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Isopullulanase (Aspergillus niger)

Isopullulanase Aspergillus niger E-ISPUAN
Product code: E-ISPUAN
€162.00

2,000 Units at 40oC

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Available for shipping

Content: 2,000 Units at 40oC
Shipping Temperature: Ambient
Storage Temperature: Below -10oC
Formulation: In 50% (v/v) glycerol
Physical Form: Solution
Stability: > 4 years at 4oC
Enzyme Activity: Pullulanase/Limit-dextrinase
EC Number: 3.2.1.57
CAZy Family: GH49
CAS Number: 37288-43-0
Synonyms: Pullulan 4-glucanohydrolase (isopanose-forming)
Source: Aspergillus niger
Molecular Weight: 60,500
Concentration: Supplied at ~ 1,000 U/mL
Expression: Recombinant from Aspergillus niger
Specificity: Hydrolysis of pullulan to isopanose (6-α-maltosylglucose).
Specific Activity: ~ 65 U/mg (40oC, pH 3.5 on pullulan)
Unit Definition: One Unit of isopullulanase activity is defined as the amount of enzyme required to release one µmole of glucose reducing sugar equivalents per minute from pullulan (10 mg/mL) in formic acid buffer (100 mM), pH 3.5 at 40oC.
Temperature Optima: 40oC
pH Optima: 3.5
Application examples: For use in applications that involve hydrolysis of pullulan.

High purity recombinant Isopullulanase (Aspergillus niger) for use in research, biochemical enzyme assays and in vitro diagnostic analysis.

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Documents
Certificate of Analysis
Safety Data Sheet
Booklet
Publications
Publication

Structural characterization of mixed-linkage α-glucans produced by mutants of Lactobacillus reuteri TMW 1.106 dextransucrase.

Münkel, F., Fischer, A., & Wefers, D. (2020). Carbohydrate Polymers, 231, 115697.

Dextrans and other bacterial α-glucans are versatile and structurally diverse polysaccharides which can be enzymatically synthesized by using glucansucrases. By substituting certain amino acids in the active site of these enzymes, the structure of the synthesized polysaccharides can be modified. In this study, such amino acid substitutions were applied (single and combined) to the dextransucrase from Lactobacillus reuteri TMW 1.106 and the structures of the synthesized polysaccharides were subsequently characterized in detail. Besides methylation analysis, α-glucans were hydrolyzed by several glycoside hydrolases and the liberated oligosaccharides were identified by comparison to standard compounds or by isolation and NMR spectroscopic characterization. Furthermore, two-dimensional NMR spectroscopy was used to analyze the untreated polysaccharides. The results demonstrated that structurally different α-glucans were formed, for example different highly O4-branched dextrans or several reuteran-like polymers with varying fine structures. Consequently, mutant Lactobacillus reuteri TMW 1.106 dextransucrases can be used to form structurally unique polysaccharides.

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Safety Information
Symbol : Not Applicable
Signal Word : Not Applicable
Hazard Statements : Not Applicable
Precautionary Statements : Not Applicable
Safety Data Sheet
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