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Synthesis of New Hyperbranched alpha-Glucans from Sucrose by Lactobacillus reuteri 180 Glucansucrase Mutants

机译:罗伊氏乳杆菌180葡聚糖酶突变体由蔗糖合成新的超支链α-葡聚糖

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摘要

alpha-Glucans produced by glucansucrase enzymes of lactic acid bacteria attract strong attention as novel ingredients and functional biopolymers in the food industry. In the present study, alpha-helix 4 amino acid residues D1085, R1088, and N1089 of glucansucrase GTF180 of Lactobacillus reuteri 180 were targeted for mutagenesis both jointly and separately. Analysis of the mutational effects on enzyme function revealed that all D1085 and R1088 mutants catalyzed the synthesis of hyperbranched alpha-glucans with 15-22% branching (a1 -> 3,6) linkages, compared to 13% in the wild-type GTF180. In addition, besides native (a1 -> 6) and (a1 -> 3) linkages, all of the mutations introduced a small amount of (a1 -> 4) linkages (5% at most) in the polysaccharides produced. We conclude that alpha-helix 4 residues, especially D1085 and R1088, constituting part of the +2 acceptor binding subsite, are important determinants for the linkage specificity. The new hyperbranched alpha-glucans provide very interesting structural diversities and may find applications in the food industry.
机译:由乳酸菌的葡糖核酸酶生产的α-葡聚糖作为食品工业中的新型成分和功能性生物聚合物引起了广泛的关注。在本研究中,将路氏乳杆菌180的葡聚糖酶GTF180的α-螺旋4个氨基酸残基D1085,R1088和N1089共同和分别作为诱变靶标。突变对酶功能的影响分析表明,所有D1085和R1088突变体均催化具有15-22%分支(a1-> 3,6)键的超支化α-葡聚糖的合成,而野生型GTF180中为13%。另外,除了天然的(a1→6)和(a1→3)键外,所有的突变都在产生的多糖中引入了少量的(a1→4)键(最多5%)。我们得出结论,构成+2受体结合亚位点的一部分的α-螺旋4残基,尤其是D1085和R1088,是决定连接特异性的重要决定因素。新的超支化α-葡聚糖提供了非常有趣的结构多样性,并可能在食品工业中找到应用。

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