Cargando…
A Proterozoic microbial origin of extant cyanide-hydrolyzing enzyme diversity
In addition to its role as a toxic environmental contaminant, cyanide has been hypothesized to play a key role in prebiotic chemistry and early biogeochemical evolution. While cyanide-hydrolyzing enzymes have been studied and engineered for bioremediation, the extant diversity of these enzymes remai...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10098168/ https://www.ncbi.nlm.nih.gov/pubmed/37065136 http://dx.doi.org/10.3389/fmicb.2023.1130310 |
_version_ | 1785024744126414848 |
---|---|
author | Schwartz, Sarah L. Rangel, L. Thiberio Payette, Jack G. Fournier, Gregory P. |
author_facet | Schwartz, Sarah L. Rangel, L. Thiberio Payette, Jack G. Fournier, Gregory P. |
author_sort | Schwartz, Sarah L. |
collection | PubMed |
description | In addition to its role as a toxic environmental contaminant, cyanide has been hypothesized to play a key role in prebiotic chemistry and early biogeochemical evolution. While cyanide-hydrolyzing enzymes have been studied and engineered for bioremediation, the extant diversity of these enzymes remains underexplored. Additionally, the age and evolution of microbial cyanide metabolisms is poorly constrained. Here we provide comprehensive phylogenetic and molecular clock analyses of the distribution and evolution of the Class I nitrilases, thiocyanate hydrolases, and nitrile hydratases. Molecular clock analyses indicate that bacterial cyanide-reducing nitrilases were present by the Paleo- to Mesoproterozoic, and were subsequently horizontally transferred into eukaryotes. These results present a broad diversity of microbial enzymes that could be optimized for cyanide bioremediation. |
format | Online Article Text |
id | pubmed-10098168 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100981682023-04-14 A Proterozoic microbial origin of extant cyanide-hydrolyzing enzyme diversity Schwartz, Sarah L. Rangel, L. Thiberio Payette, Jack G. Fournier, Gregory P. Front Microbiol Microbiology In addition to its role as a toxic environmental contaminant, cyanide has been hypothesized to play a key role in prebiotic chemistry and early biogeochemical evolution. While cyanide-hydrolyzing enzymes have been studied and engineered for bioremediation, the extant diversity of these enzymes remains underexplored. Additionally, the age and evolution of microbial cyanide metabolisms is poorly constrained. Here we provide comprehensive phylogenetic and molecular clock analyses of the distribution and evolution of the Class I nitrilases, thiocyanate hydrolases, and nitrile hydratases. Molecular clock analyses indicate that bacterial cyanide-reducing nitrilases were present by the Paleo- to Mesoproterozoic, and were subsequently horizontally transferred into eukaryotes. These results present a broad diversity of microbial enzymes that could be optimized for cyanide bioremediation. Frontiers Media S.A. 2023-03-30 /pmc/articles/PMC10098168/ /pubmed/37065136 http://dx.doi.org/10.3389/fmicb.2023.1130310 Text en Copyright © 2023 Schwartz, Rangel, Payette and Fournier. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Schwartz, Sarah L. Rangel, L. Thiberio Payette, Jack G. Fournier, Gregory P. A Proterozoic microbial origin of extant cyanide-hydrolyzing enzyme diversity |
title | A Proterozoic microbial origin of extant cyanide-hydrolyzing enzyme diversity |
title_full | A Proterozoic microbial origin of extant cyanide-hydrolyzing enzyme diversity |
title_fullStr | A Proterozoic microbial origin of extant cyanide-hydrolyzing enzyme diversity |
title_full_unstemmed | A Proterozoic microbial origin of extant cyanide-hydrolyzing enzyme diversity |
title_short | A Proterozoic microbial origin of extant cyanide-hydrolyzing enzyme diversity |
title_sort | proterozoic microbial origin of extant cyanide-hydrolyzing enzyme diversity |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10098168/ https://www.ncbi.nlm.nih.gov/pubmed/37065136 http://dx.doi.org/10.3389/fmicb.2023.1130310 |
work_keys_str_mv | AT schwartzsarahl aproterozoicmicrobialoriginofextantcyanidehydrolyzingenzymediversity AT rangellthiberio aproterozoicmicrobialoriginofextantcyanidehydrolyzingenzymediversity AT payettejackg aproterozoicmicrobialoriginofextantcyanidehydrolyzingenzymediversity AT fourniergregoryp aproterozoicmicrobialoriginofextantcyanidehydrolyzingenzymediversity AT schwartzsarahl proterozoicmicrobialoriginofextantcyanidehydrolyzingenzymediversity AT rangellthiberio proterozoicmicrobialoriginofextantcyanidehydrolyzingenzymediversity AT payettejackg proterozoicmicrobialoriginofextantcyanidehydrolyzingenzymediversity AT fourniergregoryp proterozoicmicrobialoriginofextantcyanidehydrolyzingenzymediversity |