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红豆杉酰基转移酶cDNA的克隆与表达

Cloning and expression of Taxus acyltransferase cDNA.

作者信息

Tu Jun, Zhu Ping, Cheng Ke-Di, Liu Jiangguo

机构信息

Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College, 1 Xian Nong Tan Street, Beijing 100050, P. R. China.

出版信息

Z Naturforsch C J Biosci. 2004 Sep-Oct;59(9-10):755-61. doi: 10.1515/znc-2004-9-1022.

Abstract

A new full-length acyltransferase cDNA was obtained from Taxus chinensis by homology-based cloning strategy. The cDNA has an open-reading frame of 1,275 nucleotides, which encodes 425 amino acids with a calculated molecular weight of 47,241 Da and an estimated pI value of 5.93. The deduced amino acid sequence resembles the sequences of other cloned acyltransferases (56-61% identity; 71-75% similarity) involved directly in taxol biosynthetic pathways. This cDNA was expressed in Escherichia coli using the expression vector pET32a(+). The expression band corresponds to the calculated mass plus the N-terminal fusion protein derived from the vector.

摘要

通过基于同源性的克隆策略,从中国红豆杉中获得了一个新的全长酰基转移酶cDNA。该cDNA具有1275个核苷酸的开放阅读框,编码425个氨基酸,计算分子量为47241Da,估计pI值为5.93。推导的氨基酸序列与其他直接参与紫杉醇生物合成途径的克隆酰基转移酶序列相似(同一性为56 - 61%;相似性为71 - 75%)。使用表达载体pET32a(+)在大肠杆菌中表达该cDNA。表达条带对应于计算出的分子量加上来自载体的N端融合蛋白。

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