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木瓜(哈妮德瓦品种)愈伤组织培养和小植株生产。

Callus culture and plantlet production in Carica papaya (Var. Honey Dew).

机构信息

Department of Botany, Bose Institute, 93/1, APC Road, 700 009, Calcutta, India.

出版信息

Plant Cell Rep. 1994 Apr;13(7):390-3. doi: 10.1007/BF00234144.

Abstract

In order to develop techniques for efficient callus production and regeneration in Carica papaya (Var. Honey Dew), lamina, petiole, stem and root explants from in vitro plantlets were cultured in media supplemented with 2.0 mg/1 IBA and 0.5 mg/1 BAP. Use of in vitro-grown plantlets as an explant source helped to avoid contamination common in papaya tissue culture. Callusing was maximum in root explants cultured in a modified MS (half-strength) medium. Shoot reganeration was maxium in root-derived callus grown in full-strength modified MS medium supplemented with 0.5 mg/1 IBA and 1 to 2 mg/1 kinetin. A histological study indicated that shoot buds originated from peripheral cell layers of the callus. Each shoot regenerated from callus was subcultured using a multiplication medium. Root formation was induced in all shoots treated in half-strength of modified MS medium containing 2 mg/1 IBA and rooted shoots were transferred successfully to the field.

摘要

为了在 Carica papaya(Var. Honey Dew)中开发高效愈伤组织生产和再生技术,将来自体外幼苗的叶片、叶柄、茎和根外植体培养在添加 2.0mg/1 IBA 和 0.5mg/1 BAP 的培养基中。使用体外生长的幼苗作为外植体来源有助于避免木瓜组织培养中常见的污染。在改良 MS(半强度)培养基中培养的根外植体的愈伤组织形成最多。在添加 0.5mg/1 IBA 和 1 至 2mg/1 激动素的全强度改良 MS 培养基中生长的根衍生愈伤组织中,芽再生最多。组织学研究表明,芽原基起源于愈伤组织的外周细胞层。从愈伤组织再生的每个芽都使用增殖培养基进行继代培养。所有在含有 2mg/1 IBA 的改良 MS 半强度培养基中处理的芽都诱导生根,生根的芽成功移栽到田间。

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