Enhanced virulence of Beauveria bassiana against Diatraea saccharalis using a soluble recombinant enzyme with endo- and exochitinase activity

Beauveria bassiana chitinases are involved in degrading the chitin in insects’ exoskeletons and internal structures, and thus are important virulence factors as they participate in initial to final steps of infection. In this work, the B. bassiana (Bv062 isolate) open reading frame (ORF) encoding a...

Full description

Autores:
Tipo de recurso:
Fecha de publicación:
2020
Institución:
Universidad del Rosario
Repositorio:
Repositorio EdocUR - U. Rosario
Idioma:
eng
OAI Identifier:
oai:repository.urosario.edu.co:10336/23524
Acceso en línea:
https://doi.org/10.1016/j.biocontrol.2020.104211
https://repository.urosario.edu.co/handle/10336/23524
Palabra clave:
Beauveria bassiana
Chitinase
Diatraea saccharalis
Recombinant protein
Virulence
Rights
License
Abierto (Texto Completo)
id EDOCUR2_42bd51a7b14fa668672de457fb3f1f4d
oai_identifier_str oai:repository.urosario.edu.co:10336/23524
network_acronym_str EDOCUR2
network_name_str Repositorio EdocUR - U. Rosario
repository_id_str
spelling d4f2eb49-82bf-4776-86aa-0b81a5f295e0-1e86f85c4-2132-42de-97b3-e9aaa56c02f0-1e81874bd-6409-4309-8825-a100ffc5849d-179653065-1f92a261c-8bfb-49fa-b4fc-3e5a502cd904-12020-05-26T00:02:47Z2020-05-26T00:02:47Z2020Beauveria bassiana chitinases are involved in degrading the chitin in insects’ exoskeletons and internal structures, and thus are important virulence factors as they participate in initial to final steps of infection. In this work, the B. bassiana (Bv062 isolate) open reading frame (ORF) encoding a chitinase identified as Chit37 (orthologous Bvchit1) was molecularly cloned and expressed in Escherichia coli, and the potential of the recombinant protein (rChit37) to enhance the insecticidal activity of Bv062 conidia against second instar Diatraea saccharalis larvae was studied. rChit37 was produced in both soluble and insoluble fractions of an E. coli culture. Both fractions expressing endo- (90 mU/µL) and exochitinase (170 mU/µL) enzymatic activity, with optimum conditions for enzyme activity of 45 °C and pH 5.0. His-tag affinity chromatography was used to purify the rChit37 from the soluble fraction. Purified rChit37 was then diluted to 200 and 300 µg/mL for use as Bv062 conidia additive (1x106con/mL) in a laboratory bioassay against D. saccharalis larvae. No significant differences were observed between the efficacy of Bv062 conidia applied alone or mixed with 200 µg/mL purified rChit37. However, 300 µg/mL rChit37 increased BV062 conidia insecticidal activity, achieving 96.7% efficacy (14 days post-infection) and 6.2 days median lethal time (LT50), compared to 60% efficacy and 8.9 days for conidia alone. rChit37 addition did not affect conidial viability in terms of germination (96.6% after 24 h) or vigour estimated as germ-tube elongation rate. This work provides proof of concept about soluble recombinant chitinase as an additive to enhance B. bassiana virulence against D. saccharalis. © 2020 The Authorsapplication/pdfhttps://doi.org/10.1016/j.biocontrol.2020.1042111090211210499644https://repository.urosario.edu.co/handle/10336/23524engAcademic Press Inc.Biological ControlVol. 144Biological Control, ISSN:10902112, 10499644, Vol.144,(2020)https://www.scopus.com/inward/record.uri?eid=2-s2.0-85081201691&doi=10.1016%2fj.biocontrol.2020.104211&partnerID=40&md5=99d599274343399325574b6c778fe6b9Abierto (Texto Completo)http://purl.org/coar/access_right/c_abf2instname:Universidad del Rosarioreponame:Repositorio Institucional EdocURBeauveria bassianaChitinaseDiatraea saccharalisRecombinant proteinVirulenceEnhanced virulence of Beauveria bassiana against Diatraea saccharalis using a soluble recombinant enzyme with endo- and exochitinase activityarticleArtículohttp://purl.org/coar/version/c_970fb48d4fbd8a85http://purl.org/coar/resource_type/c_6501Lovera, AndreaBelaich, MarianoVillamizar, LauraPatarroyo, Manuel A.Barrera, GloriaORIGINAL1-s2-0-S1049964419308163-main.pdfapplication/pdf1441379https://repository.urosario.edu.co/bitstreams/a029deec-a110-4142-b7fb-ccbbf7812b71/downloade32585255affe58ec7e7b5aedcf5dbbbMD51TEXT1-s2-0-S1049964419308163-main.pdf.txt1-s2-0-S1049964419308163-main.pdf.txtExtracted texttext/plain64098https://repository.urosario.edu.co/bitstreams/1ed100cc-1d89-448c-8ed3-94d7819f8a17/download38be70459fc3445ddee7608eb6db7356MD52THUMBNAIL1-s2-0-S1049964419308163-main.pdf.jpg1-s2-0-S1049964419308163-main.pdf.jpgGenerated Thumbnailimage/jpeg4190https://repository.urosario.edu.co/bitstreams/19decded-e3bd-441e-a3db-f20421b073a9/download3d6a9b2fe4d74403f851d85fb3aec0d1MD5310336/23524oai:repository.urosario.edu.co:10336/235242022-05-02 07:37:14.614519https://repository.urosario.edu.coRepositorio institucional EdocURedocur@urosario.edu.co
dc.title.spa.fl_str_mv Enhanced virulence of Beauveria bassiana against Diatraea saccharalis using a soluble recombinant enzyme with endo- and exochitinase activity
title Enhanced virulence of Beauveria bassiana against Diatraea saccharalis using a soluble recombinant enzyme with endo- and exochitinase activity
spellingShingle Enhanced virulence of Beauveria bassiana against Diatraea saccharalis using a soluble recombinant enzyme with endo- and exochitinase activity
Beauveria bassiana
Chitinase
Diatraea saccharalis
Recombinant protein
Virulence
title_short Enhanced virulence of Beauveria bassiana against Diatraea saccharalis using a soluble recombinant enzyme with endo- and exochitinase activity
title_full Enhanced virulence of Beauveria bassiana against Diatraea saccharalis using a soluble recombinant enzyme with endo- and exochitinase activity
title_fullStr Enhanced virulence of Beauveria bassiana against Diatraea saccharalis using a soluble recombinant enzyme with endo- and exochitinase activity
title_full_unstemmed Enhanced virulence of Beauveria bassiana against Diatraea saccharalis using a soluble recombinant enzyme with endo- and exochitinase activity
title_sort Enhanced virulence of Beauveria bassiana against Diatraea saccharalis using a soluble recombinant enzyme with endo- and exochitinase activity
dc.subject.keyword.spa.fl_str_mv Beauveria bassiana
Chitinase
Diatraea saccharalis
Recombinant protein
Virulence
topic Beauveria bassiana
Chitinase
Diatraea saccharalis
Recombinant protein
Virulence
description Beauveria bassiana chitinases are involved in degrading the chitin in insects’ exoskeletons and internal structures, and thus are important virulence factors as they participate in initial to final steps of infection. In this work, the B. bassiana (Bv062 isolate) open reading frame (ORF) encoding a chitinase identified as Chit37 (orthologous Bvchit1) was molecularly cloned and expressed in Escherichia coli, and the potential of the recombinant protein (rChit37) to enhance the insecticidal activity of Bv062 conidia against second instar Diatraea saccharalis larvae was studied. rChit37 was produced in both soluble and insoluble fractions of an E. coli culture. Both fractions expressing endo- (90 mU/µL) and exochitinase (170 mU/µL) enzymatic activity, with optimum conditions for enzyme activity of 45 °C and pH 5.0. His-tag affinity chromatography was used to purify the rChit37 from the soluble fraction. Purified rChit37 was then diluted to 200 and 300 µg/mL for use as Bv062 conidia additive (1x106con/mL) in a laboratory bioassay against D. saccharalis larvae. No significant differences were observed between the efficacy of Bv062 conidia applied alone or mixed with 200 µg/mL purified rChit37. However, 300 µg/mL rChit37 increased BV062 conidia insecticidal activity, achieving 96.7% efficacy (14 days post-infection) and 6.2 days median lethal time (LT50), compared to 60% efficacy and 8.9 days for conidia alone. rChit37 addition did not affect conidial viability in terms of germination (96.6% after 24 h) or vigour estimated as germ-tube elongation rate. This work provides proof of concept about soluble recombinant chitinase as an additive to enhance B. bassiana virulence against D. saccharalis. © 2020 The Authors
publishDate 2020
dc.date.accessioned.none.fl_str_mv 2020-05-26T00:02:47Z
dc.date.available.none.fl_str_mv 2020-05-26T00:02:47Z
dc.date.created.spa.fl_str_mv 2020
dc.type.eng.fl_str_mv article
dc.type.coarversion.fl_str_mv http://purl.org/coar/version/c_970fb48d4fbd8a85
dc.type.coar.fl_str_mv http://purl.org/coar/resource_type/c_6501
dc.type.spa.spa.fl_str_mv Artículo
dc.identifier.doi.none.fl_str_mv https://doi.org/10.1016/j.biocontrol.2020.104211
dc.identifier.issn.none.fl_str_mv 10902112
10499644
dc.identifier.uri.none.fl_str_mv https://repository.urosario.edu.co/handle/10336/23524
url https://doi.org/10.1016/j.biocontrol.2020.104211
https://repository.urosario.edu.co/handle/10336/23524
identifier_str_mv 10902112
10499644
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.citationTitle.none.fl_str_mv Biological Control
dc.relation.citationVolume.none.fl_str_mv Vol. 144
dc.relation.ispartof.spa.fl_str_mv Biological Control, ISSN:10902112, 10499644, Vol.144,(2020)
dc.relation.uri.spa.fl_str_mv https://www.scopus.com/inward/record.uri?eid=2-s2.0-85081201691&doi=10.1016%2fj.biocontrol.2020.104211&partnerID=40&md5=99d599274343399325574b6c778fe6b9
dc.rights.coar.fl_str_mv http://purl.org/coar/access_right/c_abf2
dc.rights.acceso.spa.fl_str_mv Abierto (Texto Completo)
rights_invalid_str_mv Abierto (Texto Completo)
http://purl.org/coar/access_right/c_abf2
dc.format.mimetype.none.fl_str_mv application/pdf
dc.publisher.spa.fl_str_mv Academic Press Inc.
institution Universidad del Rosario
dc.source.instname.spa.fl_str_mv instname:Universidad del Rosario
dc.source.reponame.spa.fl_str_mv reponame:Repositorio Institucional EdocUR
bitstream.url.fl_str_mv https://repository.urosario.edu.co/bitstreams/a029deec-a110-4142-b7fb-ccbbf7812b71/download
https://repository.urosario.edu.co/bitstreams/1ed100cc-1d89-448c-8ed3-94d7819f8a17/download
https://repository.urosario.edu.co/bitstreams/19decded-e3bd-441e-a3db-f20421b073a9/download
bitstream.checksum.fl_str_mv e32585255affe58ec7e7b5aedcf5dbbb
38be70459fc3445ddee7608eb6db7356
3d6a9b2fe4d74403f851d85fb3aec0d1
bitstream.checksumAlgorithm.fl_str_mv MD5
MD5
MD5
repository.name.fl_str_mv Repositorio institucional EdocUR
repository.mail.fl_str_mv edocur@urosario.edu.co
_version_ 1814167536008167424