首页> 外文期刊>Biochimica et biophysica acta. Gene structure and expression >Cloning and sequence of a type I pullulanase from an extremely thermophilic anaerobic bacterium, Caldicellulosiruptor saccharolyticus
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Cloning and sequence of a type I pullulanase from an extremely thermophilic anaerobic bacterium, Caldicellulosiruptor saccharolyticus

机译:嗜热厌氧细菌嗜热卡尔德酵母的克隆和I型支链淀粉酶的序列

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摘要

A gene coding for a pullulanase from the obligately anaerobic, extremely thermophilic bacterium Caldicellulosiruptor saccharolyticus has been cloned in Escherichia coli. It consists of an open reading frame (pulA) of 2478 bp which codes for an enzyme of 95 732 Da and is flanked by two other open reading frames. A truncated version of the gene which lacks 381 bp of 5′-sequence also has pullulanase activity and it appears that the amino-terminal portion of the gene is not essential for either activity or thermostability. Amino acid sequence comparisons with other published amylases and pullulanases showed that it possesses homology to the four key regions common to these enzymes.
机译:已经从大肠杆菌中克隆了一种来自专性厌氧的,嗜热性极强的细菌卡尔迪纤维素分解酶糖酶的支链淀粉酶的基因。它由一个2478 bp的开放阅读框(pulA)组成,其编码95 732 Da的酶,两侧是另外两个开放阅读框。缺少381 bp的5'序列的基因的截短形式也具有支链淀粉酶活性,并且看来该基因的氨基末端部分对于活性或热稳定性不是必需的。与其他已发表的淀粉酶和支链淀粉酶的氨基酸序列比较表明,它与这些酶共有的四个关键区域具有同源性。

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