Issue 8, 2015

Resveratrol improves fungal ribosylation capacity through a unique mechanism

Abstract

Ribosylation is a significant modification conferring new complex and broadened cellular roles of compounds, but small organic molecules are rarely ribosylated. Here, we report the 3-O- and 4′-O-α-ribosylation of resveratrol, a phytoalexin that is exogenous to the fungus Daldinia eschscholzii IFB-TL01. The ribosylation is mechanistically due to the resveratrol-activated expression of the silent or less active fungal genes governing the ribosylation of non-fungal phytophenols. The resveratrol-induced ribosylation is also characterized by an increased expression of ribosyltransferases in concert with a rare ribosylating reaction using nicotinamide mononucleotide (NMN) as a ribose donor. The ribosylation-reduced toxicity of resveratrol to D. eschscholzii, along with the involvement of at least two p-glycoproteins in the glycosylation, suggests that such a glycosylation process may be a general strategy for the fungal detoxification of phenolic chemicals. The findings present an updated view of the ribosylation of small molecules, and provide direct chemogenetic evidence that will aid understanding of how phytophenols such as resveratrol function differently in the plant, microbial and animal kingdoms.

Graphical abstract: Resveratrol improves fungal ribosylation capacity through a unique mechanism

Supplementary files

Article information

Article type
Paper
Submitted
21 Oct 2014
Accepted
04 Dec 2014
First published
05 Dec 2014

RSC Adv., 2015,5, 5657-5663

Author version available

Resveratrol improves fungal ribosylation capacity through a unique mechanism

G. Zhao, J. Fan, C. Hua, W. Yan, C. Chen, Y. Lu, R. Jiao and R. Tan, RSC Adv., 2015, 5, 5657 DOI: 10.1039/C4RA12851F

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements