Difference between revisions of "Part:BBa K3767001"
(→Characterization) |
(→Characterization) |
||
Line 20: | Line 20: | ||
<partinfo>BBa_K3767001 SequenceAndFeatures</partinfo> | <partinfo>BBa_K3767001 SequenceAndFeatures</partinfo> | ||
− | |||
Revision as of 21:18, 18 October 2021
Alkaline Phosphatase optimized for E. Coli w/ 40x catalytic activity
This part is being registered as an improvement on a previously registered part BBa_K1216001. Our contribution altered the sequence to improve enzymatic activity and expression rates in E. Coli.
Usage and Biology
Alkaline phosphatase are plasma membrane-bound glycoproteins which are capable of hydrolyzing monophosphate esters resulting in the release of inorganic phosphate[3]. Dephosphorylation activity is catalyzed by two Zn2+ and one Mg2+ ions within the active site with both ions being required for enzymatic activity. In addition to this, both metal ions aid in structure conformation stability and subunit-subunit interactions.
The varying reaction mechanisms of this enzyme are well-conserved across animal and bacteria variants with either Ser, Thr, or Cys being modified within the active site during transfer (the residue used depends on the activity type)[4]. Additionally, the final phosphate receptor is conserved being either H2O, a secondary substrate, or another hydroxyl group within the same molecule. An illustration of the transfer of the phosphate group is depicted below.
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
References
1. Lowe, D., Sanvictores, T., and John, S. (2021) Alkaline Phosphatase, StatPearls Publishing, [online] http://www.ncbi.nlm.nih.gov/pubmed/29083622 (Accessed June 8, 2021)
2. Part:BBa K1216001 - parts.igem.org [online] https://parts.igem.org/Part:BBa_K1216001#References (Accessed June 8, 2021)
3. Sharma, U., Pal, D., and Prasad, R. (2014) Alkaline phosphatase: An overview. Indian J. Clin. Biochem. 29, 269–278
4. Millán, J. L. (2006) Alkaline phosphatases. Purinergic Signal. 2, 335–341
5. Du, M. H. L., Lamoure, C., Muller, B. H., Bulgakov, O. V., Lajeunesse, E., Ménez, A., and Boulain, J. C. (2002) Artificial evolution of an enzyme active site: Structural studies of three highly active mutants of Escherichia coli alkaline phosphatase. J. Mol. Biol. 316, 941–953