Difference between revisions of "Part:BBa K2753002"
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<partinfo>BBa_K2753002 short</partinfo> | <partinfo>BBa_K2753002 short</partinfo> | ||
− | <p>GPPS: Geranyl diphosphate (GPP), the entry point to the formation of terpene moiety, is a product of the condensation of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP) by GPP synthase (GPPS)<sup>[1]</sup>. IPP and DMAPP are supplied by either MVA pathway or MEP pathway or both depending on species. This parts originated from the species Abies Grandis, and it’s codon-optimized for the use in E. coli.</p | + | <p>GPPS: Geranyl diphosphate (GPP), the entry point to the formation of terpene moiety, is a product of the condensation of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP) by GPP synthase (GPPS)<sup>[1]</sup>. IPP and DMAPP are supplied by either MVA pathway or MEP pathway or both depending on species. This parts originated from the species Abies Grandis, and it’s codon-optimized for the use in E. coli.</p> |
<html> | <html> | ||
<center> | <center> | ||
<Figure> | <Figure> | ||
− | <img width="70%" src=" | + | <img width="70%" src="https://static.igem.org/mediawiki/2018/9/97/T--GreatBay_China--_GPPS_pathway.png"> |
<figcaption>Fig.1 The biosynthesis pathway for GPP <sup>[2]</sup>.</figcaption> | <figcaption>Fig.1 The biosynthesis pathway for GPP <sup>[2]</sup>.</figcaption> | ||
</figure> | </figure> | ||
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<br/> | <br/> | ||
+ | ===Characterization=== | ||
+ | <p>In our study, to investigate the optimal expression level of GPPS and GES for geraniol production, we assembled GPPS and obGES to make a geraniol-generating operon without a promoter(Part#), We employed three different promoters: </p><br> | ||
+ | <ul> | ||
+ | <li>pTALE sp1 (https://parts.igem.org/Part:BBa_K2753000), copy number-independent promoter of medium strength</li> | ||
+ | <li>pTALE sp2 (https://parts.igem.org/Part:BBa_K2753001), copy number-independent promoter of low strength</li> | ||
+ | <li>pTac (https://parts.igem.org/Part:BBa_K180000), IPTG inducible promoter</li> | ||
+ | </ul> | ||
+ | <p>And three vectors of unique copy number:</p><br> | ||
+ | <ul> | ||
+ | <li>pUC20: ~500</li> | ||
+ | <li>pR6K: ~15</li> | ||
+ | <li>pSC101: ~1<li> | ||
+ | </ul> | ||
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− | |||
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− | |||
<span class='h3bb'>Sequence and Features</span> | <span class='h3bb'>Sequence and Features</span> | ||
<partinfo>BBa_K2753002 SequenceAndFeatures</partinfo> | <partinfo>BBa_K2753002 SequenceAndFeatures</partinfo> |
Revision as of 10:00, 1 October 2018
pSB1C3-GPPS cds
GPPS: Geranyl diphosphate (GPP), the entry point to the formation of terpene moiety, is a product of the condensation of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP) by GPP synthase (GPPS)[1]. IPP and DMAPP are supplied by either MVA pathway or MEP pathway or both depending on species. This parts originated from the species Abies Grandis, and it’s codon-optimized for the use in E. coli.
Characterization
In our study, to investigate the optimal expression level of GPPS and GES for geraniol production, we assembled GPPS and obGES to make a geraniol-generating operon without a promoter(Part#), We employed three different promoters:
- pTALE sp1 (https://parts.igem.org/Part:BBa_K2753000), copy number-independent promoter of medium strength
- pTALE sp2 (https://parts.igem.org/Part:BBa_K2753001), copy number-independent promoter of low strength
- pTac (https://parts.igem.org/Part:BBa_K180000), IPTG inducible promoter
And three vectors of unique copy number:
- pUC20: ~500
- pR6K: ~15
- pSC101: ~1
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Referece
[1]: Rai, A., Smita, S. S., Singh, A. K., Shanker, K., & Nagegowda, D. A. (2013). Heteromeric and Homomeric Geranyl Diphosphate Synthases from Catharanthus roseus and Their Role in Monoterpene Indole Alkaloid Biosynthesis. Molecular Plant, 6(5), 1531–1549. doi:10.1093/mp/sst058
[2]: Zebec, Z., Wilkes, J., Jervis, A. J., Scrutton, N. S., Takano, E., & Breitling, R. (n.d.). Towards synthesis of monoterpenes and derivatives using synthetic biology. Current Opinion in Chemical Biology, 34, 37–43. https://doi.org/10.1016/j.cbpa.2016.06.002