BtRgl9B(Rhamnogalacturonan lyase)

BtRgl9B

En-Rgl0180 

(EC. 4.2.2.23) Rhamnogalacturonan lyase

CAZy Family: PL9

 

PROPERTIES

1. ELECTROPHORETIC PURITY

-Single band on SDS-gel electrophoresis (MW ~47 kDa)

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Figure 1. Electrophoresis analysis of BtRgl9B. 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, BtRgl9B purified from Ni sepharose fast flow column.

 

2. SPECIFIC ACTIVITY

2.0 U/mg protein (on RG-I-AT from Adenophora tetraphylla(Thunb.)Fisch.) at pH 8.0 and 37°C.

One unit of RGL activity was defined as the amount of enzyme required to generate 1 mmol of 4,5-unsaturated galacturonic acid in 1 min.

 

3. RELATIVE RATES OF HYDROLYSIS OF SUBSTRATES

Table 1 Activity of BtRgl9B

Substrate

kcat(min-1)

Km (mM)

kcat/Km (mM-1min-1)

AM-RG-I

174.1 ± 5.0

0.020 ± 0.002

8.8 x 103 ± 1.2 x 103

Sugar beet arabinan

350.1 ± 10.2

0.059 ± 0.005

6.0 x 103 ± 706

P-RG-I

NA

 

4. PHYSICOCHEMICAL PROPERTIES

pH Optima: 7.5

Temperature Optima: 37°C

 

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Figure 2. Effect of pH on the activity of recombinant BtRgl9B. Assays were carried out at 37°C for 10 min in buffers ranging in pH from 5.5 to 11.0. The activity at optimum pH was defifined as 100%.

 

5. STORAGE CONDITIONS

The enzyme should be stored at -20°C. For assay, this enzyme should be diluted in phosphate buffer (50 mM) pH 8.0. Swirl to mix the enzyme immediately prior to use.

 

6. REFERENCE

[1] Luís A S. Microbial pectin recognition and utilization of the mammalian gastrointestinal tract[D]. Newcastle University, 2017.

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RGI果胶降解酶

BtRgl9B(Rhamnogalacturonan lyase)

BtRgl9B

En-Rgl0180 

(EC. 4.2.2.23) Rhamnogalacturonan lyase

CAZy Family: PL9

 

PROPERTIES

1. ELECTROPHORETIC PURITY

-Single band on SDS-gel electrophoresis (MW ~47 kDa)

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Figure 1. Electrophoresis analysis of BtRgl9B. 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, BtRgl9B purified from Ni sepharose fast flow column.

 

2. SPECIFIC ACTIVITY

2.0 U/mg protein (on RG-I-AT from Adenophora tetraphylla(Thunb.)Fisch.) at pH 8.0 and 37°C.

One unit of RGL activity was defined as the amount of enzyme required to generate 1 mmol of 4,5-unsaturated galacturonic acid in 1 min.

 

3. RELATIVE RATES OF HYDROLYSIS OF SUBSTRATES

Table 1 Activity of BtRgl9B

Substrate

kcat(min-1)

Km (mM)

kcat/Km (mM-1min-1)

AM-RG-I

174.1 ± 5.0

0.020 ± 0.002

8.8 x 103 ± 1.2 x 103

Sugar beet arabinan

350.1 ± 10.2

0.059 ± 0.005

6.0 x 103 ± 706

P-RG-I

NA

 

4. PHYSICOCHEMICAL PROPERTIES

pH Optima: 7.5

Temperature Optima: 37°C

 

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Figure 2. Effect of pH on the activity of recombinant BtRgl9B. Assays were carried out at 37°C for 10 min in buffers ranging in pH from 5.5 to 11.0. The activity at optimum pH was defifined as 100%.

 

5. STORAGE CONDITIONS

The enzyme should be stored at -20°C. For assay, this enzyme should be diluted in phosphate buffer (50 mM) pH 8.0. Swirl to mix the enzyme immediately prior to use.

 

6. REFERENCE

[1] Luís A S. Microbial pectin recognition and utilization of the mammalian gastrointestinal tract[D]. Newcastle University, 2017.