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Optimization of culture conditions for improved plant regeneration efficiency from wheat microspore culture

机译:优化培养条件以提高小麦小孢子培养的植物再生效率

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摘要

The production of haploid plants through microspore culture is a very important tool for plant breeding. However, progress in microspore culture for many species has been hampered by a number of factors that have resulted in low recovery of regenerated green plants. In this study, a series of experiments were conducted to increase the regeneration of haploid green plants from isolated wheat microspores. The use of different basal media and variations in media components resulted in the increased recovery (approximately double) of regenerated haploid wheat plants. Our findings demonstrate that CHB medium, in combination with 2,4-d, was a better medium for embryoids induction and plant regeneration than medium MC17 with either 2,4-d or PAA growth hormones. Wheat microspores cultured without ovary co-cultivation did not respond. Furthermore, high efficiency of microspore derived embryoids (up to 296 MDEs per 100 anthers) and green plant regeneration (up to 71 green plants per 100 anthers) were achieved by the use of gelrite instead of agarose as a gelling agent, and by the addition of media additives such as spent medium or MET.
机译:通过小孢子培养产生单倍体植物是植物育种的重要工具。但是,许多物种的小孢子培养进展受到许多因素的阻碍,这些因素导致再生绿色植物的回收率低。在这项研究中,进行了一系列实验,以提高分离的小麦小孢子中单倍体绿色植物的再生。使用不同的基础培养基和培养基成分的变化会导致再生单倍体小麦植株的回收率提高(大约翻倍)。我们的发现表明,与含2,4-d或PAA生长激素的MC17培养基相比,与2,4-d结合的CHB培养基是更好的胚状体诱导和植物再生培养基。未经卵巢共培养的小麦小孢子无反应。此外,通过使用胶凝剂代替琼脂糖作为胶凝剂,并通过添加胶凝剂,可以实现高效的小孢子来源胚状体(每100支花药最多296 MDEs)和绿色植物再生(每100支花药最多71株绿色植物)。培养基添加剂,例如用过的培养基或MET。

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