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不同处理诱导新海16号体细胞胚胎同步化发生
引用本文:郭家雁,张霞,丁喜莲,李娟,邓莉,陈全家,孙国清,曲延英.不同处理诱导新海16号体细胞胚胎同步化发生[J].棉花学报,2017,29(4):385-392.
作者姓名:郭家雁  张霞  丁喜莲  李娟  邓莉  陈全家  孙国清  曲延英
作者单位:1. 新疆农业大学农学院/农业生物技术重点实验室,乌鲁木齐,830052;2. 中国农业科学院生物技术研究所,北京,100081
基金项目:国家自然科学基金(31660078),棉花生物学国家重点实验室开放课题基金(CB2015A24)
摘    要:【目的】旨在探索诱导海岛棉体细胞胚胎同步化发生的有效方法。【方法】以海岛棉品种新海16号的胚性愈伤组织为材料,研究了低温、饥饿和渗透处理诱导体细胞胚胎同步化发生的效果。【结果】在低温处理组中,4℃诱导时体细胞胚胎发生的数量随着低温诱导时间的延长而显著增加;10℃诱导时,不同诱导时间下各处理体细胞胚胎发生的数量差异不显著,但都显著高于对照(28℃);缺磷、缺氮、缺肌醇3种饥饿处理的体细胞胚胎的数量都随着处理时间的延长而减少;渗透处理组中,在含40 g·L-1葡萄糖的培养基上诱导7 d的效果最佳。【结论】4℃处理3 d、缺磷处理5 d、缺氮处理5 d以及40 g·L-1葡萄糖诱导7 d可以显著促进新海16号的体细胞胚胎同步化发生,其中4℃处理3 d的诱导效果最佳。

关 键 词:海岛棉  体细胞胚胎  诱导  同步化

Synchronized Somatic Embryogenesis of 'Xinhai 16'Induced by Different Treatments
Guo Jiayan,Zhang Xia,Ding Xilian,Li Juan,Deng Li,Chen Quanjia,Sun Guoqing,Qu Yanying.Synchronized Somatic Embryogenesis of 'Xinhai 16'Induced by Different Treatments[J].Cotton Science,2017,29(4):385-392.
Authors:Guo Jiayan  Zhang Xia  Ding Xilian  Li Juan  Deng Li  Chen Quanjia  Sun Guoqing  Qu Yanying
Institution:1. College of Agriculture/Key Laboratory of Agricultural Biotechnology, Xinjiang Agricultural University, Urumqi 830052, China; 2. Biotechnology Research Institute, Chinese Academy of Agricultural Sciences, Beijing 100081, China
Abstract:Objective] The aim of this study was to develop an efficient method for synchronizing the somatic embryogenesis of Gossypium barbadense L.Method] We attempted to synchronize the somatic embryogenesis of G.barbadense L.cv.'Xinhai 16'embryonic calli.The somatic embryos induced by low temperature,starvation,and osmotic pressure were counted and analyzed.Result] In the low-temperature treatment group,the number of somatic embryos increased significantly at 4 ℃.While,them were no significant differences in the number of somatic embryos between treatment times at 10 ℃.Nevertheless,more somatic embryos were produced at 10 ℃ than at 28 ℃ (control temperature).Somatic embryogenesis was inhibited by the nutrient starvation treatment (i.e.,phosphate,nitrogen,or inositol deficiency).In the osmotic stress group,the best results were observed following a 7-day culture in medium containing 40 g·L-1 glucose.Conclusion]'Xinhai 16'somatic embryogenesis can be synchronized by incubating calli at 4 ℃ for 3 days,simulating phosphate or nitrogen starvation conditions for 5 days,or maintaining calli in a medium containing 40 g· L-1 glucose for 7 days.The low-temperature treatment may provide optimal synchronization conditions.
Keywords:Gossypium barbadense L    somatic embryogenesis  inducement  synchronization
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