Matching Items (3)
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Description
Microbial Potentiometric Sensors (MPS) utilize endemic biofilms to generate a signal using a measurable potentiometric difference, without the use of cleaning, maintenance, and reagents of conventional sensor monitoring methods. These advantages are suitable for monitoring bioreactions in water distribution systems, soils, and wastewater treatment. In controlled fermentation processes, monitoring seeks

Microbial Potentiometric Sensors (MPS) utilize endemic biofilms to generate a signal using a measurable potentiometric difference, without the use of cleaning, maintenance, and reagents of conventional sensor monitoring methods. These advantages are suitable for monitoring bioreactions in water distribution systems, soils, and wastewater treatment. In controlled fermentation processes, monitoring seeks to avoid contamination and degradation, which results in loss of productivity. MPS have yet to be applied to monitor the fermentation of milk to yogurt. This study examined the feasibility of using MPS technology to monitor the progress of milk fermentation in real-time with a bench-scale model bioreactor. Signal data obtained by the MPS was analyzed and assessed for the ability to model and predict the time of complete fermentation. Analysis of complete fermentation times in conjunction with pH and MPS signal values found characteristics indicative of complete fermentation. The method detection limit was assessed to inform of the method’s capacity to distinguish complete fermentation time. A sensitivity analysis was conducted to develop a more robust method for predicting complete fermentation time. At this proof-of-concept scale, MPS successfully performed in this capacity to monitor bioreaction conditions continuously. MPS captured information as fermentation progressed, was completed, and as the yogurt product naturally began to decay. Analysis of the data obtained with the technology found predictions of complete fermentation time within a two hour range, with further assessment in the sensitivity analysis narrowing this timeframe to less than 45 minutes. This study revealed the challenges in precisely predicting complete fermentation;however, advancement of a robust analytical method and demonstration of technical feasibility promotes further MPS technology applications that seek to monitor conditions in real-time to preserve health and production.
ContributorsDieter, Lucien Andres (Author) / Hristovski, Kirl D. (Thesis advisor) / Olson, Larry W. (Committee member) / Ünver, Olcay (Committee member) / Arizona State University (Publisher)
Created2021
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Description
This work focuses on a novel approach to combine electrical current with cyanobacterial technology, called microbial electrophotosynthesis (MEPS). It involves using genetically modified PSII-less Synechocystis PCC 6803 cells to avoid photoinhibition, a problem that hinders green energy. In the work, a cathodic electron delivery system is employed for growth and

This work focuses on a novel approach to combine electrical current with cyanobacterial technology, called microbial electrophotosynthesis (MEPS). It involves using genetically modified PSII-less Synechocystis PCC 6803 cells to avoid photoinhibition, a problem that hinders green energy. In the work, a cathodic electron delivery system is employed for growth and synthesis. Photoinhibition leads to the dissipation energy and lower yield, and is a major obstacle to preventing green energy from competing with fossil fuels. However, the urgent need for alternative energy sources is driven by soaring energy consumption and rising atmospheric carbon dioxide levels. When developed, MEPS can contribute to a carbon capture technology while helping with energy demands. It is thought that if PSII electron flux can be replaced with an alternative source photosynthesis could be enhanced for more effective production. MEPS has the potential to address these challenges by serving as a carbon capture technology while meeting energy demands. The idea is to replace PSII electron flux with an alternative source, which can be enhanced for higher yields in light intensities not tolerated with PSII. This research specifically focuses on creating the initiation of electron flux between the cathode and the MEPS cells while controlling and measuring the system in real time. The successful proof-of-concept work shows that MEPS can indeed generate high-light-dependent current at intensities up to 2050 µmol photons m^‒2 s^‒1, delivering 113 µmol electrons h^‒1 mg-chl^‒1. The results were further developed to characterize redox tuning for electron delivery of flux to the photosynthetic electron transport chain and redox-based kinetic analysis to model the limitations of the MEPS system.
ContributorsLewis, Christine Michelle (Author) / Torres, César I (Thesis advisor) / Fromme, Petra (Thesis advisor) / Woodbury, Neal (Committee member) / Hayes, Mark (Committee member) / Arizona State University (Publisher)
Created2023
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Description
The study was to analyze the extent of bacterial transport in a two-dimensional tank under saturated conditions. The experiments were done in a 2-D tank packed with 3,700 in3 of fine grained, homogenous, chemically inert sand under saturated conditions. The tank used for transport was decontaminated by backwashing with 0.6%

The study was to analyze the extent of bacterial transport in a two-dimensional tank under saturated conditions. The experiments were done in a 2-D tank packed with 3,700 in3 of fine grained, homogenous, chemically inert sand under saturated conditions. The tank used for transport was decontaminated by backwashing with 0.6% chlorine solution with subsequent backwashing with chlorine-neutral water (tap water and Na2S2O3) thus ensuring no residual chlorine in the tank. The transport of bacteria was measured using samples collected from ports at vertical distances of 5, 15 and 25 inches (12.7, 38.1 and 63.5 cm) from the surface of the sand on both sides for the 2-D tank. An influent concentration of 105 CFU/mL was set as a baseline for both microbes and the percolation rate was set at 11.37 inches/day using a peristaltic pump at the bottom outlet. At depths of 5, 15 and 25 inches, E. coli breakthroughs were recorded at 5, 17 and 28 hours for the ports on the right side and 7, 17 and 29 hours for the ports on the left sides, respectively. At respective distances Legionella breakthroughs were recorded at 8, 22 and 35 hours for the ports on the right side and 9, 24, 36 hours for the ports on the left side, respectively which is homologous to its pleomorphic nature. A tracer test was done and the visual breakthroughs were recorded at the same depths as the microbes. The breakthroughs for the dye at depths of 5, 15 and 25 inches, were recorded at 13.5, 41 and 67 hours for the ports on the right side and 15, 42.5 and 69 hours for the ports on the left side, respectively. However, these are based on visual estimates and the physical breakthrough could have happened at the respective heights before the reported times. This study provided a good basis for the premise that transport of bacterial cells and chemicals exists under recharge practices.
ContributorsMondal, Indrayudh (Author) / Abbaszadegan, Morteza (Thesis advisor) / Dahlen, Paul (Committee member) / Delgado, Anca (Committee member) / Arizona State University (Publisher)
Created2019