莽草激酶II表达体系的构建及莽草酸3-磷酸的制备

H. Akiyama, H. Okunuki, S. Tsuzuki, S. Arami, H. Miura, J. Sakushima, R. Teshima, Y. Goda, A. Hind, J. Sawada, M. Toyoda
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引用次数: 3

摘要

以莽草酸3-磷酸(S-3-P)为底物检测转基因大豆中表达的5-烯醇丙酮基莽草酸3-磷酸合成酶(CP4EPSPS)的酶活性。因此,我们尝试在大肠杆菌中过表达莽草酸激酶II (SK-II),以生物合成获得S-3-P。在表达载体pET22b(+)中构建了编码SK-II的aroL基因。用电穿孔法将aroL表达载体转染大肠杆菌BL21。所得aroL蛋白的活性通过高效液相色谱(HPLC)用氨基硅胶柱和标记ATP的[32P]掺入莽草酸中证实。反应产物采用碳柱-高碘酸盐处理的液相色谱/质谱法测定。采用碳柱的高效液相色谱法不使用非挥发性缓冲液作为流动相。因此,该方法可用于从SK-II的粗反应混合物中制备S-3-P。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Construction of an Expression System of Shikimate Kinase II and Preparation of Shikimic Acid 3-Phosphate
Shikimic acid 3-phosphate (S-3-P) is needed as a substrate to detect the enzyme activity of 5-enolpyruvylshikimic acid 3-phosphate synthase (CP4EPSPS), which is expressed in genetically modified soybeans. Therefore, we attempted the over-expression of shikimate kinase II (SK-II) in E. coli to biosynthetically obtain S-3-P. The aroL gene encoding SK-II was constructed in the expression vector pET22b(+). The aroL expression vector was then transfected into E. coli strain BL21 using the electroporation method. The activity of the obtained aroL protein was confirmed by HPLC using an amino-silica column and incorporation of [32P] from labeled ATP to shikimic acid. The determination of the reaction product was performed by LC/MS using a carbon column and periodate treatment.HPLC using a carbon column does not use a non-volatile buffer as the mobile phase. Thus, this method should be useful for preparing S-3-P from the crude reaction mixture of SK-II.
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