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转基因大豆中的植酸酶表达:利用无载体构建体的稳定转化

Phytase expression in transgenic soybeans: stable transformation with a vector-less construct.

作者信息

Gao Xiao Rong, Wang Guo Kun, Su Qiao, Wang Yan, An Li Jia

机构信息

Department of Bioscience and Biotechnology, Dalian University of Technology, Dalian, 116024, P.R. China.

出版信息

Biotechnol Lett. 2007 Nov;29(11):1781-7. doi: 10.1007/s10529-007-9439-x. Epub 2007 Jul 4.

Abstract

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.

摘要

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。

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