Boscariol R L, Almeida W A B, Derbyshire M T V C, Mourão Filho F A A, Mendes B M J
Laboratório de Biotecnologia Vegetal, Centro de Energia Nuclear na Agricultura, Universidade de São Paulo, Piracicaba 13 400-970 São Paulo, Brazil.
Plant Cell Rep. 2003 Sep;22(2):122-8. doi: 10.1007/s00299-003-0654-1. Epub 2003 Jul 19.
A new method for obtaining transgenic sweet orange plants was developed in which positive selection (Positech) based on the Escherichia coli phosphomannose-isomerase (PMI) gene as the selectable marker gene and mannose as the selective agent was used. Epicotyl segments from in vitro-germinated plants of Valencia, Hamlin, Natal and Pera sweet oranges were inoculated with Agrobacterium tumefaciens EHA101-pNOV2116 and subsequently selected on medium supplemented with different concentrations of mannose or with a combination of mannose and sucrose as a carbon source. Genetic transformation was confirmed by PCR and Southern blot. The transgene expression was evaluated using a chlorophenol red assay and isoenzymes. The transformation efficiency rate ranged from 3% to 23.8%, depending on cultivar. This system provides an efficient manner for selecting transgenic sweet orange plants without using antibiotics or herbicides.
开发了一种获得转基因甜橙植株的新方法,该方法使用基于大肠杆菌磷酸甘露糖异构酶(PMI)基因作为选择标记基因以及甘露糖作为选择剂的正向选择(Positech)。用根癌农杆菌EHA101-pNOV2116接种来自瓦伦西亚、哈姆林、纳塔尔和佩拉甜橙的体外萌发植株的上胚轴切段,随后在补充有不同浓度甘露糖或甘露糖与蔗糖组合作为碳源的培养基上进行选择。通过PCR和Southern印迹确认遗传转化。使用氯酚红测定法和同工酶评估转基因表达。转化效率范围为3%至23.8%,取决于品种。该系统为选择转基因甜橙植株提供了一种无需使用抗生素或除草剂的有效方式。