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作 者:王利虎 胡兰[1] 李登科 刘平[1,2] 刘孟军[1]
机构地区:[1]河北农业大学中国枣研究中心,河北保定071001 [2]果树种质创制与利用山西省重点实验室,太原030031
出 处:《果树学报》2016年第10期1307-1314,共8页Journal of Fruit Science
基 金:国家自然科学基金(31372029);国家科技支撑项目(2013BAD14B03);河北省百名优秀创新人才支持计划(Ⅱ)(2014-2016);河北省自然科学基金(C2014204047);山西省重点实验室开放基金课题(2015012001-12)
摘 要:【目的】检验建立的枣田间愈伤组织途径芽再生技术的通用性并对其进一步优化。【方法】将其在115个枣和4个酸枣基因型上进行应用,进而分析基因型、愈伤组织状态、枝条粗度和位置等对田间愈伤途径芽再生的影响。【结果】发现80.67%的基因型能够实现芽再生,其中‘北京酸枣’‘龙壶枣’‘北京马牙枣’的平均单枝截面出芽数分别高达10.33、9.40、8.00个;芽再生能力随着愈伤发育等级的增加而升高,以5级愈伤的芽再生能力最强;直径为1.4~1.9 cm的枝条平均单枝截面出芽数达2.16个,显著高于其他粗度枝条的出芽数;树冠上部枝条的单枝截面出芽数显著高于中下部枝条的出芽数。【结论】枣田间愈伤组织途径芽再生技术在不同枣和酸枣基因型上有良好的通用性;影响田间愈伤组织途径芽再生的最主要因素为基因型,其次是愈伤组织状态及枝条粗度和垂直位置,枝条角度及水平位置对于芽再生的影响不显著。进一步优化了枣田间愈伤组织途径芽再生技术体系。[ Objective ] Asexual polyploidization is an effective way for creating new germplasm in jujube. The occurrence and purification of mixoploid is always the bottleneck of polyploid induction breeding in fruit tree and could be avoided by combing bud regeneration via callus with chromosome number doubling using colchicines, by which pure polyploid could be acquired directly. Bud regeneration is the basis and key point of field in vivo polyploid induction via callus. This study is to examine the universality of in vivo Bud Regeneration Technique via Callus (IVBRTC) we previously created in Chinese jujube and to make a optimization of the approach. [ Methods ] A total of 115 Chinese jujube (Ziziphus jujuba Mill.) and 4 sour ju- jube (Z. acidojujuba Cheng et Liu) genotypes were employed for IVBRTC application. The 119 genotypes covered a wide genetic diversity including the main cuhivars (such as 'Huizao' 'Junzao' 'Zanhuangda- zao' ‘ Jinsixiaozao'‘ Linyilizao' ‘ Yuanlingzao.'), newly released cuhivars (‘ Jingzao39' ' Lengbaiyu' ' Jin- gudazao' 'Liuyuexian', et al), famous local cultivars (‘Fengmiguan' 'Changxindianbaizao', et al), South Korea cuhivars (' Wudeng' ' Hongyan' ‘ Jincheng'‘ Fuzao' and ‘ Yuechu') as well as sour jujube (‘ Taigu- dasuanza'‘ Yesuanzao', and so on). The protocols of IVBRTC are as follows: First, cutting the randomly selected strong branches with branch shears or hand saw; Second, treating the cross sections of branches with 1.5 mL inducer (4.0 mg·L-1 TDZ+ 2.0 rag. U1 AgNO3) for 24 h; At last, putting wet mud on the cross section and then covering the wet mud with white plastic bag to keep moisture; Fourth, replacing the wet mud about every 10 days; Fifth, removing the wet mud after the adventitious buds formed from callus reaching 2 cm long and making them growing naturally. The callus status on the cross section were ob- served 20 days after the branches being cut. The bud numb
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