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拟南芥中编码α1,3-岩藻糖基转移酶同源物的cDNA的克隆与表达

Cloning and expression of cDNAs encoding alpha1,3-fucosyltransferase homologues from Arabidopsis thaliana.

作者信息

Wilson I B, Rendić D, Freilinger A, Dumić J, Altmann F, Mucha J, Müller S, Hauser M T

机构信息

Institut für Chemie, Universität für Bodenkultur, Vienna, Austria.

出版信息

Biochim Biophys Acta. 2001 Jul 2;1527(1-2):88-96. doi: 10.1016/s0304-4165(01)00151-9.

Abstract

The core alpha1,3-fucosyltransferases are involved in the synthesis of glycans specific to plants and invertebrates which are known to be immunogenic and allergenic. We report the identification, isolation and characterisation of the cDNAs of three genes (FucTA, FucTB and FucTC) encoding proteins similar to alpha1,3-fucosyltransferases in Arabidopsis thaliana. Reverse transcription-polymerase chain reaction was used to amplify the full length coding sequence of FucTA. The FucTA gene, which consists of seven exons, encodes a presumptive protein of 501 amino acids showing an overall sequence identity of 66% to the protein encoded by the recently isolated mung bean Fuc-T C3 cDNA. FucTA was expressed in Pichia pastoris under the control of the AOX1 gene promoter. The soluble enzyme was found to catalyse the same reaction as mung bean core alpha1,3-fucosyltransferase as judged by analyses of the products by MALDI-TOF and high-performance liquid chromatography. The FucTB cDNA was isolated from a lambda-ZAP library, but the clone used an alternative splicing site between the second and third exon resulting in a premature stop codon. The FucTC gene encodes a protein with less than 40% identity to FucTA across 115 amino acids of a total of 401 amino acids and is a member of a new sub-family of plant alpha1,3/4-fucosyltransferase homologues.

摘要

核心α1,3-岩藻糖基转移酶参与植物和无脊椎动物特有的聚糖合成,而这些聚糖具有免疫原性和致敏性。我们报告了在拟南芥中鉴定、分离和表征编码与α1,3-岩藻糖基转移酶相似蛋白质的三个基因(FucTA、FucTB和FucTC)的cDNA。采用逆转录-聚合酶链反应扩增FucTA的全长编码序列。FucTA基因由七个外显子组成,编码一个推定的501个氨基酸的蛋白质,与最近分离的绿豆Fuc-T C3 cDNA编码的蛋白质整体序列同一性为66%。FucTA在AOX1基因启动子的控制下在毕赤酵母中表达。通过基质辅助激光解吸电离飞行时间质谱和高效液相色谱对产物进行分析判断,发现可溶性酶催化与绿豆核心α1,3-岩藻糖基转移酶相同的反应。FucTB cDNA是从λ-ZAP文库中分离得到的,但该克隆在第二和第三外显子之间使用了一个替代剪接位点,导致提前出现终止密码子。FucTC基因编码的蛋白质在总共401个氨基酸中的115个氨基酸上与FucTA的同一性小于40%,是植物α1,3/4-岩藻糖基转移酶同源物新亚家族的成员。

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