Yu Shuhuai, Wang Xiao, Zhang Tao, Stressler Timo, Fischer Lutz, Jiang Bo, Mu Wanmeng
State Key Laboratory of Food Science and Technology, Jiangnan University, Wuxi, 214122, Jiangsu, People's Republic of China.
Synergetic Innovation Center of Food Safety and Nutrition, Jiangnan University, Wuxi, 214122, Jiangsu, People's Republic of China.
PLoS One. 2015 Nov 10;10(11):e0142640. doi: 10.1371/journal.pone.0142640. eCollection 2015.
Previously, a di-D-fructofuranose 1,2':2,3' dianhydride (DFA III)-producing strain, Arthrobacter aurescens SK8.001, was isolated from soil, and the gene cloning and characterization of the DFA III-forming enzyme was studied. In this study, a DFA III hydrolysis enzyme (DFA IIIase)-encoding gene was obtained from the same strain, and the DFA IIIase gene was cloned and expressed in Escherichia coli. The SDS-PAGE and gel filtration results indicated that the purified enzyme was a homotrimer holoenzyme of 145 kDa composed of subunits of 49 kDa. The enzyme displayed the highest catalytic activity for DFA III at pH 5.5 and 55°C, with specific activity of 232 U mg-1. Km and Vmax for DFA III were 30.7 ± 4.3 mM and 1.2 ± 0.1 mM min-1, respectively. Interestingly, DFA III-forming enzymes and DFA IIIases are highly homologous in amino acid sequence. The molecular modeling and docking of DFA IIIase were first studied, using DFA III-forming enzyme from Bacillus sp. snu-7 as a template. It was suggested that A. aurescens DFA IIIase shared a similar three-dimensional structure with the reported DFA III-forming enzyme from Bacillus sp. snu-7. Furthermore, their catalytic sites may occupy the same position on the proteins. Based on molecular docking analysis and site-directed mutagenesis, it was shown that D207 and E218 were two potential critical residues for the catalysis of A. aurescens DFA IIIase.
此前,从土壤中分离出一株产二 - D - 呋喃果糖1,2':2,3' 二酐(DFA III)的菌株——金色节杆菌SK8.001,并对DFA III合成酶进行了基因克隆和特性研究。在本研究中,从同一菌株中获得了一个编码DFA III水解酶(DFA IIIase)的基因,并将DFA IIIase基因克隆到大肠杆菌中进行表达。SDS - PAGE和凝胶过滤结果表明,纯化后的酶是一种由49 kDa亚基组成的145 kDa同三聚体全酶。该酶在pH 5.5和55°C时对DFA III表现出最高催化活性,比活性为232 U mg-1。DFA III的Km和Vmax分别为30.7 ± 4.3 mM和1.2 ± 0.1 mM min-1。有趣的是,DFA III合成酶和DFA IIIase在氨基酸序列上高度同源。首次以芽孢杆菌属snu - 7的DFA III合成酶为模板,对DFA IIIase进行了分子建模和对接研究。结果表明,金色节杆菌DFA IIIase与已报道的芽孢杆菌属snu - 7的DFA III合成酶具有相似的三维结构。此外,它们的催化位点可能在蛋白质上占据相同位置。基于分子对接分析和定点诱变,结果表明D207和E218是金色节杆菌DFA IIIase催化的两个潜在关键残基。