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利用噻苯隆诱导杂种紫草(Royle)完整叶片直接再生。

Direct shoot regeneration from intact leaves of Arnebia euchroma (Royle) Johnston using thidiazuron.

机构信息

Division of Biotechnology, Institute of Himalayan Bioresource Technology CSIR, Palampur, HP, India.

出版信息

Cell Biol Int. 2010 Apr 8;34(5):537-42. doi: 10.1042/CBI20090372.

Abstract

The present study highlights the importance of preculture time and concentration of TDZ (thidiazuron) for direct regeneration from in vitro leaves (attached to shoots) in Arnebia euchroma. Shoot buds proliferated to form multiple shoots on MS medium (Murashige and Skoog medium) with 5.0 microM Kn. Different additives viz. ascorbic acid, PVP (polyvinylpyrrolidone), PVPP (polyvinylpolypyrrolidone) or activated charcoal (50, 100 and 250 mg/l each) were used to check the phenolic exudations. Direct shoot regeneration was obtained when shoots were initially precultured for 40 days on medium with a higher concentration of TDZ (20.0 muM) and then transferred to a lower concentration (5.0 microM TDZ). The identity of shoot buds was confirmed by histological studies. Regenerated shoots were cultured for 30 days on medium containing Kn (5.0 microM) for proliferation and then transferred to IBA (0.25 microM)-containing medium for rooting. Rooted plantlets were transferred to greenhouse with 45-50% survival.

摘要

本研究强调了预培养时间和 TDZ(噻苯隆)浓度对从体外叶片(附生在芽上)直接再生的重要性,在 Arnebia euchroma 中。芽在含有 5.0 microM Kn 的 MS 培养基(Murashige 和 Skoog 培养基)上增殖形成多个芽。使用不同的添加剂,如抗坏血酸、PVP(聚乙烯吡咯烷酮)、PVPP(聚乙烯聚吡咯烷酮)或活性炭(50、100 和 250 mg/l),以检查酚类分泌物。当芽在含有较高浓度 TDZ(20.0 μM)的培养基中预培养 40 天时,可获得直接芽再生,然后转移到较低浓度(5.0 μM TDZ)的培养基中。芽的身份通过组织学研究得到确认。再生芽在含有 Kn(5.0 μM)的培养基上培养 30 天以增殖,然后转移到含有 IBA(0.25 μM)的培养基中生根。生根的组培苗在 45-50%的存活率下转移到温室中。

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