Supporting Information Figure S1. Representative lateral deflection images (20 µm x 20 µm) in SW as obtained by AFM analysis of PDC (A), PCB5 (B), PCB10 (C), PCB15 (D) and PCB100 (E). Note the difference in z-height of PDC in respect to the other polymer coatings.
Holographic 3D tracking was applied to record and analyze the swimming behavior of Pseudomonas aeruginosa. The obtained trajectories allow to qualitatively and quantitatively analyze the free swimming behavior of the bacterium. This can be classified into five distinct swimming patterns. In addition to the previously reported smooth and oscillatory swimming motions, three additional patterns are distinguished. We show that Pseudomonas aeruginosa performs helical movements which were so far only described for larger microorganisms. Occurrence of the swimming patterns was determined and transitions between the patterns were analyzed.
Methacrylate and acrylate monomers are popular building blocks for antifouling (AF) and fouling-release (FR) coatings to counteract marine biofouling. They are used in various combinations and often combined into amphiphilic materials. This study investigated the FR properties of amphiphilic ethylene glycol dicyclopentenyl ether acrylate (DCPEA) and the corresponding methacrylate (DCPEMA) blended with 5 wt % zwitterionic carboxybetaine acrylate (CBA) and the corresponding methacrylate (CBMA). A series of (co)polymers with different acrylate/methacrylate compositions were synthesized and tested against the attachment of the diatom Navicula perminuta and in short-term dynamic field exposure experiments. The more hydrophobic methacrylate DCPEMA homopolymer outperformed its acrylate counterpart DCPEA. Incorporated zwitterionic functionality of both CBMA and CBA imparted ultralow fouling capability in the amphiphilic polymers toward diatom attachment, whereas in the real ocean environment, only the employment of CBMA reduced marine biofouling. Moreover, it was observed that CBA-containing coatings showed different surface morphologies and roughnesses compared to the CBMA analogues. Particularly, a high impact was found when acrylic CBA was mixed with methacrylic DCPEMA. While the wettability of the coatings was comparable, investigated methacrylates in general exhibited superior fouling resistance compared to the acrylates.
Dendritic
polyglycerol (PG) was covalently coupled to 2-hydroxyethyl
methacrylate (HEMA) by an anionically catalyzed ring-opening polymerization
generating a dendritic PG-HEMA with four PG repetition units (PG4MA). Coatings of the methacrylate monomer were prepared by
grafting-through and compared against commercially available hydrophilic
monomers of HEMA, poly(ethylene) glycol methacrylate (PEGMA), and
poly(propylene) glycol methacrylate (PPGMA). The obtained coatings
were characterized by modern surface analytical techniques, including
water contact angle goniometry (sessile and captive bubble), attenuated
total internal reflection Fourier transform infrared spectroscopy,
and atomic force microscopy. The antifouling (AF) and fouling-release
(FR) properties of the coatings were tested against the model organisms Cobetia marina and Navicula perminuta in laboratory-scale dynamic accumulation assays as well as in a
dynamic short-term field exposure (DSFE) in the marine environment.
In addition, the hydration of the coatings and their susceptibility
toward silt uptake were evaluated, revealing a strong correlation
between water uptake, silt incorporation, and field assay performance.
While all glycol derivatives showed good resistance in laboratory
settlement experiments, PPGMA turned out to be less susceptible to
silt incorporation and outperformed PEGMA and PG4MA in
the DSFE assay.
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