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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Perfusion microbioreactor system with permeable membranes to monitor bacterial growth

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Autor(es):
Vit, Franciele Flores [1] ; Oliveira, Aline Furtado [1] ; Osorio Rodriguez, Daniel Andres [2] ; de Carvalho, Hernandes F. [2] ; Lancellotti, Marcelo [3] ; de la Torre, Lucimara Gaziola [1]
Número total de Autores: 6
Afiliação do(s) autor(es):
[1] Univ Estadual Campinas, Sch Chem Engn, Dept Bioproc & Mat Engn, Albert Einstein Ave 500, BR-13083852 Campinas, SP - Brazil
[2] Univ Estadual Campinas, Inst Biol, Dept Cell Biol, Campinas, SP - Brazil
[3] Univ Estadual Campinas, Sch Pharmaceut Sci, Dept Pharmaceut Sci, Campinas, SP - Brazil
Número total de Afiliações: 3
Tipo de documento: Artigo Científico
Fonte: JOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY; v. 94, n. 3, p. 712-720, MAR 2019.
Citações Web of Science: 2
Resumo

BACKGROUND Microfluidics offers itself as a potential platform for optimizing microbial growth in different substrate concentrations using a single assay. The aim of this study was to construct a reversible microfluidic device for monitoring the bacterial growth in chambers with different substrate concentrations with its respective technical triplicates. The convective concentration gradient generator (CCG) system was constructed with three inlets for solutions with different concentrations that distributed them to the sequential cultivation chambers (CCs). A perfusion microbioreactor system (PM) was constructed using a commercial polydimethylsiloxane (PDMS) sheet and glass, with an adapted semi-permeable membrane system to constrain the cells within the CC. Cell growth of a fluorescent Escherichia coli JM109 was monitored by fluorescence microscope with time-lapse technique. RESULTS The growth profile of E. coli with different streptomycin concentrations and its specific growth rates (mu(x)) in the microfluidics device (mu(x) of 0.0088 and 0.0092 h(-1)) were compared in batch cultivations, which show no significant difference between the two methods. In addition, the half maximal inhibitory concentration (IC50) values indicate that continuous perfusion surpasses consumption of the tested drug. CONCLUSION The results demonstrate the efficiency of the microfluidic device for cell cultivation and its applicability in industrial biotechnology, allowing rapid screening of multiple parameters. (c) 2018 Society of Chemical Industry (AU)

Processo FAPESP: 15/26701-0 - Microfluídica como estratégia tecnológica para nano&biotecnologia aplicada: (i) lipossomas catiônicos, nanopartículas de quitosana e baseadas em poliaminoácidos para terapia gênica e rotas alternativas de investigação de bioprocessos
Beneficiário:Lucimara Gaziola de la Torre
Modalidade de apoio: Auxílio à Pesquisa - Regular