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Recombinant E. coli N-Acetyl-D-Glucosamine Kinase/NAGK, CF 25 UG

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產(chǎn)品介紹

    基本參數(shù)

    詳細(xì)說(shuō)明

    • Purity

      >90%, by SDS-PAGE under reducing conditions and visualized by Colloidal Coomassie? Blue stain at 5 μg per lane

    • Endotoxin Level

      <0.01 EU per 1 μg of the protein by the LAL method.  

    • Activity

      Measured by its ability to phosphorylate N-acetyl-D-glucosamine. The specific activity is >10,000 pmol/min/μg, as measured under the described conditions. See Activity Assay Protocol on .

    • Source

      E. coli-derived Met1-Asp303 with C-terminal 6-His tag

    • Accession #

    • N-terminal Sequence    
      Analysis

      Met1

    • Predicted Molecular Mass

      34 kDa

    • SDS-PAGE

      37-38 kDa, reducing conditions

    8020-GK

     

    Formulation Supplied as a 0.2 μm filtered solution in Tris, NaCl, Glycerol, Brij-35 and DTT.





    Shipping The product is shipped with dry ice or equivalent. Upon receipt, store it immediately at the temperature recommended below.


    Stability & Storage:       Use a manual defrost freezer and avoid repeated freeze-thaw cycles.      

    • 6 months from date of receipt, -70 °C as supplied.

    • 3 months, -70 °C under sterile conditions after opening.


    Assay Procedure

    Materials

    • Assay Buffer: 25 mM HEPES, 150 mM NaCl, 10 mM MgCl2, 10 mM CaCl2, pH 7.0

    • Recombinant E.coli N?Acetyl?D?Glucosamine Kinase/NAGK (rE.coli NAGK) (Catalog # 8020-GK)

    • Adenosine triphosphate (ATP) (Sigma, Catalog # A7699), 10 mM stock in deionized water

    • N-acetyl-alpha -D-glucosamine (GlcNAc)  (Calbiochem, Catalog # 1079), 1 M stock in deionized water

    • Universal Kinase Activity Kit (Catalog # )

    • 96-well Clear Plate (Costar, Catalog # 92592)

    • Plate Reader (Model: SpectraMax Plus by Molecular Devices) or equivalent

    1. Dilute 1 mM Phosphate Standard provided by the Universal Kinase Activity Kit by adding 40 μL of the 1 mM Phosphate Standard to 360 μL of Assay Buffer for a 100 μM stock.

    2. Prepare standard curve by performing six one-half serial dilutions of the 100 μM Phosphate stock in Assay Buffer. The standard curve has a range of 0.078 to 5 nmol per well.

    3. Prepare a reaction mixture composed of 0.5 mM ATP and 12.5 mM GlcNAc in Assay Buffer.

    4. Dilute Coupling Phosphatase 4 (supplied in kit) to 10 μg/mL in Assay Buffer.

    5. Dilute rE.coli NAGK to 1 μg/mL in Assay Buffer.

    6. Load 50 μL of each dilution of the standard curve into a plate. Include a curve blank containing 50 μL of Assay Buffer.

    7. Load 20 μL of the 1 μg/mL rE.coli NAGK into the plate. Include a control containing 20 μL of Assay Buffer.

    8. Add 10 μL of 10 μg/mL Coupling Phosphatase 4 to the wells, excluding the standard curve.

    9. Add 20 μL of reaction mixture to the wells, excluding the standard curve.

    10. Cover the plate with a plate sealer and incubate at room temperature for 10 minutes.

    11. Add 30 μL of the Malachite Green Reagent A to all wells. Mix briefly.

    12. Add 100 μL of deionized water to all wells. Mix briefly.

    13. Add 30 μL of the Malachite Green Reagent B to all wells.  Mix and incubate for 20 minutes at room temperature.

    14. Read plate at 620 nm (absorbance) in endpoint mode.

    15. Calculate specific activity:

         Specific Activity (pmol/min/μg) =

    Phosphate released* (nmol) x (1000 pmol/nmol)
    Incubation time (min) x amount of enzyme (μg) x Coupling Rate**

         *Derived from the phosphate standard curve using linear or 4-parameter fitting and adjusted for control.
         ** Under these conditions, the coupling rate is 0.475.

    Per Reaction:

    • rE.coli NAGK: 0.020 μg

    • Coupling Phosphatase 4: 0.1 ug

    • ATP: 0.2 mM

    • GlcNAc: 5 mM

    Background: N-Acetyl-D-Glucosamine Kinase/NAGK

    N-acetylglucosamine (GlcNAc) and N-acetylmuramic acid (MurNAc) are repeating sugar units of peptidoglycan, the major component of bacterial cell wall structure and a drug target of various antibiotics including penicillin (1). Recently, interest has been generated regarding cell wall peptidoglycan catabolism, because as much as 50% of the peptidoglycan is turned over in one generation of bacterial growth (2). N-acetylglycosamine kinase (nagK) is a key enzyme for the recycling of GlcNAc in   E. coli (3). Due to its high activity, it can be used for efficient conversion of GlcNAc to GlcNAc-6-phosphate. The enzyme is assayed using a phosphatase-coupled kinase assay (4).

    • References:

      1. Plumbridge, J. (2009). J. Bacteriol. 191:5641.

      2. Reith, J. et al (2011). J. Bacteriol. 193:5386.

      3. Uehara, T. and Park, J.T.(2011) J. Bacteriol. 186:7273.

      4. Wu, Z.L. (2011) PLoS One 6:e23172.

    • Long Name:

      N-Acetyl-D-Glucosamine Kinase

    • Entrez Gene IDs:

      55577 (Human); 56174 (Mouse); 297393 (Rat); 945664 (E. coli)

    • Alternate Names:

      EC 2.7.1.59; GlcNAc Kinase; GNK; GNKGlcNAc kinase; N-acetyl-D-glucosamine kinase; N-Acetylglucosamine Kinase; N-acetylglucosamine kinaseHSA242910; NAGK



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