BtGal27C (exo-α-Galactosidase)

BtGal27C

Ex-Gal0034

(EC.3.2.1.22) exo-α-Galactosidase

CAZy Family: GH27


PROPERTIES

1.ELECTROPHORETIC PURITY

-Single band on SDS-gel electrophoresis (MW ~74kDa)

Figure 1. Electrophoresis analysis ofBtGal27C. M, molecular weight marker (PageRuler Prestained Protein Ladder, Thermo Scientific); lane 1, culture lysate before IPTG induction; lane 2, culture lysate after IPTG induction; lane 3,BtGal27C purified from Ni sepharose fastflow column.


2.SPECIFIC ACTIVITY

0.89 U/mg protein (on pNP-α-gal) at pH 7.0 and 37°C.

One Unit of pNP-α-gal activity is defined as the amount of enzyme required to release 1 μmol of p-nitrophenyl per minute from pNP-α-gal (5 mM) insodium phosphatebuffer(20 mM) pH7.0.



3.RELATIVE RATES OF HYDROLYSIS OF SUBSTRATES

Table 1. Relative activity of BtGal27C on different substratesa.

Substrateb

Relative activity (%)c

pNPαGlc

_

pNPβGlc

_

pNPαGal

100±0.0

pNPβGal

_

pNPαMan

_

pNPβMan

_

pNPαXyl

_

pNPβXyl

_

pNPαAraf

_

pNPαArap

_

pNPαRha

_

pNPαFuc

_

aReactions were performed with 5mM substrate, pH7.0, at 37°C for 5 min.

bAbsorption caused by released p-nitrophenol was measured at 405 nm. The relative activity on pNPαGal was taken as 100%.

cThe data are reported as means±standard errors from the mean for three independent experiments.


4.PHYSICOCHEMICAL PROPERTIES

pH Optima:7.0

Temperature Optima:37°C



5.STORAGE CONDITIONS

The enzyme should be stored at -20 °C. For assay, this enzyme should be diluted insodium phosphate buffer(20 mM) pH 7.0. Swirl to mix the enzyme immediately prior to use.

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BtGal27C (exo-α-Galactosidase)

BtGal27C

Ex-Gal0034

(EC.3.2.1.22) exo-α-Galactosidase

CAZy Family: GH27


PROPERTIES

1.ELECTROPHORETIC PURITY

-Single band on SDS-gel electrophoresis (MW ~74kDa)

Figure 1. Electrophoresis analysis ofBtGal27C. M, molecular weight marker (PageRuler Prestained Protein Ladder, Thermo Scientific); lane 1, culture lysate before IPTG induction; lane 2, culture lysate after IPTG induction; lane 3,BtGal27C purified from Ni sepharose fastflow column.


2.SPECIFIC ACTIVITY

0.89 U/mg protein (on pNP-α-gal) at pH 7.0 and 37°C.

One Unit of pNP-α-gal activity is defined as the amount of enzyme required to release 1 μmol of p-nitrophenyl per minute from pNP-α-gal (5 mM) insodium phosphatebuffer(20 mM) pH7.0.



3.RELATIVE RATES OF HYDROLYSIS OF SUBSTRATES

Table 1. Relative activity of BtGal27C on different substratesa.

Substrateb

Relative activity (%)c

pNPαGlc

_

pNPβGlc

_

pNPαGal

100±0.0

pNPβGal

_

pNPαMan

_

pNPβMan

_

pNPαXyl

_

pNPβXyl

_

pNPαAraf

_

pNPαArap

_

pNPαRha

_

pNPαFuc

_

aReactions were performed with 5mM substrate, pH7.0, at 37°C for 5 min.

bAbsorption caused by released p-nitrophenol was measured at 405 nm. The relative activity on pNPαGal was taken as 100%.

cThe data are reported as means±standard errors from the mean for three independent experiments.


4.PHYSICOCHEMICAL PROPERTIES

pH Optima:7.0

Temperature Optima:37°C



5.STORAGE CONDITIONS

The enzyme should be stored at -20 °C. For assay, this enzyme should be diluted insodium phosphate buffer(20 mM) pH 7.0. Swirl to mix the enzyme immediately prior to use.