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首页> 外文期刊>Electronic Journal of Biotechnology >Rapid multiplication and in vitro production of leaf biomass in Kaempferia galanga through tissue culture
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Rapid multiplication and in vitro production of leaf biomass in Kaempferia galanga through tissue culture

机译:通过组织培养快速扩增和生产高加索无性系的叶片生物量

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An efficient protocol has been established for rapid multiplication and in vitro production of leaf biomass in Kaempferia galanga L, a rare medicinal plant. Different plant growth regulators like Benzyladenine (BA), Indoleacetic acid (IAA), Indolebutyric acid (IBA), Napthaleneacetic acid (NAA) and adenine sulphates (Ads) have been tried for induction of multiple shoots using lateral bud of rhizome as explants. The highest rate of shoot multiplication (11.5 ± 0.6) shoot/explant as well as leaf biomass production (7.4 ± 0.3) gram/explant was observed on Murashige and Skoog medium supplemented with Benzyladenine (1 mg/l) and Indoleacetic acid (0.5 mg/l). Data of shoot multiplication and leaf biomass production were statistically analysed. Upon excission of leaves after 2 months of culture under sterile condition, the base of each plantlet was transferred to fresh media which could produce the same leaf biomass within another 2 months in a 50 ml culture tube containing 20 ml and 250 ml conical flasks containing 30 ml Murashige and Skoog medium. The rate of multiplication and leaf biomass production remained unchanged in subsequent subcultures. The regenerated plantlets were acclimatized in greenhouse and subsequently transferred to the field. Survival rate of the plantlets under ex vitro condition was 95 percent. Genetic fidelity of the regenerants was confirmed using random amplified polymorphic DNA (RAPD) marker. The protocol could be commercially utilized for large scale production of true-to-type plantlets and as an alternative method of leaf biomass production in Kaempferia galanga.
机译:已经建立了一种有效的方案,用于在稀有的药用植物Kaempferia galanga L中快速繁殖和体外生产叶片生物量。尝试使用不同的植物生长调节剂,如苯并亚麻腺素(BA),吲哚乙酸(IAA),吲哚丁酸(IBA),萘乙酸(NAA)和腺嘌呤硫酸盐(Ads),以根茎的侧芽为外植体来诱导多芽。在补充了苄基腺嘌呤(1 mg / l)和吲哚乙酸(0.5 mg)的Murashige和Skoog培养基上观察到最高的芽繁殖率(11.5±0.6)芽/叶片生物量产生(7.4±0.3)克/株/ l)。对枝条繁殖和叶片生物量产生的数据进行统计分析。在无菌条件下培养2个月后叶片消失后,将每株苗的基部转移到新鲜培养基中,该培养基可以在装有20 ml的50 ml培养管和装有30 ml的250 ml锥形烧瓶中的另外2个月内产生相同的叶片生物量ml Murashige和Skoog培养基。在随后的亚培养中,繁殖速率和叶片生物量的产生保持不变。再生的幼苗在温室中适应环境,随后转移到田间。离体条件下小苗成活率为95%。使用随机扩增多态性DNA(RAPD)标记确认了再生子的遗传保真度。该协议可用于商业化大规模生产真实型小植株,并作为一种替代方法在高倍生Kaempferia galanga中生产叶片生物量。

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