Cargando…

Dynamic succession of microbial compost communities and functions during Pleurotus ostreatus mushroom cropping on a short composting substrate

Cultivating oyster mushrooms (Pleurotus ostreatus), a typical primary decomposer of lignocellulose, on a short composting substrate is a novel procedure which possesses energy conserves, reduced the chance of infection by competitive species, shorter production duration and achieved high production...

Descripción completa

Detalles Bibliográficos
Autores principales: Liu, Qin, Kong, Weili, Cui, Xiao, Hu, Sujuan, Shi, Ziwen, Wu, Jie, Zhang, Yuting, Qiu, Liyou
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9433973/
https://www.ncbi.nlm.nih.gov/pubmed/36060741
http://dx.doi.org/10.3389/fmicb.2022.946777
_version_ 1784780755805667328
author Liu, Qin
Kong, Weili
Cui, Xiao
Hu, Sujuan
Shi, Ziwen
Wu, Jie
Zhang, Yuting
Qiu, Liyou
author_facet Liu, Qin
Kong, Weili
Cui, Xiao
Hu, Sujuan
Shi, Ziwen
Wu, Jie
Zhang, Yuting
Qiu, Liyou
author_sort Liu, Qin
collection PubMed
description Cultivating oyster mushrooms (Pleurotus ostreatus), a typical primary decomposer of lignocellulose, on a short composting substrate is a novel procedure which possesses energy conserves, reduced the chance of infection by competitive species, shorter production duration and achieved high production efficiency. However, the microbiome and microbial metabolic functions in the composting substrate during the mushroom cropping is unknown. In the present study, the contents of hemicellulose, cellulose and lignin and the activities of protease, laccase and cellulase were evaluated in the corncob short composting substrate from before oyster mushroom spawning to first flush fructification; meanwhile the changes in the microbiome and microbial metabolic functions were surveyed by using metagenomic sequencing. Results showed that the hemicellulose, cellulose and lignin in the short composting substrate were decomposed of 42.76, 34.01, and 30.18%, respectively, during the oyster mushroom cropping process. In addition, the contents of hemicellulose, cellulose and lignin in the composting substrate were reduced rapidly and negatively correlated with the abundance of the Actinobacteria phylum. The activities of protease, laccase and cellulase fastly increased in the period of before oyster mushroom spawning to full colonization and were positively correlated to the abundance of Actinobacteria phylum. The total abundance of bacteria domain gradually decreased by only approximately 15%, while the abundance of Actinobacteria phylum increased by 68% and was positively correlated with that of oyster mushroom. The abundance of oyster mushroom increased by 50 times from spawning to first flush fructification. The dominant genera, all in the order of Actinomycetales, were Cellulosimicrobium, Mycobacterium, Streptomyces and Saccharomonospora. The total abundance of genes with functions annotated in the Clusters of Orthologous Groups of proteins (COG) for Bacteria and Archaea and Kyoto Encyclopedia of Genes and Genomes (KEGG) database for all three life domains was positively correlated. The three metabolic pathways for carbohydrates, amino acids and energy were the primary enrichment pathways in KEGG pathway, accounting for more than 30% of all pathways, during the mushroom cropping in which the glycine metabolic pathway, carbon fixation pathways in prokaryotes and methane metabolism were all dominated by bacteria. The genes of cellulolytic enzymes, hemicellulolytic enzymes, laccase, chitinolytic enzymes, peptidoglycanlytic enzymes and ammonia assimilation enzymes with abundances from 0.28 to 0.24%, 0.05 to 0.02%, 0.02 to 0.01%, 0.14 to 0.08%, 0.39 to 0.16%, and 0.13 to 0.12% during the mushroom cropping identified in the Evolutionary Genealogy of Genes: Non-supervised Orthologous Groups (eggNOG) database for all three life domains were all aligned to COG database. These results indicated that bacteria, especially Actinomycetales, were the main metabolism participants in the short composting substrate during the oyster mushroom cropping. The relationship between oyster mushrooms and bacteria was cooperative, Actinomycetales were oyster mushroom growth promoting bacteria (OMGPB).
format Online
Article
Text
id pubmed-9433973
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-94339732022-09-02 Dynamic succession of microbial compost communities and functions during Pleurotus ostreatus mushroom cropping on a short composting substrate Liu, Qin Kong, Weili Cui, Xiao Hu, Sujuan Shi, Ziwen Wu, Jie Zhang, Yuting Qiu, Liyou Front Microbiol Microbiology Cultivating oyster mushrooms (Pleurotus ostreatus), a typical primary decomposer of lignocellulose, on a short composting substrate is a novel procedure which possesses energy conserves, reduced the chance of infection by competitive species, shorter production duration and achieved high production efficiency. However, the microbiome and microbial metabolic functions in the composting substrate during the mushroom cropping is unknown. In the present study, the contents of hemicellulose, cellulose and lignin and the activities of protease, laccase and cellulase were evaluated in the corncob short composting substrate from before oyster mushroom spawning to first flush fructification; meanwhile the changes in the microbiome and microbial metabolic functions were surveyed by using metagenomic sequencing. Results showed that the hemicellulose, cellulose and lignin in the short composting substrate were decomposed of 42.76, 34.01, and 30.18%, respectively, during the oyster mushroom cropping process. In addition, the contents of hemicellulose, cellulose and lignin in the composting substrate were reduced rapidly and negatively correlated with the abundance of the Actinobacteria phylum. The activities of protease, laccase and cellulase fastly increased in the period of before oyster mushroom spawning to full colonization and were positively correlated to the abundance of Actinobacteria phylum. The total abundance of bacteria domain gradually decreased by only approximately 15%, while the abundance of Actinobacteria phylum increased by 68% and was positively correlated with that of oyster mushroom. The abundance of oyster mushroom increased by 50 times from spawning to first flush fructification. The dominant genera, all in the order of Actinomycetales, were Cellulosimicrobium, Mycobacterium, Streptomyces and Saccharomonospora. The total abundance of genes with functions annotated in the Clusters of Orthologous Groups of proteins (COG) for Bacteria and Archaea and Kyoto Encyclopedia of Genes and Genomes (KEGG) database for all three life domains was positively correlated. The three metabolic pathways for carbohydrates, amino acids and energy were the primary enrichment pathways in KEGG pathway, accounting for more than 30% of all pathways, during the mushroom cropping in which the glycine metabolic pathway, carbon fixation pathways in prokaryotes and methane metabolism were all dominated by bacteria. The genes of cellulolytic enzymes, hemicellulolytic enzymes, laccase, chitinolytic enzymes, peptidoglycanlytic enzymes and ammonia assimilation enzymes with abundances from 0.28 to 0.24%, 0.05 to 0.02%, 0.02 to 0.01%, 0.14 to 0.08%, 0.39 to 0.16%, and 0.13 to 0.12% during the mushroom cropping identified in the Evolutionary Genealogy of Genes: Non-supervised Orthologous Groups (eggNOG) database for all three life domains were all aligned to COG database. These results indicated that bacteria, especially Actinomycetales, were the main metabolism participants in the short composting substrate during the oyster mushroom cropping. The relationship between oyster mushrooms and bacteria was cooperative, Actinomycetales were oyster mushroom growth promoting bacteria (OMGPB). Frontiers Media S.A. 2022-08-18 /pmc/articles/PMC9433973/ /pubmed/36060741 http://dx.doi.org/10.3389/fmicb.2022.946777 Text en Copyright © 2022 Liu, Kong, Cui, Hu, Shi, Wu, Zhang and Qiu. 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
Liu, Qin
Kong, Weili
Cui, Xiao
Hu, Sujuan
Shi, Ziwen
Wu, Jie
Zhang, Yuting
Qiu, Liyou
Dynamic succession of microbial compost communities and functions during Pleurotus ostreatus mushroom cropping on a short composting substrate
title Dynamic succession of microbial compost communities and functions during Pleurotus ostreatus mushroom cropping on a short composting substrate
title_full Dynamic succession of microbial compost communities and functions during Pleurotus ostreatus mushroom cropping on a short composting substrate
title_fullStr Dynamic succession of microbial compost communities and functions during Pleurotus ostreatus mushroom cropping on a short composting substrate
title_full_unstemmed Dynamic succession of microbial compost communities and functions during Pleurotus ostreatus mushroom cropping on a short composting substrate
title_short Dynamic succession of microbial compost communities and functions during Pleurotus ostreatus mushroom cropping on a short composting substrate
title_sort dynamic succession of microbial compost communities and functions during pleurotus ostreatus mushroom cropping on a short composting substrate
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9433973/
https://www.ncbi.nlm.nih.gov/pubmed/36060741
http://dx.doi.org/10.3389/fmicb.2022.946777
work_keys_str_mv AT liuqin dynamicsuccessionofmicrobialcompostcommunitiesandfunctionsduringpleurotusostreatusmushroomcroppingonashortcompostingsubstrate
AT kongweili dynamicsuccessionofmicrobialcompostcommunitiesandfunctionsduringpleurotusostreatusmushroomcroppingonashortcompostingsubstrate
AT cuixiao dynamicsuccessionofmicrobialcompostcommunitiesandfunctionsduringpleurotusostreatusmushroomcroppingonashortcompostingsubstrate
AT husujuan dynamicsuccessionofmicrobialcompostcommunitiesandfunctionsduringpleurotusostreatusmushroomcroppingonashortcompostingsubstrate
AT shiziwen dynamicsuccessionofmicrobialcompostcommunitiesandfunctionsduringpleurotusostreatusmushroomcroppingonashortcompostingsubstrate
AT wujie dynamicsuccessionofmicrobialcompostcommunitiesandfunctionsduringpleurotusostreatusmushroomcroppingonashortcompostingsubstrate
AT zhangyuting dynamicsuccessionofmicrobialcompostcommunitiesandfunctionsduringpleurotusostreatusmushroomcroppingonashortcompostingsubstrate
AT qiuliyou dynamicsuccessionofmicrobialcompostcommunitiesandfunctionsduringpleurotusostreatusmushroomcroppingonashortcompostingsubstrate