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Modeling biofilms with dual extracellular electron transfer mechanisms

机译:用双胞外电子转移机制模拟生物膜

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摘要

Electrochemically active biofilms have a unique form of respiration in which they utilize solid external materials as terminal electron acceptors for their metabolism. Currently, two primary mechanisms have been identified for long-range extracellular electron transfer (EET): a diffusion- and a conduction-based mechanism. Evidence in the literature suggests that some biofilms, particularly Shewanella oneidensis, produce the requisite components for both mechanisms. In this study, a generic model is presented that incorporates the diffusion- and the conduction-based mechanisms and allows electrochemically active biofilms to utilize both simultaneously. The model was applied to S. oneidensis and Geobacter sulfurreducens biofilms using experimentally generated data found in the literature. Our simulation results show that 1) biofilms having both mechanisms available, especially if they can interact, may have a metabolic advantage over biofilms that can use only a single mechanism; 2) the thickness of G. sulfurreducens biofilms is likely not limited by conductivity; 3) accurate intrabiofilm diffusion coefficient values are critical for current generation predictions; and 4) the local biofilm potential and redox potential are two distinct parameters and cannot be assumed to have identical values. Finally, we determined that simulated cyclic and squarewave voltammetry based on our model are currently not capable of determining the specific percentages of extracellular electron transfer mechanisms in a biofilm. The developed model will be a critical tool for designing experiments to explain EET mechanisms.
机译:电化学活性生物膜具有独特的呼吸形式,其中它们利用固体外部材料作为新陈代谢的末端电子受体。当前,已经确定了用于远程细胞外电子转移(EET)的两种主要机制:扩散机制和基于传导的机制。文献证据表明,某些生物膜,特别是希瓦氏菌,产生了这两种机制的必要成分。在这项研究中,提出了一个通用模型,该模型结合了基于扩散和传导的机制,并允许电化学活性生物膜同时利用两者。使用在文献中发现的实验生成的数据,将该模型应用于沙门氏菌和降低土壤杆菌的生物膜。我们的模拟结果表明:1)具有两种可用机制的生物膜,尤其是它们可以相互作用的生物膜,与仅使用单一机制的生物膜相比,可能具有代谢优势; 2)硫还原菌生物膜的厚度可能不受电导率的限制; 3)准确的生物膜内扩散系数值对于当前的预测至关重要; 4)局部生物膜电势和氧化还原电势是两个不同的参数,不能假定它们具有相同的值。最后,我们确定基于我们的模型的模拟循环伏安法和方波伏安法目前尚无法确定生物膜中细胞外电子转移机制的特定百分比。开发的模型将成为设计实验以解释EET机制的关键工具。

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