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Initiation, proliferation and development of micro-propagation system for mass scale production of banana through meristem culture

机译:通过分生组织培养大规模生产香蕉的微繁殖系统的启动,增殖和发展

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摘要

Explants were taken from field grown plants in 2010. The shoot apical meristem of different sizes was cultured on Murashige and skoog’s (MS) medium supplemented with different concentrations and combinations of 6-benzylamino-purine (BAP), kinetin (Kin) and α- naphthaleneacetic acid (NAA) either alone or in combination with each other under different temperature conditions ranging from 23 to 27°C. Shoot formation response from shoot apical meristem showed that MS medium containing 1.0 mg/l BAP showed best response for shoot formation. For shoot multiplication,?MS medium containing 1.0 mg/l BAP + 0.25 mg/l kin provided?thebest multiplication response which was 8 shoot per culture vial within 21.6 days after inoculation into shoot multiplication medium. Shoot formation and multiplication response was also affected by temperature variations. The best results were obtained at 27°C ± 1°C. By increase or decrease in temperature,?the?rate of?in vitroresponse was also decreased. For rooting of well developed?in vitro?shoots MS medium supplemented with 1.0 mg/l?Indole-3- butyric acid?(IBA)+ 0.5 mg/l NAA showed 3.6 roots per plant after 6.8 days of inoculation into rooting medium with an average root length of 2.4 cm. 100% hardening response was obtained in Peat moss after 21 days of transplantation in glass house.?The?experiments were designed in completely randomized pattern.
机译:外植体取自2010年的田间种植植物。在不同浓度的Murashige和skoog's(MS)培养基上培养了不同大小的茎尖分生组织,6-6-氨基氨基嘌呤(BAP),激动素(Kintin)和α-萘乙酸(NAA)可以单独使用,也可以在23至27°C的不同温度条件下相互组合使用。芽顶分生组织的芽形成响应表明,含有1.0 mg / l BAP的MS培养基显示出最佳的芽形成响应。对于芽繁殖,包含1.0 mg / l BAP + 0.25 mg / l kin的?MS培养基提供了最佳的增殖反应,接种到芽增殖培养基中后的21.6天内,每个培养瓶有8个芽。芽的形成和繁殖反应也受温度变化的影响。在27°C±1°C下可获得最佳结果。通过升高或降低温度,体外反应的速率也降低了。为使发育良好的“体外”枝条生根,补充1.0 mg / l“吲哚-3-丁酸”(IBA)+ 0.5 mg / l NAA的MS培养基接种6.8天后,每株植株有3.6根。平均根长为2.4厘米。在玻璃温室中移植21天后,泥炭藓获得了100%的硬化反应。实验设计为完全随机的模式。

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