Turnover dependent phenotypic simulation: a quantitative constraint-based simulation method that accommodates all main strain design strategies
Autor(a) principal: | |
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Data de Publicação: | 2019 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/1822/62535 |
Resumo: | The uncertain relationship between genotype and phenotype can make strain engineering an arduous trial and error process. To identify promising gene targets faster, constraint-based modelling methodologies are often used, although they remain limited in their predictive power. Even though the search for gene knock-outs is fairly established in constraint-based modelling, most strain design methods still model gene up/down-regulations by forcing the corresponding flux values to fixed levels without taking in consideration the availability of resources. Here, we present a constraint-based algorithm, the Turnover Dependent Phenotypic Simulation (TDPS) that quantitatively simulates phenotypes in a resource conscious manner. Unlike other available algorithms, TDPS does not force flux values and considers resource availability, using metabolite production turnovers as an indicator of metabolite abundance. TDPS can simulate up-regulation of metabolic reactions as well as the introduction of heterologous genes, alongside gene deletion and down-regulation scenarios. TDPS simulations were validated using engineered Saccharomyces cerevisiae strains available in the literature by comparing the simulated and experimental production yields of the target metabolite. For many of the strains evaluated, the experimental production yields were within the simulated intervals and the relative strain performance could be predicted with TDPS. However, the algorithm failed to predict some of the production changes observed experimentally, suggesting that further improvements are necessary. The results also showed that TDPS may be helpful in finding metabolic bottlenecks, but further experiments would be required to confirm these findings. |
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Turnover dependent phenotypic simulation: a quantitative constraint-based simulation method that accommodates all main strain design strategiesGenome-scale modelsMetabolic engineeringMetabolite turnoversNetwork rigidityPhenotype simulationSaccharomyces cerevisiaeCiências Médicas::Biotecnologia MédicaEngenharia e Tecnologia::Biotecnologia IndustrialScience & TechnologyThe uncertain relationship between genotype and phenotype can make strain engineering an arduous trial and error process. To identify promising gene targets faster, constraint-based modelling methodologies are often used, although they remain limited in their predictive power. Even though the search for gene knock-outs is fairly established in constraint-based modelling, most strain design methods still model gene up/down-regulations by forcing the corresponding flux values to fixed levels without taking in consideration the availability of resources. Here, we present a constraint-based algorithm, the Turnover Dependent Phenotypic Simulation (TDPS) that quantitatively simulates phenotypes in a resource conscious manner. Unlike other available algorithms, TDPS does not force flux values and considers resource availability, using metabolite production turnovers as an indicator of metabolite abundance. TDPS can simulate up-regulation of metabolic reactions as well as the introduction of heterologous genes, alongside gene deletion and down-regulation scenarios. TDPS simulations were validated using engineered Saccharomyces cerevisiae strains available in the literature by comparing the simulated and experimental production yields of the target metabolite. For many of the strains evaluated, the experimental production yields were within the simulated intervals and the relative strain performance could be predicted with TDPS. However, the algorithm failed to predict some of the production changes observed experimentally, suggesting that further improvements are necessary. The results also showed that TDPS may be helpful in finding metabolic bottlenecks, but further experiments would be required to confirm these findings.ortuguese Foundation forScience and Technology (FCT) under the scope of thestrategic funding of UID/BIO/04469/2019 unit and Bio-TecNorte operation (NORTE-01-0145-FEDER-000004)funded by the European Regional Development Fund under the scope of Norte2020−Programa Operacional Regional doNorte. This project has received funding from the EuropeanUnion’s Horizon 2020 research and innovation programmeunder Grant Agreement No. 686070 and from the NovoNordisk Foundation. The work of Rui Pereira was supported by a PhD grant from FCT (ref SFRH/BD/51111/2010)info:eu-repo/semantics/publishedVersionAmerican Chemical SocietyUniversidade do MinhoPereira, Rui Miguel Pinheiro SilvaVilaça, P.Maia, PauloNielsen, JensRocha, I.2019-03-292019-03-29T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/1822/62535engPereira, R.; Vilaça, P.; Maia, Paulo; Nielsen, Jens; Rocha, Isabel, Turnover dependent phenotypic simulation: a quantitative constraint-based simulation method that accommodates all main strain design strategies. ACS Synthetic Biology, 8(5), 976-988, 20192161-50632161-506310.1021/acssynbio.8b0024830925047https://pubs.acs.org/doi/abs/10.1021/acssynbio.8b00248info: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:RCAAP2023-07-21T12:30:30Zoai:repositorium.sdum.uminho.pt:1822/62535Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T19:25:41.656465Repositório 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 |
Turnover dependent phenotypic simulation: a quantitative constraint-based simulation method that accommodates all main strain design strategies |
title |
Turnover dependent phenotypic simulation: a quantitative constraint-based simulation method that accommodates all main strain design strategies |
spellingShingle |
Turnover dependent phenotypic simulation: a quantitative constraint-based simulation method that accommodates all main strain design strategies Pereira, Rui Miguel Pinheiro Silva Genome-scale models Metabolic engineering Metabolite turnovers Network rigidity Phenotype simulation Saccharomyces cerevisiae Ciências Médicas::Biotecnologia Médica Engenharia e Tecnologia::Biotecnologia Industrial Science & Technology |
title_short |
Turnover dependent phenotypic simulation: a quantitative constraint-based simulation method that accommodates all main strain design strategies |
title_full |
Turnover dependent phenotypic simulation: a quantitative constraint-based simulation method that accommodates all main strain design strategies |
title_fullStr |
Turnover dependent phenotypic simulation: a quantitative constraint-based simulation method that accommodates all main strain design strategies |
title_full_unstemmed |
Turnover dependent phenotypic simulation: a quantitative constraint-based simulation method that accommodates all main strain design strategies |
title_sort |
Turnover dependent phenotypic simulation: a quantitative constraint-based simulation method that accommodates all main strain design strategies |
author |
Pereira, Rui Miguel Pinheiro Silva |
author_facet |
Pereira, Rui Miguel Pinheiro Silva Vilaça, P. Maia, Paulo Nielsen, Jens Rocha, I. |
author_role |
author |
author2 |
Vilaça, P. Maia, Paulo Nielsen, Jens Rocha, I. |
author2_role |
author author author author |
dc.contributor.none.fl_str_mv |
Universidade do Minho |
dc.contributor.author.fl_str_mv |
Pereira, Rui Miguel Pinheiro Silva Vilaça, P. Maia, Paulo Nielsen, Jens Rocha, I. |
dc.subject.por.fl_str_mv |
Genome-scale models Metabolic engineering Metabolite turnovers Network rigidity Phenotype simulation Saccharomyces cerevisiae Ciências Médicas::Biotecnologia Médica Engenharia e Tecnologia::Biotecnologia Industrial Science & Technology |
topic |
Genome-scale models Metabolic engineering Metabolite turnovers Network rigidity Phenotype simulation Saccharomyces cerevisiae Ciências Médicas::Biotecnologia Médica Engenharia e Tecnologia::Biotecnologia Industrial Science & Technology |
description |
The uncertain relationship between genotype and phenotype can make strain engineering an arduous trial and error process. To identify promising gene targets faster, constraint-based modelling methodologies are often used, although they remain limited in their predictive power. Even though the search for gene knock-outs is fairly established in constraint-based modelling, most strain design methods still model gene up/down-regulations by forcing the corresponding flux values to fixed levels without taking in consideration the availability of resources. Here, we present a constraint-based algorithm, the Turnover Dependent Phenotypic Simulation (TDPS) that quantitatively simulates phenotypes in a resource conscious manner. Unlike other available algorithms, TDPS does not force flux values and considers resource availability, using metabolite production turnovers as an indicator of metabolite abundance. TDPS can simulate up-regulation of metabolic reactions as well as the introduction of heterologous genes, alongside gene deletion and down-regulation scenarios. TDPS simulations were validated using engineered Saccharomyces cerevisiae strains available in the literature by comparing the simulated and experimental production yields of the target metabolite. For many of the strains evaluated, the experimental production yields were within the simulated intervals and the relative strain performance could be predicted with TDPS. However, the algorithm failed to predict some of the production changes observed experimentally, suggesting that further improvements are necessary. The results also showed that TDPS may be helpful in finding metabolic bottlenecks, but further experiments would be required to confirm these findings. |
publishDate |
2019 |
dc.date.none.fl_str_mv |
2019-03-29 2019-03-29T00:00:00Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/1822/62535 |
url |
http://hdl.handle.net/1822/62535 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Pereira, R.; Vilaça, P.; Maia, Paulo; Nielsen, Jens; Rocha, Isabel, Turnover dependent phenotypic simulation: a quantitative constraint-based simulation method that accommodates all main strain design strategies. ACS Synthetic Biology, 8(5), 976-988, 2019 2161-5063 2161-5063 10.1021/acssynbio.8b00248 30925047 https://pubs.acs.org/doi/abs/10.1021/acssynbio.8b00248 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
American Chemical Society |
publisher.none.fl_str_mv |
American Chemical Society |
dc.source.none.fl_str_mv |
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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RCAAP |
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RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
collection |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
repository.name.fl_str_mv |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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1799132742056673280 |