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4 protocols using lipozyme calb

1

Synthesis of Hybrid Catalysts

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Lipase B from Candida antarctica (Lipozyme® CALB), Thermomyces lanuginosus lipase (Lipozyme® TL 100L, TLL), catalase from Aspergillus niger (Catazyme® 25L, CAT), and β-galactosidase from Kluyveromyces lactis (Lactozyme® pure 6500L, LAC) solutions were from Novozymes (Denmark). 4-Methoxybenzenediazonium tetrafluoroborate (MBDFB), iodobenzene, palladium acetate, sodium tetrachloropalladate (Na2[PdCl4]), and CuSO4·5H2O were from Sigma-Aldrich (now Merk). N-Acetyl-l-tryptophan methyl ester (TrpOMe) was from Alfa Aesar. Methanol and acetonitrile of HPLC grade were purchased from Scharlab (Scharlab, S.L., Barcelona, Spain). Cu-FOS2 and Cu-NR hybrids were synthesized following the previously reported strategy.18 (link)
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2

Enzyme-Catalyzed Ring-Opening Polymerization

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5-Hydroxymetyl-2-furancarboxylic acid (HMFA, >97%), was acquired from Carbosynth Compton, Berkshire, UK). ε-Caprolactone (ECL, ≥98%), tetrahydrofuran (THF, >99%), toluene (>99%), chloroform (CHCl3, >99%), dichloromethane (CH2Cl2, ≥99,8%), acetonitrile (>99%), sodium sulphate (Na2SO4, >99%) were from Sigma Aldrich (Steinheim am Albuch, Germany). Magnesium chloride (MgCl2, 98%) and potassium carbonate (K2CO3, 99%) were purchased from Chimopar S.A. (Bucharest, Romania), while sodium chloride (NaCl, >99%) and potassium sulfate (K2SO4, 99%) were products of VWR Chemicals (Leuven, Belgium) and Alfa Aesar GmbH & Co KG (Karlsruhe, Germany), respectively. All chemicals were used as purchased, without further purification.
Three commercially available immobilized enzymes were utilized as biocatalysts for the polymerization reactions: Novozyme 435 (lipase from Candida antarctica B immobilized on acrylic resin) and Lipozyme CalB, (from C. antarctica) were products of Novozymes (Bagsværd, Denmark), while GF-CalB-IM (lipase B from C. antarctica immobilized on microporous ion exchange resin) was purchased from GenoFocus (Daejeon, South Korea). Lipase from porcine pancreas (Sigma-Aldrich, Steinheim, Germany) was used for the enzymatic degradation studies.
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3

Lipase-Catalyzed Biocatalysis: A Comparative Study

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Lipase from Candida rugosa Type VII, ≥700 U/mg (CRL) was purchased from Merck Life Science S.L.U. (Madrid, Spain). Lipase B from Candida antarctica (Lipozyme®, CAL-B), lipase A from Candida antarctica (NovoCor®AD L, CAL-A), lipase from Rhizomucor miehei (Palatase 20000; RML), lipase from Thermomyces lanuginosus (TLL) and Lecitase®ultra (LU, chimera produced through the fusion of the genes of the lipase from Thermomyces lanuginosus and the phospholipase A1 from Fusarium oxysporum) were kindly gifted from Novozymes Spain.
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4

Enzymatic Production of Cocoa Soapstock Lipids

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The raw material used in the experiments was an olein from cocoa (Theobroma cocoa) soapstocks, obtained from OLEOFAT TRADER S.L. (Tudela -Navarra -Spain) by acid fat-splitting. Cocoa soapstocks were provided by Moner Cocoa S.A. (La Selva del Camp -Tarragona -Spain). The enzymes Lipozyme CALB and Eversa transform 2.0 were purchased from Novozymes (Bagsvaerd -Copenhagen). Glycerol (99.9%) was purchased from Labbox, NaOH, KOH and the solvents used for analysis (ethanol, n-hexane, diethyl ether, methanol and acetone) were from Scharlab. The HMDS+TMCS+Pyridine 3:1:9 (Sylon HTP) mix used to quantify MAG, DAG and TAG and the internal standards such as 1,2,4-butanetriol and tricaprin were purchased from Supelco (Sigma Chemical Co., St Louis, MO). The standards for the calibration curves in the GC analysis, 1-Monolarin, Diolein, Triolein and Glycerol, were purchased from Larodan and the 30 mg/ml FAME mix (28 components) was purchased from Restek.
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