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1.
J R Soc Interface ; 3(6): 37-43, 2006 Feb 22.
Article in English | MEDLINE | ID: mdl-16849215

ABSTRACT

Mussels (Mytilus edulis) are economically important in their role as an aquaculture species and also with regard to marine biofouling. They attach tenaciously to a wide variety of submerged surfaces by virtue of collagenous attachment threads termed 'byssi'. The aim of this study was to characterize the spreading of the byssal attachment plaque, which mediates attachment to the surface, on a range of surfaces in response to changes in wettability. To achieve this, well characterized self-assembled monolayers of omega-terminated alkanethiolates on gold were used, allowing correlation of byssal plaque spreading with a single surface characteristic--wettability. The present results were inconsistent with those from previous studies, in that there was a positive correlation between plaque size and surface wettability; a trend which is not explained by conventional wetting theory for a three-phase system. A recent extension to wetting theory with regard to hydrophilic proteins is discussed and the results of settlement assays are used to attempt reconciliation of these results with those of similar previous studies and, also, with recent data presented for the spreading of Ulva linza spore adhesive.


Subject(s)
Crystallization/methods , Models, Chemical , Models, Molecular , Mytilus edulis/chemistry , Proteins/chemistry , Adhesiveness , Animals , Computer Simulation , Molecular Conformation , Phase Transition , Surface Properties
2.
J R Soc Interface ; 2(4): 319-25, 2005 Sep 22.
Article in English | MEDLINE | ID: mdl-16849189

ABSTRACT

The environmental scanning electron microscope has been used to image the adhesive pads secreted by zoospores of the marine alga Ulva linza as they settle on a range of self-assembled and grafted monolayers of different wettability, under natural, hydrated conditions. Results reveal that the diameter of the adhesive pad is strongly influenced by surface wettability, the adhesive spreading more (i.e. wetting the surface better) on the more hydrophilic surfaces. This is in direct contrast to previous observations on the spreading of marine bioadhesives and is in apparent contradiction to the predictions of the Young-Dupre equation for three-phase systems. In this paper, we attempt an explanation based upon thermodynamic analysis of the wetting properties of hydrophilic proteins.


Subject(s)
Cell Adhesion Molecules/chemistry , Cell Adhesion Molecules/physiology , Cell Adhesion/physiology , Models, Biological , Models, Chemical , Ulva/chemistry , Ulva/physiology , Adhesiveness , Computer Simulation , Energy Transfer , Hydrophobic and Hydrophilic Interactions , Spores/chemistry , Spores/physiology , Surface Properties , Wettability
3.
Nucleic Acids Res ; 29(21): E107-7, 2001 Nov 01.
Article in English | MEDLINE | ID: mdl-11691944

ABSTRACT

The field of DNA microarray technology has necessitated the cooperative efforts of interdisciplinary scientific teams to achieve its primary goal of rapidly measuring global gene expression patterns. A collaborative effort was established to produce a chemically reactive surface on glass slide substrates to which unmodified DNA will covalently bind for improvement of cDNA microarray technology. Using the p-aminophenyl trimethoxysilane (ATMS)/diazotization chemistry that was developed, microarrays were fabricated and analyzed. This immobilization method produced uniform spots containing equivalent or greater amounts of DNA than commercially available immobilization techniques. In addition, hybridization analyses of microarrays made with ATMS/diazotization chemistry showed very sensitive detection of the target sequence, two to three orders of magnitude more sensitive than the commercial chemistries. Repeated stripping and re-hybridization of these slides showed that DNA loss was minimal, allowing multiple rounds of hybridization. Thus, the ATMS/diazotization chemistry facilitated covalent binding of unmodified DNA, and the reusable microarrays that were produced showed enhanced levels of hybridization and very low background fluorescence.


Subject(s)
DNA/metabolism , Oligonucleotide Array Sequence Analysis/methods , Adsorption , Carbocyanines/metabolism , DNA/chemistry , DNA/genetics , DNA Probes/chemistry , DNA Probes/genetics , DNA Probes/metabolism , DNA, Fungal/chemistry , DNA, Fungal/genetics , DNA, Fungal/metabolism , Fluorescence , Fluorescent Dyes/metabolism , Gene Expression Profiling/methods , Glass , Neurospora crassa/genetics , Nucleic Acid Hybridization , Polylysine/metabolism , Reproducibility of Results , Silanes/chemistry , Silanes/metabolism
4.
Appl Environ Microbiol ; 66(8): 3249-54, 2000 Aug.
Article in English | MEDLINE | ID: mdl-10919777

ABSTRACT

We investigated surface selection and adhesion of motile zoospores of a green, macrofouling alga (Enteromorpha) to self-assembled monolayers (SAMs) having a range of wettabilities. The SAMs were formed from alkyl thiols terminated with methyl (CH(3)) or hydroxyl (OH) groups or mixtures of CH(3)- and OH-terminated alkyl thiols and were characterized by measuring the advancing contact angles and by X-ray photoelectron spectroscopy. There was a positive correlation between the number of spores that attached to the SAMs and increasing contact angle (hydrophobicity). Moreover, the sizes of the spore groups (adjacent spores touching) were larger on the hydrophobic SAMs. Video microscopy of a patterned arrangement of SAMs showed that more zoospores were engaged in swimming and "searching" above the hydrophobic sectors than above the hydrophilic sectors, suggesting that the cells were able to "sense" that the hydrophobic surfaces were more favorable for settlement. The results are discussed in relation to the attachment of microorganisms to substrata having different wettabilities.


Subject(s)
Cell Adhesion , Chlorophyta/physiology , Spores/physiology , Microscopy, Video , Surface Properties , Time Factors , Wettability
5.
Appl Environ Microbiol ; 65(4): 1603-9, 1999 Apr.
Article in English | MEDLINE | ID: mdl-10103257

ABSTRACT

Controlling bacterial biofouling is desirable for almost every human enterprise in which solid surfaces are introduced into nonsterile aqueous environments. One approach that is used to decrease contamination of manufactured devices by microorganisms is using materials that easily slough off accumulated material (i.e., fouling release surfaces). The compounds currently used for this purpose rely on low surface energy to inhibit strong attachment of organisms. In this study, we examined the possible use of environmentally responsive (or "smart") polymers as a new class of fouling release agents; a surface-grafted thermally responsive polymer, poly(N-isopropylacrylamide) (PNIPAAM), was used as a model compound. PNIPAAM is known to have a lower critical solubility temperature of approximately 32 degrees C (i.e., it is insoluble in water at temperatures above 32 degrees C and is soluble at temperatures below 32 degrees C). Under experimental conditions, >90% of cultured microorganisms (Staphylococcus epidermidis, Halomonas marina) and naturally occurring marine microorganisms that attached to grafted PNIPAAM surfaces during 2-, 18-, 36-, and 72-h incubations were removed when the hydration state of the polymer was changed from a wettability that was favorable for attachment to a wettability that was less favorable. Of particular significance is the observation that an organism known to attach in the greatest numbers to hydrophobic substrata (i.e., H. marina) was removed when transition of PNIPAAM to a more hydrated state occurred, whereas an organism that attaches in the greatest numbers to hydrophilic substrata (i.e., S. epidermidis) was removed when the opposite transition occurred. Neither solvated nor desolvated PNIPAAM exhibited intrinsic fouling release properties, indicating that the phase transition was the important factor in removal of organisms. Based on our observations of the behavior of this model system, we suggest that environmentally responsive polymers represent a new approach for controlling biofouling release.


Subject(s)
Acrylamides/pharmacology , Bacterial Adhesion , Biofilms/drug effects , Biofilms/growth & development , Water Microbiology , Acrylamides/chemistry , Halobacterium/drug effects , Halobacterium/physiology , Staphylococcus epidermidis/drug effects , Staphylococcus epidermidis/physiology , Surface Properties
6.
FEMS Microbiol Lett ; 142(1): 59-63, 1996 Aug 15.
Article in English | MEDLINE | ID: mdl-8759791

ABSTRACT

Bacterial cell attachment to the surfaces of self-assembled monolayers formed by the adsorption of omega-substituted alkanethiols on transparent gold films has been studied under defined bacterial culture and flow conditions. Phase contrast microscopy was used to quantify the attachment of two organisms, one of medical (Staphylococcus epidermidis) and one of marine (Deleya marina) importance. Self-assembled monolayers terminated with hexa(ethylene glycol), methyl, carboxylic acid and fluorocarbon groups were investigated. Over the range of experimental conditions, self-assembled monolayers formed from HS(CH2)11(OCH2CH2)6OH were found to be uniformly resistant to bacterial attachment, with a 99.7% reduction of attachment for both organisms when compared to the most fouled surface for each organism. On other surfaces, S. epidermidis and D. marina were shown to exhibit very different attachment responses to the wettability of the substratum. While the attachment of S. epidermidis correlated positively with surface hydrophilicity, D. marina showed a preference for hydrophobic surfaces. This study suggests that surfaces incorporating high densities of oligo(ethylene glycol) are good candidates for surfaces that interact minimally with bacteria.


Subject(s)
Bacterial Adhesion/drug effects , Ethylene Glycols/pharmacology , Ethylene Glycols/chemistry , Gram-Negative Aerobic Bacteria/drug effects , Gram-Negative Aerobic Bacteria/growth & development , Models, Biological , Staphylococcus epidermidis/drug effects , Staphylococcus epidermidis/growth & development , Surface Properties
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