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<p>In March of 2016, an article was released about the discovery of a bacterium that could degrade PET, polyethylene terephthalate. Ideonella sakaiensis 201-F6 was found to contain a PET hydrolase and a MHET hydrolase, named PETase and MHETase respectively. PETase introduced on a PET film degraded PET into MHET, a monomer of the PET chain, along with minimal amounts of terephthalic acid. In combination with MHETase, the PET film was degraded into the final products of terephthalic acid and ethylene glycol. After 6 weeks, the PET film was almost completely degraded. [2] <br><br> | <p>In March of 2016, an article was released about the discovery of a bacterium that could degrade PET, polyethylene terephthalate. Ideonella sakaiensis 201-F6 was found to contain a PET hydrolase and a MHET hydrolase, named PETase and MHETase respectively. PETase introduced on a PET film degraded PET into MHET, a monomer of the PET chain, along with minimal amounts of terephthalic acid. In combination with MHETase, the PET film was degraded into the final products of terephthalic acid and ethylene glycol. After 6 weeks, the PET film was almost completely degraded. [2] <br><br> | ||
− | Two years later, in April of 2018, an article was released with extensive research on wild-type PETase and select PETase mutations. The W159H/S238F double mutant of PETase showed significant improvement in crystallinity reduction and product release over the wild-type in just 96 hours. The percent crystallinity change is a result of the pitting on the film caused by the PET degradation. [3] </p> | + | Two years later, in April of 2018, an article was released with extensive research on wild-type PETase and select PETase mutations. The W159H/S238F double mutant of PETase showed significant improvement in crystallinity reduction and product release over the wild-type in just 96 hours. The percent crystallinity change is a result of the pitting on the film caused by the PET degradation. [3] </p> <br> |
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− | <img src = "https://static.igem.org/mediawiki/2018/2/21/T--RHIT--DescGraph.jpg" style="width: | + | <img src = "https://static.igem.org/mediawiki/2018/2/21/T--RHIT--DescGraph.jpg" style="width:50%"> |
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<center> Figure 1. A comparison of the previous PETase sequence and the double-mutated sequence. Image included from the April 2018 article. [3] | <center> Figure 1. A comparison of the previous PETase sequence and the double-mutated sequence. Image included from the April 2018 article. [3] | ||
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<p>For our project, we have designed a plasmid that secretes MHETase and the double mutant PETase to increase the rate at which PET is degraded compared to the previous PETase sequence. We inserted the plasmid into an E. coli MG1655 strain. Because of the toxicity of ethylene glycol, a second plasmid was designed to allow the bacteria to break down the ethylene glycol and utilize its products as a carbon source. These enzymes include glycolaldehyde reductase, glycolaldehyde dehydrogenase, glycolate oxidase, and malate synthase. This series of enzymes will turn the ethylene glycol, released from the breakdown of PET, into malate which can be used by the cell as a carbon source via the citric acid cycle. <br><br> | <p>For our project, we have designed a plasmid that secretes MHETase and the double mutant PETase to increase the rate at which PET is degraded compared to the previous PETase sequence. We inserted the plasmid into an E. coli MG1655 strain. Because of the toxicity of ethylene glycol, a second plasmid was designed to allow the bacteria to break down the ethylene glycol and utilize its products as a carbon source. These enzymes include glycolaldehyde reductase, glycolaldehyde dehydrogenase, glycolate oxidase, and malate synthase. This series of enzymes will turn the ethylene glycol, released from the breakdown of PET, into malate which can be used by the cell as a carbon source via the citric acid cycle. <br><br> | ||
− | Much of the inspiration for our project came from the many changes that have taken place on Rose-Hulman’s campus. Within the last few years, recycling and decreasing plastic waste have become important aspects of campus. Many of these changes are due to the Six Sigma class. Six Sigma does projects where the students collect data before and after an improvement phase. Some of their past projects have included collecting data on the amount of recyclables in the trash and the use of plastic straws on campus. Recycling areas were set up throughout the academic buildings, and the campus community was educated about what and how to recycle. The plastic straw project initiated a decline in plastic straw use around campus by offering a biodegradable alternative to plastic straws at the eateries on campus and selling reusable straws to students. Figure 2 and Figure 3 show data collected by the Six Sigma class during their recycling project. Figure 2 is before the improvement phase and Figure 3 is after. This data shows a noticeable change in the campus community. [4] </p> | + | Much of the inspiration for our project came from the many changes that have taken place on Rose-Hulman’s campus. Within the last few years, recycling and decreasing plastic waste have become important aspects of campus. Many of these changes are due to the Six Sigma class. Six Sigma does projects where the students collect data before and after an improvement phase. Some of their past projects have included collecting data on the amount of recyclables in the trash and the use of plastic straws on campus. Recycling areas were set up throughout the academic buildings, and the campus community was educated about what and how to recycle. The plastic straw project initiated a decline in plastic straw use around campus by offering a biodegradable alternative to plastic straws at the eateries on campus and selling reusable straws to students. Figure 2 and Figure 3 show data collected by the Six Sigma class during their recycling project. Figure 2 is before the improvement phase and Figure 3 is after. This data shows a noticeable change in the campus community. [4] </p> <br> |
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Revision as of 17:55, 2 August 2018