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Purpose(Empty Backbone) Plasmid for gene replacement using kanamycin/sucrose selection/counterselection. Derived from pK18mobsacB but reduced in size.
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 177839 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepK18sB
- Backbone size (bp) 3282
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Vector typeBacterial gene replacement
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Selectable markersCounterselection: Sucrose
Growth in Bacteria
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Bacterial Resistance(s)Kanamycin, 50 μg/mL
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Growth Temperature37°C
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Growth Strain(s)DH5alpha
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Copy numberUnknown
Cloning Information
- Cloning method Gibson Cloning
- 5′ sequencing primer Special M13R binding site, M13R: CAGGAAACAGCTATGAC
- 3′ sequencing primer M13F: TGTAAAACGACGGCCAGT (Common Sequencing Primers)
Resource Information
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Supplemental Documents
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A portion of this plasmid was derived from a plasmid made bySequences were derived from pK18mobsacB (ATCC 87097)
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.
Depositor Comments
The sequence for this plasmid has been deposited with Genbank (Accession # OK423783).
Sequences were derived from pK18mobsacB (ATCC 87097), which was originally described in Schäfer, A., Tauch, A., Jäger, W., Kalinowski, J., Thierbach, G., Pühler, A., 1994. Small mobilizable multi-purpose cloning vectors derived from the Escherichia coli plasmids pK18 and pK19: selection of defined deletions in the chromosome of Corynebacterium glutamicum. Gene 145, 69–73. doi:10.1016/0378-1119(94)90324-7
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:
pK18msB was a gift from Christopher Johnson (Addgene plasmid # 177839 ; http://n2t.net/addgene:177839 ; RRID:Addgene_177839) -
For your References section:
Muconic acid production from glucose and xylose in Pseudomonas putida via evolution and metabolic engineering. Ling C, Peabody GL, Salvachua D, Kim YM, Kneucker CM, Calvey CH, Monninger MA, Munoz NM, Poirier BC, Ramirez KJ, St John PC, Woodworth SP, Magnuson JK, Burnum-Johnson KE, Guss AM, Johnson CW, Beckham GT. Nat Commun. 2022 Aug 22;13(1):4925. doi: 10.1038/s41467-022-32296-y. 10.1038/s41467-022-32296-y PubMed 35995792