Differential Colonization Dynamics of Marine Biofilm-Forming Eukaryotic Microbes on Different Protective Coating Materials

In this study, the actual anti-biofouling (AF) efficacy of three protective coatings, including a chlorinated rubber-based coating (C₀) and two polydimethylsiloxane (PDMS)-based coatings (P₀ and P ), were estimated via the static field exposure assays. The surface properties of these protective coat...

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Published inPolymers Vol. 11; no. 1; p. 161
Main Authors Lang, Yanhe, Sun, Yuan, Yu, Miao, Ji, Yubin, Wang, Lei, Zhang, Zhizhou
Format Journal Article
LanguageEnglish
Published Switzerland MDPI AG 17.01.2019
MDPI
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Summary:In this study, the actual anti-biofouling (AF) efficacy of three protective coatings, including a chlorinated rubber-based coating (C₀) and two polydimethylsiloxane (PDMS)-based coatings (P₀ and P ), were estimated via the static field exposure assays. The surface properties of these protective coatings, including surface wettability and morphology features, were characterized using the static water contact angle (WCA) and scanning electron microscope (SEM). The colonization and succession dynamics of the early-adherent biofilm-forming eukaryotic microbial communities occupied on these protective coatings were explored using the Single-stranded Conformation Polymorphism (SSCP) technique. The field data clearly revealed that coating P₀ and P performed better in the long-term static submergence, as compared with the C₀ surface, while coating P showed excellent AF efficacy in the field. Fingerprinting analysis suggested that the diversity, abundance, the clustering patterns, and colonization dynamics of the early-colonized eukaryotic microbes were significantly perturbed by these protective coatings, particularly by the P surfaces. These differential AF efficacy and perturbation effects would be largely ascribed to the differences in the wettability and surface nanostructures between the C₀, P₀ and P surfaces, as evidenced by WCA and SEM analysis.
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These authors contributed equally to this work.
ISSN:2073-4360
2073-4360
DOI:10.3390/polym11010161