Plantlet formation via somatic embryogenesis and LC ESI Q-TOF MS determination of secondary metabolites in Butea monosperma (Lam.) Kuntze

• Autorzy: Sharma C. , Kumari T. , Pant G. , Bajpai V. , Srivastava M. , Mitra K. , Kumar B. , Arya K.R.
• Języki publikacji: EN

Abstrakty

EN

Medicinal properties of Butea monosperma (BM) and overexploitation of bark as a rich source of flavonoids for different biological activities, development of efficient method for high frequency somatic embryos and in vitro synthesis of bioactive secondary metabolites using plant tissue culture technology is important. Initially, callus was induced from leaf explants of BM on Murashige and Skoog (MS) medium containing 0.25 mg L-1 2,4-Ddichlorophenoxyacetic acid (2,4-D) with 0.1 mg L-1 kinetin (Kn) and ascorbic acid (AA). MS half strength macronutrients and full strength micronutrients containing 0.25 mg L-1 2,4-D with 0.1 mg L-1 Kn, and 0.5 mg L-1 AA provided fragile callus with 84.0 ± 1.00 % optimal growth response. Shoot formation occurred via somatic embryogenesis through an intermediary callus phase. However, 2.1 mg L-1 thidiazuron with 0.5 mg L-1 AA provides high frequency (79.6 ± 2.02 %) of somatic embryogenesis within 5 weeks. Developed embryos when transferred to woody plant medium containing 0.5 mg L-1 AA with 3.0 mg L-1 Kn and 0.5 mg L-1 a naphthalene acetic acid responded 44.0 ± 0.00 % embryo maturation, whereas 0.5 mg L-1 Kn, 0.3 mg L-1 indole-3-butyric acid, and 0.25 mg L-1 AA induced rooting within 6 and 8 weeks, respectively. Liquid chromatography electro spray ionization quadrupole time of flight mass spectrometry (LC ESI Q-TOF MS) analysis of in vitro cultures showed similarity to those compounds identified in wild grown leaf samples known for osteogenic activity. Histological investigation through scanning electron microscopy demonstrates the developmental stages of somatic embryos, shoot bud formation, and induction of root primordial.

• Wydawca: -
• Czasopismo: Acta Physiologiae Plantarum
• Rocznik: 2015
• Tom: 37
• Numer: 11
• Opis fizyczny: Article: 239 [10 p.], fig.,ref.

Twórcy

autor

Sharma C.

• Botany Division, CSIR-Central Drug Research Institute, Sector-10, Jankipuram Extension, Sitapur Road, Lucknow, Uttar Pradesh, 226031, India

autor

Kumari T.

• Botany Division, CSIR-Central Drug Research Institute, Sector-10, Jankipuram Extension, Sitapur Road, Lucknow, Uttar Pradesh, 226031, India

autor

Pant G.

• Electron Microscopy Unit, CSIR-Central Drug Research Institute, Lucknow, 226031, India

autor

Bajpai V.

• Sophisticated Analytical Instrument Facility, CSIR-Central Drug Research Institute, Lucknow, 226031, India

autor

Srivastava M.

• Biometry and Statistics Division, CSIR-Central Drug Research Institute, Lucknow, 226031, India

autor

Mitra K.

• Electron Microscopy Unit, CSIR-Central Drug Research Institute, Lucknow, 226031, India

autor

Kumar B.

• Sophisticated Analytical Instrument Facility, CSIR-Central Drug Research Institute, Lucknow, 226031, India

autor

Arya K.R.

• Botany Division, CSIR-Central Drug Research Institute, Sector-10, Jankipuram Extension, Sitapur Road, Lucknow, Uttar Pradesh, 226031, India

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Identyfikatory

DOI

10.1007/s11738-015-1973-x