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PurposeBglBrick plasmid (=pBbA5a-MTSAe-T1f-MBI(f)-T1002i-Ptrc-trGPPS(co)-LS) coding for MEV pathway enzymes to produce limonene from glucose in E. coli
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 47049 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepBbA5a
- Backbone size w/o insert (bp) 3500
- Total vector size (bp) 15146
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Vector typeBacterial Expression, Synthetic Biology ; BglBrick
Growth in Bacteria
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Bacterial Resistance(s)Ampicillin, 100 μg/mL
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Growth Temperature37°C
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Growth Strain(s)DH10B
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Copy numberHigh Copy
Gene/Insert
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Gene/Insert nameCodon-optimized sequences for MEV pathway expression in E. coli to produce limonene
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SpeciesS. cerevisiae (budding yeast); Mentha spicata, Abies grandis and Staphylococcus aureus
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Insert Size (bp)11500
- Promoter PlacUV5
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site EcoRI, BglII (not destroyed)
- 3′ cloning site BamHI, XhoI (not destroyed)
- 5′ sequencing primer F1
- 3′ sequencing primer R1 (Common Sequencing Primers)
Resource Information
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Supplemental Documents
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Articles Citing this Plasmid
Terms and Licenses
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Academic/Nonprofit Terms
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Industry Terms
- Not Available to Industry
Trademarks:
- Zeocin® is an InvivoGen trademark.
These plasmids were created by your colleagues. Please acknowledge the Principal Investigator, cite the article in which the plasmids were described, and include Addgene in the Materials and Methods of your future publications.
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For your Materials & Methods section:
pJBEI-6410 was a gift from Taek Soon Lee (Addgene plasmid # 47049 ; http://n2t.net/addgene:47049 ; RRID:Addgene_47049) -
For your References section:
Metabolic engineering of Escherichia coli for limonene and perillyl alcohol production. Alonso-Gutierrez J, Chan R, Batth TS, Adams PD, Keasling JD, Petzold CJ, Lee TS. Metab Eng. 2013 May 29;19C:33-41. doi: 10.1016/j.ymben.2013.05.004. 10.1016/j.ymben.2013.05.004 PubMed 23727191