Discovery of the gut microbial enzyme responsible for bilirubin reduction to urobilinogen.


Journal

bioRxiv : the preprint server for biology
Titre abrégé: bioRxiv
Pays: United States
ID NLM: 101680187

Informations de publication

Date de publication:
08 Feb 2023
Historique:
pubmed: 18 2 2023
medline: 18 2 2023
entrez: 17 2 2023
Statut: epublish

Résumé

The degradation of heme and the interplay of its catabolic derivative, bilirubin, between humans and their gut microbiota is an essential facet of human health. However, the hypothesized bacterial enzyme that reduces bilirubin to urobilinogen, a key step that produces the excretable waste products of this pathway, has remained unidentified. In this study, we used a combination of biochemical analyses and comparative genomics to identify a novel enzyme, BilR, that can reduce bilirubin to urobilinogen. We delineated the BilR sequences from other members of the Old Yellow Enzyme family through the identification of key residues in the active site that are critical for bilirubin reduction and found that BilR is predominantly encoded by Firmicutes in the gut microbiome. Our analysis of human gut metagenomes showed that BilR is a common feature of a healthy adult human microbiome but has a decreased prevalence in neonates and IBD patients. This discovery sheds new light on the role of the gut microbiome in bilirubin metabolism and highlights the significance of the gut-liver axis in maintaining bilirubin homeostasis.

Identifiants

pubmed: 36798240
doi: 10.1101/2023.02.07.527579
pmc: PMC9934709
pii:
doi:

Types de publication

Preprint

Langues

eng

Auteurs

Brantley Hall (B)

Department of Cell Biology and Molecular Genetics, University of Maryland, College Park, College Park, MD 20742, United States.
Center for Bioinformatics and Computational Biology, University of Maryland, College Park, College Park, MD 20742, United States.

Sophia Levy (S)

Department of Cell Biology and Molecular Genetics, University of Maryland, College Park, College Park, MD 20742, United States.

Keith Dufault-Thompson (K)

National Library of Medicine, National Institutes of Health, Bethesda, MD 20894, United States.

Glory Minabou Ndjite (GM)

Department of Cell Biology and Molecular Genetics, University of Maryland, College Park, College Park, MD 20742, United States.

Ashley Weiss (A)

Department of Cell Biology and Molecular Genetics, University of Maryland, College Park, College Park, MD 20742, United States.

Domenick Braccia (D)

Center for Bioinformatics and Computational Biology, University of Maryland, College Park, College Park, MD 20742, United States.

Conor Jenkins (C)

Department of Chemistry and Biochemistry, University of Maryland, College Park, MD 20742, USA.

Yiyan Yang (Y)

National Library of Medicine, National Institutes of Health, Bethesda, MD 20894, United States.

Gabi Arp (G)

Department of Cell Biology and Molecular Genetics, University of Maryland, College Park, College Park, MD 20742, United States.

Stephenie Abeysinghe (S)

Department of Cell Biology and Molecular Genetics, University of Maryland, College Park, College Park, MD 20742, United States.

Madison Jermain (M)

Department of Cell Biology and Molecular Genetics, University of Maryland, College Park, College Park, MD 20742, United States.

Chih Hao Wu (CH)

Program of Computational Biology, Bioinformatics, and Genomics, University of Maryland, College Park, MD 20742, United States.

Xiaofang Jiang (X)

National Library of Medicine, National Institutes of Health, Bethesda, MD 20894, United States.

Classifications MeSH