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The lowest concentrations without visible growth (at the binocular microscope) were defined as MICs.
The lowest concentrations without visible growth (at the binocular microscope) were defined as MIC.
The lowest concentrations without visible growth (at the binocular microscope) were defined as concentrations that completely inhibited bacterial growth (MICs).
Brown granules in cells under microscope were defined as positive signals and observed at 400x magnification of light microscopy.
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The resolution of a microscope is defined as the full width at half maximum (FWHM) of the point spread function (PSF) [ 34].
CECs extracted in this way were counted using a Nageotte chamber on a fluorescence microscope and were defined as Ulex europaeus lectin (Sigma-Aldrich, Doset, UK) bright cells that were > 10 μm in size, with five or more magnetic beads attached.
Colonies, which were defined as clusters of more than 40 cells, were counted after 7 days using an inverted microscope.
The optics of the microscope objective are defined by the focal length, N.A., and field of view.
Furthermore, the microscope scanning direction can be defined which is important for the correct 3D reconstruction of image stacks from image cross sections files (Fig 6B).
The colonies were stained with Giemsa (Sigma) and scored under microscope, where a cluster of more than 50 cells was defined as one colony.
'Fluorescence' was defined as 'visible fluorescence using the operating microscope' as described above.
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