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dc.contributor.authorXavier, Joao B.
dc.contributor.authorPicioreanu, Cristian
dc.contributor.authorRani, Suriani A.
dc.contributor.authorvan Loosdrecht, Mark C. M.
dc.contributor.authorStewart, Philip S.
dc.date.accessioned2017-07-13T22:38:34Z
dc.date.available2017-07-13T22:38:34Z
dc.date.issued2005-12
dc.identifier.citationXavier JB, Picioreanu C, Abdul Rani S, van Loosdrecht MCM, Stewart PS, "Biofilm control strategies based on enzymic disruption of the extracellular polymeric substance matrix - a modeling study," Microbiology, 2005 151(12):3817-3832en_US
dc.identifier.issn1350-0872
dc.identifier.urihttps://scholarworks.montana.edu/xmlui/handle/1/13308
dc.description.abstractA kinetic model is proposed to assess the feasibility of strategies for the removal of biofilms by using substances that induce detachment by affecting the cohesiveness of the matrix of extracellular polymeric substances (EPSs). The model uses a two-state description of the EPS (natural EPS and compromised EPS) to provide a unified representation of diverse mechanisms of action of detachment-promoting agents (DPAs), which include enzymes that degrade the EPS and other agents described in the literature. A biofilm-cohesiveness factor describes local increases in detachment rates resultant from losses in cohesive strength. The kinetic model was implemented in an individual-based biofilm-modeling framework, including detachment rates dependent on local cohesiveness. The efficacy of treatments with DPAs was assessed by three-dimensional model simulations. Changes in treatment efficacy were evaluated quantitatively by using a Thiele modulus, which quantifies the relationship between diffusion of the DPA through the biofilm matrix and DPA decay rate, and a Damköhler number relating the rate of EPS reaction with a DPA and the rate of EPS production by the micro-organisms in the biofilm. This study demonstrates the feasibility and limits of implementing biofilm-control strategies based on attacking the EPS.en_US
dc.titleBiofilm control strategies based on enzymic disruption of the extracellular polymeric substance matrix - a modeling studyen_US
dc.typeArticleen_US
mus.citation.extentfirstpage3817en_US
mus.citation.extentlastpage3832en_US
mus.citation.issue12en_US
mus.citation.journaltitleMicrobiologyen_US
mus.citation.volume151en_US
mus.identifier.categoryEngineering & Computer Scienceen_US
mus.identifier.doi10.1099/mic.0.28165-0en_US
mus.relation.collegeCollege of Engineeringen_US
mus.relation.departmentCenter for Biofilm Engineering.en_US
mus.relation.departmentChemical & Biological Engineering.en_US
mus.relation.departmentChemical Engineering.en_US
mus.relation.universityMontana State University - Bozemanen_US
mus.relation.researchgroupCenter for Biofilm Engineering.en_US
mus.data.thumbpage12en_US


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