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首页> 外文期刊>British Biotechnology Journal >Effect of Desiccation and Chilling Treatment onSomatic Embryo Development and Germinationin Rough Lemon (Citrus jambhiri Lush)
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Effect of Desiccation and Chilling Treatment onSomatic Embryo Development and Germinationin Rough Lemon (Citrus jambhiri Lush)

机译:干燥和低温处理对粗糙柠檬(Citrus jambhiri Lush)体细胞胚发育和萌发的影响

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The goal of this study was to evaluate the effect of desiccation and chilling treatments on somatic embryogenesis of rough lemon (Citrus jambhiri Lush.). Styles were cultured on seven culture media (MS I-MS VII) containing Benzylaminopurine (BAP), Kinetin (KN) and Malt Extract for cell proliferation and somatic embryo development. Cell proliferation was maximum on MS IV media but maximum cultures showing somatic embryogenesis (52.08 %) was observed on MS VII media. Embryogenic callus proliferated on MS VII media was subjected to desiccation and chilling treatment for 24, 48, 72 and 96 hours. Embryogenic callus desiccated for 24 and 48 hours in sterile petriplates showed 58.33 and 56.94 % somatic embryogenesis respectively as compared to undesiccated callus (51.98%). Average number of cotyledonary embryos (6.80/culture) in embryogenic cultures from desiccated callus (48 hrs) was more as compared to untreated callus (2.26/culture). There was significantly less number of abnormal embryos (0.60-0.53/culture) in desiccated callus for 48, 72 and 96 hours as compared to untreated callus (7.20/culture). Chilling treatment also improves the average number of cotyledonary embryos and reduces the abnormal development of embryos. Among all the treatments desiccation of embryogenic callus for 48 hrs proved beneficial for improvement of somatic embryo development and germination.
机译:这项研究的目的是评估干燥和冷冻处理对粗糙柠檬(Citrus jambhiri Lush。)体细胞胚发生的影响。在含有苄基氨基嘌呤(BAP),激动素(KN)和麦芽提取物的七种培养基(MS I-MS VII)上培养花样,以促进细胞增殖和体细胞胚发育。在MS IV培养基上细胞增殖最大,但是在MS VII培养基上观察到显示出体细胞胚发生的最大培养物(52.08%)。将在MS VII培养基上增殖的胚性愈伤组织进行干燥,冷冻处理24、48、72和96小时。与未干燥的愈伤组织(51.98%)相比,在无菌培养皿中干燥24和48小时的胚性愈伤组织分别显示出58.33和56.94%的体细胞胚发生。与未处理的愈伤组织(2.26 /培养物)相比,来自干燥愈伤组织(48小时)的胚发生培养物中子叶胚的平均数目(6.80 /培养物)更多。与未处理的愈伤组织(7.20 /培养物)相比,干燥的愈伤组织中48、72和96小时内的异常胚胎数量(0.60-0.53 /培养物)明显减少。低温处理还可以提高子叶胚的平均数量,并减少胚的异常发育。在所有处理中,证明胚胎发生愈伤组织的干燥48小时有助于改善体细胞胚的发育和发芽。

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