Difference between revisions of "Part:BBa K5089003:Design"
Line 16: | Line 16: | ||
===References=== | ===References=== | ||
+ | 1. Hajighasemi, M., et al., 2016. Biochemical and Structural Insights into Enzymatic. Depolymerization of Polylactic Acid and Other Polyesters by Microbial Carboxylesterases. Biomacromolecules, 17(6), 2027–2039. https://doi.org/10.1021/acs.biomac.6b00223 |
Latest revision as of 20:40, 29 September 2024
MGS0156
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NotI site found at 457
- 21INCOMPATIBLE WITH RFC[21]Illegal XhoI site found at 1059
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 159
Illegal NgoMIV site found at 330 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 843
Design Notes
This expression system is codon optimized for expression in E.coli.
Source
MGS0156 is a serine-dependent ⍺/β hydrolase originally identified from an environmental metagenomic analysis study to look for enzymes to degrade PLA[1]
References
1. Hajighasemi, M., et al., 2016. Biochemical and Structural Insights into Enzymatic. Depolymerization of Polylactic Acid and Other Polyesters by Microbial Carboxylesterases. Biomacromolecules, 17(6), 2027–2039. https://doi.org/10.1021/acs.biomac.6b00223