Difference between revisions of "Part:BBa K5226008"
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__NOTOC__ | __NOTOC__ | ||
<partinfo>BBa_K5226008 short</partinfo> | <partinfo>BBa_K5226008 short</partinfo> | ||
− | + | ===Sequence and Features=== | |
+ | <partinfo>BBa_K5226008 SequenceAndFeatures</partinfo> | ||
+ | <br> | ||
===Introduction=== | ===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 | + | One of the goals of iGEM24-SCUT-China-A is to use synthetic biology tools to obtain <i>Halomonas</i> TD strains that can <b>metabolize formate</b>. We chose to <b>introduce the formate assimilation pathway</b> to enable it to utilize formate, a difficult-to-recover product in CDE. For the first method, <b>based on previous studies obtained from literature research</b>, we <b>selected the tetrahydrofolate (THF) cycle imported from <i>Methylobacterium extorquens</i> AM1 and strengthened the endogenous C2 and C3 modules of <i>Halomonas</i> TD</b>. |
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===Usage and Biology=== | ===Usage and Biology=== | ||
− | TD-SdaA is L-serine dehydratase.The protein sequence is from Halomonas sp. TD01 strain.This protein catalyzes the conversion of L-serine into pyruvate during the glycine assimilation(C3M) | + | TD-SdaA is <b>L-serine dehydratase<ib>.The protein sequence is from <i>Halomonas sp.</b> TD01 strain.This protein <b>catalyzes the conversion of L-serine into pyruvate during the glycine assimilation(C3M)</b> . |
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<!-- Uncomment this to enable Functional Parameter display | <!-- Uncomment this to enable Functional Parameter display |
Latest revision as of 09:18, 13 September 2024
TD-sdaA
Sequence and Features
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal XbaI site found at 1119
Illegal SpeI site found at 646 - 12INCOMPATIBLE WITH RFC[12]Illegal SpeI site found at 646
- 21COMPATIBLE WITH RFC[21]
- 23INCOMPATIBLE WITH RFC[23]Illegal XbaI site found at 1119
Illegal SpeI site found at 646 - 25INCOMPATIBLE WITH RFC[25]Illegal XbaI site found at 1119
Illegal SpeI site found at 646 - 1000COMPATIBLE WITH RFC[1000]
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 and strengthened the endogenous C2 and C3 modules of Halomonas TD.
Usage and Biology
TD-SdaA is L-serine dehydratase<ib>.The protein sequence is from Halomonas sp.</b> TD01 strain.This protein <b>catalyzes the conversion of L-serine into pyruvate during the glycine assimilation(C3M)</b> .