State Key Laboratory for Conservation and Utilization of Subtropical Agro-Bioresources, Guangxi Research Center for Microbial and Enzyme Engineering Technology, College of Life Science and Technology, Guangxi University, Nanning 530004, China.
Int J Mol Sci. 2024 Nov 7;25(22):11986. doi: 10.3390/ijms252211986.
Rapeseed meal is severely restricted in its utilization as unconventional animal feed due to anti-nutritive compounds, such as glucosinolate, that are degraded to toxic nitriles such as 3-butenenitrile and 4-pentenenitrile in animals. Few studies on nitrilases that can degrade glucosinolate-derived nitriles have been reported thus far. In the present study, a nitrilase gene from was over-expressed in and the purified recombinant nitrilase rGiNIT showed specific activities of 134.48 U/mg and 122.16 U/mg when using 3-butenenitrile and 4-pentenenitrile as substrates at the optimal pH, 7.5, and temperature, 45 °C, which is the highest reported in the literature. The conversion of 3-butenenitrile and 4-pentenenitrile by rGiNIT reached 81.89% and 80.23% after hydrolysis for 15 min and 300 min, respectively. Site-directed mutagenesis and molecular docking analysis revealed that the catalytic ability of rGiNIT depended on the substrate binding pocket comprising 13 key amino acid residues. These results provide a potential enzyme resource for rapeseed meal detoxification and theoretical guidance for protein engineering.
菜粕由于含有芥子碱等抗营养成分,在非常规动物饲料中的应用受到严重限制,这些抗营养成分在动物体内降解会产生有毒的腈类物质,如丙烯腈和戊烯腈。目前,关于能够降解芥子碱衍生腈类物质的腈酶的研究较少。本研究在 中过表达了来自 的腈酶基因,纯化后的重组腈酶 rGiNIT 在最适 pH 值 7.5 和最适温度 45°C 下,以丙烯腈和戊烯腈为底物时的比活力分别为 134.48 U/mg 和 122.16 U/mg,这是文献中报道的最高值。rGiNIT 水解 300 min 后,丙烯腈和戊烯腈的转化率分别达到 81.89%和 80.23%。定点突变和分子对接分析表明,rGiNIT 的催化能力取决于包含 13 个关键氨基酸残基的底物结合口袋。这些结果为菜粕解毒提供了潜在的酶资源,并为蛋白质工程提供了理论指导。