Difference between revisions of "Part:BBa K4759001:Design"
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===Design Notes=== | ===Design Notes=== | ||
− | Co-expressed with other components,and Olep is selected to synthesize the above gene by adding histidine tags at the C-terminus through E. coli codon optimization and subcloning the above genes onto the plasmid pET-28a to obtain the recombinant plasmid pET-28a-oleP. | + | Co-expressed with other components,and Olep is selected to synthesize the above gene by adding histidine tags at the C-terminus through <i>E. coli</i> codon optimization and subcloning the above genes onto the plasmid pET-28a to obtain the recombinant plasmid pET-28a-oleP. |
===Source=== | ===Source=== | ||
− | P450 enzyme CYP107D1 derived from Streptomyces, abbreviated as Olep | + | P450 enzyme CYP107D1 derived from <i>Streptomyces</i>, abbreviated as Olep |
===References=== | ===References=== | ||
− | [1] G P, I F, C E, et al. Dissecting the Cytochrome P450 OleP Substrate Specificity: Evidence for a Preferential Substrate[J]. Biomolecules, 2020, 10(10). | + | [1] G P, I F, C E, et al. Dissecting the Cytochrome P450 OleP Substrate Specificity: Evidence for a Preferential Substrate[J]. Biomolecules, 2020, 10(10).<br> |
[2] B H, H Y, J Z, et al. Whole-Cell P450 Biocatalysis Using Engineered Escherichia coli with Fine-Tuned Heme Biosynthesis[J]. Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2023, 10(6): e2205580 | [2] B H, H Y, J Z, et al. Whole-Cell P450 Biocatalysis Using Engineered Escherichia coli with Fine-Tuned Heme Biosynthesis[J]. Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2023, 10(6): e2205580 |
Latest revision as of 06:43, 12 October 2023
OleP
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 16
Illegal AgeI site found at 114 - 1000COMPATIBLE WITH RFC[1000]
Design Notes
Co-expressed with other components,and Olep is selected to synthesize the above gene by adding histidine tags at the C-terminus through E. coli codon optimization and subcloning the above genes onto the plasmid pET-28a to obtain the recombinant plasmid pET-28a-oleP.
Source
P450 enzyme CYP107D1 derived from Streptomyces, abbreviated as Olep
References
[1] G P, I F, C E, et al. Dissecting the Cytochrome P450 OleP Substrate Specificity: Evidence for a Preferential Substrate[J]. Biomolecules, 2020, 10(10).
[2] B H, H Y, J Z, et al. Whole-Cell P450 Biocatalysis Using Engineered Escherichia coli with Fine-Tuned Heme Biosynthesis[J]. Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2023, 10(6): e2205580