Acid proteinase enzyme activity in Candida albicans strains: A comparison of spectrophotometry and plate methods

dc.contributor.buuauthorAkçağlar, Sevim
dc.contributor.buuauthorEner, Beyza
dc.contributor.buuauthorTöre, Okan
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Mikrobiyoloji ve Enfeksiyon Hastalıkları Anabilim Dalı.tr_TR
dc.contributor.orcid0000-0002-4803-8206tr_TR
dc.contributor.researcheridAAG-8523-2021tr_TR
dc.contributor.scopusid6506194958tr_TR
dc.contributor.scopusid15053025300tr_TR
dc.contributor.scopusid6505909596tr_TR
dc.date.accessioned2022-01-06T11:47:12Z
dc.date.available2022-01-06T11:47:12Z
dc.date.issued2011
dc.description.abstractIn recent years, the incidence of fungal infections has been rising all over the world. Although the amount of research in the field of pathogenic fungi has also increased, there is still a need for studies on fungal virulence. In this investigation, we focused on testing bloodstream-identified Candida albicans in experimental in vitro virulence assays. The proteinase enzyme activities of 30 C. albicans strains isolated from the bloodstream and sterile body fluids were investigated (15 colonizations, 15 infections). The spectrophotometric and plate methods were used to determine proteinase activity. The correlations between the 2 methods were compared. This study indicates that, in terms of proteinase activity, there were no statistically significant differences between strains obtained from infection and colonization sites by either method (P > 0.05).en_US
dc.identifier.citationAkçağlar, S. vd. (2011). "Acid proteinase enzyme activity in Candida albicans strains: A comparison of spectrophotometry and plate methods". Turkish Journal of Biology, 35(5), 556-567.tr_TR
dc.identifier.endpage567tr_TR
dc.identifier.issn1300-0152
dc.identifier.issn1303-6092
dc.identifier.issue5tr_TR
dc.identifier.scopus2-s2.0-80052680173tr_TR
dc.identifier.startpage559tr_TR
dc.identifier.urihttps://doi.org/10.3906/biy-1002-39
dc.identifier.urihttps://journals.tubitak.gov.tr/biology/issues/biy-11-35-5/biy-35-5-4-1002-39.pdf
dc.identifier.urihttp://hdl.handle.net/11452/23906
dc.identifier.volume35tr_TR
dc.identifier.wos000295771900004
dc.indexed.scopusScopusen_US
dc.indexed.trdizinTrDizintr_TR
dc.indexed.wosSCIEen_US
dc.language.isoenen_US
dc.publisherTÜBİTAKtr_TR
dc.relation.journalTurkish Journal of Biologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectLife sciences & biomedicine - other topicsen_US
dc.subjectCandida albicansen_US
dc.subjectSecreted aspartyl proteinase (SAP) activityen_US
dc.subjectVirulenceen_US
dc.subjectBlood-stream infectionsen_US
dc.subjectPhospholipase-activityen_US
dc.subjectVirulence factorsen_US
dc.subjectUnited-statesen_US
dc.subjectVaginitisen_US
dc.subjectSusceptibilityen_US
dc.subjectPathogenicityen_US
dc.subjectFrequencyen_US
dc.subjectCandida albicansen_US
dc.subjectFungien_US
dc.subject.scopusAspartic Acid Proteases; Candida; Virulence Factorsen_US
dc.subject.wosBiologyen_US
dc.titleAcid proteinase enzyme activity in Candida albicans strains: A comparison of spectrophotometry and plate methodsen_US
dc.typeArticle
dc.wos.quartileQ3en_US

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