Evaluation of solid and submerged fermentations for the production of cyclodextrin glycosyltransferase by Paenibacillus campinasensis H69-3 and characterization of crude enzyme

Detalhes bibliográficos
Autor(a) principal: Alves-Prado, Heloiza Ferreira [UNESP]
Data de Publicação: 2006
Outros Autores: Gomes, Eleni [UNESP], Da Silva, Roberto [UNESP]
Tipo de documento: Artigo de conferência
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1007/978-1-59745-268-7_18
http://hdl.handle.net/11449/224760
Resumo: Cyclodextrin glycosyltransferase (CGTase) is an enzyme that produces cyclodextrins from starch by an intramolecular transglycosylation reaction. Cyclodextrins have been shown to have a number of applications in the food, cosmetic, pharmaceutical, and chemical industries. In the current study, the production of CGTase by Paenibacillus campinasensis strain H69-3 was examined in submerged and solid-state fermentations. P. campinasensis strain H69-3 was isolated from the soil, which grows at 45°C, and is a Gram-variable bacterium. Different substrate sources such as wheat bran, soybean bran, soybean extract, cassava solid residue, cassava starch, corn starch, and other combinations were used in the enzyme production. CGTase activity was highest in submerged fermentations with the greatest production observed at 48-72 h. The physical and chemical properties of CGTase were determined from the crude enzyme produced from submerged fermentations. The optimum temperature was found to be 70-75°C, and the activity was stable at 55°C for 1 h. The enzyme displayed two optimum pH values, 5.5 and 9.0 and was found to be stable between a pH of 4.5 and 11.0. Copyright © 2006 by Humana Press Inc. All rights of any nature whatsoever reserved.
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spelling Evaluation of solid and submerged fermentations for the production of cyclodextrin glycosyltransferase by Paenibacillus campinasensis H69-3 and characterization of crude enzymeCyclodextrin glycosyltransferasePaenibacillus campinasensisSolid-state fermentationSubmerged fermentationCyclodextrin glycosyltransferase (CGTase) is an enzyme that produces cyclodextrins from starch by an intramolecular transglycosylation reaction. Cyclodextrins have been shown to have a number of applications in the food, cosmetic, pharmaceutical, and chemical industries. In the current study, the production of CGTase by Paenibacillus campinasensis strain H69-3 was examined in submerged and solid-state fermentations. P. campinasensis strain H69-3 was isolated from the soil, which grows at 45°C, and is a Gram-variable bacterium. Different substrate sources such as wheat bran, soybean bran, soybean extract, cassava solid residue, cassava starch, corn starch, and other combinations were used in the enzyme production. CGTase activity was highest in submerged fermentations with the greatest production observed at 48-72 h. The physical and chemical properties of CGTase were determined from the crude enzyme produced from submerged fermentations. The optimum temperature was found to be 70-75°C, and the activity was stable at 55°C for 1 h. The enzyme displayed two optimum pH values, 5.5 and 9.0 and was found to be stable between a pH of 4.5 and 11.0. Copyright © 2006 by Humana Press Inc. All rights of any nature whatsoever reserved.UNESP-State University of São Paulo Biochemistry and Applied Microbiology Laboratory, R. Cristovao Colombo no. 2265, 15054-000, S. Jose do Rio PretoUNESP-State University of São Paulo Biology Institute, Rio Claro, SPUNESP-State University of São Paulo Biochemistry and Applied Microbiology Laboratory, R. Cristovao Colombo no. 2265, 15054-000, S. Jose do Rio PretoUNESP-State University of São Paulo Biology Institute, Rio Claro, SPUniversidade Estadual Paulista (UNESP)Alves-Prado, Heloiza Ferreira [UNESP]Gomes, Eleni [UNESP]Da Silva, Roberto [UNESP]2022-04-28T20:07:44Z2022-04-28T20:07:44Z2006-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/conferenceObject234-246http://dx.doi.org/10.1007/978-1-59745-268-7_18Applied Biochemistry and Biotechnology, v. 129, n. 1-3, p. 234-246, 2006.0273-2289http://hdl.handle.net/11449/22476010.1007/978-1-59745-268-7_182-s2.0-33646919626Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengApplied Biochemistry and Biotechnologyinfo:eu-repo/semantics/openAccess2022-04-28T20:07:44Zoai:repositorio.unesp.br:11449/224760Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T19:49:58.449121Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Evaluation of solid and submerged fermentations for the production of cyclodextrin glycosyltransferase by Paenibacillus campinasensis H69-3 and characterization of crude enzyme
title Evaluation of solid and submerged fermentations for the production of cyclodextrin glycosyltransferase by Paenibacillus campinasensis H69-3 and characterization of crude enzyme
spellingShingle Evaluation of solid and submerged fermentations for the production of cyclodextrin glycosyltransferase by Paenibacillus campinasensis H69-3 and characterization of crude enzyme
Alves-Prado, Heloiza Ferreira [UNESP]
Cyclodextrin glycosyltransferase
Paenibacillus campinasensis
Solid-state fermentation
Submerged fermentation
title_short Evaluation of solid and submerged fermentations for the production of cyclodextrin glycosyltransferase by Paenibacillus campinasensis H69-3 and characterization of crude enzyme
title_full Evaluation of solid and submerged fermentations for the production of cyclodextrin glycosyltransferase by Paenibacillus campinasensis H69-3 and characterization of crude enzyme
title_fullStr Evaluation of solid and submerged fermentations for the production of cyclodextrin glycosyltransferase by Paenibacillus campinasensis H69-3 and characterization of crude enzyme
title_full_unstemmed Evaluation of solid and submerged fermentations for the production of cyclodextrin glycosyltransferase by Paenibacillus campinasensis H69-3 and characterization of crude enzyme
title_sort Evaluation of solid and submerged fermentations for the production of cyclodextrin glycosyltransferase by Paenibacillus campinasensis H69-3 and characterization of crude enzyme
author Alves-Prado, Heloiza Ferreira [UNESP]
author_facet Alves-Prado, Heloiza Ferreira [UNESP]
Gomes, Eleni [UNESP]
Da Silva, Roberto [UNESP]
author_role author
author2 Gomes, Eleni [UNESP]
Da Silva, Roberto [UNESP]
author2_role author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (UNESP)
dc.contributor.author.fl_str_mv Alves-Prado, Heloiza Ferreira [UNESP]
Gomes, Eleni [UNESP]
Da Silva, Roberto [UNESP]
dc.subject.por.fl_str_mv Cyclodextrin glycosyltransferase
Paenibacillus campinasensis
Solid-state fermentation
Submerged fermentation
topic Cyclodextrin glycosyltransferase
Paenibacillus campinasensis
Solid-state fermentation
Submerged fermentation
description Cyclodextrin glycosyltransferase (CGTase) is an enzyme that produces cyclodextrins from starch by an intramolecular transglycosylation reaction. Cyclodextrins have been shown to have a number of applications in the food, cosmetic, pharmaceutical, and chemical industries. In the current study, the production of CGTase by Paenibacillus campinasensis strain H69-3 was examined in submerged and solid-state fermentations. P. campinasensis strain H69-3 was isolated from the soil, which grows at 45°C, and is a Gram-variable bacterium. Different substrate sources such as wheat bran, soybean bran, soybean extract, cassava solid residue, cassava starch, corn starch, and other combinations were used in the enzyme production. CGTase activity was highest in submerged fermentations with the greatest production observed at 48-72 h. The physical and chemical properties of CGTase were determined from the crude enzyme produced from submerged fermentations. The optimum temperature was found to be 70-75°C, and the activity was stable at 55°C for 1 h. The enzyme displayed two optimum pH values, 5.5 and 9.0 and was found to be stable between a pH of 4.5 and 11.0. Copyright © 2006 by Humana Press Inc. All rights of any nature whatsoever reserved.
publishDate 2006
dc.date.none.fl_str_mv 2006-01-01
2022-04-28T20:07:44Z
2022-04-28T20:07:44Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/conferenceObject
format conferenceObject
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1007/978-1-59745-268-7_18
Applied Biochemistry and Biotechnology, v. 129, n. 1-3, p. 234-246, 2006.
0273-2289
http://hdl.handle.net/11449/224760
10.1007/978-1-59745-268-7_18
2-s2.0-33646919626
url http://dx.doi.org/10.1007/978-1-59745-268-7_18
http://hdl.handle.net/11449/224760
identifier_str_mv Applied Biochemistry and Biotechnology, v. 129, n. 1-3, p. 234-246, 2006.
0273-2289
10.1007/978-1-59745-268-7_18
2-s2.0-33646919626
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Applied Biochemistry and Biotechnology
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 234-246
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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