Difference between revisions of "Part:BBa K5226004"
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<partinfo>BBa_K5226004 short</partinfo> | <partinfo>BBa_K5226004 short</partinfo> | ||
+ | ===Introduction=== | ||
+ | One of the goals of iGEM24-SCUT-China-A is to use synthetic biology tools to obtain Halomonas TD strains that can metabolize formate. We chose to introduce the formate assimilation pathway to enable it to utilize formate, a difficult-to-recover product in CDE. For the first method, based on previous studies obtained from literature research, we selected the tetrahydrofolate (THF) cycle imported from Methylobacterium extorquens AM1(parts:) and strengthened the endogenous C2 and C3 modules of Halomonas TD(parts:). | ||
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===Usage and Biology=== | ===Usage and Biology=== | ||
+ | TD-GcvT is Aminomethyltransferase.The protein sequence is from Halomonas sp. TD01 strain.This protein catalyzes the conversion of S-aminomethyl-dihydrolipoyllysine into dihydrolipoyllysine during the glycine cleavage system(C2M) . This part is used in BBa_xx and BBa_xx. | ||
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Revision as of 13:48, 1 August 2024
TD-gcvT
Introduction
One of the goals of iGEM24-SCUT-China-A is to use synthetic biology tools to obtain Halomonas TD strains that can metabolize formate. We chose to introduce the formate assimilation pathway to enable it to utilize formate, a difficult-to-recover product in CDE. For the first method, based on previous studies obtained from literature research, we selected the tetrahydrofolate (THF) cycle imported from Methylobacterium extorquens AM1(parts:) and strengthened the endogenous C2 and C3 modules of Halomonas TD(parts:).
Usage and Biology
TD-GcvT is Aminomethyltransferase.The protein sequence is from Halomonas sp. TD01 strain.This protein catalyzes the conversion of S-aminomethyl-dihydrolipoyllysine into dihydrolipoyllysine during the glycine cleavage system(C2M) . This part is used in BBa_xx and BBa_xx.
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal PstI site found at 436
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 627
Illegal PstI site found at 436 - 21COMPATIBLE WITH RFC[21]
- 23INCOMPATIBLE WITH RFC[23]Illegal PstI site found at 436
- 25INCOMPATIBLE WITH RFC[25]Illegal PstI site found at 436
- 1000COMPATIBLE WITH RFC[1000]