通过改造底物结合区氨基酸疏水性提高氨肽酶热稳定性

Enhancing Thermostability of Aminopeptidase by Improving the Hydrophobic Interactions in the Substrate Binding Region

DOI：10.3969/j.issn.1673-1689.2020.03.002

中文关键词: 氨肽酶 定点突变 疏水性 热稳定性

英文关键词: aminopeptidase,site-directed mutagenesis,hydrophobic interactions,thermostability

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中文摘要:

通过提高枯草芽孢杆菌来源的氨肽酶底物结合区域氨基酸的疏水性，提高氨肽酶YwaD的热稳定性。基于氨肽酶底物结合区域氨基酸特性分析，选定亲水性氨基酸残基N385为目标，通过定点突变使其突变为疏水氨基酸残基L385，获得突变体N385L。结果表明，与野生型ywaD相比，突变体N385L酶热稳定性明显提高，在80 ℃放置30 min，野生型YwaD完全失活，而突变体N385L仍保留20%的酶活力。另外，突变型N385L对底物氨基酰基-硝基苯胺的亲和力提高了47.4%，催化效率提高了28.5%。该研究有利于提高氨基肽酶工业应用前景。

英文摘要:

The increase of thermostability of aminopeptidase by creating hydrophobic interactions in the substrate binding region was exploited in Bacillus subtilis 168. The hydrophilic residue N385 was targeted and substituted by hydrophobic residue L385. Based on thermostability analysis，N385L mutant was found to retain 20% while the relative activity of the wild type was reduced to 0% at the same temperature（80 ℃）in 30 min. Furthermore，the affinity and catalytic efficiency of the mutant N385L for the subtrate of L-Leu-pNA increased by 47.4% and 28.5%，respectively，compared to wild type. This study will inspire the production of thermostable aminopeptidase for industrial application.

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