Wilkie S E, Roper J M, Smith A G, Warren M J
School of Biological Sciences, Queen Mary and Westfield College, London, UK.
Plant Mol Biol. 1995 Mar;27(6):1227-33. doi: 10.1007/BF00020897.
A clone encoding aspartate aminotransferase (AAT, EC 2.6.1.1) was isolated from an Arabidopsis thaliana leaf cDNA library. This clone contains a 1365 bp open reading frame encoding a polypeptide of 49.8 kDa, designated Ataat1. The clone was shown to contain a chloroplastic isoenzyme as an in organellar protein import assay demonstrated that a radiolabelled transcription/translation product of 49.8 kDa was imported into viable pea chloroplasts and was subsequently processed to yield a mature protein of 45 kDa. The open reading frame corresponding to the predicted mature AAT was manipulated into an expression construct (pEC14). Transformed Escherichia coli cells containing pEC14 expressed up to 16 times more AAT activity than vector only controls, thus demonstrating conclusively that the clone encoded AAT.
从拟南芥叶片cDNA文库中分离出一个编码天冬氨酸转氨酶(AAT,EC 2.6.1.1)的克隆。该克隆含有一个1365 bp的开放阅读框,编码一个49.8 kDa的多肽,命名为Ataat1。由于细胞器内蛋白质导入试验表明,一个49.8 kDa的放射性标记转录/翻译产物被导入到活的豌豆叶绿体中,随后加工产生一个45 kDa的成熟蛋白,因此该克隆被证明含有一种叶绿体同工酶。将对应于预测成熟AAT的开放阅读框构建到一个表达载体(pEC14)中。含有pEC14的转化大肠杆菌细胞表达的AAT活性比仅含载体的对照高16倍,从而确凿地证明该克隆编码AAT。