Team:Washington/Alkanes/Future

From 2011.igem.org

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[https://2011.igem.org/Team:Washington/Alkanes/Future/DecarbDesign Decarbonylase Redesign]  
[https://2011.igem.org/Team:Washington/Alkanes/Future/DecarbDesign Decarbonylase Redesign]  
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:<nowiki>One way to diversify the kind of alkanes produced is to alter the substrate specificity of the proteins involved. Since an alternative alkane-producing enzyme has not been found, we decided to mutate the aldehyde decarbonylase to produce shorter-chain alkanes.</nowiki>
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Revision as of 00:02, 23 September 2011


Future Directions

Our current in vivo system only efficiently makes C15 alkanes. To be efficient enough for factory production, there are two broad goals to be done:

  1. Increase production efficiency
  2. Diversity the range of alkanes for the system.
  3. Increase scale of system for industrial processes.

We have already begun efforts to expand the efficiency and scope of alkane production.

UW 2011 Alkane Future Work Image.png
Washington 2011 Optimization.png

System Optimization

The efficiency of this system was reported to be much higher than our initial system, but the growth conditions of the assay and the DNA was not available to us. We increased production efficiency by altering the initial environmental conditions in the assay.
Washington 2011 ADC Redesign.png

Decarbonylase Redesign

One way to diversify the kind of alkanes produced is to alter the substrate specificity of the proteins involved. Since an alternative alkane-producing enzyme has not been found, we decided to mutate the aldehyde decarbonylase to produce shorter-chain alkanes.
Washington 2011 LuxCDE.png

Alternate Aldehyde Production

Another way to diversify our system is to use alternative proteins. Our current system uses acyl-ACP reductase, and we've identified an hypothetical alternative system that produces aldehydes: LuxCDE, made from parts from the 2010 competition.
Washington 2011 fabh2 branch.png

Branched Alkanes Production

Our system is only capable of producing unbranched alkanes, as the cell mainly utilizes straight chained fatty acids. However, fuel we use are also composed largely of branched alkanes that affect very important properties of the fuel such as flash point and freezing point. If our fuels are truly intended to be synthesized in bacteria, we need to work on methods of making those crucial branched chained alkanes. We explored FabH2, a protein that when involved in fatty acid synthesis makes branched fatty acids.
Washington 2011 Protein Localization.png

Enzyme Localization

The easiest way to increase yield is to increase the concentration; if the number of molecules remained the same but the volume decreased, the reaction speed increases with occurrences of molecular collisions. However, this is only easily done with purified protein assays. However, there are ways to "increase the concentration" of reactions in cells. We cannot make the cells literally denser, but we can localize the enzymes involved in the reaction, which either decreases the volume of the cell in which the enzymes reside and/or limit the number of reaction steps.
Washington 2011 Alternate Chassis.png

Alternative Chasis

By synthesizing alkanes in organisms, alkanes can become a useful renewable energy source; CO2 emitted from burning the alkanes are converted to glucose through photosynthesis, and then the glucose can be fed to alkane-synthesizing organisms to restart the cycle. This cycle can be drastically improved if there were fewer steps in the cycle. We explored the possibility of optimizing the alkane biosynthesis system in different micro-organisms, with the idea that perhaps with autotrophic organisms, we do not need to obtain glucose for the reaction.