Optimizing pectin lyase production using the one-factor-at-a-time method and response surface methodology

dc.contributor.authorGul, Ertugrul
dc.contributor.authorDursun, Arzu Yadigar
dc.contributor.authorTepe, Ozlem
dc.contributor.authorAkaslan, Gonca
dc.contributor.authorPampal, Fadile Gul
dc.date.accessioned2026-08-12T17:21:37Z
dc.date.issued2025
dc.departmentFırat Üniversitesi
dc.description.abstractPectinases are commonly industrially synthesized by molds. This study aimed to optimize pectin lyase synthesis by a bacterium, Pseudomonas fluorescens, using both the one-factor-at-a-time (OFAT) method and response surface methodology. First, on optimization of pectin lyase fermentation by the OFAT method, the effects of pectin, peptone, yeast extract, (NH4)(2)SO4, pH, and salts were investigated. The highest pectin lyase activity was determined to be 28.63 U/mL at pH 8, 30 degrees C, with 1% (w/v) pectin and 0.14% (w/v) (NH4)(2)SO4 concentration at the 90th hour. The effect of substrate inhibition on the microbial growth was also investigated, and the results showed that the process can be described by noncompetitive inhibition model. The values of kinetic constants were determined as mu (m) = 0.175 h(-1), K-S = 6.931 g/L, and, K-I = 6.932 g/L by nonlinear regression analysis. It was reported that pectin lyase enzymes exhibited peak activity at 50 degrees C and pH 8. Finally, response surface methodology (RSM) was utilized to optimize pH, concentrations of ammonium sulfate, and pectin, which were chosen as independent variables. The interactions between these variables were also examined. According to RSM, the optimum values of the parameters to achieve a maximum pectin lyase activity of 35.62 U/mL were determined to be pH 7.97, 1.25% (w/v) pectin concentration, and 0.25% (w/v) (NH4)(2)SO4 concentration.
dc.description.sponsorshipFirat University Scientific Research Projects Unit (FUBAP), Turkey [FUBAP MF. 12.11]
dc.description.sponsorshipFirat University Scientific Research Projects Unit (FUBAP), Turkey,Grant/Award Number: FUBAP MF. 12.11
dc.identifier.doi10.1002/bab.2686
dc.identifier.endpage651
dc.identifier.issn0885-4513
dc.identifier.issn1470-8744
dc.identifier.issue3
dc.identifier.orcid0000-0001-8611-2983
dc.identifier.orcid0000-0001-8336-3699
dc.identifier.pmid39434440
dc.identifier.scopus2-s2.0-85206942843
dc.identifier.scopusqualityQ1
dc.identifier.startpage638
dc.identifier.urihttps://doi.org/10.1002/bab.2686
dc.identifier.urihttps://hdl.handle.net/11508/54004
dc.identifier.volume72
dc.identifier.wosWOS:001339684300001
dc.identifier.wosqualityQ3
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherWiley
dc.relation.ispartofBiotechnology and Applied Biochemistry
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WoS_20260511
dc.subjectenzyme stability
dc.subjectmicrobial kinetic
dc.subjectoptimization
dc.subjectpectin lyase
dc.subjectPseudomonas fluorescens
dc.subjectresponse surface methodology
dc.titleOptimizing pectin lyase production using the one-factor-at-a-time method and response surface methodology
dc.typeArticle

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