lipase from candida rugosa
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Catalysts ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 744
Author(s):  
Laura Chronopoulou ◽  
Viviana Couto Sayalero ◽  
Hassan Rahimi ◽  
Aurelia Rughetti ◽  
Cleofe Palocci

Recent advances in nanotechnology techniques enable the production of polymeric nanoparticles with specific morphologies and dimensions and, by tailoring their surfaces, one can manipulate their characteristics to suit specific applications. In this work we report an innovative approach for the immobilization of a commercial lipase from Candida rugosa (CRL) which employs nanostructured polymeric carriers conjugated with anti-lipase monoclonal antibodies (MoAbs). MoAbs were chemically conjugated on the surface of polymeric nanoparticles and used to selectively adsorb CRL molecules. Hydrolytic enzymatic assays evidenced that such immobilization technique afforded a significant enhancement of enzymatic activity in comparison to the free enzyme.


2020 ◽  
Vol 30 ◽  
pp. 101812
Author(s):  
Renata Deda Mendonca Ferreira ◽  
Rodrigo Brackmann ◽  
Ernandes Benedito Pereira ◽  
Raquel Dalla Costa da Rocha

2018 ◽  
Vol 35 (11) ◽  
pp. 2220-2231 ◽  
Author(s):  
Agnieszka Kołodziejczak-Radzimska ◽  
Jakub Zdarta ◽  
Filip Ciesielczyk ◽  
Teofil Jesionowski

LWT ◽  
2018 ◽  
Vol 93 ◽  
pp. 534-541 ◽  
Author(s):  
Hamed Hosseini ◽  
Mohammad Ghorbani ◽  
Seid Mahdi Jafari ◽  
Alireza Sadeghi Mahoonak

Fuel ◽  
2018 ◽  
Vol 215 ◽  
pp. 705-713 ◽  
Author(s):  
Elisa D.C. Cavalcanti ◽  
Érika C.G. Aguieiras ◽  
Priscila R. da Silva ◽  
Jaqueline G. Duarte ◽  
Eliane P. Cipolatti ◽  
...  

2017 ◽  
Vol 41 (16) ◽  
pp. 8222-8231 ◽  
Author(s):  
Zafar Ali ◽  
Lei Tian ◽  
Baoliang Zhang ◽  
Nisar Ali ◽  
Muhammad khan ◽  
...  

Paramagnetic mesoporous fibrous silica (Fe3O4@KCC-1) was prepared and its surface was functionalized with 3-aminopropyltriethoxysilane (APTES).


2016 ◽  
Vol 11 (9) ◽  
pp. 1934578X1601100 ◽  
Author(s):  
Stefano Serra ◽  
Davide De Simeis

We here describe a study of the enzyme-mediated acylation reaction of 6,7-dihydroxy-linalool stereoisomers, which are natural triols occurring in different vegetal species. We found that only few lipases are able to catalyze the acylation of the secondary hydroxy group present in these isomers and only lipase from Candida rugosa and novozyme 435 provide either (3 R,6 R)-6-acetoxy-7-hydroxylinalool or (3 R,6 S)-6-acetoxy-7-hydroxylinalool in moderate and very good isomeric purity, respectively Even for these favorable cases the reaction proceeds very sluggishly. Our finding can give a sensible interpretation to the fact that 6-acyl-7-hydroxy-linalool derivatives do not occur in nature, whereas the corresponding glycosides, whose formation is catalyzed by glycosidase, are very common.


2016 ◽  
Vol 130 ◽  
pp. 32-39 ◽  
Author(s):  
Susana Velasco-Lozano ◽  
Fernando López-Gallego ◽  
Javier Rocha-Martin ◽  
José Manuel Guisán ◽  
Ernesto Favela-Torres

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