The integrative omics of white-rot fungus Pycnoporus coccineus reveals co-regulated CAZymes for orchestrated lignocellulose breakdown.

Innovative green technologies are of importance for converting plant wastes into renewable sources for materials, chemicals and energy. However, recycling agricultural and forestry wastes is a challenge. A solution may be found in the forest. Saprotrophic white-rot fungi are able to convert dead pla...

Full description

Bibliographic Details
Main Authors: Shingo Miyauchi, David Navarro, Sacha Grisel, Didier Chevret, Jean-Guy Berrin, Marie-Noelle Rosso
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2017-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5386290?pdf=render
id doaj-067d1bbd44ec475bbd8edc174483b4e1
record_format Article
spelling doaj-067d1bbd44ec475bbd8edc174483b4e12020-11-25T01:46:00ZengPublic Library of Science (PLoS)PLoS ONE1932-62032017-01-01124e017552810.1371/journal.pone.0175528The integrative omics of white-rot fungus Pycnoporus coccineus reveals co-regulated CAZymes for orchestrated lignocellulose breakdown.Shingo MiyauchiDavid NavarroSacha GriselDidier ChevretJean-Guy BerrinMarie-Noelle RossoInnovative green technologies are of importance for converting plant wastes into renewable sources for materials, chemicals and energy. However, recycling agricultural and forestry wastes is a challenge. A solution may be found in the forest. Saprotrophic white-rot fungi are able to convert dead plants into consumable carbon sources. Specialized fungal enzymes can be utilized for breaking down hard plant biopolymers. Thus, understanding the enzymatic machineries of such fungi gives us hints for the efficient decomposition of plant materials. Using the saprotrophic white-rot fungus Pycnoporus coccineus as a fungal model, we examined the dynamics of transcriptomic and secretomic responses to different types of lignocellulosic substrates at two time points. Our integrative omics pipeline (SHIN+GO) enabled us to compress layers of biological information into simple heatmaps, allowing for visual inspection of the data. We identified co-regulated genes with corresponding co-secreted enzymes, and the biological roles were extrapolated with the enriched Carbohydrate-Active Enzyme (CAZymes) and functional annotations. We observed the fungal early responses for the degradation of lignocellulosic substrates including; 1) simultaneous expression of CAZy genes and secretion of the enzymes acting on diverse glycosidic bonds in cellulose, hemicelluloses and their side chains or lignin (i.e. hydrolases, esterases and oxido-reductases); 2) the key role of lytic polysaccharide monooxygenases (LPMO); 3) the early transcriptional regulation of lignin active peroxidases; 4) the induction of detoxification processes dealing with biomass-derived compounds; and 5) the frequent attachments of the carbohydrate binding module 1 (CBM1) to enzymes from the lignocellulose-responsive genes. Our omics combining methods and related biological findings may contribute to the knowledge of fungal systems biology and facilitate the optimization of fungal enzyme cocktails for various industrial applications.http://europepmc.org/articles/PMC5386290?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Shingo Miyauchi
David Navarro
Sacha Grisel
Didier Chevret
Jean-Guy Berrin
Marie-Noelle Rosso
spellingShingle Shingo Miyauchi
David Navarro
Sacha Grisel
Didier Chevret
Jean-Guy Berrin
Marie-Noelle Rosso
The integrative omics of white-rot fungus Pycnoporus coccineus reveals co-regulated CAZymes for orchestrated lignocellulose breakdown.
PLoS ONE
author_facet Shingo Miyauchi
David Navarro
Sacha Grisel
Didier Chevret
Jean-Guy Berrin
Marie-Noelle Rosso
author_sort Shingo Miyauchi
title The integrative omics of white-rot fungus Pycnoporus coccineus reveals co-regulated CAZymes for orchestrated lignocellulose breakdown.
title_short The integrative omics of white-rot fungus Pycnoporus coccineus reveals co-regulated CAZymes for orchestrated lignocellulose breakdown.
title_full The integrative omics of white-rot fungus Pycnoporus coccineus reveals co-regulated CAZymes for orchestrated lignocellulose breakdown.
title_fullStr The integrative omics of white-rot fungus Pycnoporus coccineus reveals co-regulated CAZymes for orchestrated lignocellulose breakdown.
title_full_unstemmed The integrative omics of white-rot fungus Pycnoporus coccineus reveals co-regulated CAZymes for orchestrated lignocellulose breakdown.
title_sort integrative omics of white-rot fungus pycnoporus coccineus reveals co-regulated cazymes for orchestrated lignocellulose breakdown.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2017-01-01
description Innovative green technologies are of importance for converting plant wastes into renewable sources for materials, chemicals and energy. However, recycling agricultural and forestry wastes is a challenge. A solution may be found in the forest. Saprotrophic white-rot fungi are able to convert dead plants into consumable carbon sources. Specialized fungal enzymes can be utilized for breaking down hard plant biopolymers. Thus, understanding the enzymatic machineries of such fungi gives us hints for the efficient decomposition of plant materials. Using the saprotrophic white-rot fungus Pycnoporus coccineus as a fungal model, we examined the dynamics of transcriptomic and secretomic responses to different types of lignocellulosic substrates at two time points. Our integrative omics pipeline (SHIN+GO) enabled us to compress layers of biological information into simple heatmaps, allowing for visual inspection of the data. We identified co-regulated genes with corresponding co-secreted enzymes, and the biological roles were extrapolated with the enriched Carbohydrate-Active Enzyme (CAZymes) and functional annotations. We observed the fungal early responses for the degradation of lignocellulosic substrates including; 1) simultaneous expression of CAZy genes and secretion of the enzymes acting on diverse glycosidic bonds in cellulose, hemicelluloses and their side chains or lignin (i.e. hydrolases, esterases and oxido-reductases); 2) the key role of lytic polysaccharide monooxygenases (LPMO); 3) the early transcriptional regulation of lignin active peroxidases; 4) the induction of detoxification processes dealing with biomass-derived compounds; and 5) the frequent attachments of the carbohydrate binding module 1 (CBM1) to enzymes from the lignocellulose-responsive genes. Our omics combining methods and related biological findings may contribute to the knowledge of fungal systems biology and facilitate the optimization of fungal enzyme cocktails for various industrial applications.
url http://europepmc.org/articles/PMC5386290?pdf=render
work_keys_str_mv AT shingomiyauchi theintegrativeomicsofwhiterotfunguspycnoporuscoccineusrevealscoregulatedcazymesfororchestratedlignocellulosebreakdown
AT davidnavarro theintegrativeomicsofwhiterotfunguspycnoporuscoccineusrevealscoregulatedcazymesfororchestratedlignocellulosebreakdown
AT sachagrisel theintegrativeomicsofwhiterotfunguspycnoporuscoccineusrevealscoregulatedcazymesfororchestratedlignocellulosebreakdown
AT didierchevret theintegrativeomicsofwhiterotfunguspycnoporuscoccineusrevealscoregulatedcazymesfororchestratedlignocellulosebreakdown
AT jeanguyberrin theintegrativeomicsofwhiterotfunguspycnoporuscoccineusrevealscoregulatedcazymesfororchestratedlignocellulosebreakdown
AT marienoellerosso theintegrativeomicsofwhiterotfunguspycnoporuscoccineusrevealscoregulatedcazymesfororchestratedlignocellulosebreakdown
AT shingomiyauchi integrativeomicsofwhiterotfunguspycnoporuscoccineusrevealscoregulatedcazymesfororchestratedlignocellulosebreakdown
AT davidnavarro integrativeomicsofwhiterotfunguspycnoporuscoccineusrevealscoregulatedcazymesfororchestratedlignocellulosebreakdown
AT sachagrisel integrativeomicsofwhiterotfunguspycnoporuscoccineusrevealscoregulatedcazymesfororchestratedlignocellulosebreakdown
AT didierchevret integrativeomicsofwhiterotfunguspycnoporuscoccineusrevealscoregulatedcazymesfororchestratedlignocellulosebreakdown
AT jeanguyberrin integrativeomicsofwhiterotfunguspycnoporuscoccineusrevealscoregulatedcazymesfororchestratedlignocellulosebreakdown
AT marienoellerosso integrativeomicsofwhiterotfunguspycnoporuscoccineusrevealscoregulatedcazymesfororchestratedlignocellulosebreakdown
_version_ 1725021406880595968