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Laccase-mediated Synthesis of Bioactive Natural Products and Their Analogues

Overview
Journal RSC Chem Biol
Specialty Biology
Date 2022 Jun 27
PMID 35755186
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Abstract

Laccases are a class of multicopper oxidases that catalyse the one-electron oxidation of four equivalents of a reducing substrate, with the concomitant four-electron reduction of dioxygen to water. Typically, they catalyse many anabolic reactions, in which mostly phenolic metabolites were subjected to oxidative coupling. Alternatively, laccases catalyse the degradation or modification of biopolymers like lignin in catabolic processes. In recent years, laccases have proved valuable and green biocatalysts for synthesising compounds with therapeutic value, including antitumor, antibiotic, antimicrobial, and antioxidant agents. Further up to date applications include oxidative depolymerisation of lignin to gain new biomaterials and bioremediation processes of industrial waste. This review summarizes selected examples from the last decade's literature about the laccase-mediated synthesis of biologically active natural products and their analogues; these will include lignans and neolignans, dimeric stilbenoids, biflavonoids, biaryls and other compounds of potential interest for the pharmaceutical industry. In addition, a short section about applications of laccases in natural polymer modification has been included.

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References
1.
Keshmiri-Neghab H, Goliaei B . Therapeutic potential of gossypol: an overview. Pharm Biol. 2013; 52(1):124-8. DOI: 10.3109/13880209.2013.832776. View

2.
Dillies J, Vivien C, Chevalier M, Rulence A, Chataigne G, Flahaut C . Enzymatic depolymerization of industrial lignins by laccase-mediator systems in 1,4-dioxane/water. Biotechnol Appl Biochem. 2020; 67(5):774-782. DOI: 10.1002/bab.1887. View

3.
Hahn V, Mikolasch A, Weitemeyer J, Petters S, Davids T, Lalk M . Ring-Closure Mechanisms Mediated by Laccase to Synthesize Phenothiazines, Phenoxazines, and Phenazines. ACS Omega. 2020; 5(24):14324-14339. PMC: 7315418. DOI: 10.1021/acsomega.0c00719. View

4.
Mori K . Bioactive natural products and chirality. Chirality. 2011; 23(6):449-62. DOI: 10.1002/chir.20930. View

5.
Benedict C, Liu J, Stipanovic R . The peroxidative coupling of hemigossypol to (+)- and (-)-gossypol in cottonseed extracts. Phytochemistry. 2006; 67(4):356-61. DOI: 10.1016/j.phytochem.2005.11.015. View