Screening polymeric ionic liquids for chromatography-based purification of bacteriophage M13

Detalhes bibliográficos
Autor(a) principal: Jacinto, M.J.
Data de Publicação: 2021
Outros Autores: Wagner, Alexandra, Sá, Inês M., Patinha, David J.S., Marrucho, Isabel M., Gonçalves, João, Willson, Richard C., Azevedo, A.M., Aires-Barros, M.R.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10773/37758
Resumo: M13 bacteriophage is a key instrument in phage display applications, as well as a possible antibacterial therapeutic agent due to its highly restrictive bacterial pathogenesis, and other applications. The traditional phage purification process is usually achieved by gradient ultracentrifugation or a combination of precipitation, centrifugation and microfiltration. These approaches easily lead to long process times, high operational costs, phage aggregation and consequent product loss (approximately 60%). This work is thus focused on an alternative potential large-scale process to achieve high yield and purity while minimizing the operational costs. Electrostatic-based separation processes are also common biomolecules purification techniques. Although anion exchange chromatography has been used before to purify several viral particles, this technique has been poorly reported for the purification of M13 phage. In a recent work, our group has demonstrated the use of a predominant anion exchange process, where a polymeric ionic liquid (PIL) was used as an alternative separation matrix for M13 bacteriophage. In this work, a variety of system parameters was studied, including chemical structure of the cation and the anion, the crosslinker nature and its concentration, either in batch adsorption/elution or chromatographic operation mode. The PIL-based chromatographic operation mode revealed to be a suitable separation process for M13 from directly filtered E. coli supernatant, reaching over 70% M13 recovery and 4.6 purification factor in a single step. To our knowledge, this is the first time that PILs have been reported as separation agents for bioproducts from complex mixtures.
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spelling Screening polymeric ionic liquids for chromatography-based purification of bacteriophage M13Polymeric ionic liquidsBacteriophage M13Batch adsorptionChromatographyAnion-exchangeM13 bacteriophage is a key instrument in phage display applications, as well as a possible antibacterial therapeutic agent due to its highly restrictive bacterial pathogenesis, and other applications. The traditional phage purification process is usually achieved by gradient ultracentrifugation or a combination of precipitation, centrifugation and microfiltration. These approaches easily lead to long process times, high operational costs, phage aggregation and consequent product loss (approximately 60%). This work is thus focused on an alternative potential large-scale process to achieve high yield and purity while minimizing the operational costs. Electrostatic-based separation processes are also common biomolecules purification techniques. Although anion exchange chromatography has been used before to purify several viral particles, this technique has been poorly reported for the purification of M13 phage. In a recent work, our group has demonstrated the use of a predominant anion exchange process, where a polymeric ionic liquid (PIL) was used as an alternative separation matrix for M13 bacteriophage. In this work, a variety of system parameters was studied, including chemical structure of the cation and the anion, the crosslinker nature and its concentration, either in batch adsorption/elution or chromatographic operation mode. The PIL-based chromatographic operation mode revealed to be a suitable separation process for M13 from directly filtered E. coli supernatant, reaching over 70% M13 recovery and 4.6 purification factor in a single step. To our knowledge, this is the first time that PILs have been reported as separation agents for bioproducts from complex mixtures.Elsevier2023-05-16T13:29:25Z2021-02-15T00:00:00Z2021-02-15info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10773/37758eng1383-586610.1016/j.seppur.2020.117906Jacinto, M.J.Wagner, AlexandraSá, Inês M.Patinha, David J.S.Marrucho, Isabel M.Gonçalves, JoãoWillson, Richard C.Azevedo, A.M.Aires-Barros, M.R.info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2024-02-22T12:13:47Zoai:ria.ua.pt:10773/37758Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T03:08:21.760514Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Screening polymeric ionic liquids for chromatography-based purification of bacteriophage M13
title Screening polymeric ionic liquids for chromatography-based purification of bacteriophage M13
spellingShingle Screening polymeric ionic liquids for chromatography-based purification of bacteriophage M13
Jacinto, M.J.
Polymeric ionic liquids
Bacteriophage M13
Batch adsorption
Chromatography
Anion-exchange
title_short Screening polymeric ionic liquids for chromatography-based purification of bacteriophage M13
title_full Screening polymeric ionic liquids for chromatography-based purification of bacteriophage M13
title_fullStr Screening polymeric ionic liquids for chromatography-based purification of bacteriophage M13
title_full_unstemmed Screening polymeric ionic liquids for chromatography-based purification of bacteriophage M13
title_sort Screening polymeric ionic liquids for chromatography-based purification of bacteriophage M13
author Jacinto, M.J.
author_facet Jacinto, M.J.
Wagner, Alexandra
Sá, Inês M.
Patinha, David J.S.
Marrucho, Isabel M.
Gonçalves, João
Willson, Richard C.
Azevedo, A.M.
Aires-Barros, M.R.
author_role author
author2 Wagner, Alexandra
Sá, Inês M.
Patinha, David J.S.
Marrucho, Isabel M.
Gonçalves, João
Willson, Richard C.
Azevedo, A.M.
Aires-Barros, M.R.
author2_role author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Jacinto, M.J.
Wagner, Alexandra
Sá, Inês M.
Patinha, David J.S.
Marrucho, Isabel M.
Gonçalves, João
Willson, Richard C.
Azevedo, A.M.
Aires-Barros, M.R.
dc.subject.por.fl_str_mv Polymeric ionic liquids
Bacteriophage M13
Batch adsorption
Chromatography
Anion-exchange
topic Polymeric ionic liquids
Bacteriophage M13
Batch adsorption
Chromatography
Anion-exchange
description M13 bacteriophage is a key instrument in phage display applications, as well as a possible antibacterial therapeutic agent due to its highly restrictive bacterial pathogenesis, and other applications. The traditional phage purification process is usually achieved by gradient ultracentrifugation or a combination of precipitation, centrifugation and microfiltration. These approaches easily lead to long process times, high operational costs, phage aggregation and consequent product loss (approximately 60%). This work is thus focused on an alternative potential large-scale process to achieve high yield and purity while minimizing the operational costs. Electrostatic-based separation processes are also common biomolecules purification techniques. Although anion exchange chromatography has been used before to purify several viral particles, this technique has been poorly reported for the purification of M13 phage. In a recent work, our group has demonstrated the use of a predominant anion exchange process, where a polymeric ionic liquid (PIL) was used as an alternative separation matrix for M13 bacteriophage. In this work, a variety of system parameters was studied, including chemical structure of the cation and the anion, the crosslinker nature and its concentration, either in batch adsorption/elution or chromatographic operation mode. The PIL-based chromatographic operation mode revealed to be a suitable separation process for M13 from directly filtered E. coli supernatant, reaching over 70% M13 recovery and 4.6 purification factor in a single step. To our knowledge, this is the first time that PILs have been reported as separation agents for bioproducts from complex mixtures.
publishDate 2021
dc.date.none.fl_str_mv 2021-02-15T00:00:00Z
2021-02-15
2023-05-16T13:29:25Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10773/37758
url http://hdl.handle.net/10773/37758
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 1383-5866
10.1016/j.seppur.2020.117906
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dc.publisher.none.fl_str_mv Elsevier
publisher.none.fl_str_mv Elsevier
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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