Liu Jingran, Li Ren, Miao Jincheng, Sun Hongxu, Chen Qiwei, Song Haiyan, Peng Hui, Chang Yanhong, Luo Hui
Department of Environmental Science and Engineering University of Science and Technology Beijing Beijing China.
Department of Biological Science and Engineering University of Science and Technology Beijing Beijing China.
Eng Life Sci. 2025 Feb 28;25(3):e70013. doi: 10.1002/elsc.70013. eCollection 2025 Mar.
Combined cross-linked enzyme aggregates (combi-CLEAs) represent a promising carrier-free immobilized enzyme technology. This study describes the preparation of combi-CLEAs comprising leucine dehydrogenase (LeuDH) and formate dehydrogenase (FDH) for the regeneration of cofactor nicotinamide adenine dinucleotide necessary for 2-aminobutyric acid production. Different from traditional methods using ammonium sulfate or organic reagents as precipitant, this work utilized low concentrations of calcium ions to purify and precipitate the histidine-tagged enzymes. We developed a simple and environmentally friendly protocol for combi-CLEAs formation, involving precipitation with 10 mM calcium ions at an enzyme activity ratio of 1:2 for LeuDH and FDH, respectively, followed by cross-linking with 0.15% (w/v) glutaraldehyde at 20°C for 2 h at pH 7.5. The optimal catalytic reaction temperature and pH value for the combi-CLEAs were determined to be a temperature of 37°C and a pH of 7.5. The combi-CLEAs demonstrated enhanced thermal and pH tolerance compared to the free enzyme mixture. Moreover, the combi-CLEAs showed good operational stability, retaining 40% of its initial activity after seven cycles of reuse. These findings suggest that the combi-CLEAs of LeuDH and FDH are an efficient and cost-effective option for 2-aminobutyric acid production.
复合交联酶聚集体(combi-CLEAs)代表了一种很有前景的无载体固定化酶技术。本研究描述了用于制备包含亮氨酸脱氢酶(LeuDH)和甲酸脱氢酶(FDH)的combi-CLEAs,用于生产2-氨基丁酸所需的辅因子烟酰胺腺嘌呤二核苷酸的再生。与使用硫酸铵或有机试剂作为沉淀剂的传统方法不同,这项工作利用低浓度的钙离子来纯化和沉淀带有组氨酸标签的酶。我们开发了一种简单且环保的combi-CLEAs形成方案,包括分别以1:2的酶活性比例用10 mM钙离子沉淀LeuDH和FDH,然后在20°C、pH 7.5条件下用0.15%(w/v)戊二醛交联2小时。combi-CLEAs的最佳催化反应温度和pH值分别确定为37°C和7.5。与游离酶混合物相比,combi-CLEAs表现出增强的热耐受性和pH耐受性。此外,combi-CLEAs显示出良好的操作稳定性,在重复使用七个循环后仍保留其初始活性的40%。这些发现表明,LeuDH和FDH的combi-CLEAs是生产2-氨基丁酸的一种高效且经济的选择。