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dc.contributor.authorBinahmed, Sara
dc.contributor.authorHasane, Anissa
dc.contributor.authorWang, Zhaoxing
dc.contributor.authorMansurov, Aslan
dc.contributor.authorRomero-Vargas Castrillon, Santiago
dc.date.accessioned2019-08-28T13:17:30Z
dc.date.available2019-08-28T13:17:30Z
dc.date.created2018-12-07T16:55:24Z
dc.date.issued2018
dc.identifier.citationEnvironmental Science and Technology. 2018, 52 (1), 162-172.nb_NO
dc.identifier.issn0013-936X
dc.identifier.urihttp://hdl.handle.net/11250/2611463
dc.description.abstractInsight into the mechanisms underlying bacterial adhesion is critical to the formulation of membrane biofouling control strategies. Using AFM-based single-cell force spectroscopy, we investigated the interaction between Pseudomonas fluorescens, a biofilm-forming bacterium, and polysulfone (PSF) ultrafiltration (UF) membranes to unravel the mechanisms underlying early stage membrane biofouling. We show that hydrophilic polydopamine (PDA) coatings decrease bacterial adhesion forces at short bacterium-membrane contact times. Further, we find that adhesion forces are weakened by the presence of natural organic matter (NOM) conditioning films, owing to the hydrophilicity of NOM. Investigation of the effect of adhesion contact time revealed that PDA coatings are less effective at preventing bioadhesion when the contact time is prolonged to 2–5 s, or when the membranes are exposed to bacterial suspensions under stirring. These results therefore challenge the notion that simple hydrophilic surface coatings are effective as a biofouling control strategy. Finally, we present evidence that adhesion to the UF membrane surface is mediated by cell-surface macromolecules (likely to be outer membrane proteins and pili) which, upon contacting the membrane, undergo surface-induced unfolding.nb_NO
dc.language.isoengnb_NO
dc.publisherAmerican Chemical Societynb_NO
dc.titleBacterial Adhesion to Ultrafiltration Membranes: Role of Hydrophilicity, Natural Organic Matter, and Cell-Surface Macromoleculesnb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionpublishedVersionnb_NO
dc.source.pagenumber162-172nb_NO
dc.source.volume52nb_NO
dc.source.journalEnvironmental Science and Technologynb_NO
dc.source.issue1nb_NO
dc.identifier.doi10.1021/acs.est.7b03682
dc.identifier.cristin1640526
dc.description.localcodeThis article will not be available due to copyright restrictions © 2018 by American Chemical Societynb_NO
cristin.unitcode194,64,91,0
cristin.unitnameInstitutt for bygg- og miljøteknikk
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2


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