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
Specific activity:
≥23,000 U/g, pH 7.0, 50 °C (Optimum pH and temperature)
specific activity
≥23,000 U/g, pH 7.0, 50 °C (Optimum pH and temperature)
Quality Level
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.
signalword
Danger
hcodes
pcodes
Hazard Classifications
Resp. Sens. 1
Storage Class
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
常规特殊物品
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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)
Lipase-catalyzed enantioselective transesterification of prochiral 1-((1, 3-dihydroxypropan-2-yloxy) methyl)-5, 6, 7, 8-tetrahydroquinazoline-2, 4 (1H, 3H)-dione in ionic liquids.
Kolodziejska, et al.
Chirality, 30(2), 206-214 (2018)
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
Articles
Efficient epimerization catalyst for enzyme mediated dynamic kinetic resolution (DKR).
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