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首页> 外文期刊>Indian Journal of Horticulture >In vitro regeneration of tuberose through petals and immature flower buds.
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In vitro regeneration of tuberose through petals and immature flower buds.

机译:通过花瓣和未成熟花蕾的晚香玉再生。

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摘要

Unlike many other bulbous flower crops, where in vitro propagation techniques have been perfected, tuberose does not have enough background studies. A study was carried out to establish aseptic cultures and to standardize in vitro propagation protocol with petal segment and immature flower bud as explants. The explants pre-treated with carbendazim 0.1%+mancozeb 0.1% and 8-HQC (200 mg l-1) for 2 1/2 h and surface sterilized with HgCl2 (0.1%)+NaOCl (1.0%) for 8 min., respectively were found to be the best in getting aseptic culture. The best medium for shoot multiplication was MS medium supplemented with 6.0 mg/l BAP+0.5 mg/l NAA+0.7 mg/l 2,4-D+0.5 mg/l TDZ for both petals (4.0) and immature flower bud (4.33) enhanced shoot multiplication. Irrespective of explants, maximum roots were observed on half-strength MS medium+1.0 mg/l IBA. The in vitro regenerated micro-plant lets were successfully acclimatized in glass jar with polypropylene cap.
机译:与许多其他鳞茎类花卉作物一样,它们的体外繁殖技术已得到完善,晚香玉没有足够的背景研究。进行了一项研究,以建立无菌培养物并标准化以花瓣段和未成熟花芽为外植体的体外繁殖方案。外植体分别用0.1%多菌灵+ 0.1%代森锰锌和8-HQC(200 mg l -1 )预处理2 1/2 h,并用HgCl 2 进行表面灭菌发现(0.1%)+ NaOCl(1.0%)处理8分钟分别是无菌培养的最佳方法。对于花瓣(4.0)和未成熟花蕾(4.33)而言,最好的芽繁殖培养基是MS培养基,添加6.0 mg / l BAP + 0.5 mg / l NAA + 0.7 mg / l 2,4-D + 0.5 mg / l TDZ )增强芽繁殖。不考虑外植体,在半强度MS培养基+1.0 mg / l IBA上观察到最大根。 体外再生的微植株在带有聚丙烯盖的玻璃罐中成功地驯化。

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