534730
Amano Lipase from Pseudomonas fluorescens
beige-brown, ≥20,000 U/g
Sinônimo(s):
Lipase, triacylglycerol, Triacylglycerol lipase
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About This Item
Produtos recomendados
fonte biológica
Pseudomonas fluorescens
Nível de qualidade
atividade específica
≥20,000 U/g, pH 8.0, 55 °C (Optimum pH and temperature)
≥20,000 U/g
cor
beige-brown
InChI
1S/C11H9N3O2.Na/c15-8-4-5-9(10(16)7-8)13-14-11-3-1-2-6-12-11;/h1-7,16H,(H,12,14);/q;+1/b13-9-;
chave InChI
QWZUIMCIEOCSJF-CHHCPSLASA-N
Aplicação
Amano Lipase from Pseudomonas fluorescens can be used as a biocatalyst in the:
Amano Lipase can also immobilized on silk fibroin spheres to prepare optically active epoxides by enzymatic kinetic resolution of halohydrins.
- Hydrolysis and transesterification of parabens (para-hydroxybenzoic acid esters).
- Enzymatic kinetic resolution of chlorohydrins.
- Regio-selective acylation of andrographolide with different acylating agents to synthesize andrographolide derivatives.
Amano Lipase can also immobilized on silk fibroin spheres to prepare optically active epoxides by enzymatic kinetic resolution of halohydrins.
Palavra indicadora
Danger
Frases de perigo
Declarações de precaução
Classificações de perigo
Resp. Sens. 1
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 1
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
Eyeshields, Gloves, type N95 (US)
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Immobilization of Amano lipase from Pseudomonas fluorescens on silk fibroin spheres: an alternative protocol for the enantioselective synthesis of halohydrins
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Lei Wang et al.
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Hydrolysis is generally considered as the main pathway for the degradation of ester-type pollutants in aquatic environments. In this study, we found that when methanol or ethanol presented as the external carbon in the activated sludge, transesterification is very important
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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
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