Wind-hydrogen systems for remote area power supply are an early niche application of sustainable hydrogen energy. Optimal direct coupling between a wind turbine and an electrolyser stack is essential for maximum electrical energy transfer and hydrogen production. In addition, system costs need to be minimised if wind-hydrogen systems are to become competitive. This paper investigates achieving near maximum power transfer between a fixed pitched variable-speed wind turbine and a Proton Exchange Membrane (PEM) electrolyser without the need for intervening voltage converters and maximum power point tracking electronics. The approach investigated involves direct coupling of the wind turbine with suitably configured generator coils to an optimal series-parallel configuration of PEM electrolyser cells so that the I-V characteristics of both the wind turbine and electrolyser stack are closely matched for maximum power transfer. A procedure for finding these optimal con figurations and hence maximising hydrogen production from the system is described. For the case of an Air 403 400 W wind turbine located at a typical coastal site in south-eastern Australia and directly coupled to an optimally configured 400 W stack of PEM electrolysers, it is estimated that up to 95% of the maximum achievable energy can be transferred to the electrolyser over an annual period. The results of an extended experiment to test this theoretical prediction for an actual Air 403 wind turbine are reported. The implications of optimal coupling between a PEM electrolyser and an aerogenerator for the performance and overall economics of wind-energy hydrogen systems for RAPS applications are discussed.

Renewable energy-hydrogen systems for remote area power supply (RAPS) constitute an early niche market for sustainable hydrogen energy. The primary objective of this research has been to investigate the possibility of direct coupling of a PV array to a proton exchange membrane (PEM) electrolyser by appropriate matching of the current-voltage characteristics of both the components. The degree to which optimal matching can be achieved by direct coupling has been studied both theoretically and experimentally. A procedure for matching the maximum power point output of a PV array with the PEM electrolyser load to maximise the energy transfer between them has been presented. The key element of the matching strategy proposed is to vary the series-parallel stacking of individual cells in both the PV array and the PEM electrolyser so that the characteristic current (I) -voltage (V) curves of both the components align as closely as possible. This procedure is applied to a case study of direct coupling a PV array comprising 75 W panels (BP275) to a PEM electrolyser bank assembled from 50 W PEM electrolyser stacks (h-tec StaXX7). It was estimated theoretically that the optimal PV-electrolyser combination would yield an energy transfer of over 94% of the theoretical maximum on annual basis. This combination also gave the lowest hydrogen production cost on a lifecycle basis. An experimental test of this theoretical result for direct coupling was conducted over a period of 728 hours, with an effective direct-coupling operational time of about 467 hours (omitting the hours of zero solar radiation). Close agreement between the theoretically predicted and actual energy transfer from the PV array to the electrolyser bank in this trial was found. The difference between theoretical and experimental hydrogen production was less then 1.2%. The overall solar-to-hydrogen energy conversion efficiency was found to be 7.8%. The electrolysers were characterised before and after the direct coupling experiment, and showed a small decline in Faraday efficiency and energy efficiency. But this decline was less than the uncertainties in the measured values, so that no firm conclusions about electrolyser degradation can be drawn at this stage. Another direct-coupling experiment, using a larger scale PV-electrolyser system, that is, a 2.4 kW PV array at RMIT connected to the 'Oreion Alpha 1' stand-alone 2 kW PEM electrolyser developed by the CSIRO Energy Technology, was also successfully conducted for a period of 1519 hours (with 941 hours of effective operational time of the electrolyser). Energy-efficient direct coupling of a PV array and electrolyser as examined in this thesis promises to improve the economic viability of solar-hydrogen systems for remote power supply since the costs of an electronic coupling system employing a maximum power point tracker (MPPT) and dc-to-dc converter (around US$ 700/ kW) are avoided.

Phosphate is an essential nutrient for all forms of life. Escherichia coli has a PhoR/PhoB two component regulatory system that controls the expression of various genes whose products allow the cell to thrive in low phosphate environments. The signaling mechanism of the PhoR/PhoB system has been studied and the phosphorylation cascade that controls gene expression is well understood. What is still unknown is how PhoR senses the phosphate level of the environment. The PstS, PstC, PstA, PstB, and PhoU proteins play a role in this signal sensing. This work confirms the hypothesis that the PstSCAB complex senses the environmental phosphate and that phosphate signal is passed through PhoU to PhoR. Further, this work characterizes residues important for interaction on PhoU and PhoR and identifies a structural model for interaction. This model points to a potential mechanism for PhoU mediated signaling to PhoR. We tested this model with direct coupling analysis and obtained further confirmation. Further use of these techniques may elucidate more of the interactions necessary for proper phosphate signaling.

Hydrogen energy sector has gained significant attention worldwide but one of the key enabling components for its success would be cheaper and sustainable hydrogen production. Hydrogen could be produced directly from natural gas or coal etc; alternatively it could be produced by electrolysis of water powered by renewable energy sources, nuclear energy or fossil fuel. Wind energy is growing rapidly, which can produce cheap hydrogen. Electrolysers can be employed to control the frequency of the electricity grid while also making fuel as a by-product. This thesis concerns the intricacies of hydrogen production by electrolysers from renewable energy sources. A generalised, input-based mathematical model of the electrolyser has been developed for various subsystems, such as current-voltage, Faraday efficiency, gas production, gas purity, differential pressure, temperature subsystem, parasitic losses, gas losses and efficiencies at various stages of operation. Some empirical equations have been developed and some adjusted parameters have been used in the model. The model has been tested and verified against the experimental measurements. A generic method has been developed for modelling the Faraday efficiency. Model simulations have been carried out to investigate the sensitivity of the results to the value of the capacitance and how this affects the dynamic response of the electrolyser. A new sizing method of the electrolyser has been developed for a stand-alone energy system such as the HARI project. The electrolyser model has also been simulated for maximum and efficient hydrogen production in a directly coupled mode of electrolysers with solar PV arrays without the maximum power point (MPP) tracker, which leads to an interesting finding that "electrolysers should not be operated at MPP". It has also been found that the dynamic and intermittent power supply from renewables can damage the stability of electrolysers and reduce the energy capture. This is especially true for pressurised electrolysers, which are favoured by the industry at present. The in-depth theoretical and practical analysis of several aspects confirms - contrary to industry trends - that "Pressurised electrolysers are less energy efficient, less durable, more costly and not adequately compatible for renewable energy powered operation, especially in the stand-alone energy systems, compared to atmospheric electrolysers".

Nutrient sensing kinases lie at the heart of cellular health and homeostasis, allowing cells to quickly adapt to changing environments. Target of Rapamycin (TOR) and PAS kinase (PASK, or PASKIN) are two such nutrient kinases, conserved from yeast to man. In yeast, these kinases each have paralogs. The two TOR paralogs in yeast mimic the mammalian TORC1 and TORC2 complexes, except both Tor1 and Tor2 may contribute to TORC1 or TORC2 function. The two PAS kinase paralogs are paired with the TOR paralogs, meaning that both Psk1 and Psk2 regulate TORC1, while Psk2 suppresses a temperature-sensitive allele of Tor2. Herein we review the evolutionary models for these paralogs, their function in yeast and mammalian cells, as well as the overlapping function of PAS kinase and TOR. We also use Rice University’s Direct Coupling Analysis algorithms to analyze co-evolutionary relationships and identify potential interaction sites between PAS kinase and several of its substrates.

Does the active membrane transporter, Na+,K+-ATPase dimerize? If it does, whatis the functional benefit? Does it increase or decrease the turnover rate? Theseare still unanswered questions and current research topics. Previous studies havedemonstrated dimerizations in closely related proteins of the P-type ATPase family.For the Na+, K+-ATPase a first indication of dimerization has been shown viaFluorescence lifetime imaging microscopy (FLIM) or Fluorescence resonance energytransfer - Fluorescence correlation spectroscopy (FRET-FCS) experiments. Theprecise dimer structure, dimerization process, and its ultimate functional effecthowever, remain to be found. This master thesis approaches those questions froma co-evolutionary standpoint. It predicts a possible dimer structure by starting with amultiple sequence alignment, direct coupling analysis, and structural contact filteringalgorithm. This model would strengthen the dimerization model of a decreasedturnover rate due to a competitive behavior of two Na+, K+-ATPases for its energysource ATP. / Dimeriserar den aktiva membrantransporten Na+,K+-ATPas? Om den gör det,vad är den funktionella nyttan? Ökar eller minskar det omsättningshastigheten?Dessa är obesvarade frågor och rådande forskningsämnen. Tidigare studier hardemonstrerat dimeriseringar i nära relaterade proteiner av P-typ ATPas-familjen.För Na+, K+-ATPas har en första indikation av dimerisering visats via ”Flourescencelifetime imaging microscopy (FLIM)” eller ”Flourescence resonance energy transfer- Flourescence correlation spectroscopy (FRET-FCS)”. Den precisa dimerstrukturen,dimeriseringsprocessen och dess slutgiltiga funktionella effekt emellertid, återståratt ses. Detta examensarbete på masternivå närmar sig dessa frågor från ettsamevolutionärt perspektiv. Det förutser en möjlig dimerstruktur genom att utgåfrån en flersekvenslinjering, direkt kopplingsanalys och en strukturell kontaktfiltreringsalgoritm. Denna modell skulle stärka dimeriseringsmodellen av minskadomsättningshastighet till följd av tävlingsbeteende mellan två Na+,K+-ATPaser fördess energikälla ATP.