Cargando…
Anaerobic 4-hydroxyproline utilization: Discovery of a new glycyl radical enzyme in the human gut microbiome uncovers a widespread microbial metabolic activity
The discovery of enzymes responsible for previously unappreciated microbial metabolic pathways furthers our understanding of host-microbe and microbe-microbe interactions. We recently identified and characterized a new gut microbial glycyl radical enzyme (GRE) responsible for anaerobic metabolism of...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219649/ https://www.ncbi.nlm.nih.gov/pubmed/29405826 http://dx.doi.org/10.1080/19490976.2018.1435244 |
_version_ | 1783368691586433024 |
---|---|
author | Huang, Yolanda Y. Martínez-del Campo, Ana Balskus, Emily P. |
author_facet | Huang, Yolanda Y. Martínez-del Campo, Ana Balskus, Emily P. |
author_sort | Huang, Yolanda Y. |
collection | PubMed |
description | The discovery of enzymes responsible for previously unappreciated microbial metabolic pathways furthers our understanding of host-microbe and microbe-microbe interactions. We recently identified and characterized a new gut microbial glycyl radical enzyme (GRE) responsible for anaerobic metabolism of trans-4-hydroxy-l-proline (Hyp). Hyp dehydratase (HypD) catalyzes the removal of water from Hyp to generate Δ(1)-pyrroline-5-carboxylate (P5C). This enzyme is encoded in the genomes of a diverse set of gut anaerobes and is prevalent and abundant in healthy human stool metagenomes. Here, we discuss the roles HypD may play in different microbial metabolic pathways as well as the potential implications of this activity for colonization resistance and pathogenesis within the human gut. Finally, we present evidence of anaerobic Hyp metabolism in sediments through enrichment culturing of Hyp-degrading bacteria, highlighting the wide distribution of this pathway in anoxic environments beyond the human gut. |
format | Online Article Text |
id | pubmed-6219649 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-62196492018-11-07 Anaerobic 4-hydroxyproline utilization: Discovery of a new glycyl radical enzyme in the human gut microbiome uncovers a widespread microbial metabolic activity Huang, Yolanda Y. Martínez-del Campo, Ana Balskus, Emily P. Gut Microbes Addendum The discovery of enzymes responsible for previously unappreciated microbial metabolic pathways furthers our understanding of host-microbe and microbe-microbe interactions. We recently identified and characterized a new gut microbial glycyl radical enzyme (GRE) responsible for anaerobic metabolism of trans-4-hydroxy-l-proline (Hyp). Hyp dehydratase (HypD) catalyzes the removal of water from Hyp to generate Δ(1)-pyrroline-5-carboxylate (P5C). This enzyme is encoded in the genomes of a diverse set of gut anaerobes and is prevalent and abundant in healthy human stool metagenomes. Here, we discuss the roles HypD may play in different microbial metabolic pathways as well as the potential implications of this activity for colonization resistance and pathogenesis within the human gut. Finally, we present evidence of anaerobic Hyp metabolism in sediments through enrichment culturing of Hyp-degrading bacteria, highlighting the wide distribution of this pathway in anoxic environments beyond the human gut. Taylor & Francis 2018-06-04 /pmc/articles/PMC6219649/ /pubmed/29405826 http://dx.doi.org/10.1080/19490976.2018.1435244 Text en © 2018 Yolanda Y. Huang, Ana Martínez-del Campo, and Emily P. Balskus. Published with license by Taylor & Francis http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License http://creativecommons.org/licenses/by-nc-nd/4.0/, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted. |
spellingShingle | Addendum Huang, Yolanda Y. Martínez-del Campo, Ana Balskus, Emily P. Anaerobic 4-hydroxyproline utilization: Discovery of a new glycyl radical enzyme in the human gut microbiome uncovers a widespread microbial metabolic activity |
title | Anaerobic 4-hydroxyproline utilization: Discovery of a new glycyl radical enzyme in the human gut microbiome uncovers a widespread microbial metabolic activity |
title_full | Anaerobic 4-hydroxyproline utilization: Discovery of a new glycyl radical enzyme in the human gut microbiome uncovers a widespread microbial metabolic activity |
title_fullStr | Anaerobic 4-hydroxyproline utilization: Discovery of a new glycyl radical enzyme in the human gut microbiome uncovers a widespread microbial metabolic activity |
title_full_unstemmed | Anaerobic 4-hydroxyproline utilization: Discovery of a new glycyl radical enzyme in the human gut microbiome uncovers a widespread microbial metabolic activity |
title_short | Anaerobic 4-hydroxyproline utilization: Discovery of a new glycyl radical enzyme in the human gut microbiome uncovers a widespread microbial metabolic activity |
title_sort | anaerobic 4-hydroxyproline utilization: discovery of a new glycyl radical enzyme in the human gut microbiome uncovers a widespread microbial metabolic activity |
topic | Addendum |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219649/ https://www.ncbi.nlm.nih.gov/pubmed/29405826 http://dx.doi.org/10.1080/19490976.2018.1435244 |
work_keys_str_mv | AT huangyolanday anaerobic4hydroxyprolineutilizationdiscoveryofanewglycylradicalenzymeinthehumangutmicrobiomeuncoversawidespreadmicrobialmetabolicactivity AT martinezdelcampoana anaerobic4hydroxyprolineutilizationdiscoveryofanewglycylradicalenzymeinthehumangutmicrobiomeuncoversawidespreadmicrobialmetabolicactivity AT balskusemilyp anaerobic4hydroxyprolineutilizationdiscoveryofanewglycylradicalenzymeinthehumangutmicrobiomeuncoversawidespreadmicrobialmetabolicactivity |