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Simultaneous enumeration of yeast and bacterial cells in the context of industrial bioprocesses

dc.contributor.authorMartins, Carolina Teixeira
dc.contributor.authorJacobus, Ana Paula [UNESP]
dc.contributor.authorConceição, Renilson
dc.contributor.authorBarbin, Douglas Fernandes
dc.contributor.authorBolini, Helena
dc.contributor.authorGombert, Andreas Karoly
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionUniversidade Estadual de Campinas (UNICAMP)
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.date.accessioned2025-04-29T18:37:39Z
dc.date.issued2024-01-01
dc.description.abstractIn scenarios where yeast and bacterial cells coexist, it is of interest to simultaneously quantify the concentrations of both cell types, since traditional methods used to determine these concentrations individually take more time and resources. Here, we compared different methods for quantifying the fuel ethanol Saccharomyces cerevisiae PE-2 yeast strain and cells from the probiotic Lactiplantibacillus plantarum strain in microbial suspensions. Individual suspensions were prepared, mixed in 1:1 or 100:1 yeast-to-bacteria ratios, covering the range typically encountered in sugarcane biorefineries, and analyzed using bright field microscopy, manual and automatic Spread-plate and Drop-plate counting, flow cytometry (at 1:1 and 100:1 ratios), and a Coulter Counter (at 1:1 and 100:1 ratios). We observed that for yeast cell counts in the mixture (1:1 and 100:1 ratios), flow cytometry, the Coulter Counter, and both Spread-plate options (manual and automatic CFU counting) yielded statistically similar results, while the Drop-plate and microscopy-based methods gave statistically different results. For bacterial cell quantification, the microscopy-based method, Drop-plate, and both Spread-plate plating options and flow cytometry (1:1 ratio) produced no significantly different results (p > .05). In contrast, the Coulter Counter (1:1 ratio) and flow cytometry (100:1 ratio) presented results statistically different (p < .05). Additionally, quantifying bacterial cells in a mixed suspension at a 100:1 ratio wasn’t possible due to an overlap between yeast cell debris and bacterial cells. We conclude that each method has limitations, advantages, and disadvantages. One-sentence summary: This study compares methods for simultaneously quantifying yeast and bacterial cells in a mixed sample, highlighting that in different cell proportions, some methods cannot quantify both cell types and present distinct advantages and limitations regarding time, cost, and precision.en
dc.description.affiliationUniversidade de São Paulo Programa de Pós-Graduação Interunidades em Biotecnologia Cidade Universitária, Avenida Prof. Lineu Prestes, 2415 - Edifício ICB - III, SP
dc.description.affiliationFaculdade de Engenharia de Alimentos Universidade Estadual de Campinas, Rua Monteiro Lobato 80, SP
dc.description.affiliationInstituto de Pesquisa em Bioenergia Universidade Estadual Paulista “Júlio de Mesquita Filho”, Rua 10 2527, SP
dc.description.affiliationUnespInstituto de Pesquisa em Bioenergia Universidade Estadual Paulista “Júlio de Mesquita Filho”, Rua 10 2527, SP
dc.identifierhttp://dx.doi.org/10.1093/jimb/kuae029
dc.identifier.citationJournal of Industrial Microbiology and Biotechnology, v. 51.
dc.identifier.doi10.1093/jimb/kuae029
dc.identifier.issn1476-5535
dc.identifier.issn1367-5435
dc.identifier.scopus2-s2.0-85203807483
dc.identifier.urihttps://hdl.handle.net/11449/298626
dc.language.isoeng
dc.relation.ispartofJournal of Industrial Microbiology and Biotechnology
dc.sourceScopus
dc.subjectCell counting
dc.subjectLactic acid bacteria
dc.subjectMixed culture
dc.subjectYeast
dc.titleSimultaneous enumeration of yeast and bacterial cells in the context of industrial bioprocessesen
dc.typeArtigopt
dspace.entity.typePublication
unesp.author.orcid0000-0003-2429-8422 0000-0003-2429-8422[1]
unesp.author.orcid0000-0001-9557-3773[6]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Pesquisa em Bioenergia, Rio Claropt

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