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
Recommended Products
Quality Level
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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Enantiomer selective acylation of racemic alcohols by lipases in continuous-flow bioreactors.
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Reverse Stereoselectivity in the Lipase-Catalyzed Hydrolysis of Diacetylated Pyrimidine Acyclonucleosides.
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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.
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Journal of Molecular Catalysis. B, Enzymatic, 109, 94-100 (2014)
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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
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