Unraveling the Molecular Basis of Mycosporine Biosynthesis in Fungi

Autores
Sepúlveda, Dionisia; Campusano, Sebastián; Moline, Martin; Barahona, Salvador; Baeza, Marcelo; Alcaíno, Jennifer; Colabella, Fernando; Urzúa, Blanca; Libkind Frati, Diego; Cifuentes, Víctor
Año de publicación
2023
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
The Phaffia rhodozyma UCD 67-385 genome harbors a 7873 bp cluster containing DDGS, OMT, and ATPG, encoding 2-desmethy-4-deoxygadusol synthase, O-methyl transferase, and ATPgrasp ligase, respectively, of the mycosporine glutaminol (MG) biosynthesis pathway. Homozygous deletion mutants of the entire cluster, single-gene mutants, and the ∆ddgs−/−;∆omt−/− and ∆omt−/−;∆atpg−/− double-gene mutants did not produce mycosporines. However, ∆atpg−/− accumulated the intermediate 4-deoxygadusol. Heterologous expression of the DDGS and OMT or DDGS, OMT, and ATPG cDNAs in Saccharomyces cerevisiae led to 4-deoxygadusol or MG production, respectively. Genetic integration of the complete cluster into the genome of the non-mycosporine-producing CBS 6938 wild-type strain resulted in a transgenic strain (CBS 6938_MYC) that produced MG and mycosporine glutaminol glucoside. These results indicate the function of DDGS, OMT, and ATPG in the mycosporine biosynthesis pathway. The transcription factor gene mutants ∆mig1−/−, ∆cyc8−/−, and ∆opi1−/− showed upregulation, ∆rox1−/− and ∆skn7−/− showed downregulation, and ∆tup6−/− and ∆yap6−/− showed no effect on mycosporinogenesis in glucose-containing medium. Finally, comparative analysis of the cluster sequences in several P. rhodozyma strains and the four newly described species of the genus showed the phylogenetic relationship of the P. rhodozyma strains and their differentiation from the other species of the genus Phaffia.
Fil: Sepúlveda, Dionisia. Universidad de Chile; Chile
Fil: Campusano, Sebastián. Universidad de Chile; Chile
Fil: Moline, Martin. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Patagonia Norte. Instituto Andino Patagónico de Tecnologías Biológicas y Geoambientales. Universidad Nacional del Comahue. Instituto Andino Patagónico de Tecnologías Biológicas y Geoambientales; Argentina
Fil: Barahona, Salvador. Universidad de Chile; Chile
Fil: Baeza, Marcelo. Universidad de Chile; Chile
Fil: Alcaíno, Jennifer. Universidad de Chile; Chile
Fil: Colabella, Fernando. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Urzúa, Blanca. Universidad de Chile; Chile
Fil: Libkind Frati, Diego. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Patagonia Norte. Instituto Andino Patagónico de Tecnologías Biológicas y Geoambientales. Universidad Nacional del Comahue. Instituto Andino Patagónico de Tecnologías Biológicas y Geoambientales; Argentina
Fil: Cifuentes, Víctor. Universidad de Chile; Chile
Materia
PHAFFIA
GENE CLUSTER
MYCOSPORINE
SECONDARY METABOLITE
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/235559

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network_acronym_str CONICETDig
repository_id_str 3498
network_name_str CONICET Digital (CONICET)
spelling Unraveling the Molecular Basis of Mycosporine Biosynthesis in FungiSepúlveda, DionisiaCampusano, SebastiánMoline, MartinBarahona, SalvadorBaeza, MarceloAlcaíno, JenniferColabella, FernandoUrzúa, BlancaLibkind Frati, DiegoCifuentes, VíctorPHAFFIAGENE CLUSTERMYCOSPORINESECONDARY METABOLITEhttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1The Phaffia rhodozyma UCD 67-385 genome harbors a 7873 bp cluster containing DDGS, OMT, and ATPG, encoding 2-desmethy-4-deoxygadusol synthase, O-methyl transferase, and ATPgrasp ligase, respectively, of the mycosporine glutaminol (MG) biosynthesis pathway. Homozygous deletion mutants of the entire cluster, single-gene mutants, and the ∆ddgs−/−;∆omt−/− and ∆omt−/−;∆atpg−/− double-gene mutants did not produce mycosporines. However, ∆atpg−/− accumulated the intermediate 4-deoxygadusol. Heterologous expression of the DDGS and OMT or DDGS, OMT, and ATPG cDNAs in Saccharomyces cerevisiae led to 4-deoxygadusol or MG production, respectively. Genetic integration of the complete cluster into the genome of the non-mycosporine-producing CBS 6938 wild-type strain resulted in a transgenic strain (CBS 6938_MYC) that produced MG and mycosporine glutaminol glucoside. These results indicate the function of DDGS, OMT, and ATPG in the mycosporine biosynthesis pathway. The transcription factor gene mutants ∆mig1−/−, ∆cyc8−/−, and ∆opi1−/− showed upregulation, ∆rox1−/− and ∆skn7−/− showed downregulation, and ∆tup6−/− and ∆yap6−/− showed no effect on mycosporinogenesis in glucose-containing medium. Finally, comparative analysis of the cluster sequences in several P. rhodozyma strains and the four newly described species of the genus showed the phylogenetic relationship of the P. rhodozyma strains and their differentiation from the other species of the genus Phaffia.Fil: Sepúlveda, Dionisia. Universidad de Chile; ChileFil: Campusano, Sebastián. Universidad de Chile; ChileFil: Moline, Martin. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Patagonia Norte. Instituto Andino Patagónico de Tecnologías Biológicas y Geoambientales. Universidad Nacional del Comahue. Instituto Andino Patagónico de Tecnologías Biológicas y Geoambientales; ArgentinaFil: Barahona, Salvador. Universidad de Chile; ChileFil: Baeza, Marcelo. Universidad de Chile; ChileFil: Alcaíno, Jennifer. Universidad de Chile; ChileFil: Colabella, Fernando. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Urzúa, Blanca. Universidad de Chile; ChileFil: Libkind Frati, Diego. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Patagonia Norte. Instituto Andino Patagónico de Tecnologías Biológicas y Geoambientales. Universidad Nacional del Comahue. Instituto Andino Patagónico de Tecnologías Biológicas y Geoambientales; ArgentinaFil: Cifuentes, Víctor. Universidad de Chile; ChileMolecular Diversity Preservation International2023-03info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/235559Sepúlveda, Dionisia; Campusano, Sebastián; Moline, Martin; Barahona, Salvador; Baeza, Marcelo; et al.; Unraveling the Molecular Basis of Mycosporine Biosynthesis in Fungi; Molecular Diversity Preservation International; International Journal of Molecular Sciences; 24; 6; 3-2023; 1-191422-0067CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://www.mdpi.com/1422-0067/24/6/5930info:eu-repo/semantics/altIdentifier/doi/10.3390/ijms24065930info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T09:43:49Zoai:ri.conicet.gov.ar:11336/235559instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-03 09:43:49.427CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Unraveling the Molecular Basis of Mycosporine Biosynthesis in Fungi
title Unraveling the Molecular Basis of Mycosporine Biosynthesis in Fungi
spellingShingle Unraveling the Molecular Basis of Mycosporine Biosynthesis in Fungi
Sepúlveda, Dionisia
PHAFFIA
GENE CLUSTER
MYCOSPORINE
SECONDARY METABOLITE
title_short Unraveling the Molecular Basis of Mycosporine Biosynthesis in Fungi
title_full Unraveling the Molecular Basis of Mycosporine Biosynthesis in Fungi
title_fullStr Unraveling the Molecular Basis of Mycosporine Biosynthesis in Fungi
title_full_unstemmed Unraveling the Molecular Basis of Mycosporine Biosynthesis in Fungi
title_sort Unraveling the Molecular Basis of Mycosporine Biosynthesis in Fungi
dc.creator.none.fl_str_mv Sepúlveda, Dionisia
Campusano, Sebastián
Moline, Martin
Barahona, Salvador
Baeza, Marcelo
Alcaíno, Jennifer
Colabella, Fernando
Urzúa, Blanca
Libkind Frati, Diego
Cifuentes, Víctor
author Sepúlveda, Dionisia
author_facet Sepúlveda, Dionisia
Campusano, Sebastián
Moline, Martin
Barahona, Salvador
Baeza, Marcelo
Alcaíno, Jennifer
Colabella, Fernando
Urzúa, Blanca
Libkind Frati, Diego
Cifuentes, Víctor
author_role author
author2 Campusano, Sebastián
Moline, Martin
Barahona, Salvador
Baeza, Marcelo
Alcaíno, Jennifer
Colabella, Fernando
Urzúa, Blanca
Libkind Frati, Diego
Cifuentes, Víctor
author2_role author
author
author
author
author
author
author
author
author
dc.subject.none.fl_str_mv PHAFFIA
GENE CLUSTER
MYCOSPORINE
SECONDARY METABOLITE
topic PHAFFIA
GENE CLUSTER
MYCOSPORINE
SECONDARY METABOLITE
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.6
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv The Phaffia rhodozyma UCD 67-385 genome harbors a 7873 bp cluster containing DDGS, OMT, and ATPG, encoding 2-desmethy-4-deoxygadusol synthase, O-methyl transferase, and ATPgrasp ligase, respectively, of the mycosporine glutaminol (MG) biosynthesis pathway. Homozygous deletion mutants of the entire cluster, single-gene mutants, and the ∆ddgs−/−;∆omt−/− and ∆omt−/−;∆atpg−/− double-gene mutants did not produce mycosporines. However, ∆atpg−/− accumulated the intermediate 4-deoxygadusol. Heterologous expression of the DDGS and OMT or DDGS, OMT, and ATPG cDNAs in Saccharomyces cerevisiae led to 4-deoxygadusol or MG production, respectively. Genetic integration of the complete cluster into the genome of the non-mycosporine-producing CBS 6938 wild-type strain resulted in a transgenic strain (CBS 6938_MYC) that produced MG and mycosporine glutaminol glucoside. These results indicate the function of DDGS, OMT, and ATPG in the mycosporine biosynthesis pathway. The transcription factor gene mutants ∆mig1−/−, ∆cyc8−/−, and ∆opi1−/− showed upregulation, ∆rox1−/− and ∆skn7−/− showed downregulation, and ∆tup6−/− and ∆yap6−/− showed no effect on mycosporinogenesis in glucose-containing medium. Finally, comparative analysis of the cluster sequences in several P. rhodozyma strains and the four newly described species of the genus showed the phylogenetic relationship of the P. rhodozyma strains and their differentiation from the other species of the genus Phaffia.
Fil: Sepúlveda, Dionisia. Universidad de Chile; Chile
Fil: Campusano, Sebastián. Universidad de Chile; Chile
Fil: Moline, Martin. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Patagonia Norte. Instituto Andino Patagónico de Tecnologías Biológicas y Geoambientales. Universidad Nacional del Comahue. Instituto Andino Patagónico de Tecnologías Biológicas y Geoambientales; Argentina
Fil: Barahona, Salvador. Universidad de Chile; Chile
Fil: Baeza, Marcelo. Universidad de Chile; Chile
Fil: Alcaíno, Jennifer. Universidad de Chile; Chile
Fil: Colabella, Fernando. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Urzúa, Blanca. Universidad de Chile; Chile
Fil: Libkind Frati, Diego. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Patagonia Norte. Instituto Andino Patagónico de Tecnologías Biológicas y Geoambientales. Universidad Nacional del Comahue. Instituto Andino Patagónico de Tecnologías Biológicas y Geoambientales; Argentina
Fil: Cifuentes, Víctor. Universidad de Chile; Chile
description The Phaffia rhodozyma UCD 67-385 genome harbors a 7873 bp cluster containing DDGS, OMT, and ATPG, encoding 2-desmethy-4-deoxygadusol synthase, O-methyl transferase, and ATPgrasp ligase, respectively, of the mycosporine glutaminol (MG) biosynthesis pathway. Homozygous deletion mutants of the entire cluster, single-gene mutants, and the ∆ddgs−/−;∆omt−/− and ∆omt−/−;∆atpg−/− double-gene mutants did not produce mycosporines. However, ∆atpg−/− accumulated the intermediate 4-deoxygadusol. Heterologous expression of the DDGS and OMT or DDGS, OMT, and ATPG cDNAs in Saccharomyces cerevisiae led to 4-deoxygadusol or MG production, respectively. Genetic integration of the complete cluster into the genome of the non-mycosporine-producing CBS 6938 wild-type strain resulted in a transgenic strain (CBS 6938_MYC) that produced MG and mycosporine glutaminol glucoside. These results indicate the function of DDGS, OMT, and ATPG in the mycosporine biosynthesis pathway. The transcription factor gene mutants ∆mig1−/−, ∆cyc8−/−, and ∆opi1−/− showed upregulation, ∆rox1−/− and ∆skn7−/− showed downregulation, and ∆tup6−/− and ∆yap6−/− showed no effect on mycosporinogenesis in glucose-containing medium. Finally, comparative analysis of the cluster sequences in several P. rhodozyma strains and the four newly described species of the genus showed the phylogenetic relationship of the P. rhodozyma strains and their differentiation from the other species of the genus Phaffia.
publishDate 2023
dc.date.none.fl_str_mv 2023-03
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/235559
Sepúlveda, Dionisia; Campusano, Sebastián; Moline, Martin; Barahona, Salvador; Baeza, Marcelo; et al.; Unraveling the Molecular Basis of Mycosporine Biosynthesis in Fungi; Molecular Diversity Preservation International; International Journal of Molecular Sciences; 24; 6; 3-2023; 1-19
1422-0067
CONICET Digital
CONICET
url http://hdl.handle.net/11336/235559
identifier_str_mv Sepúlveda, Dionisia; Campusano, Sebastián; Moline, Martin; Barahona, Salvador; Baeza, Marcelo; et al.; Unraveling the Molecular Basis of Mycosporine Biosynthesis in Fungi; Molecular Diversity Preservation International; International Journal of Molecular Sciences; 24; 6; 3-2023; 1-19
1422-0067
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/url/https://www.mdpi.com/1422-0067/24/6/5930
info:eu-repo/semantics/altIdentifier/doi/10.3390/ijms24065930
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
application/pdf
dc.publisher.none.fl_str_mv Molecular Diversity Preservation International
publisher.none.fl_str_mv Molecular Diversity Preservation International
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
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instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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