Difference between revisions of "Part:BBa K5477047"

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<partinfo>BBa_K5477047 short</partinfo>
 
<partinfo>BBa_K5477047 short</partinfo>
  
In our system, we have integrated two detoxification modules in yeast to create a highly efficient platform for the removal of environmental pollutants, including polycyclic aromatic hydrocarbons (PAHs), dioxins, and polychlorinated biphenyls (PCBs). These modules, CYP1A1-pGAL1/10-POR and UDPD-pGAL1/10-UGT1A1, work in tandem under the control of the pGAL1/10 bidirectional promoter, which allows for the coordinated expression of key enzymes in opposite directions.
+
In our system, we have integrated two detoxification modules in yeast to create a highly efficient platform for the removal of environmental pollutants, including dioxins and polychlorinated biphenyls (PCBs). These modules, CYP1A1-pGAL1/10-POR and UDPD-pGAL1/10-UGT1A1, work in tandem under the control of the pGAL1/10 bidirectional promoter, which allows for the coordinated expression of key enzymes in opposite directions.
  
The CYP1A1-pGAL1/10-POR module addresses phase I metabolism. CYP1A1 catalyzes the oxidation of carcinogenic compounds like PAHs and PCBs, converting these toxic hydrophobic molecules into more reactive and soluble intermediates. This reaction requires electrons supplied by cytochrome P450 oxidoreductase (POR), which transfers electrons from NADPH to CYP1A1, ensuring efficient oxidation. This step transforms hydrophobic environmental pollutants into more hydrophilic compounds, preparing them for further processing.
+
The CYP1A1-pGAL1/10-POR module addresses phase I metabolism. CYP1A1 catalyzes the oxidation of compounds like dioxin and PCBs, converting these toxic hydrophobic molecules into more reactive and soluble intermediates. This reaction requires electrons supplied by cytochrome P450 oxidoreductase (POR), which transfers electrons from NADPH to CYP1A1, ensuring efficient oxidation. This step transforms hydrophobic environmental pollutants into more hydrophilic compounds, preparing them for further processing.
 
The UDPD-pGAL1/10-UGT1A1 module complements this system by facilitating phase II metabolism. UGT1A1 (UDP-glucuronosyltransferase 1A1) conjugates glucuronic acid to the oxidized intermediates produced by CYP1A1, making them even more soluble and ready for excretion. However, for this reaction to proceed, a constant supply of UDP-glucuronic acid is needed, which is generated by UDP-glucose dehydrogenase (UDPD). UDPD converts UDP-glucose into UDP-glucuronic acid, providing UGT1A1 with the necessary substrate for the glucuronidation process. This modification significantly enhances the excretion of the pollutants via bile or urine, effectively detoxifying the yeast cells and reducing the toxicity of these compounds (1).
 
The UDPD-pGAL1/10-UGT1A1 module complements this system by facilitating phase II metabolism. UGT1A1 (UDP-glucuronosyltransferase 1A1) conjugates glucuronic acid to the oxidized intermediates produced by CYP1A1, making them even more soluble and ready for excretion. However, for this reaction to proceed, a constant supply of UDP-glucuronic acid is needed, which is generated by UDP-glucose dehydrogenase (UDPD). UDPD converts UDP-glucose into UDP-glucuronic acid, providing UGT1A1 with the necessary substrate for the glucuronidation process. This modification significantly enhances the excretion of the pollutants via bile or urine, effectively detoxifying the yeast cells and reducing the toxicity of these compounds (1).
  
 
https://static.igem.wiki/teams/5477/for-registry/correct-ones/detox-47.png
 
https://static.igem.wiki/teams/5477/for-registry/correct-ones/detox-47.png
  
Together, these two modules, regulated by the bidirectional pGAL1/10 promoter, form an integrated detoxification system that mimics both phase I (oxidation) and phase II (conjugation) of human metabolism. By expressing these systems in yeast, we can efficiently detoxify environmental pollutants such as PAHs, dioxins, and PCBs, transforming them into less toxic, more water-soluble metabolites that can be readily excreted. The following composites were used to build this device: [https://parts.igem.org/Part:BBa_K5477037 BBa_K5477037] and [https://parts.igem.org/Part:BBa_K5477036 BBa_K5477036]
+
Together, these two modules, regulated by the bidirectional pGAL1/10 promoter, form an integrated detoxification system that mimics both phase I (oxidation) and phase II (conjugation) of human metabolism. By expressing these systems in yeast, we can efficiently detoxify environmental pollutants such as dioxins, and PCBs, transforming them into less toxic, more water-soluble metabolites that can be readily excreted. The following composites were used to build this device: [https://parts.igem.org/Part:BBa_K5477037 BBa_K5477037] and [https://parts.igem.org/Part:BBa_K5477036 BBa_K5477036]
  
  

Revision as of 06:03, 1 October 2024


Detoxification device against dioxin and PCBs

In our system, we have integrated two detoxification modules in yeast to create a highly efficient platform for the removal of environmental pollutants, including dioxins and polychlorinated biphenyls (PCBs). These modules, CYP1A1-pGAL1/10-POR and UDPD-pGAL1/10-UGT1A1, work in tandem under the control of the pGAL1/10 bidirectional promoter, which allows for the coordinated expression of key enzymes in opposite directions.

The CYP1A1-pGAL1/10-POR module addresses phase I metabolism. CYP1A1 catalyzes the oxidation of compounds like dioxin and PCBs, converting these toxic hydrophobic molecules into more reactive and soluble intermediates. This reaction requires electrons supplied by cytochrome P450 oxidoreductase (POR), which transfers electrons from NADPH to CYP1A1, ensuring efficient oxidation. This step transforms hydrophobic environmental pollutants into more hydrophilic compounds, preparing them for further processing. The UDPD-pGAL1/10-UGT1A1 module complements this system by facilitating phase II metabolism. UGT1A1 (UDP-glucuronosyltransferase 1A1) conjugates glucuronic acid to the oxidized intermediates produced by CYP1A1, making them even more soluble and ready for excretion. However, for this reaction to proceed, a constant supply of UDP-glucuronic acid is needed, which is generated by UDP-glucose dehydrogenase (UDPD). UDPD converts UDP-glucose into UDP-glucuronic acid, providing UGT1A1 with the necessary substrate for the glucuronidation process. This modification significantly enhances the excretion of the pollutants via bile or urine, effectively detoxifying the yeast cells and reducing the toxicity of these compounds (1).

detox-47.png

Together, these two modules, regulated by the bidirectional pGAL1/10 promoter, form an integrated detoxification system that mimics both phase I (oxidation) and phase II (conjugation) of human metabolism. By expressing these systems in yeast, we can efficiently detoxify environmental pollutants such as dioxins, and PCBs, transforming them into less toxic, more water-soluble metabolites that can be readily excreted. The following composites were used to build this device: BBa_K5477037 and BBa_K5477036


Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal EcoRI site found at 7148
    Illegal PstI site found at 232
    Illegal PstI site found at 1434
    Illegal PstI site found at 2548
    Illegal PstI site found at 2745
    Illegal PstI site found at 3129
    Illegal PstI site found at 3569
    Illegal PstI site found at 3629
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal EcoRI site found at 7148
    Illegal PstI site found at 232
    Illegal PstI site found at 1434
    Illegal PstI site found at 2548
    Illegal PstI site found at 2745
    Illegal PstI site found at 3129
    Illegal PstI site found at 3569
    Illegal PstI site found at 3629
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal EcoRI site found at 7148
    Illegal BglII site found at 5440
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal EcoRI site found at 7148
    Illegal PstI site found at 232
    Illegal PstI site found at 1434
    Illegal PstI site found at 2548
    Illegal PstI site found at 2745
    Illegal PstI site found at 3129
    Illegal PstI site found at 3569
    Illegal PstI site found at 3629
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal EcoRI site found at 7148
    Illegal PstI site found at 232
    Illegal PstI site found at 1434
    Illegal PstI site found at 2548
    Illegal PstI site found at 2745
    Illegal PstI site found at 3129
    Illegal PstI site found at 3569
    Illegal PstI site found at 3629
    Illegal NgoMIV site found at 326
    Illegal NgoMIV site found at 413
    Illegal NgoMIV site found at 2951
    Illegal NgoMIV site found at 3070
    Illegal AgeI site found at 1956
    Illegal AgeI site found at 6146
  • 1000
    COMPATIBLE WITH RFC[1000]


References

1. 1. Inui H, Itoh T, Yamamoto K, Ikushiro S, Sakaki T. Mammalian cytochrome P450-dependent metabolism of polychlorinated dibenzo-p-dioxins and coplanar polychlorinated biphenyls. Int J Mol Sci. 2014 Aug 13;15(8):14044-57. doi: 10.3390/ijms150814044. PMID: 25123135; PMCID: PMC4159838.