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Biofilm-control strategies based on enzymic disruption of the extracellular polymeric substance matrix – a modelling study

机译:基于酶促破坏细胞外聚合物物质基质的生物膜控制策略 - 建模研究

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A 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-modelling 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 Damk?hler 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.
机译:提出了一种动力学模型来评估通过使用诱导脱离的物质来评估策略的可行性,通过影响脱离的物质来影响细胞外聚合物物质(EPS)的基质的凝聚性。该模型使用EPS(自然eps和损害的EPS)的两个状态描述,以提供脱离促进剂(DPA)的各种作用机制的统一表示,其包括降解所述EPS和所述其他药剂的酶文学。生物膜凝聚因子描述了局部拆分率的局部增加,从而产生了粘性强度的损失。动力学模型在基于个体的生物膜建模框架中实施,包括依赖于局部内聚的分离率。通过三维模型模拟评估DPA治疗的疗效。通过使用硫醚模量定量评估治疗效能的变化,这通过生物膜基质和DPA衰减率来定量DPA的扩散之间的关系,以及与DPA的EPS反应率和率的差距和差距通过生物膜中的微生物产生的EPS生产。本研究展示了基于攻击EPS实施生物膜控制策略的可行性和限制。

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