
@article {229,
	title = {Applications of an inactive Dispersin B probe to monitor biofilm polysaccharide production.},
	journal = {Methods Enzymol},
	volume = {665},
	year = {2022},
	month = {2022},
	pages = {209-231},
	abstract = {<p>Bacterial biofilms consist of surface-attached communities that secrete polymeric substances to form a biofilm matrix, generating a local microenvironment which helps protect from external factors. One such matrix component produced by a diverse list of microorganisms is the polysaccharide poly-β-1,6-N-acetylglucosamine (PNAG). Dispersin B is a PNAG-specific glycosyl hydrolase, which by leveraging its unique specificity, can be used to design a macromolecular fluorescent PNAG binding probe. An active site mutant of Dispersin B was fused to a fluorescent protein, to generate a probe that bound PNAG but did not hydrolyze its polysaccharide target. The ease and versatility of this strategy has made it possible to study PNAG in the context of maturing biofilms, as the probe tends to sequester in regions of high PNAG density. In this chapter, typical workflows from probe construction to cell-binding and imaging experiments are described.</p>},
	keywords = {Acetylglucosamine, Bacterial Proteins, Biofilms, Catalytic Domain, Polysaccharides},
	issn = {1557-7988},
	doi = {10.1016/bs.mie.2021.11.006},
	author = {Eddenden, Alexander and Nitz, Mark}
}
