4EEX
Crystal Structure of Lactococcus lactis Alcohol Dehydrogenase
4EEX の概要
| エントリーDOI | 10.2210/pdb4eex/pdb |
| 関連するPDBエントリー | 4EEZ |
| 分子名称 | Alcohol dehydrogenase 1, ZINC ION, TETRAETHYLENE GLYCOL, ... (4 entities in total) |
| 機能のキーワード | alcohol dehydrogenase, site-saturation mutagenesis, directed evolution, isobutyraldehyde, biofuel, oxidoreductase |
| 由来する生物種 | Lactococcus lactis subsp. lactis |
| タンパク質・核酸の鎖数 | 2 |
| 化学式量合計 | 74226.32 |
| 構造登録者 | Liu, X.,Bastian, S.,Snow, C.D.,Brustad, E.M.,Saleski, T.,Xu, J.H.,Meinhold, P.,Arnold, F.H. (登録日: 2012-03-28, 公開日: 2012-09-26, 最終更新日: 2024-02-28) |
| 主引用文献 | Liu, X.,Bastian, S.,Snow, C.D.,Brustad, E.M.,Saleski, T.E.,Xu, J.H.,Meinhold, P.,Arnold, F.H. Structure-guided engineering of Lactococcus lactis alcohol dehydrogenase LlAdhA for improved conversion of isobutyraldehyde to isobutanol. J.Biotechnol., 164:188-195, 2012 Cited by PubMed Abstract: We have determined the X-ray crystal structures of the NADH-dependent alcohol dehydrogenase LlAdhA from Lactococcus lactis and its laboratory-evolved variant LlAdhA(RE1) at 1.9Å and 2.5Å resolution, respectively. LlAdhA(RE1), which contains three amino acid mutations (Y50F, I212T, and L264V), was engineered to increase the microbial production of isobutanol (2-methylpropan-1-ol) from isobutyraldehyde (2-methylpropanal). Structural comparison of LlAdhA and LlAdhA(RE1) indicates that the enhanced activity on isobutyraldehyde stems from increases in the protein's active site size, hydrophobicity, and substrate access. Further structure-guided mutagenesis generated a quadruple mutant (Y50F/N110S/I212T/L264V), whose KM for isobutyraldehyde is ∼17-fold lower and catalytic efficiency (kcat/KM) is ∼160-fold higher than wild-type LlAdhA. Combining detailed structural information and directed evolution, we have achieved significant improvements in non-native alcohol dehydrogenase activity that will facilitate the production of next-generation fuels such as isobutanol from renewable resources. PubMed: 22974724DOI: 10.1016/j.jbiotec.2012.08.008 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.2 Å) |
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