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首页> 外文期刊>Frontiers in Molecular Biosciences >SacB-SacR Gene Cassette As the Negative Selection Marker to Suppress Agrobacterium Overgrowth in Agrobacterium-Mediated Plant Transformation
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SacB-SacR Gene Cassette As the Negative Selection Marker to Suppress Agrobacterium Overgrowth in Agrobacterium-Mediated Plant Transformation

机译:SacB-SacR基因盒作为抑制农杆菌介导的植物转化中农杆菌过度生长的阴性选择标记

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Agrobacterium overgrowth is a common problem in Agrobacterium-mediated plant transfor-mation. To suppress the Agrobacterium overgrowth, various antibiotics have been used during plant tissue culture steps. The antibiotics are expensive and may adversely affect plant cell differentiation and reduce plant transformation efficiency. The SacB-SacR proteins are toxic to most Agrobacterium tumefaciens strains when they are grown on culture medium sup?plemented with sucrose. Therefore, SacB-SacR genes can be used as negative selection markers to suppress the overgrowth of Agrobacterium tumefaciens in the plant tissue culture process. We generated a mutant Agrobacterium tumefaciens strain GV2260 (recA-SacB/R) that has the SacB-SacR cassette inserted into the bacterial genome at the recA gene locus. The mutant Agrobacterium strain is sensitive to sucrose but maintains its ability to transform plant cells in both transient and stable transformation assays. We demonstrated that the mutant strain GV2260 (recA-SacB/R) can be inhibited by sucrose that reduces the overgrowth of Agrobacterium and therefore improves the plant transformation efficiency. We employed GV2260 (recA-SacB/R) to generate stable transgenic N. benthamiana plants expressing a CRISPR-Cas9 for knocking out a WRKY transcrip?tion factor.
机译:农杆菌过度生长是农杆菌介导的植物转化中的普遍问题。为了抑制土壤杆菌的过度生长,在植物组织培养步骤中使用了多种抗生素。抗生素是昂贵的,并且可能不利地影响植物细胞分化并降低植物转化效率。当SacB-SacR蛋白在补充有蔗糖的培养基上生长时,它们对大多数根癌农杆菌菌株均具有毒性。因此,SacB-SacR基因可以用作负选择标记,以抑制植物组织培养过程中根癌农杆菌的过度生长。我们生成了一个突变的根癌农杆菌菌株GV2260(recA-SacB / R),该菌株具有在recA基因位点插入细菌基因组的SacB-SacR盒。突变农杆菌菌株对蔗糖敏感,但在瞬时和稳定转化试验中均保持其转化植物细胞的能力。我们证明了蔗糖可以抑制突变株GV2260(recA-SacB / R),从而减少农杆菌的过度生长,从而提高植物转化效率。我们使用GV2260(recA-SacB / R)生成表达CRISPR-Cas9的稳定转基因本氏烟草植物,以敲除WRKY转录因子。

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