Zhu Ben-Wei, Huang Li-Shu-Xin, Tan Hai-Dong, Qin Yu-Qi, Du Yu-Guang, Yin Heng
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.
Biotechnol Lett. 2015 Feb;37(2):409-15. doi: 10.1007/s10529-014-1685-0. Epub 2014 Sep 26.
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.
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。