Registry
Module Specifications
Current Academic Year 2012 - 2013
Please note that this information is subject to change.
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| Description | |||||||||||||||||||||||||||||||||||||||||||||||||
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The purpose of this module is to provide students with the skills and understanding necessary for handling and quantitation of micro-organisms in a laboratory environment. To this end, you will work through Standard Operating Procedures commonly used in food and water microbiology and use procedures for surfaces to quantify microbial contamination. This is a continuously assessed laboratory module and attendance is compulsory and will be monitered. | |||||||||||||||||||||||||||||||||||||||||||||||||
| Learning Outcomes | |||||||||||||||||||||||||||||||||||||||||||||||||
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1. Analyse food and water samples for microbes and use these findings to determine the quality of food and water samples. 2. Culture microbes in batch and continuous culture, graphically analyse the results and use these to calculate microbial growth parameters. 3. Carry out a sequential 'multistep' protein purification scheme including ion-exchange and gel filtration chromatography and calculate yield and purification. 4. Carry out HPLC analysis to determine the concentration of an analyte and its purity. 5. Write up reports, to be viewed by an experimental scientist and by the general public, detailing their experimental findings and the conclusions that may be drawn from them. | |||||||||||||||||||||||||||||||||||||||||||||||||
All module information is indicative and subject to change. For further information,students are advised to refer to the University's Marks and Standards and Programme Specific Regulations at: http://www.dcu.ie/registry/examinations/index.shtml |
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| Indicative Content and Learning Activities | |||||||||||||||||||||||||||||||||||||||||||||||||
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Assay for lyzozyme activity and protein. Preparation of crude lyzozyme from egg-white. Salt precipitation of lyzozyme by gel-filtration chromatography on sephadex G-100. Purification of 'partially-purified' lyzozyme by cation-exchange chromatography. Concentration of lyzozyme by reverse dialysis using solid polyethylene glycol. Analysis of lyzozyme fractions by native and SDS Polyacrylamide electrophoresis. Analysis of lyzozyme fractions and standards by Isoelectric focusing. Computer learning system for teaching the use of HPLC and its applications. Techniques to prepare and analyse samples for the HPLC analysis of drugs. Determination of molar growth yield in batch and continuous microbial fermentation. Food microbiology - analysis of samples by pour plates and spread plates. Water microbiology - analysis of samples by MPN and membrane filtration. | |||||||||||||||||||||||||||||||||||||||||||||||||
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| Indicative Reading List | |||||||||||||||||||||||||||||||||||||||||||||||||
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| Other Resources | |||||||||||||||||||||||||||||||||||||||||||||||||
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| Programme or List of Programmes | |||||||||||||||||||||||||||||||||||||||||||||||||
| AS | BSc in Analytical Science | ||||||||||||||||||||||||||||||||||||||||||||||||
| Timetable this semester: Timetable for BE353 | |||||||||||||||||||||||||||||||||||||||||||||||||
| Date of Last Revision | 01-OCT-08 | ||||||||||||||||||||||||||||||||||||||||||||||||
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