普鲁兰酶
热稳定性
普鲁兰
枯草芽孢杆菌
生物化学
大肠杆菌
麦芽三糖
分子克隆
生物
脂肪酶
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重组DNA
基因
酶
化学
淀粉酶
细菌
基因表达
肽序列
遗传学
多糖
作者
Youran Li,Liang Zhang,Dandan Niu,Zhengxiang Wang,Guiyang Shi
摘要
The pulA1 gene, encoding a novel thermostable type I pullulanase PulA1 from Bacillus sp. CICIM 263, was identified from genomic DNA. The open reading frame of the pulA1 gene was 2655 base pairs long and encoded a polypeptide (PulA1) of 885 amino acids with a calculated molecular mass of 100,887 Da. The pulA1 gene was expressed in Escherichia coli and Bacillus subtilis. Recombinant PuLA1 showed optimal activity at pH 6.5 and 70 °C. The enzyme demonstrated moderate thermostability as PuLA1 maintained more than 88% of its acitivity when incubated at 70 °C for 1 h. The enzyme could completely hydrolyze pullulan to maltotriose, and hydrolytic activity was also detected with glycogen, starch and amylopection, but not with amylose, which is consistent with the property of type I pullulanase. PulA1 may be suitable for industrial applications to improve the yields of fermentable sugars for bioethanol production.
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