BfAra43B (exo-α-Arabinofuranosidase)

BfAra43B

Endo-Gal0157

(EC. 3.2.1) exo-α-Arabinofuranosidase

CAZy Family: GH43


PROPERTIES

ELECTROPHORETIC PURITY

-Single band on SDS-gel electrophoresis (MW ~34 kDa)

Figure 1. Electrophoresis analysis of BfAra43B. 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, BfAra43B purified from Ni sepharose fastflow column.



RELATIVE RATES OF HYDROLYSIS OF SUBSTRATES

Table 1. Relative activity of BfAra43B on different substratesa.

Substrateb

Relative activity (%)c

pNPβGlc

_

pNPβGal

91.2±0.6

pNPβMan

_

pNPβXyl

_

pNPαGlc

_

pNPαGal

_

pNPαMan

_

pNPαAraf

100.0±0.6

pNPαArap

_

aReactions were performed with 5 mM substrate, pH 7.0, at 37°C for 5 min.

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

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


PHYSICOCHEMICAL PROPERTIES


pH Optima: suggested use 7.0

Temperature Optima: suggested use 37°C



STORAGE CONDITIONS

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

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BfAra43B (exo-α-Arabinofuranosidase)

BfAra43B

Endo-Gal0157

(EC. 3.2.1) exo-α-Arabinofuranosidase

CAZy Family: GH43


PROPERTIES

ELECTROPHORETIC PURITY

-Single band on SDS-gel electrophoresis (MW ~34 kDa)

Figure 1. Electrophoresis analysis of BfAra43B. 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, BfAra43B purified from Ni sepharose fastflow column.



RELATIVE RATES OF HYDROLYSIS OF SUBSTRATES

Table 1. Relative activity of BfAra43B on different substratesa.

Substrateb

Relative activity (%)c

pNPβGlc

_

pNPβGal

91.2±0.6

pNPβMan

_

pNPβXyl

_

pNPαGlc

_

pNPαGal

_

pNPαMan

_

pNPαAraf

100.0±0.6

pNPαArap

_

aReactions were performed with 5 mM substrate, pH 7.0, at 37°C for 5 min.

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

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


PHYSICOCHEMICAL PROPERTIES


pH Optima: suggested use 7.0

Temperature Optima: suggested use 37°C



STORAGE CONDITIONS

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