Difference between revisions of "Competition/Tracks/Manufacturing"

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<h2>Manufacturing Track</h2>
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<h1>Manufacturing Track</h1>
 
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Manufacturing is already an area of demonstrable success in synthetic biology. It is built on diverse history of previous work in metabolic pathway engineering with work such as the production of human insulin using recombinant DNA technologies, starting in the early 1980's. The most well known current example is likely Amyris' engineering of the antimalarial drug precursor, artemisinic acid. Other companies are demonstrating the production of transportation fuels using algal systems in photobioreactors on non-arable land.  
 
Manufacturing is already an area of demonstrable success in synthetic biology. It is built on diverse history of previous work in metabolic pathway engineering with work such as the production of human insulin using recombinant DNA technologies, starting in the early 1980's. The most well known current example is likely Amyris' engineering of the antimalarial drug precursor, artemisinic acid. Other companies are demonstrating the production of transportation fuels using algal systems in photobioreactors on non-arable land.  
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<li><a href ="https://igem.org/Team_Tracks?year=2016"> iGEM 2016 Manufacturing team list</a></li>
 
<li><a href ="https://igem.org/Team_Tracks?year=2015"> iGEM 2015 Manufacturing team list</a></li>
 
<li><a href ="https://igem.org/Team_Tracks?year=2015"> iGEM 2015 Manufacturing team list</a></li>
 
<li><a href ="https://igem.org/Team_Tracks?year=2014"> iGEM 2014 Manufacturing team list</a></li>
 
<li><a href ="https://igem.org/Team_Tracks?year=2014"> iGEM 2014 Manufacturing team list</a></li>
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<h2>Recent Manufacturing projects to win best in track</h2>
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<h3>Winning Manufacturing project in 2013 Undergrad: Plasticity: Engineering microbes to make environmentally friendly plastics from non-recyclable waste</h3>
 
  
<h3><a href="https://2013.igem.org/Team:Imperial_College">Imperial College</a></h3>
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<img src="https://static.igem.org/mediawiki/2017/f/f1/HQ_manufacturing_aachen2015.jpg">
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<h3><a href="https://2015.igem.org/Team:Aachen"> Aachen  2015 </a></h3>
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<h4> Upcycling Methanol into a Universal Carbon Source  </h4>
  
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<strong>Project abstract:</strong>
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Nowadays, mankind uses 94 million barrels of oil per day. But as agreed on by various nations, we have to become independent from fossil resources during the next decades. As a consequence, not only fuels, but many other products including drugs, fine chemicals and plastic will have to be produced from renewable carbon sources. In parallel, we observe arable land per capita shrinking and more frequent droughts. But even by increasing agricultural productivity, plants will not be able to meet our massive demands. Therefore, we are developing an alternative route to sustainably produce complex carbon which significantly reduces the space and water needs. By using new synthetic pathways, we are upcycling a simple, renewable chemical into a universal carbon source.
Accumulation of waste represents a considerable problem to humanity. Over the next 50 years, the global community will produce approximately 2 trillion tonnes of waste, or 2.5 times the weight of Mount Everest. Traditionally, mixed non-recyclable waste is sent to landfill or for incineration, both of which result in environmental damage. The detrimental effects are perpetrated by the plastic degradation into toxic byproducts and the production of greenhouse gases by these processes. As an alternative we propose to upcycle this mixed waste into the bioplastic poly-3-hydroxybutyrate (P3HB) to create a closed loop recycling system. Our engineered E. coli will operate within sealed bioreactors. In the future we picture the use of our system in a variety of contexts as part of our M.A.P.L.E. (Modular And Plastic Looping E.coli) system.
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<h3>Winning Manufacturing project in 2012: Arachnicoli</h3>
 
  
<h3><a href="https://2012.igem.org/Team:Utah_State">Utah State</a></h3>
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<img src="https://static.igem.org/mediawiki/2017/3/36/HQ_manufacturing_stanfordbrown2015.jpg">
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<h3><a href="https://2015.igem.org/Team:Stanford-Brown">Stanford-Brown 2015 </a></h3>
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<h4>  biOrigami: A New Approach to Reduce the Cost of Space Missions </h4>
  
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<strong>Project abstract </strong>:
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Space exploration lies at the inquisitive core of human nature, yet high costs hinder the advancement of this frontier. We are harnessing the replicative properties of biology to create biOrigami—biological, self-folding origami—to reduce the mass, volume, and assembly time of materials needed for space missions. biOrigami consists of two main components: manufacturing substrates biologically and bioengineering folding mechanisms. For substrates, we are developing new BioBricks to synthesize two thermoplastics: polystyrene and polyhydroxyalkanoates. For folding mechanisms, we are using heat-induced contraction of thermoplastics and the contractile properties of bacterial spores. After consulting with experts, we believe that biOrigami could be incorporated into rovers, solar sails, and more. In addition to biOrigami, we are creating a novel method to efficiently transform bacteria by using the CRISPR/Cas9 system, benefitting the broader synthetic biology community. Our project integrates and improves manufacturing processes for space exploration on both the micro and macro levels.
Spider silk is the strongest known biomaterial, with a large variety of applications. These applications include artificial tendons and ligaments, biomedical sutures, athletic gear, parachute cords, air bags, and other yet discovered products which require a high tensile strength with amazing extendibility. Spiders however cannot be farmed because they are territorial and cannibalistic. Thus, an alternative to producing spider silk must be found. We aim to engineer spider silk genes into E. coli to produce this highly valuable product. Spider silk production in bacteria has been limited due to the highly repetitive nature of the spider silk amino acids in the protein. To overcome this obstacle we are using various synthetic biology techniques to boost spider silk protein production and increase cellular fitness. After successful production, spider silk protein is artificially spun into usable fibers and tested for physical properties.
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<h3>Winning Manufacturing project 2011: Biofactory</h3>
 
  
<h3><a href ="https://2011.igem.org/Team:Cornell">Cornell</a></h3>
 
  
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<strong>Project abstract:</strong>
 
Cornell's 2011 iGEM team has designed a new, scalable, and cell-free method to produce complex biomolecules. Current methods for purification from cellular lysate are expensive and time consuming. Biofactory utilizes modified enzymes, capable of being attached to surfaces, in the creation of a modular microfluidic chip for each enzyme. The surface bonding is performed by the well characterized biotin-avidin mechanism. When combined in series, these chips operate as a linear biochemical pathway for continous flow reactions. Additionally, we engineered E. Coli with the mechanism for light-induced apoptosis to easily lyse cultures producing the necessary enzymes. The resulting lysate is flowed through the microfluidic channels, coating them with the desired enzyme. We believe these methods will reduce unwanted side reactions, and lower the costs of producing bio-pharmaceuticals in the future.
 
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Revision as of 16:10, 16 December 2016

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Manufacturing Track

Manufacturing is already an area of demonstrable success in synthetic biology. It is built on diverse history of previous work in metabolic pathway engineering with work such as the production of human insulin using recombinant DNA technologies, starting in the early 1980's. The most well known current example is likely Amyris' engineering of the antimalarial drug precursor, artemisinic acid. Other companies are demonstrating the production of transportation fuels using algal systems in photobioreactors on non-arable land.

Manufacturing will also play a big role in tissue engineering through the production of new skin, organs and other medical substrates to treat disease and injury. While these problems may seem like medical technologies, scaling them up from the bench to the clinic will very much require innovations in manufacturing.

The potential for the manufacturing track in iGEM is immense. Biological systems can be used to make products under conditions that were previously impossible. Many enzymes can achieve reaction conditions in a tube that would otherwise require high temperatures, pressures or expensive substrates to reproduce using chemical engineering methods. Another possibility is micro-scale production of drugs, therapeutics or other high-value molecules. iGEM teams who choose to work on manufacturing have a wide range of possible projects and many large challenges to overcome.

You can find images and abstracts of the winning Manufacturing teams from 2013 to 2015 in the page below. Also, follow the links below to see projects from all the Manufacturing track teams.

Aachen 2015

Upcycling Methanol into a Universal Carbon Source

Nowadays, mankind uses 94 million barrels of oil per day. But as agreed on by various nations, we have to become independent from fossil resources during the next decades. As a consequence, not only fuels, but many other products including drugs, fine chemicals and plastic will have to be produced from renewable carbon sources. In parallel, we observe arable land per capita shrinking and more frequent droughts. But even by increasing agricultural productivity, plants will not be able to meet our massive demands. Therefore, we are developing an alternative route to sustainably produce complex carbon which significantly reduces the space and water needs. By using new synthetic pathways, we are upcycling a simple, renewable chemical into a universal carbon source.

Stanford-Brown 2015

biOrigami: A New Approach to Reduce the Cost of Space Missions

Space exploration lies at the inquisitive core of human nature, yet high costs hinder the advancement of this frontier. We are harnessing the replicative properties of biology to create biOrigami—biological, self-folding origami—to reduce the mass, volume, and assembly time of materials needed for space missions. biOrigami consists of two main components: manufacturing substrates biologically and bioengineering folding mechanisms. For substrates, we are developing new BioBricks to synthesize two thermoplastics: polystyrene and polyhydroxyalkanoates. For folding mechanisms, we are using heat-induced contraction of thermoplastics and the contractile properties of bacterial spores. After consulting with experts, we believe that biOrigami could be incorporated into rovers, solar sails, and more. In addition to biOrigami, we are creating a novel method to efficiently transform bacteria by using the CRISPR/Cas9 system, benefitting the broader synthetic biology community. Our project integrates and improves manufacturing processes for space exploration on both the micro and macro levels.