Cargando…

Zearalenone lactonohydrolase activity in Hypocreales and its evolutionary relationships within the epoxide hydrolase subset of a/b-hydrolases

BACKGROUND: Zearalenone is a mycotoxin produced by several species of Fusarium genus, most notably Fusarium graminearum and Fusarium culmorum. This resorcylic acid lactone is one of the most important toxins causing serious animal and human diseases. For over two decades it has been known that the m...

Descripción completa

Detalles Bibliográficos
Autores principales: Popiel, Delfina, Koczyk, Grzegorz, Dawidziuk, Adam, Gromadzka, Karolina, Blaszczyk, Lidia, Chelkowski, Jerzy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4021089/
https://www.ncbi.nlm.nih.gov/pubmed/24708405
http://dx.doi.org/10.1186/1471-2180-14-82
_version_ 1782316169522315264
author Popiel, Delfina
Koczyk, Grzegorz
Dawidziuk, Adam
Gromadzka, Karolina
Blaszczyk, Lidia
Chelkowski, Jerzy
author_facet Popiel, Delfina
Koczyk, Grzegorz
Dawidziuk, Adam
Gromadzka, Karolina
Blaszczyk, Lidia
Chelkowski, Jerzy
author_sort Popiel, Delfina
collection PubMed
description BACKGROUND: Zearalenone is a mycotoxin produced by several species of Fusarium genus, most notably Fusarium graminearum and Fusarium culmorum. This resorcylic acid lactone is one of the most important toxins causing serious animal and human diseases. For over two decades it has been known that the mycoparasitic fungus Clonostachys rosea (synonym: Gliocladium roseum, teleomorph: Bionectria ochroleuca) can detoxify zearalenone, however no such attributes have been described within the Trichoderma genus. RESULTS: We screened for the presence of zearalenone lactonohydrolase homologs in isolates of Clonostachys and Trichoderma genera. We report first finding of expressed zearalenone lactonohydrolase in Trichoderma aggressivum. For three isolates (T. aggressivum, C. rosea and Clonostachys catenulatum isolates), we were able to reconstruct full coding sequence and verify the biotransformation ability potential. Additionally, we assessed progression of the detoxification process (in terms of transcript accumulation and mycotoxin decomposition in vitro). In silico, search for origins of zearalenone lactonohydrolase activity in model fungal and bacterial genomes has shown that zearalenone lactonohydrolase homologs form a monophyletic fungal clade among the a/b hydrolase superfamily representatives. We corroborated the finding of functional enzyme homologs by investigating the functional sites (active site pocket with postulated, noncanonical Ser-Glu-His catalytic triad) conserved in both multiple sequence alignment and in homology-based structural models. CONCLUSIONS: Our research shows the first finding of a functional zearalenone lactonohydrolase in mycoparasitic Trichoderma aggressivum (an activity earlier characterised in the Clonostachys rosea strains). The supporting evidence for presence and activity of functional enzyme homologs is based on the chemical analyses, gene expression patterns, homology models showing conservation of key structural features and marked reduction of zearalenone content in cultured samples (containing both medium and mycelium). Our findings also show divergent strategies of zearalenone biotransformation ability (rapid induced expression and detoxification vs. gradual detoxification) present in several members of Hypocreales order (Trichoderma and Clonostachys genera). The potential for lactonhydrolase activity directed towards zearalenone and/or similar compounds is likely ancient, with homologs present in several divergent filamentous fungi among both Sordariomycetes (Bionectria sp., Trichoderma sp., Apiospora montagnei) and Leotiomycetes (Marssonina brunnea f. sp. ‘multigermtubi’).
format Online
Article
Text
id pubmed-4021089
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-40210892014-05-16 Zearalenone lactonohydrolase activity in Hypocreales and its evolutionary relationships within the epoxide hydrolase subset of a/b-hydrolases Popiel, Delfina Koczyk, Grzegorz Dawidziuk, Adam Gromadzka, Karolina Blaszczyk, Lidia Chelkowski, Jerzy BMC Microbiol Research Article BACKGROUND: Zearalenone is a mycotoxin produced by several species of Fusarium genus, most notably Fusarium graminearum and Fusarium culmorum. This resorcylic acid lactone is one of the most important toxins causing serious animal and human diseases. For over two decades it has been known that the mycoparasitic fungus Clonostachys rosea (synonym: Gliocladium roseum, teleomorph: Bionectria ochroleuca) can detoxify zearalenone, however no such attributes have been described within the Trichoderma genus. RESULTS: We screened for the presence of zearalenone lactonohydrolase homologs in isolates of Clonostachys and Trichoderma genera. We report first finding of expressed zearalenone lactonohydrolase in Trichoderma aggressivum. For three isolates (T. aggressivum, C. rosea and Clonostachys catenulatum isolates), we were able to reconstruct full coding sequence and verify the biotransformation ability potential. Additionally, we assessed progression of the detoxification process (in terms of transcript accumulation and mycotoxin decomposition in vitro). In silico, search for origins of zearalenone lactonohydrolase activity in model fungal and bacterial genomes has shown that zearalenone lactonohydrolase homologs form a monophyletic fungal clade among the a/b hydrolase superfamily representatives. We corroborated the finding of functional enzyme homologs by investigating the functional sites (active site pocket with postulated, noncanonical Ser-Glu-His catalytic triad) conserved in both multiple sequence alignment and in homology-based structural models. CONCLUSIONS: Our research shows the first finding of a functional zearalenone lactonohydrolase in mycoparasitic Trichoderma aggressivum (an activity earlier characterised in the Clonostachys rosea strains). The supporting evidence for presence and activity of functional enzyme homologs is based on the chemical analyses, gene expression patterns, homology models showing conservation of key structural features and marked reduction of zearalenone content in cultured samples (containing both medium and mycelium). Our findings also show divergent strategies of zearalenone biotransformation ability (rapid induced expression and detoxification vs. gradual detoxification) present in several members of Hypocreales order (Trichoderma and Clonostachys genera). The potential for lactonhydrolase activity directed towards zearalenone and/or similar compounds is likely ancient, with homologs present in several divergent filamentous fungi among both Sordariomycetes (Bionectria sp., Trichoderma sp., Apiospora montagnei) and Leotiomycetes (Marssonina brunnea f. sp. ‘multigermtubi’). BioMed Central 2014-04-03 /pmc/articles/PMC4021089/ /pubmed/24708405 http://dx.doi.org/10.1186/1471-2180-14-82 Text en Copyright © 2014 Popiel et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Popiel, Delfina
Koczyk, Grzegorz
Dawidziuk, Adam
Gromadzka, Karolina
Blaszczyk, Lidia
Chelkowski, Jerzy
Zearalenone lactonohydrolase activity in Hypocreales and its evolutionary relationships within the epoxide hydrolase subset of a/b-hydrolases
title Zearalenone lactonohydrolase activity in Hypocreales and its evolutionary relationships within the epoxide hydrolase subset of a/b-hydrolases
title_full Zearalenone lactonohydrolase activity in Hypocreales and its evolutionary relationships within the epoxide hydrolase subset of a/b-hydrolases
title_fullStr Zearalenone lactonohydrolase activity in Hypocreales and its evolutionary relationships within the epoxide hydrolase subset of a/b-hydrolases
title_full_unstemmed Zearalenone lactonohydrolase activity in Hypocreales and its evolutionary relationships within the epoxide hydrolase subset of a/b-hydrolases
title_short Zearalenone lactonohydrolase activity in Hypocreales and its evolutionary relationships within the epoxide hydrolase subset of a/b-hydrolases
title_sort zearalenone lactonohydrolase activity in hypocreales and its evolutionary relationships within the epoxide hydrolase subset of a/b-hydrolases
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4021089/
https://www.ncbi.nlm.nih.gov/pubmed/24708405
http://dx.doi.org/10.1186/1471-2180-14-82
work_keys_str_mv AT popieldelfina zearalenonelactonohydrolaseactivityinhypocrealesanditsevolutionaryrelationshipswithintheepoxidehydrolasesubsetofabhydrolases
AT koczykgrzegorz zearalenonelactonohydrolaseactivityinhypocrealesanditsevolutionaryrelationshipswithintheepoxidehydrolasesubsetofabhydrolases
AT dawidziukadam zearalenonelactonohydrolaseactivityinhypocrealesanditsevolutionaryrelationshipswithintheepoxidehydrolasesubsetofabhydrolases
AT gromadzkakarolina zearalenonelactonohydrolaseactivityinhypocrealesanditsevolutionaryrelationshipswithintheepoxidehydrolasesubsetofabhydrolases
AT blaszczyklidia zearalenonelactonohydrolaseactivityinhypocrealesanditsevolutionaryrelationshipswithintheepoxidehydrolasesubsetofabhydrolases
AT chelkowskijerzy zearalenonelactonohydrolaseactivityinhypocrealesanditsevolutionaryrelationshipswithintheepoxidehydrolasesubsetofabhydrolases