Team:UCL/Science/Bioprocessing

From 2014.igem.org

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<b>Case study sheet 2: Tailoring a bioprocess for a cotton dyeing plant</b>
<b>Case study sheet 2: Tailoring a bioprocess for a cotton dyeing plant</b>
<img src="https://static.igem.org/mediawiki/2014/5/53/Screen_Shot_2014-10-13_at_12.12.53_PM.png" style="float:right;margin:0 0 0 10px;" width="50%">
<img src="https://static.igem.org/mediawiki/2014/5/53/Screen_Shot_2014-10-13_at_12.12.53_PM.png" style="float:right;margin:0 0 0 10px;" width="50%">
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<b>Assuming batch (discontinuous) dyeing process:</b>
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<br><b>Assuming batch (discontinuous) dyeing process:</b>
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<br>1. Liquor ratio- <i>parameter in discontinuous dyeing</i>- weight ratio between total dry material and total liquor  -  <b>1 kg cotton : 100 L H2O</b>
<br>1. Liquor ratio- <i>parameter in discontinuous dyeing</i>- weight ratio between total dry material and total liquor  -  <b>1 kg cotton : 100 L H2O</b>
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<b>Assumptions:</b>  
<b>Assumptions:</b>  
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<br>a. Dyeing efficiency or fixation rate refers to the ability for a dye to be fixed onto a target material <i>i.e. a  dyeing efficiency of 80% therefore suggests 20% by mass of the dye is present in the effluent stream. </i>
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a. Dyeing efficiency or fixation rate refers to the ability for a dye to be fixed onto a target material <i>i.e. a  dyeing efficiency of 80% therefore suggests 20% by mass of the dye is present in the effluent stream. </i>
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<br>b. No losses or additional uses of  water <i>(Density 1000kg.m-3)</i>
<br>b. No losses or additional uses of  water <i>(Density 1000kg.m-3)</i>
<br>c. Chemical additives such as sodium chloride are not included in this analysis
<br>c. Chemical additives such as sodium chloride are not included in this analysis
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Our meeting with ETAD provided us with a more holistic understanding of typical effluent concentrations found in textile processing. We used this information to decide on process variables by considering volumes and flow rates.
Our meeting with ETAD provided us with a more holistic understanding of typical effluent concentrations found in textile processing. We used this information to decide on process variables by considering volumes and flow rates.
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The E. coli cell is treated as a biocatalyst exhibiting a kinetic behaviour modelled by Michaelis-menten:
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The E. coli cell is treated as a biocatalyst exhibiting a kinetic behaviour modelled by Michaelis-Menten:
<b><i> v = Vmax[S]/(Km + [S])</i></b>
<b><i> v = Vmax[S]/(Km + [S])</i></b>
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Revision as of 16:33, 14 October 2014

Goodbye Azodye UCL iGEM 2014

Sustainable Bioprocessing

Our Design Process

We will use rapid polymer prototyping techniques to generate microfluidic chips that will allow us to test our reaction and aid in the construction of a realistic bioprocess, which can be successfully scaled-up for industrial use. As we optimise and change our bioprocess, we can also quickly design new microfluidic chips that can mimic its development on a micro-scale. For example, it is our goal to integrate multiple downstream steps, such as chromatography, in order to isolate potential useful products. Demonstrating this in a microfluidic system is less time-consuming and far more cost effective than doing so at a larger scale.


For our microfluidic bioreactor, we will be using a magnetic free floating bar as our mixing system. This is an effective method of mixing at a microfluidic scale, as demonstrated in the video on the right. This video is of a microfluidic chemostat bioreactor designed by Davies et al. 2014 UCL, using a free-floating bar to mix two dyes.



Above are some examples of the microfluidics devices developed by our team for use in the lab at the UCL ACBE. The devices are initially designed using AutoCAD (2D and 3D computer-aided design software), once the designs are finalised they can be 3D-printed using the facilities provided by the UCL Institute of Making and UCL ACBE; allowing our bioprocess and laboratory team to experiment and improve designs.


An example of one of our microfluidic devices designed on AutoCAD can be downloaded here. This device utilises the basic concept of mixing the cells and dyes, producing a single output stream; much alike to the bioprocessing concept. During the course of designing the microfluidic device, several key considerations must be taken into account: ability to withstand high pressure without leakage; materials of construction to be inert and transparent; size constraints of inlet and outlet piping; ability to accurately 3D-print the device.


Contact Us

University College London
Gower Street - London
WC1E 6BT
Biochemical Engineering Department
Phone: +44 (0)20 7679 2000
Email: ucligem2014@gmail.com

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