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使用完整子叶节作为外植体进行高效大豆再生及农杆菌介导的转化。

Efficient soybean regeneration and Agrobacterium-mediated transformation using a whole cotyledonary node as an explant.

作者信息

Zhang Fuli, Chen Can, Ge Honglian, Liu Jinmei, Luo Yunling, Liu Kun, Chen Long, Xu Kedong, Zhang Yi, Tan Guangxuan, Li Chengwei

机构信息

Key Laboratory of Plant Genetics and Molecular Breeding, Department of Life Science, Zhoukou Normal University, Zhoukou, People's Republic of China.

出版信息

Biotechnol Appl Biochem. 2014 Sep-Oct;61(5):620-5. doi: 10.1002/bab.1207. Epub 2014 Jun 26.

Abstract

An optimized regeneration and Agrobacterium-mediated transformation protocol based on whole cotyledonary node explants was developed in soybean (Glycine max) cultivar Zhong Huang 13. Adding 6-benzylaminopurine (BAP) in a germinating medium could significantly increase regeneration efficiency; the optimal BAP concentration for shoot formation was 0.5 mg/L. The concentrations of plant growth regulators in a shoot induction medium were optimized by the orthogonal test [L9 (3(3))]. The best combination for shoot regeneration was a medium of Murashige & Skoog salts with B5 vitamins (MSB) supplemented with 3.5 mg/L BAP, 0.2 mg/L indole-3-butyric acid (IBA), and 0.2 mg/L kinetin (KT). Under this favorable condition, one node could regenerate 28-30 shoots. Soybean whole cotyledonary nodes were transformed by inoculation with A. tumefaciens strain EHA105 harboring a vector pBI121 containing a β-glucuronidase gene (gus). GUS assay, polymerase chain reaction, and Southern blot analysis indicated that the gus gene was transformed into soybean plants with 23.1% transformation efficiency. Transgenic plants could be obtained within 5-6 weeks, which was about 4 weeks less than that of a traditional single cotyledonary node method.

摘要

在大豆品种中黄13中建立了基于完整子叶节外植体的优化再生及农杆菌介导转化体系。在发芽培养基中添加6-苄基腺嘌呤(BAP)可显著提高再生效率;芽形成的最佳BAP浓度为0.5 mg/L。通过正交试验[L9(3(3))]优化了芽诱导培养基中植物生长调节剂的浓度。芽再生的最佳组合是添加了3.5 mg/L BAP、0.2 mg/L吲哚-3-丁酸(IBA)和0.2 mg/L激动素(KT)的含有Murashige & Skoog盐和B5维生素的培养基(MSB)。在此有利条件下,一个节可再生28-30个芽。用携带含有β-葡萄糖醛酸酶基因(gus)的载体pBI121的根癌农杆菌菌株EHA105接种大豆完整子叶节进行转化。GUS检测、聚合酶链反应和Southern杂交分析表明,gus基因已转化到大豆植株中,转化效率为23.1%。转基因植株可在5-6周内获得,比传统的单子叶节方法少约4周。

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