Difference between revisions of "Part:BBa M50054"
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<partinfo>BBa_M50054 short</partinfo> | <partinfo>BBa_M50054 short</partinfo> | ||
− | This is a mutant of PETase that combines two mutations designed by the 2016 iGEM Tianjin team. Wild type PETase shows | + | This is a mutant of PETase that combines two mutations designed by the 2016 iGEM Tianjin team. Wild-type PETase shows the ability to hydrolyze Polyethylene terephthalate (PET), commonly used for plastics. The two mutations are the 208th amino acid (changed from isoleucine(I) to valine(V)) and the 90th amino acid (changed from arginine (R) to alanine (A)), and each individual mutant has been showed by the Tianjin team to improve the catalytic activity of PET. This sequence combines both two mutations and is added 6 his tag at the end. The sequence is optimized for Escherichia coli. |
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Latest revision as of 07:29, 12 December 2016
PETase double mutant I208V and R90A
This is a mutant of PETase that combines two mutations designed by the 2016 iGEM Tianjin team. Wild-type PETase shows the ability to hydrolyze Polyethylene terephthalate (PET), commonly used for plastics. The two mutations are the 208th amino acid (changed from isoleucine(I) to valine(V)) and the 90th amino acid (changed from arginine (R) to alanine (A)), and each individual mutant has been showed by the Tianjin team to improve the catalytic activity of PET. This sequence combines both two mutations and is added 6 his tag at the end. The sequence is optimized for Escherichia coli.
Sequence and Features
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 633
Illegal PstI site found at 864 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 633
Illegal PstI site found at 864 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 633
- 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 633
Illegal PstI site found at 864 - 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 633
Illegal PstI site found at 864
Illegal NgoMIV site found at 220 - 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI site found at 388