Team:UCL/QWERTYtest

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<h4>Meeting with ETAD - Ecological and Toxicological Association of Dye and Pigment Manufacturers</h4>
<h4>Meeting with ETAD - Ecological and Toxicological Association of Dye and Pigment Manufacturers</h4>
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<p>ETAD - an association based in Basel represents over 35 different pigment and dyeing corporations internationally, coordinating a group initiative to limit adverse effects on health and the environment by their industry.Present at the meeting were Walter Hoffman – Director of ETAD, Dr Stefan Ehrenberg - Pigment Manufacturing R&D at Bezema, Georg Roentgen – Director of R&D Colours and Textile Effects at Huntsman.</p>
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<p>ETAD - an association based in Basel represents over 35 different pigment and dyeing corporations interna
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<p>The main reasons for this meeting were:
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    <li>To encourage industry to consider synthetic biology as a realistic, viable option when looking to reduce the toxicity of their process.
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    <li>Discuss the major concerns and problem areas the dyeing and pigments industry are currently facing.</p>
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<img width="25%" style="float:right;margin:0 0 0 10px;" src="https://static.igem.org/mediawiki/2014/4/41/1924384_10154546138020564_6502621618718289701_n.jpg"></img>
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<h4>Dye Houses vs Dye Synthesis Waste</h4>
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<p>The meeting with ETAD raised a number of points for our project. Mr Roentgen questioned how the survival of our bacterial cell would be effected in dyehouse waste as opposed to dye synthesis plant waste. The waste from a dyehouse is a complex mix of azo dyes at approximately 1%-5% concentration in a high salt concentration with the presence of metals copper and chromium. This a harsh environment compared with the waste of a dye synthesis plant, generally containing one or two azo dyes in a simple mixture at 10% concentration.</p>
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<p>This is new information for our project and has greatly influenced us to direct our research towards optimising remediation of dye synthesis waste water. Another advantage of remediation of dye synthesis plant waste water is that the low variety of azo dyes in each batch mixture will make filtration of valuable products a much easier and viable process, enhancing the economic feasibility of our device.</p>
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<h4>Sulphonated Azo Dyes</h4>
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<p>The current trend in the textile industry is to reduce the volume of water consumed, leading to a greater use of more soluble dyes. For a dye to be more soluble it must be more polar, as such, many of these soluble dyes have sulfonated groups. The sulphur atom has a electron withdrawing effect making reduction of the azo bond difficult, the industry are finding chemical processes to degrade these dyes to be ineffective. </p>
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<p>We feel we can offer an alternative since ..lignin peroxidase…. change this is known to be effective working on azo bonds with sulphur group.</p>
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<h4>Conclusions</h4>
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<p>Overall the meeting was a great success in guiding our project towards an industrial relevant direction. Running through our presentation highlighted a number of changes needed before the jamboree, specifically putting more emphasis on the novelty and innovation of our project. Ensuring our project delivers a solution that is conscious of the needs of the industry is extremely important to us, meetings such as these are invaluable to the progression of our work.</p>
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<br>
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<div class="textTitle"><h4>A Strong Commercial Strategy</h4></div>
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Assessment of commercial feasibility is widely based on evaluating the target market’s “readiness” to receive and integrate an innovative product or process. This primarily involves defining and characterising the target market and quantifying economic potential in terms of projected demand. Furthermore technical feasibility based on forecasted costs and resource requirements must be considered whilst remaining aware of potential risks and obstacles.</p>
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<div class="textTitle"><h4>Feasible Target Markets</h4></div>
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<img src="https://static.igem.org/mediawiki/2014/7/7c/Igem_Target_market_image.png" style="float:right;margin:0 0 0 10px;" width="50%">
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The potential market segmentation for this novel process is based on relative contribution to global dyeing effluent pollution. The textile industry represents a vast proportion of this contribution over other potential market segments (cosmetic, pharmaceutical, food industries) and has therefore appropriately become the thematic focus of this project. Considering the world market for textile dyeing operations, a majority of dye effluent waste can be attributed to Asia, followed by North America and Western Europe. However receptiveness to environmental initiatives and the magnitude of investment in projects of the sort are heavily skewed away from developing regions of Asia. Hence a stronger approach to achieving a realistic impact would start in the UK where socio-economic conditions are more suitable. This should be taken into consideration in further technical development and strategic commercialisation steps.
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<div class="textTitle"><h4>Value Proposition</h4></div>
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The following clarifies the net and indirect value of our bioprocessing solution to key stakeholders, and elucidates incentive for its integration into current waste management systems.
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<b>Reputation</b>
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In society, a growing culture for Eco-friendliness with an increasing political voice can be observed. Accordingly, mounting pressure to reduce harmful emissions is probing investment in effluent remediating infrastructure, not excluding that of the textile industry. Furthermore consumer demands are evolving (particularly in developed regions) to favor environmentally neutral products, with initiatives such as  being in the public eye and threatening the reputation of irresponsible manufacturers and governments.
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<h3>Why invest</h3>
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<p>In the implementation of any new product or process there exists an interplay between several elements that have the ability to effect the adoption of that product:
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jpeg.
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<br>1.Environmental: ensuring appropriate waste disposal in terms of toxicity levels and concentrations for example. Our process solution will bring forward sustainable textile processing
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<br>2.Economic: This aspect can be broken down into the financial returns of the product and the costs of goods saved through its use.
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<br>3.Legislative: Regulatory bodies and governments set emission margins and environmental burden limits for factories
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<br>4. Societal: through our public engagement campaigns (link), communicating a message to the wider society can bring about change.
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</p>
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<p>The significant economic activity of textiles and clothing in the global market makes it incredibly relevant for industrialists to consider process alterations aimed at optimizing resource allocation and reducing environmental burden.</p>
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<p><b>“According to the EIPRO study, clothing alone is responsible for 2 to 10% of the EU’s life-cycle environmental impacts. This results in textiles coming fourth in the ranking of product category which cause the greatest environmental impact”(1)’</b></p>
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<br>
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<p>The carcinogenic properties of Azodye precursors and degradation products (such as aromatic amines)(3) are exacerbated by the low susceptibility for azodye bio-degradation under aerobic conditions (4,5). This environmental burden has been going up ranks with industrial fresh water pollution due to textile treatment and dyeing reach 20% in 2010 (2).</p>
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<p>Furthermore, growing concerns regarding water consumption in textile processes due to astronomical usage of ‘potable industrial water’ (6). According to the 2010 global market report on sustainable textiles, the world used three trillion gallons of fresh water to produce 60 billion kgs of fabric. With over 80000 tonnes of reactive dyes produced and consumed each year, the heavily polluted dye baths issuing off the dyeing processes need to be treated before any reuse can be conceived (2). According to various reviews (2, , ,), conventional membrane processes and coagulation are among the suggested methods to achieve this. Implementing a water recycle strategy for a textile plant would require in-plant treatment processes (6).
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There exists an array of national and international regulations addressing ‘controlled used and allowed emissions from textile factories’ such as the EU Eco-label criteria and  REACH (Registration, Evaluation, Authorization and Restriction of Chemical substances) (regulation (EC) No 1907/2006) (7). A cost-effective process that facilitates textile companies to meet these requirements would be an ideal solution if integrated at the end of each factory, to stop short poisonous releases. Thus, by improving their performance and earning one of these eco-criteria could result in improved branding, bringing forward a strong connection with aware consumers by informing them of such sustainability initiatives.
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<div class="textTitle"><h4>Why Microfluidics?</h4></div>
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<p>Small-scale bioreactors are often the workhorse for process development. By experimenting at this scale, it is possible to determine the optimum growth conditions for E. coli. This will allow to assess costs at the required scale based on biomass requirements.We are using E. coli to cultivate the enzymes necessary for the biodegradation of azo dyes. By combining information on the production of azodyes in textile factories and stoichiometric relations, we will design an optimised cell growth (fermentation) stage.</p>
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<iframe style="padding:0.5%; border:0.5% #000;" src="//www.youtube.com/embed/0OlMfq5WT6k" allowfullscreen="" align="left" frameborder="0" height="380" width="600"></iframe></div></td><td>
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<img src="https://static.igem.org/mediawiki/2014/4/49/Microfluidic_set-up_iGEM.JPG" style="float:right;margin:0 0 0 10px;" width="35%">
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The videos above were recorded in the UCL ACBE Microfluidics labs by members of our team. The video on the left is a demonstration of laminar flow across a T-junction microfluidic device. The video on the right demonstrates one of the methods of mixing made possible by microfluidics (herring bone channels etched into the chip).
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<br><br>The image on the right displays the microfluidics set-up used by our iGEM team. This device and equipment is provided for by the UCL microfluidics lab.</p></div>
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<div class="textTitle"><h4>Our Design Process</h4></div>
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<iframe style="padding:1%; border:0.5% #000;" src="//www.youtube.com/embed/6UNpqpMS5vA" allowfullscreen="" align="right" frameborder="0" height="380" width="600"></iframe></div>
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<p>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.</p><br>
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<p>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.</p><br>
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<img src="https://static.igem.org/mediawiki/2014/thumb/b/b8/AutoCAD_Device.png/800px-AutoCAD_Device.png" width="32%">
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<img src="https://static.igem.org/mediawiki/2014/thumb/7/71/MicrofluidicsDevice.jpg/800px-MicrofluidicsDevice.jpg" style="PADDING-LEFT: 2%" "padding-right:="" 3%"="" width="32%">
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<img src="https://static.igem.org/mediawiki/2014/1/1e/Fluidics_Chip.JPG" align="right" width="32%"><br>
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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.</p></div>
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<p><img src="https://static.igem.org/mediawiki/2014/4/4c/UCLAc-2014-logo.png" align="right" width="10%">
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An example of one of our microfluidic devices designed on AutoCAD can be downloaded <a href="https://static.igem.org/mediawiki/2014/f/fa/UCL_iGEM_2014_Microfluidics_Device_Design.dwg.zip">here</a>. This device utilises the basic concept of mixing the cells and dyes, producing a single output stream; much alike to the <a href="https://2014.igem.org/Team:UCL/Science/Bioprocessing">bioprocessing</a> 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.</p><br>
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<div class="textTitle"><h4>Why Bioprocessing?</h4></div>
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<p>Bioprocess engineering is a conglomerate of fields and is extensively employed to optimize a variety of production processes. In order to cope with market forces, industries for example the pharmaceutical, have had to considerably improve their bioprocessing tools and techniques. As a result a range of novel process alternatives have been developed to harness product-specific properties, each bearing benefits, disadvantages and costs. While these can be used to drive financial returns, biological processing is becoming a gateway to eco-friendly alternatives for the treatment of recalcitrant wastewater such as industrial effluents. By providing more flexibility in supporting efficient degradation of toxic compounds and having lower operating costs, the biological treatment process brings forward key advantages over it's traditional counterpart.
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<br>A typical bioprocess involves the fermentation of a stock culture (e.g. E. coli) at a small scale which is subsequently scaled up to suitable production capacities. The products from the fermentative stages are consequently separated and purified using a variety of unit operations designed to exploit the orthogonal properties of desired products. These can then be formulated into their ultimate delivery form.
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The design of a successful bioprocess requires careful analysis of the many factors that impact choice of design parameters and process variables. It is crucial to consider the cost of the process at each stage to assess it's large scale feasibility.
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<br><br>
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Let's look at an example bioprocess
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<br>1. Upstream: Production bioreactor preceded by small-scale seed fermenters
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<br>2. Downstream: constitutes of three main stages
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<br><b>- Recovery </b>relates to primary unit operations i.e. centrifugation and filtrations. The main goal is to concentrate the desired compound within the process stream by reducing volumes and removing fermentation byproducts.
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<br><b>- Purification </b> involves unit operations such as chromatography, crystallization and ultrafiltration. The final stages are necessary to ensure purity requirements are met.
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<br><b>- Formulation</b>involves the integrating of the product into the target delivery route followed by packaging and storage.
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Revision as of 22:05, 15 October 2014

Goodbye Azodye UCL iGEM 2014

Sustainable Bioprocessing
123 Mambo no 5
A little bit of monica in my life