Difference between revisions of "Team:TU Darmstadt/Project/Bio/Monomeres/EthyleneGlycol"
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<p>Our pathway bases on the previously published paper by Liu. et. al. (1)which showed a possible EG production in <em>E. coli </em>by introducing the D-xylose dehydrogenase xylB <a href=" http://parts.igem.org/Part:BBa_K1602009" title="Opens internal link in current window" class="internal link">(BBa_K1602009)</a>. In order to provide the pathway in different model organisms we added the remaining enzymes which are normally encoded in the <em>E. coli</em> genome. Furthermore a D-xylonolactone lactonase was added.(2)</p> | <p>Our pathway bases on the previously published paper by Liu. et. al. (1)which showed a possible EG production in <em>E. coli </em>by introducing the D-xylose dehydrogenase xylB <a href=" http://parts.igem.org/Part:BBa_K1602009" title="Opens internal link in current window" class="internal link">(BBa_K1602009)</a>. In order to provide the pathway in different model organisms we added the remaining enzymes which are normally encoded in the <em>E. coli</em> genome. Furthermore a D-xylonolactone lactonase was added.(2)</p> | ||
<p> </p> | <p> </p> | ||
| − | <p>The first reaction is performed by xylB. It´s a NAD+ dependant dehydrogenase and catalyzes the reaction of D-xylose to D-xylonolactone. This lactone can either be hydrolyzed to D-xylonic acid spontaneously or actively by a D-xylonolactonase. In order to prevent a possible bottleneck at this step the lactonase http://parts.igem.org/Part: | + | <p>The first reaction is performed by xylB. It´s a NAD+ dependant dehydrogenase and catalyzes the reaction of D-xylose to D-xylonolactone. This lactone can either be hydrolyzed to D-xylonic acid spontaneously or actively by a D-xylonolactonase. In order to prevent a possible bottleneck at this step the lactonase xylC <a href=" http://parts.igem.org/Part:BBa_K1602010" title="Opens internal link in current window" class="internal link">(BBa_K1602010)</a> was added to the pathway. Both enzymes original host is <em>Caulobacter crescentus</em> and for the use in <em>E. coli</em> we used synthesized and codon optimized versions of the gene.</p> |
<p> </p> | <p> </p> | ||
<p>In the next step D-xylonic acid does react to 2-dehydro-3-deoxy-D-pentonate in a reaction catalyzed by the dehydratase yjhG. From there yagE performs a cleavage at the C3-C4 bond and forms glycoaldehyde and pyruvate. While pyruvate can be metabolized in the citric acid cycle glycoaldehyde is reduced to ethyleneglycol by the NADP+ dependent aledhyde reductase YqhD.</p> | <p>In the next step D-xylonic acid does react to 2-dehydro-3-deoxy-D-pentonate in a reaction catalyzed by the dehydratase yjhG. From there yagE performs a cleavage at the C3-C4 bond and forms glycoaldehyde and pyruvate. While pyruvate can be metabolized in the citric acid cycle glycoaldehyde is reduced to ethyleneglycol by the NADP+ dependent aledhyde reductase YqhD.</p> | ||
Revision as of 18:17, 17 September 2015
Biotechnological production of ethylene glycol in Escherichia coli
Figure 1 ethylene glycol pathway
For generating a monomer toolbox using polyesterification reactions a dialcohol is essential which builds up chains with acid groups in a condensation reaction. Ethyleneglycol (EG) is the smallest stable dialcohol and already a basic chemical for industrial polymer production. For example the widely used polyethylene terephthalate (PET) includes ethylene as a monomer.
Ethyleneglycol is currently produced in an amount of approximately 21 million tons per year by a reaction of ethyleneoxide and water. Although first biotechnological factories started production in Taiwan in 2011 their output is not comparable to the chemically synthesized amount. The used process also bases on sugarcrane which is problematic concerning the pressure this might put on prices for food products.(3)
A future production which bases on renewable non-food resources could be the fermentation of xylose with engineered E. coli expressing D-xylose dehydrogenases.(1)
Our pathway bases on the previously published paper by Liu. et. al. (1)which showed a possible EG production in E. coli by introducing the D-xylose dehydrogenase xylB (BBa_K1602009). In order to provide the pathway in different model organisms we added the remaining enzymes which are normally encoded in the E. coli genome. Furthermore a D-xylonolactone lactonase was added.(2)
The first reaction is performed by xylB. It´s a NAD+ dependant dehydrogenase and catalyzes the reaction of D-xylose to D-xylonolactone. This lactone can either be hydrolyzed to D-xylonic acid spontaneously or actively by a D-xylonolactonase. In order to prevent a possible bottleneck at this step the lactonase xylC (BBa_K1602010) was added to the pathway. Both enzymes original host is Caulobacter crescentus and for the use in E. coli we used synthesized and codon optimized versions of the gene.
In the next step D-xylonic acid does react to 2-dehydro-3-deoxy-D-pentonate in a reaction catalyzed by the dehydratase yjhG. From there yagE performs a cleavage at the C3-C4 bond and forms glycoaldehyde and pyruvate. While pyruvate can be metabolized in the citric acid cycle glycoaldehyde is reduced to ethyleneglycol by the NADP+ dependent aledhyde reductase YqhD.
- Liu H, Ramos KR, Valdehuesa KN, Nisola GM, Lee WK, Chung WJ. Biosynthesis of ethylene glycol in Escherichia coli. Appl Microbiol Biotechnol. 2013;97(8):3409-17.
- Toivari MH, Nygard Y, Penttila M, Ruohonen L, Wiebe MG. Microbial D-xylonate production. Appl Microbiol Biotechnol. 2012;96(1):1-8.
- http://www.chemicals-technology.com/projects/greencolbiomegplant/