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建立高效的农杆菌介导的盐芥叶盘转化体系。

Establishment of an efficient Agrobacterium tumefaciens-mediated leaf disc transformation of Thellungiella halophila.

作者信息

Li Hong-Qing, Xu Jie, Chen Lei, Li Mei-Ru

机构信息

Guangdong Provincial Key Lab of Biotechnology for Plant Development, South China Normal University, Guangzhou 510631, People's Republic of China.

出版信息

Plant Cell Rep. 2007 Oct;26(10):1785-9. doi: 10.1007/s00299-007-0391-y. Epub 2007 Jun 6.

Abstract

Thellungiella halophila is a salt-tolerant close relative of Arabidopsis, which is adopted as a halophytic model for stress tolerance research. We established an Agrobacterium tumefaciens-mediated transformation procedure for T. halophila. Leaf explants of T. halophila were incubated with A. tumefaciens strain EHA105 containing a binary vector pCAMBIA1301 with the hpt gene as a selectable marker for hygromycin resistance and an intron-containing beta-glucuronidase gene as a reporter gene. Following co-cultivation, leaf explants were cultured on selective medium containing 10 mg l(-1) hygromycin and 500 mg l(-1) cefotaxime. Hygromycin-resistant calluses were induced from the leaf explants after 3 weeks. Shoot regeneration was achieved after transferring the calluses onto fresh medium of the same composition. Finally, the shoots were rooted on half strength MS basal medium supplemented with 10 mg l(-1) hygromycin. Incorporation and expression of the transgenes were confirmed by PCR, Southern blot analysis and GUS histochemical assay. Using this protocol, transgenic T. halophila plants can be obtained in approximately 2 months with a high transformation frequency of 26%.

摘要

盐芥是拟南芥的耐盐近缘种,被用作耐逆性研究的盐生植物模型。我们建立了根癌农杆菌介导的盐芥转化方法。将盐芥叶片外植体与含有二元载体pCAMBIA1301的根癌农杆菌菌株EHA105共同培养,该二元载体带有作为潮霉素抗性选择标记的hpt基因和作为报告基因的含内含子的β-葡萄糖醛酸酶基因。共培养后,将叶片外植体在含有10 mg l(-1)潮霉素和500 mg l(-1)头孢噻肟的选择培养基上培养。3周后从叶片外植体诱导出潮霉素抗性愈伤组织。将愈伤组织转移到相同成分的新鲜培养基上后实现了芽再生。最后,将芽在添加有10 mg l(-1)潮霉素的1/2强度MS基本培养基上生根。通过PCR、Southern杂交分析和GUS组织化学分析证实了转基因的整合和表达。使用该方案,大约2个月内即可获得转基因盐芥植株,转化频率高达26%。

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