Difference between revisions of "Part:BBa K3866024"
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<partinfo>BBa_K3866024 short</partinfo> | <partinfo>BBa_K3866024 short</partinfo> | ||
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− | + | [[Image:T--Thessaly--YgfG0snap.png|800px|thumb|none|<I><b>Figure 1.</b> The level 0 module : pupd2- sbm (illustration from SnapGene)</i>]] | |
+ | |||
===Usage and Biology=== | ===Usage and Biology=== | ||
− | + | Catalyzes the decarboxylation of (R)-methylmalonyl-CoA to propionyl-CoA. Could be part of a pathway that converts succinate to propanoate. | |
− | + | ||
− | + | ||
+ | ===Design Notes=== | ||
+ | The sequence was domesticated. We removed BsmBI, BsaI, BtgZI, BpiI sites in order to be compatible with GoldenBraid and MoClo. The sequence is cloned in pUPD2 <bbpart>BBa_K3505007</bbpart> and has overhangs compatible for Golden Braid cloning. | ||
+ | This has position B2-B5. | ||
+ | |||
+ | [[Image: T--Thessaly--GB-AATG-GCTT.jpeg|800px|thumb|none|<i><b>Figure 1.</b>The overhangs of this part in the GoldenBraid Grammar</i>]] | ||
+ | |||
+ | ===Verification of cloning=== | ||
+ | |||
+ | [[File:T--Thessaly--YgfG0--digestion.png|800px|thumb|none|<i><b>Figure 3.</b> (C= Cut, U=Uncut) Restriction digestion of pUPD2-Sbm (C7 + C8) with: EcoRI, Expected bands: 2518bp, 1733bp, Positive result: C7 + C8</i>]] | ||
+ | |||
+ | ===Source=== | ||
+ | Synthesized by IDT. | ||
+ | |||
+ | ===Sequence and Features=== | ||
+ | <partinfo>BBa_K3866024 SequenceAndFeatures</partinfo> | ||
− | + | ===References=== | |
− | === | + | Haller T, Buckel T, Rétey J, Gerlt JA (2000). Discovering newenzymes and metabolic pathways: conversion of succinate to |
− | + | propionate by Escherichia coli. Biochemistry, 39:4622–4629. https://doi.org/10.1021/bi992888d | |
− | + |
Revision as of 21:10, 25 September 2021
ygfG - Methylmalonyl-CoA decarboxylase GB compatible with B2-B5
Usage and Biology
Catalyzes the decarboxylation of (R)-methylmalonyl-CoA to propionyl-CoA. Could be part of a pathway that converts succinate to propanoate.
Design Notes
The sequence was domesticated. We removed BsmBI, BsaI, BtgZI, BpiI sites in order to be compatible with GoldenBraid and MoClo. The sequence is cloned in pUPD2 BBa_K3505007 and has overhangs compatible for Golden Braid cloning. This has position B2-B5.
Verification of cloning
Source
Synthesized by IDT.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 173
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 632
References
Haller T, Buckel T, Rétey J, Gerlt JA (2000). Discovering newenzymes and metabolic pathways: conversion of succinate to propionate by Escherichia coli. Biochemistry, 39:4622–4629. https://doi.org/10.1021/bi992888d