Qualitative metabolomics-based characterization of a phenolic UDP-xylosyltransferase with a broad substrate spectrum from Lentinus brumalis

Author:

Jeong Eunah12ORCID,Kim Wonyong3ORCID,Son Seungju1,Yang Sungyeon1ORCID,Gwon Dasom12,Hong Jihee12ORCID,Cho Yoonhee4,Jang Chang-Young12ORCID,Steinegger Martin456ORCID,Lim Young Woon47,Kang Kyo Bin12ORCID

Affiliation:

1. College of Pharmacy, Sookmyung Women’s University, Seoul 04310, Korea

2. Research Institute of Pharmaceutical Sciences and Muscle Physiome Research Center, Sookmyung Women’s University, Seoul 04310, Korea

3. Korean Lichen Research Institute, Sunchon National University, Suncheon 57922, Korea

4. School of Biological Sciences, Seoul National University, Seoul 08826, Korea

5. Artificial Intelligence Institute, Seoul National University, Seoul 08826, Korea

6. Institute of Molecular Biology and Genetics, Seoul National University, Seoul 08826, Korea

7. Institute of Microbiology, Seoul National University, Seoul 08826, Korea

Abstract

Wood-decaying fungi are the major decomposers of plant litter. Heavy sequencing efforts on genomes of wood-decaying fungi have recently been made due to the interest in their lignocellulolytic enzymes; however, most parts of their proteomes remain uncharted. We hypothesized that wood-decaying fungi would possess promiscuous enzymes for detoxifying antifungal phytochemicals remaining in the dead plant bodies, which can be useful biocatalysts. We designed a computational mass spectrometry–based untargeted metabolomics pipeline for the phenotyping of biotransformation and applied it to 264 fungal cultures supplemented with antifungal plant phenolics. The analysis identified the occurrence of diverse reactivities by the tested fungal species. Among those, we focused on O -xylosylation of multiple phenolics by one of the species tested, Lentinus brumalis . By integrating the metabolic phenotyping results with publicly available genome sequences and transcriptome analysis, a UDP-glycosyltransferase designated UGT66A1 was identified and validated as an enzyme catalyzing O -xylosylation with broad substrate specificity. We anticipate that our analytical workflow will accelerate the further characterization of fungal enzymes as promising biocatalysts.

Funder

National Research Foundation of Korea

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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