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Somatic embryogenesis in Carica papaya through zygotic embryo derived callus culture

Tipo de material: TextoTextoSeries ; Acta Horticulturae, 851, p.201-208, 2010Trabajos contenidos:
  • Ramaswamy, A
  • Phap, P.D
  • Soorianathasundaram, K
  • Kumar, N
  • Thirugnanakumar, S
  • Sudhakar, D
  • Balasubramanian, P
Tema(s): Recursos en línea: Resumen: A rapid and efficient system for papaya (Carica papaya L. cv. Co7)regeneration through indirect somatic embryogenesis has been established. Embryogenic calli were obtained from zygotic embryos (excised from 110-120 dayold fruits)on CIM [half-strength MS (Murashige and Skoog, 1962)basal salts and vitamins, 400 mg/L of glutamine, 6 percent sucrose, 4 g/L phytagel]supplemented with varying concentrations 0.5-12.0 mg/L of 2,4-D. The frequency of somatic embryo formation was as high as 54.35 percent when cultured on medium containing 2.0 mg/L of 2,4-D. Suspension cultures were superior to static cultures (solid medium)for the maturation of somatic embryos. Matured (cotyledonary stage)somatic embryos cultured on MSR medium supplemented with 0.4 mg/L BAP and 0.02 mg/L NAA showed regeneration efficiency up to 62.32 percent. The emerging shoots with 2-3 trilobed leaves were rooted on MSL medium containing 1.0 mg/L of IBA with efficiency of 60.07 percent. Plants with well-developed shoots and roots were subsequently hardened on a potting mixture enriched with arbuscular mycorrhiza. The plantlets from zygotic embryo explants were morphologically similar and normal. No phenotypic variations have been observed in field-established plants. This regeneration protocol assures a high frequency of somatic embryogenesis, maturation and regeneration into plantlets.
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A rapid and efficient system for papaya (Carica papaya L. cv. Co7)regeneration through indirect somatic embryogenesis has been established. Embryogenic calli were obtained from zygotic embryos (excised from 110-120 dayold fruits)on CIM [half-strength MS (Murashige and Skoog, 1962)basal salts and vitamins, 400 mg/L of glutamine, 6 percent sucrose, 4 g/L phytagel]supplemented with varying concentrations 0.5-12.0 mg/L of 2,4-D. The frequency of somatic embryo formation was as high as 54.35 percent when cultured on medium containing 2.0 mg/L of 2,4-D. Suspension cultures were superior to static cultures (solid medium)for the maturation of somatic embryos. Matured (cotyledonary stage)somatic embryos cultured on MSR medium supplemented with 0.4 mg/L BAP and 0.02 mg/L NAA showed regeneration efficiency up to 62.32 percent. The emerging shoots with 2-3 trilobed leaves were rooted on MSL medium containing 1.0 mg/L of IBA with efficiency of 60.07 percent. Plants with well-developed shoots and roots were subsequently hardened on a potting mixture enriched with arbuscular mycorrhiza. The plantlets from zygotic embryo explants were morphologically similar and normal. No phenotypic variations have been observed in field-established plants. This regeneration protocol assures a high frequency of somatic embryogenesis, maturation and regeneration into plantlets.

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