4.8 Article

Scanning Ion Conductance Microscopy Reveals Differences in the Ionic Environments of Gram-Positive and Negative Bacteria

期刊

ANALYTICAL CHEMISTRY
卷 92, 期 24, 页码 16024-16032

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.analchem.0c03653

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资金

  1. EPSRC through MAS CDT [EP/L015307/1]
  2. EPSRC/Unilever
  3. European Union [790615]
  4. Royal Society
  5. Bio-Electrical Engineering Innovation Hub, University of Warwick - UK's Biological and Biotechnological Sciences [BB/S506783/1]
  6. Engineering and Physical Sciences Research Councils
  7. Marie Curie Actions (MSCA) [790615] Funding Source: Marie Curie Actions (MSCA)

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This paper reports on the use of scanning ion conductance microscopy (SICM) to locally map the ionic properties and charge environment of two live bacterial strains: the Gram-negative Escherichia coli and the Gram-positive Bacillus subtilis. SICM results find heterogeneities across the bacterial surface and significant differences among the Gram-positive and Gram-negative bacteria. The bioelectrical environment of the B. subtilis was found to be considerably more negatively charged compared to E. coli. SICM measurements, fitted to a simplified finite element method (FEM) model, revealed surface charge values of -80 to -140 mC m(-2) for the Gram-negative E. coli. The Gram-positive B. subtilis show a much higher conductivity around the cell wall, and surface charge values between -350 and -450 mC m(-2) were found using the same simplified model. SICM was also able to detect regions of high negative charge near B. subtilis, not detected in the topographical SICM response and attributed to the extracellular polymeric substance. To further explore how the B. subtilis cell wall structure can influence the SICM current response, a more comprehensive FEM model, accounting for the physical properties of the Gram-positive cell wall, was developed. The new model provides a more realistic description of the cell wall and allows investigation of the relation between its key properties and SICM currents, building foundations to further investigate and improve understanding of the Gram-positive cellular microenvironment.

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