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通过幼苗外植体培养实现臭豆(Nothapodites foetida (Wight.) Sleumer)的离体增殖。

In vitro multiplication of Nothapodites foetida (Wight.) Sleumer through seedling explant cultures.

作者信息

Satheeshkumar K, Seeni S

机构信息

Plant Biotechnology Division, Tropical Botanic Garden and Research Institute, Thiruvananthapuram, India.

出版信息

Indian J Exp Biol. 2000 Mar;38(3):273-7.

Abstract

In vitro multiplication of Nothapodites foetida (Wight.) Sleumer was achieved using axenic seedling explant cultures. Isolated nodes (1.0-1.2 cm) and shoot tips (1.0-1.5 cm) cultured in Murashige and Skoog's agar medium containing varying concentrations of TDZ, BA and combinations of 2iP and GA3. Single shoot (0.8-1.2 cm) was regenerated in each culture after 6 weeks. Axillary shoots were then excised and recultured for 8 weeks in medium containing TDZ (0.05 mgL-1) which formed shoots (about 4 in no.; 2 cm) from the basal node. Axillary branches (2) which formed on 60% of these shoots after 10-12 weeks of culture were separated and recultured in the same medium for 8 weeks. Three shoots (0.8-1.0 cm) per culture were regenerated. Shoots of 0.8-1.8 cm length were subcultured on a low cytokinin (0.01 mgL-1 TDZ) regime to induce shoot elongation (2.0-3.5 cm) in 4 weeks. Shoot cuttings were rooted (60%) in the medium containing IBA (1.5 mgL-1). Rooted plantlets established in pots (90%) after hardening resumed normal growth in 3 months.

摘要

利用无菌幼苗外植体培养实现了臭豆叶楠(Nothapodites foetida (Wight.) Sleumer)的离体增殖。将分离的节段(1.0 - 1.2厘米)和茎尖(1.0 - 1.5厘米)接种于含有不同浓度噻苯隆(TDZ)、苄氨基嘌呤(BA)以及2 - 异戊烯腺嘌呤(2iP)与赤霉素(GA3)组合的Murashige和Skoog琼脂培养基中。6周后,每个培养物中再生出单茎(0.8 - 1.2厘米)。然后切下腋芽,在含有噻苯隆(0.05毫克/升)的培养基中再培养8周,腋芽从基部节段形成茎(约4个;2厘米)。培养10 - 12周后,60%的这些茎上形成的腋枝(2个)被分离,并在相同培养基中再培养8周。每个培养物再生出三个茎(0.8 - 1.0厘米)。将长度为0.8 - 1.8厘米的茎在低细胞分裂素(0.01毫克/升噻苯隆)条件下继代培养,4周内诱导茎伸长至(2.0 - 3.5厘米)。茎插条在含有吲哚丁酸(IBA,1.5毫克/升)的培养基中生根(60%)。炼苗后,90%在花盆中定植的生根小植株在3个月内恢复正常生长。

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