Particulate adsorption by Mucor flavus and Neurospora crassa is a physical property of the cell wall, independent of both cellular metabolism and the production of extracellular polymers. Initial attractive forces responsible for particulate adsorption by N. crassa are mainly electrostatic in nature and this mechanism probably holds for M. flavus also. The outer glucan layer of the cell wall of N. crassa, although able to adsorb particulates, was not as efficient as the underlying protein layer at particle adsorption. Young, growing mycelium generally adsorbs the , -, largest amount of particles, due to the continued production of adsorption sites and the entrapment of particulates by hyphae. Factors increasing adsorption include nutrient starvation of mycelium and incubation with low concentrations of magnesium ions. Relatively high concentrations of mercury and copper ions decrease adsorption perhaps due to the precipitation and adsorption of the corresponding metal sulphides on the mycelial surface thereby effectively physically interfering with further particulate adsorption. Optimum conditions for adsorption are a temperature of 250C and a slightly acid pH value. Also, small particles are more readily adsorbed than large particles. Mucor flavus can adsorb clays and this ability may be used to treat industrial effluents which contain large amounts of clay minerals. An acid pH and a temperature of 250C are optimum conditions for clay adsorption by the fungus. Low concentrations of montmorillonite and kaolinite increase biomass production by Aspergillus niger in submerged culture, due to the inhibition of pellet formation by the fungus. The clays cause A. niger to grow in a more filamentous form and presumably would affect other fungi in a similar way. The use of clays to control fungal morphology may be important in several industrial fermentations. Low concentrations of the fungicide thiram stimulated the growth of Aspergillus niger in the presence of montmorillonite. Immobilization of fungi by magnetic means is possible due to their ability to adsorb magnetite. This method could also be used to remove fungi from fermentation media as an alternative to filtration or centrifugation. Even though older hyphae of Penicillium chrysogenum are unable to adsorb magnetite, this fungus can still be magnetically immobilized if it is grown from a spore suspension in the presence of magnetite. Either the spores or young hyphae of this fungus adsorb magnetite, producing pellets with magnetic properties. Magnetite adsorption occurs optimally at a temperature of 250C and is constant over a wide range of pH values. Waste mycelium of A. niger from the surface fermentation method of citric acid production can be magnetically removed from solution after adsorbing magnetite. Dilute solutions of sodium hydroxide and sodium bicarbonate desorbed magnetite attached to mycelial surfaces. Silver is accumulated selectively by A. niger waste mycelium produced by the surface fermentation method of citric acid production. The process is rapid, maximum uptake occurring twenty minutes after initial exposure of the mycelium to a silver solution. Silver accumulation by the mycelium is relatively insensitive to changes in pH and temperature, a slight decrease in uptake only occurring at a temperature of 800C. Dilute solutions of H2S04 and HNO3 desorb silver from the mycelial surface. However, this process is relatively inefficient and more effective desorbents need to be found to make the silver accumulation process economically viable.

Biodegradation of poorly water soluble hydrocarbons, such as n-alkanes and polycyclic aromatic hydrocarbons (PAHs) is often limited by the low availability of the pollutant to microbes. Adhesion of microorganisms to the oil-water interface can influence this availability. Our approach was to study a range of compounds and mechanisms to promote the adhesion of a hydrophilic PAH degrading bacterium, Pseudomonas fluorescens LP6a, to an oil-water interface and examine the effect on biodegradation of phenanthrene by the bacteria. The cationic surfactants cetylpyridinium chloride (CPC), poly-L-lysine and chlorhexidine gluconate (CHX) and the long chain alcohols 1-dodecanol, 2-dodecanol and farnesol increased the adhesion of P. fluorescens LP6a to n-hexadecane from ca. 30% to ca. 90% of suspended cells adhering. The alcohols also caused a dramatic change in the oil-water contact angle of the cell surface, increasing it from 24° to 104°, whereas the cationic compounds had little effect. In contrast, cationic compounds changed the electrophoretic mobility of the bacteria, reducing the mean zeta potential from –23 to –7 mV in 0.01M potassium phosphate buffer, but the alcohols had no effect on zeta potential. This results illustrate that alcohols acted through altering the cell surface hydrophobicity, whereas cationic surfactants changed the surface charge density. Phenanthrene was dissolved in heptamethylnonane and introduced to the aqueous growth medium, hence forming a two phase system. Introducing 1-dodecanol at concentrations of 217, 820 or 4100 mg/L resulted in comparable increases in phenanthrene biodegradation of about 30% after 120 h incubation with non-induced cultures. After 100 h of incubation with LP6a cultures induced with 2-aminobenzoate, 4.5% of the phenanthrene was mineralized by cultures versus more than 10% by the cultures containing initial 1-dodecanol or 2-dodecanol concentrations of 120 or 160 mg/L. The production and accumulation of metabolites in the aqueous phase responded similarly to the addition of 1-dodecanol. Further experiments showed that the positive influence of the alcohols could not be attributed to the changes in surface and interfacial tension or increase in biomass concentration. The results suggest that enhanced adhesion of bacterial cells to the oil-water interface was the main factor responsible for the observed increase in phenanthrene biodegradation by P. fluorescens LP6a. / Chemical Engineering

No description available.

The increase in microbial resistance to antibiotics underscores the need for novel antibacterial surfaces, particularly for silicone-based implants, because the hydrophobicity of silicones has been linked to undesirable microbial adhesion and biofilm formation. Unfortunately, current strategies for mitigation, such as pretreatment of surfaces with antiseptics/antibiotics, are not consistently effective. In fact, they can facilitate the prevalence of resistant pathogens by exposing bacteria to sublethal concentrations of biocides. Therefore, scientific interest has shifted to preventing initial adhesion (prior to surface colonization) by using surfactants as surface modifiers. Accordingly, Chapter 2 studied the bioactivity of ACR-008 UP (an acrylic-terminated superwetting silicone surfactant) after it was copolymerized in increasing weight percentages with butyl methacrylate (BMA) and/or methyl methacrylate (MMA). Interestingly, copolymers of 20 wt % ACR showed at least 3x less adhesion by Escherichia coli BL21 (E. coli) than any other formulation. This was not a consequence of wettability, which followed a parabolic function with ACR concentration: high contact angles (CA) with sessile water drops were observed at both low (< 20 wt %) and high (> 80 wt %) concentrations of ACR in materials. The CA at 20 wt % ACR was 66°. The lack of E. coli adhesion was ascribed to surfactant-membrane interactions; hence, the antibacterial potential of compounds related to ACR was further probed. Chapter 3, therefore, examines the structure-activity relationships of nonionic silicone polyether surfactants in solution. Azide/alkyne click chemistry was used to prepare a series of eight compounds with consistent hydrophilic tails (8- 44 poly(ethylene glycol) units), but variable hydrophobic heads (branched silicones with 3-10 siloxane linkages, and in two cases phenyl substitutions). The compounds were tested for toxicity at 0.001 w/v %, 2.5 w/v % and their critical micelle concentrations (CMCs), against different concentrations of E. coli in a 3-step assay. Surfactants with smaller head groups had as much as 4x the bioactivity of larger analogues, with the smallest hydrophobe exhibiting potency equivalent to SDS. Smaller PEG chains were similarly associated with higher potency. This data suggests that lower micelle stability, and the theoretically enhanced permeability of smaller silicone head groups in membranes, is linked to antibacterial activity. The results further demonstrate that the simple manipulation of nonionic silicone polyether structures, leads to significant changes in antibacterial action. To ensure similar results were achievable when such surfactants are immobilized on surfaces, 8 compounds with shorter, ethoxysilylpropyl-terminated PEG chains, and branched or linear hydrophobes, were incorporated into a homemade, room temperature vulcanization (RTV) silicone (Chapter 4). The materials, containing 0- 20 wt% surfactants) were then tested for contact killing and cytophobicity against the same E. coli strain. Elastomers modified with 0.5- 1 wt% of (EtO)3Si-PEG- laurate, and separately (EtO)3Si-PEG-tBS, were on average 2x more hydrophilic relative to controls (103°) and differed in their wettability by ~40°, yet both were anti-adhesive; a ~30-fold reduction in adhesion was seen on modified surfaces relative to the control PDMS. Additionally, the (EtO)3Si-PEG-tBS surface demonstrated biocidal behavior, which further highlighted the importance of surfactant chemistry- not just wettability- in observing a specific antibacterial response (if any). Based on the data collated from each Chapter, silicone surfactants seem to have great potential as bioactive agents and warrant further systematic investigations into their mechanisms of action. In so doing, their chemistry may be optimized against different microbes for a variety of applications. In particular, their potential to create non-toxic, cytophobic silicones is particularly encouraging, given the need for anti-adhesive, biofilm preventing material surfaces. / Thesis / Doctor of Philosophy (PhD)

Dans les systèmes anaérobies de traitement d'eaux usées, la biomasse microbienne complexe incluant archées et bactéries peut être maintenue au sein du procédé par l'adhésion aux supports solides sous forme de biofilm. Le but de ce travail est d'évaluer l'impact des propriétés des matériaux supports sur l'adhésion et la colonisation du consortium méthanogène. Différents matériaux (le polyéthylène, le polypropylène, le chlorure de polyvinyle, l'acrylonitrile butadiène styrène, le polycarbonate, le verre borosilicaté, l'acier inoxydable 304L et Bioflow 30 ®) sont décrits en termes de topographie par la détermination de rugosité et en termes d'énergie de surface par la mesure d'angle de contact. Le biofilm est évalué quantitativement et les structures communautaires bactériennes et archéennes sont observées grâce à l'analyse moléculaire à différents stades de sa mise en place. L'adhésion d'un consortium méthanogène sur les matériaux après deux heures de contact dans un réacteur annulaire rotatif révèle que les communautés adhérées diffèrent de l'inoculum, y compris en termes de proportion archées/bactéries. Ce résultat a un impact significatif sur le démarrage de digesteurs anaérobie car les tendances observées sont confirmées pendant l'établissement du biofilm actif. La mise en oeuvre de différents matériaux dans des réacteurs à lit fixe a permis de montrer que les populations d'archées des biofilms sont spécifiques au matériau et indépendantes de l'inoculum. / In anaerobic wastewater treatment systems, the complex microbial biomass including Archeae and Bacteria may be retained as a biofilm by attachment to solid supports. The aim of this study is to evaluate the impact of support material properties on adhesion and colonization. Various substrata (polyethylene, polypropylene, polyvinyl chloride, acrylonitrile butadiene styrene, polycarbonate, borosilicate glass, stainless steel 304L and Bioflow 30®) are described in terms of topography by determinating of roughness and in terms of surface energy by contact angle measurement. Adhesion is quantified and the bacterial and archaeal community structure are assessed by molecular analysis in various stages of the biofilm development. Adhesion of a methanogenic consortium on these substrata Is measured after two hours of contact in a rotating annular reactor. The result reveals that the adhered communities were different from the parent inocula, including the Archeae/Bacteria ratio. This result has a significant impact on the start-up of anaerobic digesters because the observed tendencies are confirmed during the establishment of the active biofilm. Start-up of anaerobic fixed-bed reactors using different substrata showed that Archeae populations in the biofilms are specific to each of the material and independent of the inoculum.

Glykane aus exokrinen Drüsen stellen ein Schutzsystem der Schleimhautoberflächen dar, indem sie an mikrobielle Adhäsine binden und dadurch Einfluß auf die mikrobielle Besiedelung und Invasion des Wirtes nehmen. 11 Patienten mit rasch fortschreitender Parodontitis (RPP) wurde über jeweils 20 Minuten in Ruhe und unter adrenerger Belastung Speichel aus den großen Speicheldrüsen entnommen und in einem kompetitiven Lektinbindungsinhibitionstest auf die Bindungsfähigkeit an 8 verschiedene Planzenlektine untersucht. Patienten mit RPP zeigen ein anderes Verteilungsmuster der antiadhäsiven Glycane als die Kontrollgruppe. Sie zernieren u.a. aus den Unterkieferdrüsen konstant signifikant mehr Glykane mit endständigen Mannosegruppen, aus der Parotis dagegen nur unter adrenerger Stimulation. Dies zeigt die unterschiedliche Funktion der Drüsen bei der Beeinflussung des Milieus in der Mundhöhle als auch einen unterschiedlichen Erregungszustand des Schleimhautschutzsystems bei Erkrankten und Kontrollen. Aus den Ergebnissen können sich diagnostische Aspekte für das Risiko und den Aktivitätszustand einer parodontalen Erkrankung ergeben. / Glycans from exocrine glands create a defense system of the mucosal surfaces by binding to microbial adhesins and interfering with colonisation and invasion of the host. Saliva from 11 patients with rapidly progressive periodontitis (RPP) was collected over a period of 20 minutes each in rest and during adrenergic stimulation. The samples were tested for binding properties to 8 different plant lectins by a competitive lectin binding inhibition test. A pattern of antiadhesive glycans different from the control group is secreted in patients with RPP. The latter constantly secrete significantly more glycans with terminal mannose from the mandibular glands. In the parotis this is only the case during adrenergic stimulation. This demonstrates the different purpose of the glands in maintaining the oral milieu as well as different states of activity of the mucosal defense system in RPP patients and controls. Diagnostic aspects for risk and activity of periodontal diseases can be drawn from these findings.

No description available.