首页> 外文期刊>FEMS Microbiology Letters >Cloning and expression of an alpha-amylase encoding gene from the hyperthermophilic archaebacterium Thermococcus hydrothermalis and biochemical characterisation of the recombinant enzyme
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Cloning and expression of an alpha-amylase encoding gene from the hyperthermophilic archaebacterium Thermococcus hydrothermalis and biochemical characterisation of the recombinant enzyme

机译:嗜热嗜热嗜热球菌α-淀粉酶编码基因的克隆表达及重组酶的生化特性

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摘要

An alpha-amylase encoding gene from the extremely thermophilic Archaea Thermococcus hydrothermalis was cloned and expressed in Escherichia coli. The encoded alpha-amylase possesses molecular characteristics specific to the Archaea, especially from Pyrococcus species, with biochemical characteristics of the alpha-amylases from Thermococcus. The gene is 1374 bp long and encodes a protein of 457 amino acids composed of a 22 amino acid putative signal peptide and a 435 amino acid mature protein (calculated molecular mass 49 236 Da). The T. hydrothermalis recombinant alpha-amylase is optimally active at 75-85 degrees C and at pH 5.0-5.5. (C) 2000 Federation of European Microbiological Societies. Published by Elsevier Science B.V. All rights reserved. [References: 18]
机译:克隆了极热嗜热古生球菌的α-淀粉酶编码基因,并在大肠杆菌中表达。编码的α-淀粉酶具有古细菌特有的分子特征,特别是来自火球菌的分子,并且具有来自嗜热球菌的α-淀粉酶的生化特征。该基因长1374 bp,编码一个457个氨基酸的蛋白质,该蛋白质由22个氨基酸的推定信号肽和435个氨基酸的成熟蛋白质组成(计算分子量49236 Da)。嗜热热菌(T.hydrothermalis)重组α-淀粉酶在75-85℃和pH 5.0-5.5下具有最佳活性。 (C)2000年欧洲微生物学会联合会。由Elsevier Science B.V.保留所有权利。 [参考:18]

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