ADP–DEPENDENT HEXOKINASE [ADP–HKPⅡ]
from Pyrococcus furiosus
(ADP: D-glucose 6-phosphotransferase, EC 2.7.1.147)
D–Glucose + ADP → D–Glucose–6–phosphate + AMP
Preparation and Specification
- Appearance
- : White amorphous powder, lyophilized
- Specific activity
- : More than 30 U/mg solid
Properties
- Substrate specificity
- : See Table 1
- Molecular weight
- : 100 kDa (gel filtration) , 51 kDa (SDS–PAGE)
- Isoelectric point
- : pH 5.1
- Michaelis constants
- : Glucose 0.64 mM (at 37℃)
ADP 0.07 mM (at 37℃)
- Optimum pH
- : 7.5Figure 1
- pH stability
- : 5.0–10.0 (37℃, 1hr) Figure 2
- Optimum temperature
- : 100℃Figure 3
- Thermal stability
- : Stable at 95℃ and belowFigure 4
- Activator
- : Mg2+, Co2+, Mn2+
Applications for Diagnostic Test
This enzyme is useful for enzymatic determination of ADP.
| ADP－HKP Ⅱ | ||
| ADP + D － Glucose | → | AMP + D－Glucose－6－phosphate |
| G6PDH | ||
| D－Glucose－6－phosphate + NADP＋ | → | D－Glucono－δ－lactone－6－phosphate + NADPH + H＋ |
Table 1. Substrate specificity
| Substrate (20mM) | Relative
activity (%) |
|---|---|
| D–Glucose | 100 |
| D–Mannose | 12 |
| D–Galactose | 7 |
| D–Fructose | 0 |
| 2–deoxy–D–Glucose | 3 |
| D–Glucosamine | 72 |
| D–1, 5–Anhydroglucitol | 68 |
| D–Sorbitol | 0 |
| D–Myoinocitol | 0 |
| D–Mannitol | 0 |
| Sucrose | 0 |
Fig.1 Optimum
〇: Acetate buffer
□: Citrate buffer
△: Phosphate buffer
●: Tris-HCI buffer
■: Glycine-NaOH buffer
□: Citrate buffer
△: Phosphate buffer
●: Tris-HCI buffer
■: Glycine-NaOH buffer
Fig.2 pH Stability
37℃, 60 min.
〇: Acetate buffer
□: Citrate buffer
△: Phosphate buffer
●: Tris-HCI buffer
■: Glycine-NaOH buffer
〇: Acetate buffer
□: Citrate buffer
△: Phosphate buffer
●: Tris-HCI buffer
■: Glycine-NaOH buffer
Fig.3 Optimum Temperature
pH 7.5
50 mM Tris-HCI buffer
50 mM Tris-HCI buffer
Fig.4 Thermal Stability
pH 7.5, 10min.
50 mM Tris-HCI buffer
50 mM Tris-HCI buffer
Assay
Principle
-
The assay is based on the increase in absorbance at 340nm as the formation of NADPH proceeds in the following reactions:
| ADP–HKP II | ||
| ADP+D–Glucose | → | AMP+D–Glucose–6–phosphate |
| Mg2+ | ||
| G6PDH | ||||
| D–Glucose–6–phosphate+NADP | → | |||
| +D–Glucono–δ–lactone–6–phosphate+NADPH+H+ | ||||
Unit definition
-
One unit is defined as the amount of enzyme which converts 1 μmole of glucose to D–Glucose–6–phosphate per minute at 37℃ under the conditions specified in the assay procedure.
Reagents
- Reaction mixture
0.1M Tris–HCl Buffer pH7.5 1.50 ml 0.2M Glucose solution 0.30 ml
-
20mM ADP solution 0.30 ml 20mM MgCl2 solution 0.30 ml 10mM NADP solution 0.30 ml 50U/ml G6PDH solution 0.30 ml - Enzyme dilution buffer
10mM Tris–HCl Buffer pH7.5 (25℃) - Reagents:
Tris (hydroxymethyl) aminomethane : Sigma Chemical Co.
#T–1503Glucose:FUJIFILM Wako Pure Chemical Corporation
#041–00595ADP (Adenosine diphosphate・2 Na) :Oriental yeast Co.,Ltd.
MgCl2・6 H2O:
FUJIFILM Wako Pure Chemical Corporation
#131–00162
NADP (Nicotinamide adenine dinucleotide oxidized form) :
FUJIFILM Wako Pure Chemical Corporation
#308–50463G6PDH Ⅱ (Glucose–6–phosphate dehydrogenase) :
Asahi Kasei Pharma Corporation #T–51
Enzyme solution
Accurately weigh about 20 mg of the sample and add enzyme dilution buffer to make a total of 20 ml.
Dilute it with enzyme dilution buffer to adjust the concentration as required.
Procedure
- Pipette accurately 3.0 ml of reaction mixture into a small test tube and preincubate at 37℃.
- After 5 min add accurately 50μl of enzyme solution and mix to start the reaction at 37℃.
※ In the case of a test blank, add 50μl of enzyme dilution buffer in place of enzyme solution. - After starting the reaction, measure the rate of increase per minutes in absorbance at 340 nm. The rate must be measured within the linear portion of the absorbance curve.
(Ex. Linear range from 2 min to 6 min)
Calculation
Activity (U/mg of powder) = {(△ A/min)/6.22} × 3.05/0.05 × 1/x-
6.22 : millimolar extinction coefficient of NADPH at 340nm ( cm2 /μmol)3.05 : final volume (ml) 0.05 : volume of enzyme solution (ml) X : concentration of the sample in enzyme solution ( mg/ml)
Storage
-
Storage at －20℃ in the presence of a desiccant is recommended.
References
- Koga, S., Yoshioka, I., Sakuraba, H., Takahashi, M., Sakasegawa, S., Shimizu S. and Ohshima T. (2000) J. Biochem. (Tokyo) , 128, 1079–1085.
- Ito, S., Fushinobu, S., Yoshioka, I., Koga, S., Matsuzawa, H. and Wakagi, T. (2001) Structure, 9, 205–214.
ADP–HKP Ⅱ活性測定法 (Japanese)
試薬液
- 反応試薬混合液
0.1M トリス–HCl 緩衝液 pH7.5 1.50 ml 0.2M グルコース溶液 0.30 ml 20mM ADP 溶液液 0.30 ml 20mM 塩化マグネシウム溶液 0.30 ml 10mM NADP 溶液 0.30 ml 50U/ml G6PDH 溶液 0.30 ml - 第二反応試薬混合液
10mM トリス–HCl 緩衝液 pH7.5 (25℃) - 試薬
トリス (ヒドロキシメチル) アミノメタン：シグマ製 #T–1503
グルコース：富士フイルム和光純薬製 特級#041–00595
ADP (アデノシン二リン酸・2Na) ：オリエンタル酵母製塩化マグネシウム (MgCl2・6H2O) ：富士フイルム和光純薬製 特級 #131–00162NADP (ニコチンアミドアデニンジヌクレオチドリン酸酸化型) ：富士フイルム和光純薬製 #308–50463
G6PDH Ⅱ (グルコース–6– リン酸脱水素酵素) ：旭化成ファーマ製 #T–51
酵素試料液
- 検品約20mg を精密に量り、酵素溶解希釈用液で溶解して全容20ml とする。
その液を酵素溶解希釈用液で適宜希釈する。
測定操作法
- 小試験管に第一反応試薬混合液1.0ml を正確に分注して37℃で予備加温する。
- 5 分経過後、酵素試料液50 μl を正確に加えて混和し、37℃で反応を開始する。
※ 盲検は酵素試料液の代わりに酵素溶解希釈用液50μl を加える。 - 反応開始後、340nm における吸光度を測定して直線的に反応している1 分間当たりの吸光度変化を求める。 (直線範囲例：2 分目から6 分目まで) 求められた吸光度変化を
-
試料液についてはAs/min
盲検液についてはAb/min とする。
※吸光度範囲
Δ A/min = (As/min－Ab/min) ≦ 0.120Abs/min
-
試料液についてはAs/min
計算
以下の計算式に従い、活性 (U/mg) を計算する。活性 (U/mg) = {(△ A/min)/6.22} × 3.05/0.05 × 1/x
| 6.22 : | NADPH の340nm におけるミリモル分子吸光係数 (cm2 / μmol) |
| 3.05 : | 反応総液量 (ml) |
| 0.05 : | 反応に供した酵素試料液量 (ml) |
| X : | 酵素試料液中の検品濃度 (mg/ml) |
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