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An Effective Protocol for Micropropagation of Edible Bamboo Species (Bambusa tulda and Melocanna baccifera) through Nodal Culture

机译:通过节节文化微繁殖食用竹种(Bambusa tulda和Melocanna baccifera)的有效协议

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摘要

High demand for edible bamboo shoots of Bambusa tulda and Melocanna baccifera in many Asian ethnic groups has led to the need for developing intensive bamboo farming. To achieve this, in vitro regeneration of bamboo plantlets is needed due to the long and irregular bamboo flowering cycle and scarcity of bamboo seeds. An effective protocol for plantlets regeneration in B. tulda and M. baccifera from nodal explants following validation of the species using the sequence of trnL-F intergenic spacer region is described. Effective axillary bud breaking was achieved at 3 mg/L of 6-benzylaminopurine (BAP) in MS medium. Importantly, combining 2 mg/L of kinetin (Kn) with 3 mg/L of BAP produced a synergistic effect for shoot multiplication in B. tulda and M. baccifera. Under optimized conditions in half-strength MS medium supplemented with 3 mg/L of indole-3-butyric acid (IBA), 10 mg/L of coumarin, and 3% sucrose, profuse production of dark-brown rhizome in B. tulda and abundant rooting (81.67%, P < 0.05, F = 15.46) for M. baccifera within 30 days were achieved. The established protocol and the validation of the reported species at the molecular level will be of help to stakeholders in edible bamboo trade to conserve gene-pool and increase productivity.
机译:在许多亚洲种族中,对班布萨图尔达(Bambusa tulda)和可食用的梅洛卡纳浆果(Melocanna baccifera)的可食用笋的大量需求导致了对发展集约化竹农的需求。为此,由于长且不规则的竹子开花周期和竹子缺乏,需要对竹子进行体外再生。描述了使用trnL-F基因间隔区序列对物种进行验证后,从结节外植体中从结节外植体再生小球藻和芽孢杆菌的有效方案。在MS培养基中以3μmg/ L的6-苄基氨基嘌呤(BAP)达到有效的腋芽破裂。重要的是,将2 µmg / L的激动素(Kn)与3 µmg / L的BAP结合在一起,对于图尔达芽孢杆菌和B. baccifera的芽繁殖具有协同作用。在优化的条件下,在半强度MS培养基中添加3μmg/ L的吲哚-3-丁酸(IBA),10μmg/ L的香豆素和3%的蔗糖,在B. tulda和在30天内为芽孢杆菌提供了丰富的生根(81.67%,P <0.05,F = 15.46)。既定的方案和分子水平上已报告物种的验证将有助于食用竹子贸易的利益相关方保护基因库并提高生产力。

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