS medium with the addition of 2.0 mg/l of BA. At the same times, shoot proliferation and root induction in such numbers were observed on MS culture medium with the addition of 0.5 mg/l BA and 0.5 mg/l kinetin (multiplication factor – 8.8±0.6 per 60-day cultivation cycle). |
Databáze: | OpenAIRE |
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