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Modified chitinase from Brevibacillus laterosporus LAK 1210 and uses thereof

机译:来自Brevibacillus Lak 1210的修饰的几丁质酶及其用途

摘要

The present invention discloses a recombinant, modified extracellular chitinase having an amino acid sequence set forth in SEQ ID NO.4 or SEQ ID NO.5. The recombinant, modified chitinase is derived by inserting two-point mutations at positions 661 and 2158 in the native chitinase gene of Brevibacillus laterosporus LAK 1210 which results in amino acid substitution of tyrosine (Y) residue with histidine (H) at positions 221 and 720. The modified chitinase exhibits both exochitinase and endochitinase activity. The recombinant, modified enzyme is thermoactive with a temperature optimum of 55-60° C. and high thermostability (Tm of 66.7° C.), functions in a broad pH range (pH 3.0-11.0) having a pH optimum of 9.0 and also exhibits improved solubility and enhanced efficacy for control of insects and phytopathogenic fungi. The invention further provides improved methods for large scale production of recombinant modified chitinase and rapid, cost-effective purification method by chitin-adsorption affinity chromatography using powdered crustacean shells.
机译:本发明公开了具有在SEQ ID No.4或SEQ ID No.5中阐述的氨基酸序列的重组,改性细胞外逐蛋白酶。通过在Brevibacillus Lak 1210的天然三丁醇酶基因中插入位置661和2158处的两个点突变来衍生重组的修饰的章节酶,这导致酪氨酸(Y)残基的氨基酸取代与组氨酸(H)在221和720时。改性的逐蛋白酶表现出脱氯糖酶和吲哚糖酶活性。重组,改性酶是热活性,温度最佳55-60℃和高热稳定性(Tm的66.7℃),在宽的pH范围(pH3.0-11.0)中具有pH最佳的pH值为9.0和表现出改善的溶解度和增强昆虫和植物疗法真菌的疗效。本发明进一步提供了通过用粉末 - 吸附亲和色谱法使用粉状甲壳类壳的大丁香蛋白吸附亲和色谱法进行大规模生产的改进方法。

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