2017
DOI: 10.24870/cjb.2017-000106
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Monochromic radiation through light-emitting diode (LED) positively augments in vitro shoot regeneration in Orchid (Dendrobium sonia)

Abstract: ORIGINAL RESEARCH PAPER OPEN ACCESS50 AbstractMonochromatic lights emitted by light-emitting diodes (LEDs) have generated great interest for efficient and controlled growth in vitro, especially of plants which are endangered or require specific intensity and wavelength of light. In the present study, we have evaluated the effect of monochromatic LEDs on in vitro morphogenesis: growth, proliferation of shoot cultures, and rooting of Dendrobium sonia. Different light sources viz. white LEDs (W), blue LEDs (B), y… Show more

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Cited by 12 publications
(11 citation statements)
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“…Mutations could generate phenotypic variations in both vegetative and reproductive characteristics and the approach is particularly useful for Dendrobium improvement because it is highly heterozygous and is genetically diverse. In our earlier study, we reported effects of monochromatic lights on growth and morphogenesis of D. sonia [21]. It is essential to study the radiosensitivity in each case to estimate lethal dose (LD50) to focus on the effective doses at which higher frequency of the mutants can be isolated [1,2].…”
Section: Resultsmentioning
confidence: 99%
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“…Mutations could generate phenotypic variations in both vegetative and reproductive characteristics and the approach is particularly useful for Dendrobium improvement because it is highly heterozygous and is genetically diverse. In our earlier study, we reported effects of monochromatic lights on growth and morphogenesis of D. sonia [21]. It is essential to study the radiosensitivity in each case to estimate lethal dose (LD50) to focus on the effective doses at which higher frequency of the mutants can be isolated [1,2].…”
Section: Resultsmentioning
confidence: 99%
“…Rhizome buds from the ex vitro plants were used as explants to initiate in vitro shoot cultures. These explants were thoroughly washed in running tap water for 10 min, surface sterilized with 0.1% mercuric chloride for 3 min followed by 70% alcohol for 30 s and finally rinsed thrice with sterilized distilled water [21]. These surface sterilized explants were then cultured on to Murashige and Skoog’s (MS) [30] basal medium supplemented with sucrose (3% w/v), 6-benzylaminopurine (BAP 2 mg/l) and gelling agent agar-agar (0.6% w/v).…”
Section: Methodsmentioning
confidence: 99%
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