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根癌农杆菌介导的欧洲黑松种子叶转化:影响uidA基因转移效率的因素评估

Agrobacterium tumefaciens-mediated transformation of Pinus pinea L. cotyledons: an assessment of factors influencing the efficiency of uidA gene transfer.

作者信息

Humara J M, López M, Ordás R J

机构信息

Dpto. Biología de Organismos y Sistemas, Unidad de Fisiología Vegetal, C/Catedrático Rodrigo Uría s/n, Universidad de Oviedo,E-33071 Oviedo, Asturias, Spain Istituto Universitario de Biotecnología de Asturias-CNB (CSIC), Universidad de Oviedo, E-33071 Oviedo, Asturias, Spain e-mail:

出版信息

Plant Cell Rep. 1999 Nov;19(1):51-58. doi: 10.1007/s002990050709.

DOI:10.1007/s002990050709
PMID:30754758
Abstract

This study is the first report of a protocol for transfer and expression of foreign chimeric genes into cotyledons excised from Pinus pinea L. embryos. Agrobacterium tumefaciens EHA105 harbouring the plasmid p35SGUSint was more infective than LBA4404 or C58 GV3850, as determined by the percentage of cotyledons showing uidA expression. Factors which significantly affected the T-DNA transfer included: (1) preinduction and concentration of bacteria, (2) days of coculture and (3) the wounding procedure applied. More efficient transfer of the uidA gene was achieved growing the bacteria in YEP medium at pH 7, infecting the cotyledons according to the sonication-assisted Agrobacterium-mediated transformation procedure with a bacterial density of 1 (OD) for 5 min, and coculture for 72 h. Using this protocol, 49.7% of the cotyledons showed a diffuse blue staining 7 days after infection. However, all were necrotic 30 days after inoculation. Since a decrease in bacterial density to 0.01 allowed the recovery of about 4% of cotyledons forming buds 1 month after inoculation, we conclude that the high mortality associated with the infection may be related to the hypersensitive response of the plant to bacterial infection.

摘要

本研究首次报道了将外源嵌合基因转入欧洲赤松胚胎切下的子叶并使其表达的实验方案。通过显示uidA表达的子叶百分比测定,携带质粒p35SGUSint的根癌农杆菌EHA105比LBA4404或C58 GV3850更具感染性。显著影响T-DNA转移的因素包括:(1)细菌的预诱导和浓度,(2)共培养天数,以及(3)采用的创伤处理方法。在pH值为7的YEP培养基中培养细菌,按照超声辅助农杆菌介导的转化程序,以细菌密度1(OD)感染子叶5分钟,并共培养72小时,可实现更高效的uidA基因转移。使用该方案,49.7%的子叶在感染7天后显示出弥漫性蓝色染色。然而,接种30天后所有子叶均坏死。由于将细菌密度降至0.01可使约4%的子叶在接种1个月后形成芽,我们得出结论,与感染相关的高死亡率可能与植物对细菌感染的超敏反应有关。

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