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Enhanced high-fructose syrup production by an hybrid fermentation/pervaporation system using a silicone rubber hollow fiber membrane module.Gagné, Isabelle. January 2001 (has links)
In this study, a mutant of the yeast Saccharomyces cerevisiae was used for the selective conversion of glucose to ethanol using feed solutions of sucrose. Batch fermentation using 30% (w/v) sucrose without membrane separation of ethanol required about 27 hours for glucose to be decreased to 2% (w/v), with a fructose yield of 99%, and an ethanol yield of 78%. Batch fermentation using 30% (w/v) sucrose with membrane separation of ethanol required about 16.5 hours for glucose to be decreased to 2% (w/v), with a fructose yield of 96.5% and an ethanol yield of 79.5%, if the membrane was started after 6 hours of batch mode. The process required about 15 hours if the membrane was started after 3 hours of batch mode, with a fructose yield of 92%, and an ethanol yield of 82%. In fed-batch mode the yeast was able to process the equivalent of a 40% (w/v) sucrose feed in 24 hours, compared to well over 40 hours without ethanol removal, with yields of, 98% fructose, and 82% ethanol. (Abstract shortened by UMI.)
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A novel method for the decrease of phenolic content in commercial canola meal using an enzyme preparation secreted by the white-rot fungus Trametes versicolor.Lacki, Karol M. January 1997 (has links)
This research project was focused on the development of a novel enzymatic method for upgrading commercial canola meal by decreasing its phenolic content. The new method is based on the enzymatic transformations of sinapic acid esters (SAE) and free sinapic acid (SA), the two main constituents of the phenolic fraction of canola meal (CM), using an enzyme preparation secreted by the white-rot fungi Trametes versicolor ATCC 42530. The study was divided into three parts: (1) enzyme production; (2) characterization of the enzyme produced--a model enzymatic system; (3) enzymatic upgrading of commercial canola meal--a canola meal system. The enzyme preparation produced was characterized in the model enzymatic system using sinapic acid (SA), sinapine (SIN) and sinapaldehyde (SALD). The results showed that the enzyme is inhibited by high concentrations of SIN and SA. Depending on the substrate, the optima temperatures and pH are in the range of 50$\sp\circ$C-60$\sp\circ$C and 3.3-4.5, respectively. The enzyme was very thermostable; the maximum thermal stability was noticed at pH values between 4.5 and 6.5. Sodium azide was a strong inhibitor of this enzyme while its activity was not affected by EDTA. Based upon the results obtained, the enzyme was characterized as a polyphenol oxidase. The overall transformation of SA was described by a mathematical model based on the Theorell-Chance Bi-Bi mechanism with oxygen as the first substrate, and the second substrate being one of the alternate phenolic compounds: SA, DAD and the unknown compound formed via the thermolysis of DAD. The modeling of sinapine transformation was also considered in this work. A mechanistic model, based on the Theorell-Chance Bi-Bi mechanism, that simultaneously predicted the effects of the concentrations of the enzyme, SIN and oxygen, for any given pH and temperature level, on the rates of the enzymatic reaction was formulated. The model parameters were estimated following the new procedure developed in this work for analyzing data concerning the effects of pH and temperature on enzyme activity. The formula relating the optimum pH of the reaction with the temperature was proposed. The enzyme preparation produced and subsequently characterized was used in the novel method to decrease the phenolic content in commercial CM, which was based on the addition of the enzyme to the meal-buffer slurry. It was found that: (1) the natural buffering capacity of CM resulted in the negligible effect of the pH of the buffer, which was used as the continuous phase in the process, on the extent of SAE decrease; (2) the system was saturated with the enzyme when the enzyme concentration was 4 nkat per mL of the continuous phase; (3) the optimum temperature was 50$\sp\circ$C. (Abstract shortened by UMI.)
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Microwave pasteurization of shell eggs-a comprehensive studyRajalakshmi Sivaramakrishnan, SatyanarayanDev January 2010 (has links)
No description available.
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Enhancement of antioxidant content of Elderberry («sambucus nigra») fruit by pulsed ultraviolet light followed by spray drying of Elderberry juiceMurugesan, Ramesh January 2010 (has links)
No description available.
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Biocatalysis of lipoxygenase in a model system using selected organic solvent mediaAlturaihi, Haydar January 2011 (has links)
No description available.
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Bioactive properties of salmon skin protein hydrolysatesAmissah, Justina January 2012 (has links)
No description available.
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Heating behavior and quality changes in canned potatoes subjected to agitation processingRattan, Navneet January 2012 (has links)
No description available.
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Thermal processing effects on total phenolic content, antioxidant activity, trypsin inhibitor activity and in-vitro protein digestibility of lentilsSampathkumar, Yamuna January 2012 (has links)
No description available.
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Practical methods for lignans quantificationNemes, Simona January 2012 (has links)
No description available.
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Biomass production, purification and characterization of selected microbial LaccasesTaqi, Marwa January 2012 (has links)
No description available.
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