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愈伤组织的形成来自培养的丹参细胞原生质体。

Callus formation from protoplasts of cultured Lithospermum erythrorhizon cells.

机构信息

Research Center for Cell and Tissue Culture, Faculty of Agriculture, Kyoto University, 606, Kyoto, Japan.

出版信息

Plant Cell Rep. 1983 Aug;2(4):179-82. doi: 10.1007/BF00270097.

Abstract

Protoplasts isolated from cell cultures of Lithospermum erythrorhizon divided repeatedly and formed callus colonies. Factors that affect protoplast division are the use of glucose as osmoticum, a new plating method with twin layers of agar-liquid medium, and the culture of protoplasts under the osmolarity lower than that in the isolation solution. When the sucrose in the protoplast-culture medium was replaced with glucose, and coconut milk was added to the medium, the frequency of colony formation markedly increased. The culture period required for colony formation also was shortened.

摘要

从紫草细胞培养物中分离出来的原生质体可以反复分裂并形成愈伤组织集落。影响原生质体分裂的因素有:使用葡萄糖作为渗透压稳定剂、采用双层琼脂液体培养基的新接种方法,以及在渗透压低于分离溶液的条件下培养原生质体。当原生质体培养基中的蔗糖被葡萄糖取代,并在培养基中添加椰子乳时,集落形成的频率显著增加。形成集落所需的培养时间也缩短了。

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