Sentence examples for binding to bacterial cell from inspiring English sources

Exact(6)

The eDNA could be incorporated during extracellular matrix development by binding to bacterial cell and to exopolymers [36], [37], possibly bridging them and allowing further glucan deposition.

The different effects of the single peptides can be explained by their varying strengths of binding to bacterial cell envelope compounds.

SpA can prevent phagocytosis by binding the complement binding portion (Fcγ) of functional antibodies thus hindering the antibody binding to bacterial cell surface components and subsequent complement dependent uptake of bacteria by phagocytic cells.

LysM-containing proteins as well as chimeric fusions of LysM domains with various other proteins have been used to investigate their (localized) binding to bacterial cell surfaces (Table  2).

First identified in intestinal Paneth cells, Omentin demonstrates low affinity binding to bacterial cell wall carbohydrates and was thought to be part of early-defense mechanisms in the gut against pathogenic bacteria [ 4].

To image the mCherry_PGRP-SA binding to bacterial cell surface by fluorescence microscopy, cells were treated as previously described (Atilano et al., 2011), except that mCherry_PGRP-SA was added to a final concentration of ≈300 µg/ml, in a reaction volume of 200 µl.

Similar(54)

Another possible mechanism of the biosurfactant anti-adhesive action relates with its ability of binding to bacterial cells, altering their hydrophobic and electrochemical properties (Neu 1996; Monteiro et al. 2011).

Additionally, the capacities for the anti-rOmpF sera binding to bacterial cells were performed among the strains of E. coli CVCC 1515, E. coli CICC 21530 (O157 H7), S. dysenteriae CMCC 51252, S. flexneri CMCC 51571, S. enteritidis CVCC 3377, S. pullorum CVCC 503, P. aeruginosa CICC 21630, and P. aeruginosa CICC 10419 in vitro.

mCherry_PGRP-SA binding to bacterial cells was also imaged by fluorescence microscopy.

To quantify mCherry_PGRP-SA binding to bacterial cells, cultures were grown to mid-exponential phase (OD600 nm 0.5), centrifuged, and resuspended in TSB to an OD of 2.5.

We have previously demonstrated that chemical structures of ammonium groups (primary, tertiary, and quaternary) determine the binding of polymers to bacterial cell membranes and antimicrobial activity against E. coli.

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