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[枸杞下胚轴原生质体的植株再生]

[Plant regeneration from hypocotyl protoplasts of Lycium barbarum L].

作者信息

Tian H Q, Xiao Y H, Liu W F

机构信息

Department of Biology, Wuhan University.

出版信息

Shi Yan Sheng Wu Xue Bao. 1993 Mar;26(1):89-93.

PMID:8356855
Abstract

The hypocotyl protoplasts of Lycium barbarum L. CV. Ningji No. 1 were isolated in an enzyme mixture solution containing 1% cellulase and 1% pectinase. The protoplasts were cultured in KM 8 p liquid medium containing 0.3 mg/L 2,4-D and 0.3 mg/L BA, The first division of regenerated cells occurred 3 days after culture. The small cell clumps could be observed by naked eyes 20 days after culture. 40 days after culture, microcalli of 1-2 mm in size were transferred to MS solid differentiation medium containing 3% sugar, 0.1-0.4 mg/L BA and 0.05-0.1 mg/L NAA. About 30 days after culture on MS solid medium, the calli with shoots were transferred to 1/2 MS medium containing 0.1 mg/L BA and 0.2 mg/L IBA, from which 80% of them differentiated roots and regenerated whole plantlets.

摘要

以枸杞品种宁杞1号的下胚轴原生质体为材料,在含有1%纤维素酶和1%果胶酶的酶混合液中进行分离。原生质体在含有0.3mg/L 2,4-D和0.3mg/L BA的KM 8 p液体培养基中培养,培养3天后再生细胞开始第一次分裂。培养20天后肉眼可见小细胞团。培养40天后,将1-2mm大小的微愈伤组织转移到含有3%蔗糖、0.1-0.4mg/L BA和0.05-0.1mg/L NAA的MS固体分化培养基上。在MS固体培养基上培养约30天后,将有芽的愈伤组织转移到含有0.1mg/L BA和0.2mg/L IBA的1/2 MS培养基上,其中80%分化出根并再生出完整植株。

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