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ORIGIN Rhizopus sp. SPECIFICATIONS Appearance White Lyophilised Powder Activity 30 U/mg powder at 40°C APPLICATION Used in the determination of alpha Amylase. UNIT DEFINITION One unit causes the formation of ten milligrams of glucose in 30 minutes at 40°C under standard assay method conditions. ASSAY PRINCIPLE Glucoamylase catalyses the following reaction: Starch + nH 2 O n Glucose + Dextrin The formation of glucose is measured as a reducing sugar by the modified Fehling-Lehmann-School Method. Glucoamylase ENZYMES CAT# GLUC-70-6881 EC# 3.2.1.1.2 CAT# GLUC-70-6881 EC# 3.2.1.1.2 ENZYMES Glucoamylase Molecular Weight: ~70kDa K m values: Maltose 11 ± 1.1 x 10 -4 M Maltotriose 3.6 ± 0.51 x 10 -4 M Maltotetraose 2.5 ± 0.33 x 10 -4 M Maltopentaose 1.6 ± 0.02 x 10 -4 M Optimum pH (Fig. 1): 4.5 to 5.0 Optimum Temperature (Fig. 2): 60°C pH Stability (Fig. 3): 4.0 to -8.5 (25°C for 20 hours) Thermal Stability (Fig. 4): Stable at 45°C and below (pH 5.5 for 10 minutes) Substrate Specificity: Hydrolyses soluble starch amylopectin, glycogen, α- or β- limit dextrin, amylose, maltooligosaccharides, and panose. CHARACTERISTICS

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O R I G I N Rhizopus sp.

� S P E C I F I C A T I O N SAppearance White Lyophilised PowderActivity ≥30 U/mg powder at 40°C

� A P P L I C A T I O NUsed in the determination of alpha Amylase.

� U N I T D E F I N I T I O NOne unit causes the formation of ten milligrams of glucose in 30 minutes at 40°C under standard assay method conditions.

� A S S AY P R I N C I P L EGlucoamylase catalyses the following reaction:

Starch + nH2O n Glucose + Dextrin

The formation of glucose is measured as a reducing sugar by the modified Fehling-Lehmann-School Method.

GlucoamylaseE N Z Y M E S

CAT# G

LUC-70-6881

EC# 3.2.1.1.2

C A T # G L U C - 7 0 - 6 8 8 1E C # 3 . 2 . 1 . 1 . 2

EN

ZY

ME

S

Glucoamylase

Molecular Weight: ~70kDa

Kmvalues: Maltose 11 ± 1.1 x 10-4 MMaltotriose 3.6 ± 0.51 x 10-4 MMaltotetraose 2.5 ± 0.33 x 10-4 MMaltopentaose 1.6 ± 0.02 x 10-4 M

Optimum pH (Fig. 1): 4.5 to 5.0

Optimum Temperature (Fig. 2): 60°C

pH Stability (Fig. 3): 4.0 to -8.5 (25°C for 20 hours)

Thermal Stability (Fig. 4): Stable at 45°C and below (pH 5.5 for 10 minutes)

Substrate Specificity: Hydrolyses soluble starch amylopectin, glycogen, α- or β- limit dextrin, amylose, maltooligosaccharides, and panose.

� C H A R A C T E R I S T I C S

CAT# G

LUC-70-6881

EC# 3.2.1.1.2

EN

ZY

ME

SRELATIVE ACTIVITY (%)

pH

120

100

80

60

40

20

0

20 30 40 50 60

F IGURE 1 : OP T IMUM pH

F IGURE 4 : pH S TAB I L I TY(pH 5 . 5 FOR 10 M INUTES )

F IGURE 2 : OP T IMUM T EMPERATURE

F IGURE 3 : THERMAL S TAB I L I TY(25 °C FOR 20 HOURS )

RELATIVE ACTIVITY (%)

TEMPERATURE (°C)

120

100

80

60

40

20

0

50 60 70

RESIDUAL ACTIVITY (%)

pH

120

100

80

60

40

20

0

3 4 5 6 7 8 9 10

RESIDUAL ACTIVITY (%)

TEMPERATURE (°C)

120

100

80

60

40

20

0

42 44 46 48 50 52 54 56 58 60

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