pTEV5_ RpMatB_1
(Plasmid
#78205)
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PurposeExpression of double-cysteine variant of Malonyl-coenzyme A synthetase, RpMatB, as scaffold for ATP biosensor
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Depositing Lab
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Sequence Information
Full plasmid sequence is not available for this item.
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 78205 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepTEV5
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Vector typeBacterial Expression
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)DH5alpha
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Growth instructionsuse OverExpress C41(DE3) for protein expression
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Copy numberHigh Copy
Gene/Insert
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Gene/Insert namematB (His6 C106A R286C Q457C K488A)
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SpeciesRhodopseudomonas palustris
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MutationC106A R286C Q457C K488A
- Promoter T7
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Tag
/ Fusion Protein
- His6 (N terminal on backbone)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site Unknown (unknown if destroyed)
- 3′ cloning site Unknown (unknown if destroyed)
- 5′ sequencing primer T7
- 3′ sequencing primer T7 terminal (Common Sequencing Primers)
Resource Information
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Supplemental Documents
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 plasmid is used to express Malonyl-coenzyme A synthetase from Rhodopseudomonas palustris (RpMatB), containing a His-tag and the mutations C106A, R286C, Q457C and K488A: (His6/C106A/R286C/Q457C/K488A)RpMatB.
The protein is modified for use as the scaffold of an ATP biosensor, Rho-RpMatB. The two cysteine mutations are for label attachment (R286C and Q457C); there is a mutation to prevent enzyme activity (K488A), a mutation to change the wild-type cysteine (C106A) and an N-terminal His-tag to aid purification.
When labelled with two 5-iodoacetamidotetramethylrhodamine (5-IATR) fluorophores, this adduct can be used as an ATP biosensor has a fluorescence intensity change of 3.7-fold. With a Kd of ~6 μM, this can be used to measure ATP formation in the range of up to ~20 micromolar, in the presence hundreds of micromolar ADP.
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:
pTEV5_ RpMatB_1 was a gift from Martin Webb (Addgene plasmid # 78205 ; http://n2t.net/addgene:78205 ; RRID:Addgene_78205) -
For your References section:
A Fluorescent, Reagentless Biosensor for ATP, Based on Malonyl-Coenzyme A Synthetase. Vancraenenbroeck R, Webb MR. ACS Chem Biol. 2015 Nov 20;10(11):2650-7. doi: 10.1021/acschembio.5b00346. Epub 2015 Sep 21. 10.1021/acschembio.5b00346 PubMed 26355992