Recombinant S. cerevisiae PPA1 Protein, CF Summary
Details of Functionality |
Measured by its ability to hydrolyze pyrophosphate. The specific activity is >125,000 pmol/min/μg, as measured under the described conditions. |
Source |
E. coli-derived yeast Inorganic Pyrophosphatase/PPA1 protein Thr2-Val287, with an N-terminal Met and 6-His tag |
Accession # |
|
N-terminal Sequence |
Met |
Protein/Peptide Type |
Recombinant Enzymes |
Gene |
IPP1 |
Purity |
>80%, by SDS-PAGE under reducing conditions and visualized by Colloidal Coomassie® Blue stain at 5 μg per lane |
Endotoxin Note |
<0.01 EU per 1 μg of the protein by the LAL method. |
Applications/Dilutions
Dilutions |
|
Theoretical MW |
33 kDa. Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors. |
SDS-PAGE |
36 kDa, reducing conditions |
Packaging, Storage & Formulations
Storage |
Use a manual defrost freezer and avoid repeated freeze-thaw cycles.- 6 months from date of receipt, -20 to -70 °C as supplied.
- 3 months, -20 to -70 °C under sterile conditions after opening.
|
Buffer |
Supplied as a 0.2 μm filtered solution in Tris, NaCl, DTT and MgCl. |
Purity |
>80%, by SDS-PAGE under reducing conditions and visualized by Colloidal Coomassie® Blue stain at 5 μg per lane |
Assay Procedure |
- Assay Buffer: 25 mM MES, 8 mM MgCl2, pH 7.0
- Recombinant Yeast Inorganic Pyrophosphatase/PPA1 (ryPPA1) (Catalog # 8088-PP)
- Substrate: Sodium Pyrophosphate (Sigma, Catalog # P8010), 125 mM stock in deionized water
- Malachite Green Phosphate Detection Kit (Catalog # DY996)
- 96-well Clear Plate (Catalog # DY990)
- Plate Reader (Model: SpectraMax Plus by Molecular Devices) or equivalent
- Dilute 1 M Phosphate Standard by adding 10 µL of the 1 M Phosphate Standard to 990 µL of deionized water for a 10 mM stock. Continue by adding 10 µL of the 10 mM Phosphate stock to 990 µL of Assay Buffer for a 100 µM stock.
- Prepare the standard curve by performing seven one-half serial dilutions of the 100 µM Phosphate stock in Assay Buffer. The standard curve has a range of 0.039 to 2.5 nmol per well.
- Dilute Substrate to 1 mM in deionized water.
- Dilute ryPPA1 to 0.01 µg/mL in Assay Buffer.
- Load 50 µL of each dilution of the standard curve into a plate. Include a curve blank containing 50 μL of Assay Buffer.
- Load 25 µL of the 0.01 µg/mL ryPPA1 into the plate. Include a Substrate Blank containing 25 µL of Assay Buffer.
- Start the reaction by adding 25 µL of 1 mM Substrate to the wells, excluding the standard curve and curve blank.
- Incubate sealed plate at room temperature for 10 minutes.
- Add 30 µL of the Malachite Green Reagent A to all wells. Mix briefly.
- Add 100 µL of deionized water to all wells. Mix briefly.
- Add 30 µL of the Malachite Green Reagent B to all wells. Mix and incubate for 20 minutes at room temperature.
- Read plate at 620 nm (absorbance) in endpoint mode.
- Calculate specific activity:
Specific Activity (pmol/min/µg) = |
Phosphate released* (nmol) x (1000 pmol/nmol) |
Incubation time (min) x amount of enzyme (µg) x 2** |
*Derived from the phosphate standard curve using linear or 4-parameter fitting and adjusted for Substrate Blank. ** Note that 2 mol of phosphate are produced for every 1 mol of Pyrophosphate consumed. Per Reaction:
- ryPPA1: 0.00025 µg
- Sodium Pyrophosphate: 0.5 mM
|
Notes
This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.
Alternate Names for Recombinant S. cerevisiae PPA1 Protein, CF
Background
Inorganic pyrophosphatases are enzymes that catalyze the hydrolysis of pyrophosphate to two phosphate ions (1). This reaction is highly exergonic, and is utilized in many biochemical pathways, such as DNA synthesis (2) and bone formation (3), to render reactions effectively irreversible (4, 5). Likewise, inorganic pyrophosphatases can be coupled to unfavorable biochemical reactions in order to drive these reactions to completion, such as in the synthesis of activated sulfur donor 3’-phosphoadenosine-5’-phosphosulfate (PAPS) (6).
-
Harold, FM (1966) Bacteriol. Rev. 30:772.
- Nelson, D.L. and Cox, M.M. (2000) Lehninger Principles of Biochemistry, 3rd ed. pp.937. ISBN 1-57259-153-6.
- Poole, K.E. and Reeve, J. (2005) Curr. Opin. Pharmacol. 5:612.
- Takahashi, K. et al (2004) Biochem. Biophys. Res. Commun. 325:203.
- Terkeltaub, R.A. (2001) Am. J. Physiol., Cell Physiol. 281:C1.
- Wu, Z.L. et al (2010) BMC Biotechnology 10:11.
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