Gao Xiao Rong, Wang Guo Kun, Su Qiao, Wang Yan, An Li Jia
Department of Bioscience and Biotechnology, Dalian University of Technology, Dalian, 116024, P.R. China.
Biotechnol Lett. 2007 Nov;29(11):1781-7. doi: 10.1007/s10529-007-9439-x. Epub 2007 Jul 4.
A minimal linear gene cassette (35S-phytase gene-nos) with T-DNA borders was acquired by PCR and directly introduced into soybean through the pollen tube pathway. A total of 13% of T(1 )plants were positive for phyA by specific PCR. Southern blot analyses showed that phyA insertions were harbored stably in T(2) progeny. Phytase expression level increased 2.5-fold over a 6-week period; its highest activity was 150 U/mg protein, compared to 56 U/mg protein in untransformed controls. Activity of phytase increased to 125 FTU/kg in T(3) transgenic seeds as compared to 64 FTU/kg in wild-type plants.
通过PCR获得了一个带有T-DNA边界的最小线性基因盒(35S-植酸酶基因-nos),并通过花粉管通道直接导入大豆。通过特异性PCR分析,共有13%的T(1)植株phyA呈阳性。Southern杂交分析表明,phyA插入片段在T(2)后代中稳定存在。植酸酶表达水平在6周内增加了2.5倍;其最高活性为150 U/mg蛋白,而未转化对照为56 U/mg蛋白。与野生型植株的64 FTU/kg相比,T(3)转基因种子中的植酸酶活性增加到125 FTU/kg。