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来自假单胞菌属的一种新型内切型聚甘露糖醛酸特异性海藻酸裂解酶的特性分析

Characterization of a new endo-type polyM-specific alginate lyase from Pseudomonas sp.

作者信息

Zhu Ben-Wei, Huang Li-Shu-Xin, Tan Hai-Dong, Qin Yu-Qi, Du Yu-Guang, Yin Heng

机构信息

Natural Products and Glyco-Biotechnology Research Group, Liaoning Provincial Key Laboratory of Carbohydrates, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, CAS, Dalian, 116023, People's Republic of China.

出版信息

Biotechnol Lett. 2015 Feb;37(2):409-15. doi: 10.1007/s10529-014-1685-0. Epub 2014 Sep 26.

Abstract

An alginate lyase gene, algA, encoding a new poly β-D-mannuronate (polyM)-specific alginate lyase AlgA, was cloned from Pseudomonas sp. E03. The recombinant AlgA with (His)6-tag, consisting of 364 amino acids (40.4 kDa),was purified using Ni-NTA Sepharose. The purified lyase had maximal activity (222 EU/mg) at pH 8 and 30 °C and also maintained activity between pH 7-9 and below 45 °C. It exclusively and endolytically depolymerized polyM by β-elimination into oligosaccharides with degrees of polymerization (DP) of 2-5. Due to its high substrate specificity, AlgA could be a valuable tool for production of polyM oligosaccharides with low DP and for determining the fine structure of alginate.

摘要

从假单胞菌属E03中克隆出一个编码新型聚β-D-甘露糖醛酸(polyM)特异性海藻酸裂解酶AlgA的海藻酸裂解酶基因algA。带有(His)6标签、由364个氨基酸(40.4 kDa)组成的重组AlgA,通过镍-亚氨基二乙酸琼脂糖凝胶进行纯化。纯化后的裂解酶在pH 8和30℃时具有最大活性(222 EU/mg),并且在pH 7-9和45℃以下也能保持活性。它通过β-消除反应将polyM特异性地、内切地解聚为聚合度(DP)为2-5的寡糖。由于其高底物特异性,AlgA可能是生产低DP的polyM寡糖以及确定海藻酸盐精细结构的有价值工具。

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