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<a href="https://2014.igem.org/Team:METU_Turkey">METU Turkey</a> | <a href="https://2014.igem.org/Team:METU_Turkey">METU Turkey</a> | ||
<ul> | <ul> | ||
− | <li>Reduced catechol to pyruvate</li> | + | <li>Reduced catechol (downstream product) to pyruvate</li> |
</ul><br> | </ul><br> | ||
<a href="https://2014.igem.org/Team:ITB_Indonesia">ITB Indonesia</a> | <a href="https://2014.igem.org/Team:ITB_Indonesia">ITB Indonesia</a> |
Revision as of 14:09, 17 October 2018
History
Past iGEM Teams involved with PET
Listed here are past iGEM teams that have worked on projects on or related to PET degredation, with condensed descriptions of their results.
2012
BAU-Indonesia
TU Darmstadt
UC Davis
- Isolation of cutinase gene from nature with primers
TU Darmstadt
- Surface display of cutinase on E. coli
- Attempted TPA transport into E. coli, further research required
- Expressed all TPH enzymes, did not attempt to measure activity
- Confirmed anaerobic conversion of PCA via AroY and XylE enzymes
UC Davis
- Confirmed cutinase activity using PNPB esterase assay
- Engineered E. coli ethylene glycol metabolism with directed evolution
2013
2014
METU Turkey
ITB Indonesia
- Reduced catechol (downstream product) to pyruvate
ITB Indonesia
- LC cutinatse activity confimed with SEM, PNPB
2015
Pasteur Paris
- PNPB assay to confirm activity of esterase EST13
- Fluorescent detection of TPA can not be accomplished when in LB broth
2016
ASIJ Tokyo
AUC Turkey
Baltimore BioCrew
BGU Israel
Harvard BioDesign
Tianjin
TJUSLS China
UESTC-China
UoA New Zealand
- Attempt at detecting PET degradation by mass change failed
AUC Turkey
- Withdrawn
Baltimore BioCrew
- Planned to weigh PET degradation, no results
BGU Israel
- PNPB and EM to confirm LC cutinase activity
- P. putida can grow on PCA as sole carbon source, but not TPA
- E. coli expressing LC-cutinase with pelB leader sequence grew on M9 plates with PET as sole carbon source. Expected to be due to consumption of ethylene glycol from PET degradation
- Unable to determine enzyme efficiency based on growth due to heterogeneity in PET distribution
- Measured fluorescence of TPA on plates, unable to quantify LC cutinase activity
Harvard BioDesign
- Petase function confirmed with PNPB
- Bacteria produced electric current when supplied with unspecified quantity of TPA
Tianjin
- EM confirmation of PETase activity of PET film degradation
- Multispectral scanning quantified PETase products for cell free system
TJUSLS China
- HPLC detection of MHET to confirm PETase activity in varying conditions
- Surface display of PETase in E. coli
UESTC-China
- SEM and PNPB to confirm PETase activity
- Possible detection of TPA by UV vis (higher absorbance across spectrum)
UoA New Zealand
- Assembled PETase part with His tag
2017
Baltimore Bio-Crew
BOKU-Vienna
ITB Indonesia
- Fluorescine diacetate hydrolysis assay to confirm PETase and MHETase hydrolytic activity
BOKU-Vienna
- Discussion of a possible method for directed evolution of PETase by culturing cells on PET film that fluoresces when degraded
ITB Indonesia
- Successful biofilm formation on PET, but biofilm matrix hampered PETase activity
- Engineered E. coli ethylene glycol metabolism with directed evolution
2018
Makerere University
OLS Canmore Canada
RHIT
ULaVerne
UMaryland
Yale
- TBA
OLS Canmore Canada
- TBA
RHIT
- TBA
ULaVerne
- TBA
UMaryland
- Check out our results on this wiki!
Yale
- TBA
Contact Us
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umarylandigem@gmail.com
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© University of Maryland 2018