Structural and Computational Biology Research Unit, Department of Biochemistry, Faculty of Science, Chulalongkorn University, Pathumwan, Bangkok 10330, Thailand.
Department of Biochemistry, Faculty of Science, Chulalongkorn University, Pathumwan, Bangkok 10330, Thailand.
J Phys Chem B. 2021 Jun 10;125(22):5766-5774. doi: 10.1021/acs.jpcb.1c02016. Epub 2021 May 28.
Levan-type fructooligosaccharides (LFOs) and levan can potentially be used as ingredients in prebiotics, skincare products, and antitumor agents. The Y246S mutant of RN-01 levansucrase (oligosaccharide-producing levansucrase, OPL) was reported to productively synthesize LFOs; however, OPL's thermostability is low at high temperatures. To enhance OPL structural stability, this study employed molecular dynamics (AMBER) to identify a highly flexible region, as measured by its average root-mean-square fluctuation (RMSF) value, on the OPL surface and computational protein design (Rosetta) to rigidify and increase favorable interactions to increase its structural stability. AMBER identified region nine (residues 277-317) as a highly flexible region that was selected for design because it has the highest number of residues and the second-highest average RMSF, and it is farthest from the active site. Rosetta designed 14 mutants with the best ΔΔ value in each position, where three mutants have better Δ than OPL. To determine whether their flexibilities and stabilities are lower than those of OPL, all 14 designed mutants were simulated at high temperature (500 K), and we found that K296E, G309S, and A310W mutants were predicted to be more stable and could retain their native structures better than OPL. Our results suggest that enhanced structural stabilities of these mutants are caused by increased hydrogen bond strengths of the designed residues and their neighboring residues. This study designed K296E, G309S, and A310W mutants of OPL with high potential for stability improvement, and they could potentially be used for the effective production of LFOs.
Levan-type 果聚糖(LFOs)和蔗果聚糖有可能被用作益生元、护肤品和抗肿瘤剂的成分。RN-01 蔗糖酶(寡糖产生蔗糖酶,OPL)的 Y246S 突变体能有效地合成 LFOs;然而,OPL 在高温下的热稳定性较低。为了提高 OPL 的结构稳定性,本研究采用分子动力学(AMBER)来识别 OPL 表面上一个高度灵活的区域,该区域的平均均方根波动(RMSF)值较高,并采用计算蛋白质设计(Rosetta)使该区域刚性化并增加有利相互作用,以提高其结构稳定性。AMBER 确定了第 9 区域(残基 277-317)作为一个高度灵活的区域,因为它具有最高数量的残基和第二高的平均 RMSF,而且距离活性位点最远。Rosetta 设计了 14 个在每个位置具有最佳ΔΔ值的突变体,其中 3 个突变体的Δ值优于 OPL。为了确定它们的灵活性和稳定性是否低于 OPL,我们在高温(500K)下模拟了所有 14 个设计的突变体,发现 K296E、G309S 和 A310W 突变体的预测稳定性更高,并且比 OPL 更能保留其天然结构。我们的研究结果表明,这些突变体的结构稳定性增强是由于设计残基及其相邻残基的氢键强度增加所致。本研究设计了 OPL 的 K296E、G309S 和 A310W 突变体,它们具有提高稳定性的潜力,并且可能用于有效生产 LFOs。