Guo Xiaojia, Wang Xueying, Hu Yinghan, Zhang Lingyun, Zhao Zongbao K
MOE Key Laboratory of Bio-Intelligent Manufacturing, School of Bioengineering, Dalian University of Technology, Dalian, 116024, China.
Laboratory of Biotechnology, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian, 116023, China.
Sci Rep. 2024 Nov 20;14(1):28701. doi: 10.1038/s41598-024-79885-z.
Formate dehydrogenase (FDH) is widely applied in regeneration of redox cofactors. There are continuing interests to engineer FDH for improved catalytic activity and cofactor preference. In the crystal structure of FDH from Pseudomonas sp. 101 (pseFDH), the C terminus with 9 amino acid residues cannot be resolved. However, our earlier work showed mutations at C terminus led pseFDH variants to favor a non-natural cofactor nicotinamide cytosine dinucleotide (NCD). Here, we investigated the role of C-terminal residues on cofactor preference by truncating their corresponding C terminus of pseFDH variants. Sequence comparison analysis showed that C-terminal residues were barely conservative among different FDHs. pseFDH and mutants with their C termini truncated were constructed, and the resulted variants showed improved preference to NCD mainly because NAD-dependent activity dropped more substantially. Further structure analysis showed that these pseFDH variants had their cofactor binding domains reconstructed to favor molecular interactions with NCD. Our work indicated that C-terminal residues of pseFDH affected enzyme activity and cofactor preference, which provides a new approach for ameliorating the performance of redox enzymes.
甲酸脱氢酶(FDH)在氧化还原辅因子的再生中有着广泛应用。人们一直在致力于改造FDH以提高其催化活性和辅因子偏好性。在来自假单胞菌属101(pseFDH)的FDH晶体结构中,包含9个氨基酸残基的C末端无法解析。然而,我们早期的工作表明,C末端的突变使pseFDH变体更倾向于一种非天然辅因子烟酰胺胞嘧啶二核苷酸(NCD)。在此,我们通过截短pseFDH变体相应的C末端来研究C末端残基在辅因子偏好性方面的作用。序列比较分析表明,不同FDH之间C末端残基几乎没有保守性。构建了pseFDH及其C末端被截短的突变体,结果变体对NCD的偏好性提高,主要是因为依赖烟酰胺腺嘌呤二核苷酸(NAD)的活性下降得更显著。进一步的结构分析表明,这些pseFDH变体的辅因子结合结构域发生了重构,以利于与NCD的分子相互作用。我们的工作表明,pseFDH的C末端残基影响酶活性和辅因子偏好性,这为改善氧化还原酶的性能提供了一种新方法。