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离体繁殖和野生阿当达 beddomei C. B. 克拉克,一种珍稀药用植物的建立。

In vitro multiplication and field establishment of Adhatoda beddomei C. B. Clarke, a rare medicinal plant.

机构信息

Plant Biotechnology Unit, Tropical Botanic Garden and Research Institute, 695 562, Thiruvananthapuram, India.

出版信息

Plant Cell Rep. 1994 Jan;13(3-4):203-7. doi: 10.1007/BF00239893.

Abstract

Clonal propagation of Adhatoda beddomei C.B. Clarke (Acanthaceae), a rare medicinal shrub, was achieved through callus-free axillary meristem proliferation from stem node explants of field-grown plants cultured in SH medium. Shoot multiplication was a function of cytokinin activity but sustained growth of the shoots was dependent on the synergistic effect with the auxin, IAA. An optimum number of 5-10 shoots per explant were obtained in 6 weeks using 3.0 mg.l(-1) BAP, 0.5 mg.l(-1) 2-ip and 1.0 mg.l(-1) IAA, Upon subculture, vertical halves of the precultured node with the differentiated shoots yielded a larger aggregate number of shoots (23-27) than the uncut precultured node left intact (15-17). Shoot multiplication was rapid and consistent over prolonged periods when the hormonal concentrations were reduced to 1.0 mg.l(-1) BAP and 0.2 mg.l(-1) IAA during subculture, and reculture of the nodal explants derived from shoot cultures. Rooting of 3-5 cm shoots thus obtained was greatly accelerated in stationary liquid medium containing 0.2 mg.l(-1) IBA or IAA. Hardening of the rooted plantlets in the humidity chamber was essential for high frequency (95%) survival. Micropropagated plants established in the field flowered after fifteen months and were free from apparent defects in cytological, growth and flowering characteristics.

摘要

贝母兰(兰科)克隆繁殖,一种稀有药用灌木,通过在 SH 培养基中培养的田间生长植株的茎节点外植体无愈伤组织腋芽增殖来实现。芽的增殖是细胞分裂素活性的功能,但芽的持续生长依赖于与生长素 IAA 的协同作用。使用 3.0 mg.l(-1) BAP、0.5 mg.l(-1) 2-ip 和 1.0 mg.l(-1) IAA,每外植体可获得 5-10 个最佳数量的芽,在 6 周内。继代培养时,用预处理的节点的垂直半部分与分化的芽一起产生比未切割的预处理节点(15-17)更大的芽总数(23-27)。当激素浓度在继代培养和芽培养衍生的节点外植体的再培养过程中降低至 1.0 mg.l(-1) BAP 和 0.2 mg.l(-1) IAA 时,芽增殖迅速且一致。如此获得的 3-5 cm 长的芽在含有 0.2 mg.l(-1) IBA 或 IAA 的静止液体培养基中生根大大加快。在湿度室中对生根的幼苗进行硬化对于高频率(95%)存活至关重要。在田间建立的微繁殖植物在十五个月后开花,并且在细胞学、生长和开花特征方面没有明显缺陷。

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