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Optimization of enzymatic synthesis of theaflavins from potato polyphenol oxidase

Authors :
Dong Li
Liang Dong
Jieyuan Li
Shiqi Zhang
Yu Lei
Mengsheng Deng
Jingya Li
Source :
Bioprocess and Biosystems Engineering. 45:1047-1055
Publication Year :
2022
Publisher :
Springer Science and Business Media LLC, 2022.

Abstract

Theaflavin (TF), a chemical component important in measuring the quality of fermented tea, has a strong natural antioxidant effect and many pharmacological functions. Enzymatic oxidation has become a widely used method for preparing TFs at the current research stage. Using plant exogenous polyphenol oxidase (PPO) to enzymatically synthesize TFs can significantly increase yield and purity. In this study, tea polyphenols were used as the reaction substrate to discuss the optimal synthesis conditions of potato PPO enzymatic synthesis of theaflavins and the main products of enzymatic synthesis of TFs. The optimal enzymatic synthesis conditions were as follows: pH of the reaction system was 5.5, reaction time was 150 min, substrate concentration was 6.0 mg/mL, reaction temperature was 20 °C, and the maximum amount of TFs produced was 651.75 μg/mL. At the same time, high-performance liquid chromatography was used to determine the content of theaflavins and catechins in the sample to be tested, and the dynamic changes and correlations of the main catechins and theaflavins in the optimal enzymatic system were analyzed. The results showed that epicatechin (EC), epigallocatechin (EGC), epicatechin gallate (ECG), and epigallocatechin gallate (EGCG) are all the main substrates synthesis of TFs. The main substrate of TFs and its strongest enzymatic catalytic effect on EGCG make theaflavin-3,3'-digallate (TFDG) the most important synthetic monomer. In this study, theaflavins were synthesized by polyphenol oxidase catalysis, which laid a foundation for industrialization of theaflavins.

Details

ISSN :
16157605 and 16157591
Volume :
45
Database :
OpenAIRE
Journal :
Bioprocess and Biosystems Engineering
Accession number :
edsair.doi.dedup.....dde3bbfe46a7f76d4dbaa2eebf956107