Difference between revisions of "Part:BBa K1921001"
 
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===Usage===
 
===Usage===
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PETase is dedicated to the role of PET degradation. Our subject of the competition for this year is to modify PETase and developing cell surface display. <br>
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MHET is dedicated to the role of PET degradation. <br>
  
 
===Biology===
 
===Biology===
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PETase was found from a kind of microorganism（Ideonella sakaiensis 201-F6） living on PET as the main carbon source. It can degrade macromolecular polymers into monomers.PETase is the only enzyme found in bacteria which can degrade PET. Compare to the other enzyme found in fungi like LCC, TfH, FsC, PETase is much more active under low temperature environment, which means its reaction conditions is feasible in practical application than the others'.Additionally, PETase has been shown to have a degrading efficiency 120 times greater than alternative enzymes.
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Like PETase, MHETase is also discovered from Ideonella sakaiensis 201-F6, it is a enzyme which can hydrolyze MHET, which is the main product of PETase when hydrolyzing PET.
  
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===Reference===
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<span style="font-size: 130%;font-weight:bold">Contribution</span>
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<span class='h3bb'>Sequence and Features</span>
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<partinfo>BBa_K1921001 SequenceAndFeatures</partinfo>
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<p>Group: Austin UTexas</p>
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<p> Summary:
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MHETase is essential for optimized PET degradation using PETase. An enzymatic synergy between PETase and MHETase exists. MHET, an intermediate in the PET degradation pathway, can be hydrolyzed by a number of PET-degrading cutinases. The form of PETase isolated from Ideonella sakaiensis, however, also requires the presence of MHETase for optimal degradation of PET into terepthalic acid (TPA) and ethylene glycol (EG), the pathway’s biodegradable products. Knot et al. showed that release rates of TPA and EG vary in samples containing different concentrations of PETase and MHETase over 96 hours at 30 °C. MHETase has no activity on PET on its own, while PETase has a moderate degradation rate of PET on its own. When MHETase and PETase are used in tandem, however, degradation rates increase. The amount of MHETase added need not be large, which suggests that presence of MHETase is more important than any particular concentration ratio to PETase.2   
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</p>
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===Reference===
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[1] Kohei Oda, Shosuke Yoshida, et al. A bacterium that degrades and assimilates poly(ethylene terephthalate)[J]. Science. Vol 351. MARCH 2016: 1196-1199
  
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[2] Knott, B. C., Erickson, E., Allen, M. D., Gado, J. E., Graham, R., Kearns, F. L., Pardo, I.,
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===Functional Parameters===
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Topuzlu, E., Anderson, J. J., Austin, H. P., Dominick, G., Johnson, C. W., Rorrer, N. A., Szostkiewicz, C. J., Copié, V., Payne, C. M., Woodcock, H. L., Donohoe, B. S., Beckham, G. T., McGeehan, J, E. (2020). Characterization and engineering of a two-enzyme system for plastics depolymerization. Proceedings of the National Academy of Sciences
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<partinfo>BBa_K1921001 parameters</partinfo>
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Latest revision as of 20:12, 30 September 2021

MHETase


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 1027
    Illegal AgeI site found at 247
    Illegal AgeI site found at 364
  • 1000
    COMPATIBLE WITH RFC[1000]


Usage

MHET is dedicated to the role of PET degradation.

Biology

Like PETase, MHETase is also discovered from Ideonella sakaiensis 201-F6, it is a enzyme which can hydrolyze MHET, which is the main product of PETase when hydrolyzing PET.

Contribution

Group: Austin UTexas

Summary: MHETase is essential for optimized PET degradation using PETase. An enzymatic synergy between PETase and MHETase exists. MHET, an intermediate in the PET degradation pathway, can be hydrolyzed by a number of PET-degrading cutinases. The form of PETase isolated from Ideonella sakaiensis, however, also requires the presence of MHETase for optimal degradation of PET into terepthalic acid (TPA) and ethylene glycol (EG), the pathway’s biodegradable products. Knot et al. showed that release rates of TPA and EG vary in samples containing different concentrations of PETase and MHETase over 96 hours at 30 °C. MHETase has no activity on PET on its own, while PETase has a moderate degradation rate of PET on its own. When MHETase and PETase are used in tandem, however, degradation rates increase. The amount of MHETase added need not be large, which suggests that presence of MHETase is more important than any particular concentration ratio to PETase.2

Reference

[1] Kohei Oda, Shosuke Yoshida, et al. A bacterium that degrades and assimilates poly(ethylene terephthalate)[J]. Science. Vol 351. MARCH 2016: 1196-1199

[2] Knott, B. C., Erickson, E., Allen, M. D., Gado, J. E., Graham, R., Kearns, F. L., Pardo, I., Topuzlu, E., Anderson, J. J., Austin, H. P., Dominick, G., Johnson, C. W., Rorrer, N. A., Szostkiewicz, C. J., Copié, V., Payne, C. M., Woodcock, H. L., Donohoe, B. S., Beckham, G. T., McGeehan, J, E. (2020). Characterization and engineering of a two-enzyme system for plastics depolymerization. Proceedings of the National Academy of Sciences