7EBO
Crystal structure of a feruloyl esterase LP_0796 from Lactobacillus plantarum
7EBO の概要
| エントリーDOI | 10.2210/pdb7ebo/pdb |
| 分子名称 | Carboxylesterase, SULFATE ION (3 entities in total) |
| 機能のキーワード | feruloyl esterase, lactobacillus plantarum, carboxylesterase, catalytic triad, hydrolase |
| 由来する生物種 | Lactiplantibacillus plantarum WCFS1 |
| タンパク質・核酸の鎖数 | 2 |
| 化学式量合計 | 56002.92 |
| 構造登録者 | |
| 主引用文献 | Zhang, H.,Wen, B.,Liu, Y.,Du, G.,Wei, X.,Imam, K.M.S.U.,Zhou, H.,Fan, S.,Wang, F.,Wang, Y.,Xin, F. A reverse catalytic triad Asp containing loop shaping a wide substrate binding pocket of a feruloyl esterase from Lactobacillus plantarum. Int.J.Biol.Macromol., 184:92-100, 2021 Cited by PubMed Abstract: Feruloyl esterase is an indispensable biocatalyst in food processing, pesticide and pharmaceutical industries, catalyzing the cleavage of the ester bond cross-linked between the polysaccharide side chain of hemicellulose and ferulic acid in plant cell walls. LP_0796 from Lactobacillus plantarum was identified as a feruloyl esterase that may have potential applications in the food industry, but the lack of the substrate recognition and catalytic mechanisms limits its application. Here, LP_0796 showed the highest activity towards methyl caffeate at pH 6.6 and 40 °C. The crystal structure of LP_0796 was determined at 2.5 Å resolution and featured a catalytic triad Asp195-containing loop facing the opposite direction, thus forming a wider substrate binding pocket. Molecular docking simulation and site-directed mutagenesis studies further demonstrated that in addition to the catalytic triad (Ser94, Asp195, His225), Arg125 and Val128 played essential roles in the function of the active site. Our data also showed that Asp mutation of Ala23 and Ile198 increased the catalytic efficiency to 4- and 5-fold, respectively. Collectively, this work provided a better understanding of the substrate recognition and catalytic mechanisms of LP_0796 and may facilitate the future protein design of this important feruloyl esterase. PubMed: 34116094DOI: 10.1016/j.ijbiomac.2021.06.033 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.5 Å) |
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