Thesis (Ph. D.)--University of Texas at Austin, 2001. / Vita. Includes bibliographical references (leaves 337-351). Available also in a digital version from Dissertation Abstracts.

This study was conducted to investigate the biofilm formation by using advanced microscopic and high-throughput sequencing techniques. The major tasks were (1) to quantitatively evaluate the initial bacterial attachment processes by Atomic Force Microscopy (AFM); (2) to characterize the chemical variation during biofilm formation by Raman microscopy; (3) to analyze the microbial structure and functions in the wastewater and drinking water biofilms by metagenomic analysis. To determine the lateral detachment force for bacteria, a quantitative method using contact mode of AFM was developed. The established method had good repeatability and sensitivity to various bacteria and substrata, and was applied to evaluate the roles of bacterial surface polymers in Phase I and II attachment, i.e. lipopolysaccharides, type 1 fimbria and capsular colanic acid. The results indicated lipopolysaccharides largely enhanced Phases I and II attachment. Fimbriae increased Phase I attachment but not significantly influence the adhesion strength in Phase II. Moreover, colanic acid had negative effect on attachment in both of Phases I and II. Surface-enhanced Raman scattering was applied to evaluate the chemical components in the biofilm matrix at different growth phases, including initial attached bacteria, colonies and mature biofilm. Three model bacteria, including Escherichia coli, Pseudomonas putida, and Bacillus subtilis, were used to cultivate biofilms. The results showed that the content of carbohydrates, proteins, and nucleic acids in biofilm matrix increased significantly along with the biofilm growth of three bacteria judging from the intensities and appearance probabilities of related marker peaks in the spectra. The content of lipids, however, only increased in the Gram-negative biofilms. Moreover, metagenomic data, coupled with PCR-based 454 pyrosequencing reads, were generated for activated sludge and biofilm from a full-scale hybrid reactor to study the microbial taxonomic and functional differences/connections between activated sludge and biofilm. The results showed that the dominant bacteria co-existed in two samples. Global functions in activated sludge and biofilm metagenomes showed quite similar pattern, revealing the limited differences of overall functions existed in two samples. For nitrogen removal, the diversity and abundance of nitrifiers and denitrifiers in biofilm did not surpass that in activated sludge. Whilst, higher abundances of nitrification and denitrification genes were indeed found in biofilm, suggesting the increased nitrogen removal by applying biofilm might be attributed to removal efficiency rather than biomass accumulation of nitrogen removal bacteria. To investigate the bacterial structure and functions of drinking water biofilm, PCR-based 454 pyrosequencing of 16S rRNA gene and Illumina metagenomic data were generated and analyzed. Significant differences of bacterial diversity and taxonomic structure were found between biofilms formed on stainless steel and plastics. Moreover, ecological succession could be obviously observed during biofilm formation. The metabolic network analysis for drinking water biofilm constructed for the first time. Moreover, the occurrence and abundance of specific genes involving in the bacterial pathway of glutathione metabolism and production/degradation of extracellular polymeric substances were also evaluated. / published_or_final_version / Civil Engineering / Doctoral / Doctor of Philosophy

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Atomic force microscopy was used to image the action of cellulolytic enzymes in situ on never-dried native cellulose films. Cellomonas fimi, CenA was used as a model enzyme for proof of concept experiments and for the identification of different enzyme action on different cellulose structures. Inactive and active Trichoderma reesei enzymes EGI and CBHI were studied to disentangle the action of the cellulose binding domain from the catalytic domain. A novel procedure, volume analysis, was developed to quantify changes in cellulose fibers as a result of this action. Volume analysis was used to compare fibers in different experiments (with different structural features and enzymes) regardless of where the change in the fiber occurred. The site-specific nature of cellulose-enzyme interactions is accessible using this analysis technique. Additionally, the reported volume change reflects a change in mass that is of interest for industrial purposes. From inactive CBHI action there was no distinguishable change between enzyme action on defect or crystalline regions of the cellulose fiber. From the active enzyme results a quantifiable degradation event was measured. Digestion was initially quick then after one hour the volume plateaued. The crystalline cellulose region plateaued at -20 ± 1% and the defect region at -31 ± 2%. The inactive EGI enzyme was found to have significant non-hydrolytic action on insoluble cellulose fibers. There was more significant swelling effect on the defect than the crystalline regions of the cellulose fiber. From the active EGI results a quantifiable degradation event was measured followed by swelling events. Degradation was initially quick with the total mass loss occurring within the first hour of the experiment. The volume then increased as the enzyme induced swelling of the fiber structure. The extent of degradation and swelling is structure limited with more disordered regions showing larger decreases in volume and predominantly crystalline regions showing mainly swelling events.

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Non-equilibrium plasma modification of polymer surfaces in an oxygen atmosphere provides a highly efficient, solventless method of raising the surface energy. The chemical and physical effects of non-equilibrium plasma treatment on polymer surfaces have been investigated. Oxygen glow discharge and silent discharge treatment of several polymers (polypropylene, polystyrene, polyphenylene oxide and polycarbonate) has been shown to cause both surface oxidation and chain scission at the polymer surface. This generates low molecular weight oxidised material on the polymer surface which conglomerates into globular features due to the difference in surface energy between the oxidised material and the untreated polymer. These features can be removed by solvent washing. Generally silent discharge treatment generates more low molecular weight oxidised material whereas oxygen glow discharge treatment generates more non-soluble oxidised material. Crystalline polymers react at a slower rate than amorphous material. During the treatment of a model crystalline polymer (hexatriacontane) the plasma attacks the edges of the crystal, rather than the surface, due to the greater chain mobility at the edge. Non-equilibrium plasma treatment of both miscible and immiscible polymer blends were investigated. The size and distribution of the globular features formed were found to be dependent on the blend composition. For the immicible polymer blend, non-equilibrium plasma treatment reveals the blend morphology mi sing from the difference in reaction rates of the parent polymers.

It is becoming clear that mechanical stimuli are critical in regulating cell biology; however, the short-term structural response of a cell to mechanical forces remains relatively poorly understood. We mechanically stimulated cells expressing actin-EGFP with controlled forces (0-20nN) in order to investigate the cell’s structural response. Two clear force dependent responses were observed: a short-term local deformation of actin stress fibres and a long-term force-induced remodelling of stress fibres at cell edges, far from the point of contact. We were also able to quantify strain dynamics occurring along stress fibres. The cell exhibits complex heterogeneous negative and positive strain fluctuations along stress fibres, indicating localized dynamic contraction and expansion. A ~50% increase in myosin contractile activity is apparent following application of 20nN force. Directly visualizing force-propagation and stress fibre strain dynamics has revealed new information about the pathways involved in mechanotransduction which ultimately govern the downstream response of a cell.

Alzheimer's Disease (AD) is a neurodegenerative disorder that is prevalent among the elderly population. Aß protein has been heavily implicated in the pathogenesis of AD. This protein in its fibrillar form is a major component in the senile plaques that form on neuronal cellular membranes during the course of AD. Despite substantial efforts the exact mechanism of Aß toxicity towards a cell membrane is not well-understood. The determination of this mechanism, however, is of utmost importance, since the membrane presents the first site of Aß interaction with neurons, which in turn maybe the origin of Aß neurotoxicity. The purpose of this study was to find a lipid composition that can be used as a model of neuronal membrane for subsequent studies of the role of topographical heterogeneity (domain formation) on Aß-membrane interaction as related to AD. The lipids used in the study were 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine (POPC), 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphoglycerol (POPG), cholesterol (Chol), sphingomyelin (SM) and ganglioside GM1 (GM1). These lipids were combined in different proportions and deposited on a mica substrate to form supported monolayers. They were then imaged with an atomic force microscope (AFM) to determine if any of them exhibited domain formation. Three of the studied samples: POPC/POPG/SM 40:40:20 +5%Chol, POPC/SM/Chol 75:20:5 and POPC/SM/GM1/Chol 74:2:1:23 were found to possess interesting topography, rich in structural features: pores and domains. The average height difference between the domain features for each sample was found to be 0.58±015 nm, 0.61±0.12 nm and 0.27±0:07 nm.

Thesis (PhDBiomedicalScience)--University of South Australia, 2001.