Coding

Part:BBa_K5226007

Designed by: Yujiao Yang   Group: iGEM24_SCUT-China-A   (2024-07-28)
Revision as of 14:18, 28 July 2024 by Admin (Talk | contribs)


TD-glyA

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-GlyA is Serine hydroxymethyltransferase .The protein sequence is from Halomonas sp. TD01 strain.This protein catalyzes the reversible interconversion of serine and glycine with tetrahydrofolate (THF) serving as the one-carbon carrier. This reaction serves as the major source of one-carbon groups required for the biosynthesis of purines, thymidylate, methionine, and other important biomolecules. Also exhibits THF-independent aldolase activity toward beta-hydroxyamino acids, producing glycine and aldehydes, via a retro-aldol mechanism.. This part is used in BBa_xx and BBa_xx.

Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal PstI site found at 626
    Illegal PstI site found at 754
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 480
    Illegal PstI site found at 626
    Illegal PstI site found at 754
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal PstI site found at 626
    Illegal PstI site found at 754
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal PstI site found at 626
    Illegal PstI site found at 754
    Illegal AgeI site found at 985
  • 1000
    COMPATIBLE WITH RFC[1000]


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Categories
Parameters
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