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An efficient protocol for rapid plant regeneration from deembryonated cotyledons of black gram [Vigna mungo (L.) Hepper]
Author(s) -
R. Anandan,
T. Deenathayalan,
R. Bhuvaneshwari,
M. Merlin Monisha,
M. Prakash
Publication year - 2019
Publication title -
indian journal of agricultural research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.241
H-Index - 8
eISSN - 0976-058X
pISSN - 0367-8245
DOI - 10.18805/ijare.a-5169
Subject(s) - vigna , shoot , explant culture , gram , murashige and skoog medium , callus , micropropagation , botany , biology , horticulture , in vitro , chemistry , bacteria , biochemistry , genetics
Here an efficient protocol for micropropagation of black gram [Vigna mungo (L.) Hepper] cv. VBN 3 is reported. The deembryonated cotyledonary explants were cultured on MS medium containing different concentrations of plant growth regulators. The maximum frequency (72%) of direct shoot regeneration (devoid of callus phase), multiple shoot induction and shoot elongation was achieved from culturing the explants on MS medium containing 3.0 mg/l of 6-benzylaminopurine (BAP). Up to 65% of the regenerated shoots were rooted on MS medium containing 0.25 mg/l of á-naphthalene acetic acid (NAA) within 3 weeks after subculturing. The in vitro-raised plantlets were successfully hardened first under culture room conditions with 62% survival rate and then in greenhouse. The identified regeneration system could be efficiently used in various in vitro manipulation studies in black gram as well.

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