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全细胞生物催化、酶法和绿色化学方法生产白藜芦醇及其衍生物。

Whole-cell biocatalytic, enzymatic and green chemistry methods for the production of resveratrol and its derivatives.

机构信息

Research Unit, Induced Resistance and Plant Bioprotection, EA 4707, SFR Condorcet FR CNRS 3417, Faculty of Sciences, University of Reims Champagne-Ardenne, PO Box 1039, 51687 Reims Cedex 2, France.

Laboratory of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Santiago de Compostela, Campus Vida, 15782 Santiago de Compostela, Spain; Instituto de Investigación e Innovación en Salud, Facultad de Ciencias de la Salud, Universidad Central de Chile, Chile.

出版信息

Biotechnol Adv. 2020 Mar-Apr;39:107461. doi: 10.1016/j.biotechadv.2019.107461. Epub 2019 Oct 31.

Abstract

Resveratrol and the biosynthetically related stilbenes are plant secondary metabolites with diverse pharmacological effects. The versatile functions of these compounds in plant defense mechanisms as phytoalexins on one hand, and in human health as potential pharmaceutical agents on the other, have attracted lots of interest in recent years to understand their biosynthetic pathways and their biological properties. Because of difficulties in obtaining resveratrol and its glucosylated derivatives as well as oligomeric forms in sufficient amounts for evaluation of their activity by plant sourcing or total synthesis, biotechnology may provide a competitive approach for the large-scale and low cost production of biologically active stilbenes. Additionally, one major limitation in the use of resveratrol and related aglycone derivatives as therapeutic agents is associated with their inherent poor aqueous solubility and low bioavailability. This article examines approaches for the synthesis of potential pharmacologically resveratrol derivatives in vivo by exploiting whole microorganisms, enzymatic and biocatalytic approaches allowing their full utilization for medicine, food and cosmetic applications. These methods also have the advantage of enabling the one-step production of stilbene compounds, compared to the time-consuming and environmentally unfriendly procedures used for their total synthesis or their extraction from plants. Increasing the desired products yield and biological activity through glucosylation (β-D-glucosides versus α-D-glucosides) and oligomerization methodologies of resveratrol including green chemistry methods in organic solvent-free media are discussed as well.

摘要

白藜芦醇和生物合成相关的芪类化合物是具有多种药理作用的植物次生代谢物。这些化合物在植物防御机制中的多功能性,一方面作为植物抗毒素,另一方面作为人类健康的潜在药物,近年来引起了人们的极大兴趣,以了解它们的生物合成途径和生物学特性。由于从植物中获取白藜芦醇及其葡萄糖苷衍生物以及低聚形式以评估其活性的数量有限,并且总合成也存在困难,因此生物技术可能为大规模、低成本生产具有生物活性的芪类化合物提供一种有竞争力的方法。此外,将白藜芦醇和相关糖苷衍生物用作治疗剂的一个主要限制是与它们固有的较差的水溶解度和低生物利用度有关。本文通过利用整个微生物、酶和生物催化方法来检查体内合成潜在药理学上有价值的白藜芦醇衍生物的方法,从而可以充分利用它们在医学、食品和化妆品中的应用。与用于其全合成或从植物中提取的耗时且对环境不友好的过程相比,这些方法还具有一步生产芪类化合物的优势。通过葡糖苷化(β-D-葡萄糖苷与α-D-葡萄糖苷)和白藜芦醇的寡聚化方法(包括有机溶剂中绿色化学方法)提高所需产物的产率和生物活性也进行了讨论。

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