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Integrative omics analyses of the ligninolytic Rhodosporidium fluviale LM-2 disclose catabolic pathways for biobased chemical production

BACKGROUND: Lignin is an attractive alternative for producing biobased chemicals. It is the second major component of the plant cell wall and is an abundant natural source of aromatic compounds. Lignin degradation using microbial oxidative enzymes that depolymerize lignin and catabolize aromatic com...

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Autores principales: Vilela, Nathália, Tomazetto, Geizecler, Gonçalves, Thiago Augusto, Sodré, Victoria, Persinoti, Gabriela Felix, Moraes, Eduardo Cruz, de Oliveira, Arthur Henrique Cavalcante, da Silva, Stephanie Nemesio, Fill, Taícia Pacheco, Damasio, André, Squina, Fabio Marcio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9830802/
https://www.ncbi.nlm.nih.gov/pubmed/36624471
http://dx.doi.org/10.1186/s13068-022-02251-6
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author Vilela, Nathália
Tomazetto, Geizecler
Gonçalves, Thiago Augusto
Sodré, Victoria
Persinoti, Gabriela Felix
Moraes, Eduardo Cruz
de Oliveira, Arthur Henrique Cavalcante
da Silva, Stephanie Nemesio
Fill, Taícia Pacheco
Damasio, André
Squina, Fabio Marcio
author_facet Vilela, Nathália
Tomazetto, Geizecler
Gonçalves, Thiago Augusto
Sodré, Victoria
Persinoti, Gabriela Felix
Moraes, Eduardo Cruz
de Oliveira, Arthur Henrique Cavalcante
da Silva, Stephanie Nemesio
Fill, Taícia Pacheco
Damasio, André
Squina, Fabio Marcio
author_sort Vilela, Nathália
collection PubMed
description BACKGROUND: Lignin is an attractive alternative for producing biobased chemicals. It is the second major component of the plant cell wall and is an abundant natural source of aromatic compounds. Lignin degradation using microbial oxidative enzymes that depolymerize lignin and catabolize aromatic compounds into central metabolic intermediates is a promising strategy for lignin valorization. However, the intrinsic heterogeneity and recalcitrance of lignin severely hinder its biocatalytic conversion. In this context, examining microbial degradation systems can provide a fundamental understanding of the pathways and enzymes that are useful for lignin conversion into biotechnologically relevant compounds. RESULTS: Lignin-degrading catabolism of a novel Rhodosporidium fluviale strain LM-2 was characterized using multi-omic strategies. This strain was previously isolated from a ligninolytic microbial consortium and presents a set of enzymes related to lignin depolymerization and aromatic compound catabolism. Furthermore, two catabolic routes for producing 4-vinyl guaiacol and vanillin were identified in R. fluviale LM-2. CONCLUSIONS: The multi-omic analysis of R. fluviale LM-2, the first for this species, elucidated a repertoire of genes, transcripts, and secreted proteins involved in lignin degradation. This study expands the understanding of ligninolytic metabolism in a non-conventional yeast, which has the potential for future genetic manipulation. Moreover, this work unveiled critical pathways and enzymes that can be exported to other systems, including model organisms, for lignin valorization. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13068-022-02251-6.
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spelling pubmed-98308022023-01-11 Integrative omics analyses of the ligninolytic Rhodosporidium fluviale LM-2 disclose catabolic pathways for biobased chemical production Vilela, Nathália Tomazetto, Geizecler Gonçalves, Thiago Augusto Sodré, Victoria Persinoti, Gabriela Felix Moraes, Eduardo Cruz de Oliveira, Arthur Henrique Cavalcante da Silva, Stephanie Nemesio Fill, Taícia Pacheco Damasio, André Squina, Fabio Marcio Biotechnol Biofuels Bioprod Research BACKGROUND: Lignin is an attractive alternative for producing biobased chemicals. It is the second major component of the plant cell wall and is an abundant natural source of aromatic compounds. Lignin degradation using microbial oxidative enzymes that depolymerize lignin and catabolize aromatic compounds into central metabolic intermediates is a promising strategy for lignin valorization. However, the intrinsic heterogeneity and recalcitrance of lignin severely hinder its biocatalytic conversion. In this context, examining microbial degradation systems can provide a fundamental understanding of the pathways and enzymes that are useful for lignin conversion into biotechnologically relevant compounds. RESULTS: Lignin-degrading catabolism of a novel Rhodosporidium fluviale strain LM-2 was characterized using multi-omic strategies. This strain was previously isolated from a ligninolytic microbial consortium and presents a set of enzymes related to lignin depolymerization and aromatic compound catabolism. Furthermore, two catabolic routes for producing 4-vinyl guaiacol and vanillin were identified in R. fluviale LM-2. CONCLUSIONS: The multi-omic analysis of R. fluviale LM-2, the first for this species, elucidated a repertoire of genes, transcripts, and secreted proteins involved in lignin degradation. This study expands the understanding of ligninolytic metabolism in a non-conventional yeast, which has the potential for future genetic manipulation. Moreover, this work unveiled critical pathways and enzymes that can be exported to other systems, including model organisms, for lignin valorization. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13068-022-02251-6. BioMed Central 2023-01-09 /pmc/articles/PMC9830802/ /pubmed/36624471 http://dx.doi.org/10.1186/s13068-022-02251-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Vilela, Nathália
Tomazetto, Geizecler
Gonçalves, Thiago Augusto
Sodré, Victoria
Persinoti, Gabriela Felix
Moraes, Eduardo Cruz
de Oliveira, Arthur Henrique Cavalcante
da Silva, Stephanie Nemesio
Fill, Taícia Pacheco
Damasio, André
Squina, Fabio Marcio
Integrative omics analyses of the ligninolytic Rhodosporidium fluviale LM-2 disclose catabolic pathways for biobased chemical production
title Integrative omics analyses of the ligninolytic Rhodosporidium fluviale LM-2 disclose catabolic pathways for biobased chemical production
title_full Integrative omics analyses of the ligninolytic Rhodosporidium fluviale LM-2 disclose catabolic pathways for biobased chemical production
title_fullStr Integrative omics analyses of the ligninolytic Rhodosporidium fluviale LM-2 disclose catabolic pathways for biobased chemical production
title_full_unstemmed Integrative omics analyses of the ligninolytic Rhodosporidium fluviale LM-2 disclose catabolic pathways for biobased chemical production
title_short Integrative omics analyses of the ligninolytic Rhodosporidium fluviale LM-2 disclose catabolic pathways for biobased chemical production
title_sort integrative omics analyses of the ligninolytic rhodosporidium fluviale lm-2 disclose catabolic pathways for biobased chemical production
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9830802/
https://www.ncbi.nlm.nih.gov/pubmed/36624471
http://dx.doi.org/10.1186/s13068-022-02251-6
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