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A broadly conserved fungal alcohol oxidase (AOX) facilitates fungal invasion of plants
Alcohol oxidases (AOXs) are ecologically important enzymes that facilitate a number of plant–fungal interactions. Within Ascomycota they are primarily associated with methylotrophy, as a peroxisomal AOX catalysing the conversion of methanol to formaldehyde in methylotrophic yeast. In this study we d...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9742500/ https://www.ncbi.nlm.nih.gov/pubmed/36251755 http://dx.doi.org/10.1111/mpp.13274 |
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author | Westrick, Nathaniel M. Park, Sung Chul Keller, Nancy P. Smith, Damon L. Kabbage, Mehdi |
author_facet | Westrick, Nathaniel M. Park, Sung Chul Keller, Nancy P. Smith, Damon L. Kabbage, Mehdi |
author_sort | Westrick, Nathaniel M. |
collection | PubMed |
description | Alcohol oxidases (AOXs) are ecologically important enzymes that facilitate a number of plant–fungal interactions. Within Ascomycota they are primarily associated with methylotrophy, as a peroxisomal AOX catalysing the conversion of methanol to formaldehyde in methylotrophic yeast. In this study we demonstrate that AOX orthologues are phylogenetically conserved proteins that are common in the genomes of nonmethylotrophic, plant‐associating fungi. Additionally, AOX orthologues are highly expressed during infection in a range of diverse pathosystems. To study the role of AOX in plant colonization, AOX knockout mutants were generated in the broad host range pathogen Sclerotinia sclerotiorum. Disease assays in soybean showed that these mutants had a significant virulence defect as evidenced by markedly reduced stem lesions and mortality rates. Chemical genomics suggested that SsAOX may function as an aromatic AOX, and growth assays demonstrated that ΔSsAOX is incapable of properly utilizing plant extract as a nutrient source. Profiling of known aromatic alcohols pointed towards the monolignol coniferyl alcohol (CA) as a possible substrate for SsAOX. As CA and other monolignols are ubiquitous among land plants, the presence of highly conserved AOX orthologues throughout Ascomycota implies that this is a broadly conserved protein used by ascomycete fungi during plant colonization. |
format | Online Article Text |
id | pubmed-9742500 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97425002022-12-13 A broadly conserved fungal alcohol oxidase (AOX) facilitates fungal invasion of plants Westrick, Nathaniel M. Park, Sung Chul Keller, Nancy P. Smith, Damon L. Kabbage, Mehdi Mol Plant Pathol Original Articles Alcohol oxidases (AOXs) are ecologically important enzymes that facilitate a number of plant–fungal interactions. Within Ascomycota they are primarily associated with methylotrophy, as a peroxisomal AOX catalysing the conversion of methanol to formaldehyde in methylotrophic yeast. In this study we demonstrate that AOX orthologues are phylogenetically conserved proteins that are common in the genomes of nonmethylotrophic, plant‐associating fungi. Additionally, AOX orthologues are highly expressed during infection in a range of diverse pathosystems. To study the role of AOX in plant colonization, AOX knockout mutants were generated in the broad host range pathogen Sclerotinia sclerotiorum. Disease assays in soybean showed that these mutants had a significant virulence defect as evidenced by markedly reduced stem lesions and mortality rates. Chemical genomics suggested that SsAOX may function as an aromatic AOX, and growth assays demonstrated that ΔSsAOX is incapable of properly utilizing plant extract as a nutrient source. Profiling of known aromatic alcohols pointed towards the monolignol coniferyl alcohol (CA) as a possible substrate for SsAOX. As CA and other monolignols are ubiquitous among land plants, the presence of highly conserved AOX orthologues throughout Ascomycota implies that this is a broadly conserved protein used by ascomycete fungi during plant colonization. John Wiley and Sons Inc. 2022-10-17 /pmc/articles/PMC9742500/ /pubmed/36251755 http://dx.doi.org/10.1111/mpp.13274 Text en © 2022 The Authors. Molecular Plant Pathology published by British Society for Plant Pathology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Westrick, Nathaniel M. Park, Sung Chul Keller, Nancy P. Smith, Damon L. Kabbage, Mehdi A broadly conserved fungal alcohol oxidase (AOX) facilitates fungal invasion of plants |
title | A broadly conserved fungal alcohol oxidase (AOX) facilitates fungal invasion of plants |
title_full | A broadly conserved fungal alcohol oxidase (AOX) facilitates fungal invasion of plants |
title_fullStr | A broadly conserved fungal alcohol oxidase (AOX) facilitates fungal invasion of plants |
title_full_unstemmed | A broadly conserved fungal alcohol oxidase (AOX) facilitates fungal invasion of plants |
title_short | A broadly conserved fungal alcohol oxidase (AOX) facilitates fungal invasion of plants |
title_sort | broadly conserved fungal alcohol oxidase (aox) facilitates fungal invasion of plants |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9742500/ https://www.ncbi.nlm.nih.gov/pubmed/36251755 http://dx.doi.org/10.1111/mpp.13274 |
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