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In vitro tetraploid induction and generation of tetraploids from mixoploids in Dioscorea zingiberensis

机译:盾叶薯os的四倍体离体诱导和四倍体的产生

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摘要

This article describes an efficient colchicine-mediated technique for the in vitro induction of tetraploids in Dioscorea zingiberensis and its confirmation by flow cytometry. Buds immersed in 0.2% colchicine solution for 36 hours prior to culture induced as high as 35.6% tetraploid plants. Colchicine-induced tetraploids remained stable after six months in soil. Leaf characteristics of diploids and tetraploids in D. zingiberensis were compared. It was determined that the leaf sizes of glasshouse-grown plants and stomatal sizes of both in vitro and glasshouse-grown plants were suitable parameters for identifying putative tetraploids in D. zingiberensis. Besides generating tetraploids, this technique generated mixoploids in D. zingiberensis. Calli derived from mixoploid leaves were induced to form buds and shoots. Individual shoots were classed as diploid, mixoploid, and tetraploid by flow cytometry. This callus-based technique could be employed when a genome-doubling agent generated mixoploids, but no tetraploids.
机译:本文介绍了一种有效的秋水仙碱介导的技术,用于体外诱导盾叶薯os中的四倍体及其通过流式细胞仪的证实。在培养之前,将芽浸入0.2%秋水仙碱溶液中36小时,然后诱导高达35.6%的四倍体植物。秋水仙碱诱导的四倍体在土壤中六个月后保持稳定。比较了金缕梅的二倍体和四倍体的叶片特性。已确定,温室栽培植物的叶片大小以及体外和温室栽培植物的气孔大小均是鉴定姜黄四倍体中假定四倍体的合适参数。除了产生四倍体之外,该技术还在金缕梅中产生了混合倍体。诱导来自混合倍体叶的愈伤组织形成芽和芽。通过流式细胞术将单个芽分为二倍体,混合倍体和四倍体。当基因组倍增剂产生混合倍体而不产生四倍体时,可以使用这种基于愈伤组织的技术。

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