534641
Amano Lipase PS, from Burkholderia cepacia
≥23,000 U/g, pH 7.0, 50 °C (Optimum pH and temperature)
Synonym(s):
APS-BCL, Pseudomonas cepacia (APS-PCL)
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About This Item
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specific activity
≥23,000 U/g, pH 7.0, 50 °C (Optimum pH and temperature)
Application
Amano Lipase PS is generally used in the enantioselective transesterification and hydrolysis. Applications include:
- Lipase catalyzed transesterification of prochiral pyrimidine acyclonucleoside.
- Lipase catalyzed hydrolysis of diacetylated pyrimidine acyclonucleosides.
- Enantiomer selective acylation of racemic alcohols in continuous-flow bioreactors.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Resp. Sens. 1
Storage Class Code
11 - Combustible Solids
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Chirality, 30(2), 206-214 (2018)
Immobilization of lipase from Burkholderia cepacia into calcium carbonate microcapsule and its use for enzymatic reactions in organic and aqueous media.
Fujiwara M, et al.
Journal of Molecular Catalysis. B, Enzymatic, 109, 94-100 (2014)
Reverse Stereoselectivity in the Lipase-Catalyzed Hydrolysis of Diacetylated Pyrimidine Acyclonucleosides.
Kolodziejska et al.
ChemCatChem, 8(23), 3644-3649 (2016)
Enantiomer selective acylation of racemic alcohols by lipases in continuous-flow bioreactors.
Csajagi C, et al.
Tetrahedron Asymmetry, 19(2), 237-246 (2008)
Dominik Koszelewski et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 25(43), 10156-10164 (2019-05-29)
A new protocol based on lipase-catalyzed tandem reaction toward α,β-enones/enoesters is presented. For the synthesis of the desired products the tandem process based on enzyme-catalyzed hydrolysis and Knoevenagel reaction starting from enol acetates and aldehyde is developed. The relevant impact
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