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 aim of this module is to provide a detailed understanding of the behaviour of proteins in solution and how their properties may be altered by changing the physical surroundings. To provide an understanding of the theory and practical techniques involved in developing a purification process. | |||||||||||||||||||||||||||||||||||||||||||||
| Learning Outcomes | |||||||||||||||||||||||||||||||||||||||||||||
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1. Discuss the principles of protein chemistry in solution. 2. Design a DSP process which is readily integrated with the USP 3. Decide how to choose the correct separation and chromatographic techniques. 4. Demonstrate an understanding of the theory and practice of chromatography and how this can help in designing the DSP. 5. Comment on the different types of chromatographic equipment and how they operate | |||||||||||||||||||||||||||||||||||||||||||||
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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Bioseparations. This module is built on the fundamental concepts of protein structure and function, physical chemistry of solutions and electrolytes/ acids/bases and pH to understand how proteins behave in solution and how their properties may be altered by changing the physical surroundings.Using examples, descriptions will be given as to how to isolate proteins from inclusion bodies or culture medium using a range of chemical and physical separation processes.The principles of developing a purification process, including theory, will be defined using a wide range of chromatographic techniques including, but not exclusive to; gel filtration, ion-exchange, hydrophobic interaction, reverse phase, metal chelate, immunoaffinity and other affinity- based techniques, microfiltration and others.The different types of equipment, fluidized versus packed-beds and how these may be scaled-up will be discussed.. | |||||||||||||||||||||||||||||||||||||||||||||
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| Indicative Reading List | |||||||||||||||||||||||||||||||||||||||||||||
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| Other Resources | |||||||||||||||||||||||||||||||||||||||||||||
| None | |||||||||||||||||||||||||||||||||||||||||||||
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| Programme or List of Programmes | |||||||||||||||||||||||||||||||||||||||||||||
| GDBE | Graduate Dip in Bioprocess Engineering | ||||||||||||||||||||||||||||||||||||||||||||
| MSBE | Master of Science in Bioprocess Engineer | ||||||||||||||||||||||||||||||||||||||||||||
| SAMPB | STAND ALONE MODULE (BIOTECHNOLOGY) | ||||||||||||||||||||||||||||||||||||||||||||
| SMPSC | Single Module Professional Science | ||||||||||||||||||||||||||||||||||||||||||||
| Timetable this semester: Timetable for BE516 | |||||||||||||||||||||||||||||||||||||||||||||
| Date of Last Revision | 10-MAR-11 | ||||||||||||||||||||||||||||||||||||||||||||
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