Modification of the 4-Hydroxyphenylacetate-3-hydroxylase Substrate Pocket to Increase Activity towards Resveratrol

• Published in: Molecules (Basel, Switzerland) Vol. 28; no. 14; p. 5602
• Main Authors: Zhang, Qianchao, Jin, Yuning, Yang, Kai, Hu, Sheng, Lv, Changjiang, Huang, Jun, Mei, Jiaqi, Zhao, Weirui, Mei, Lehe
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 01.07.2023; MDPI
• Subjects: 4-hydroxyphenylacetate-3-hydroxylase; Amino acids; Efficiency; Enzymes; Flexibility; Health insurance; Hydroxylation; Molecular dynamics; Mutagenesis; ortho-hydroxylation; piceatannol; Resveratrol; semi-rational design; substrate pocket; China; substrate pocket; semi-rational design; 4-hydroxyphenylacetate-3-hydroxylase; ortho-hydroxylation; piceatannol
• ISSN: 1420-3049; 1420-3049
• DOI: 10.3390/molecules28145602

4-Hydroxyphenylacetate-3-hydroxylase (4HPA3H; EC 1.14.14.9) is a heterodimeric flavin-dependent monooxygenase complex that catalyzes the -hydroxylation of resveratrol to produce piceatannol. Piceatannol has various health benefits and valuable applications in food, medicine, and cosmetics. Enhancing the catalytic activity of 4HPA3H toward resveratrol has the potential to benefit piceatannol production. In this study, the critical amino acid residues in the substrate pocket of 4HPA3H that affect its activity toward resveratrol were identified using semi-rational engineering. Two key amino acid sites (I157 and A211) were discovered and the simultaneous "best" mutant I157L/A211D enabled catalytic efficiency ( cat/ m-resveratrol) to increase by a factor of 4.7-fold. Molecular dynamics simulations indicated that the increased flexibility of the 4HPA3H substrate pocket has the potential to improve the catalytic activity of the enzyme toward resveratrol. On this basis, we produced 3.78 mM piceatannol by using the mutant I157L/A211D whole cells. In this study, we successfully developed a highly active 4HPA3H variant for the hydroxylation of resveratrol to piceatannol.