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通过根癌农杆菌介导下胚轴转化获得的转基因藤金合欢。

Transgenic Acacia sinuata from Agrobacterium tumefaciens-mediated transformation of hypocotyls.

作者信息

Vengadesan G, Amutha S, Muruganantham M, Anand R Prem, Ganapathi A

机构信息

Department of Biotechnology, School of Life Sciences, Bharathidasan University, Tiruchirappalli, 620024, Tamilnadu, India.

出版信息

Plant Cell Rep. 2006 Nov;25(11):1174-80. doi: 10.1007/s00299-006-0176-8. Epub 2006 Jun 29.

DOI:10.1007/s00299-006-0176-8
PMID:16807750
Abstract

Transgenic herbicide tolerant Acacia sinuata plants were produced by transformation with the bar gene conferring phosphinothricin resistance. Precultured hypocotyl explants were infected with Agrobacterium tumefaciens strain EHA105 in the presence of 100 microM acetosyringone and shoots regenerated on MS (Murashige and Skoog, 1962, Physiol Plant 15:473-497) medium with 13.3 microM benzylaminopurine, 2.6 microM indole-3-acetic acid, 1 g l(-1) activated charcoal, 1.5 mg l(-1) phosphinothricin, and 300 mg l(-1) cefotaxime. Phosphinothricin at 1.5 mg l(-1) was used for the selection. Shoots surviving selection on medium with phosphinothricin expressed GUS. Following Southern hybridization, eight independent shoots regenerated of 500 cocultivated explants were demonstrated to be transgenic, which represented transformation frequency of 1.6%. The transgenics carried one to four copies of the transgene. Transgenic shoots were propagated as microcuttings in MS medium with 6.6 microM 6-benzylaminopurine and 1.5 mg l(-1) phosphinothricin. Shoots elongated and rooted in MS medium with gibberellic acid and indole-3-butyric acid, respectively both supplemented with 1.5 mg l(-1) phosphinothricin. Micropropagation of transgenic plants by microcuttings proved to be a simple means to bulk up the material. Several transgenic plants were found to be resistant to leaf painting with the herbicide Basta.

摘要

通过用赋予草丁膦抗性的bar基因进行转化,培育出了转基因抗除草剂阿拉伯金合欢植株。将预培养的下胚轴外植体在含有100微摩尔乙酰丁香酮的条件下,用根癌农杆菌EHA105菌株进行侵染,然后在添加了13.3微摩尔苄氨基嘌呤、2.6微摩尔吲哚-3-乙酸、1克/升活性炭、1.5毫克/升草丁膦和300毫克/升头孢噻肟的MS(Murashige和Skoog,1962年,《植物生理学》15:473 - 497)培养基上再生芽。使用1.5毫克/升的草丁膦进行筛选。在含有草丁膦的培养基上筛选存活的芽表达了GUS。经过Southern杂交,在500个共培养的外植体再生的8个独立芽被证明是转基因的,转化频率为1.6%。转基因植株携带1至4个转基因拷贝。转基因芽在含有6.6微摩尔6 - 苄氨基嘌呤和1.5毫克/升草丁膦的MS培养基中作为微型插条进行繁殖。芽分别在添加了1.5毫克/升草丁膦的含有赤霉素和吲哚-3-丁酸的MS培养基中伸长和生根。通过微型插条对转基因植株进行微繁殖被证明是一种简单的扩繁材料的方法。发现几株转基因植株对用除草剂Basta进行叶片涂抹具有抗性。

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