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Influence of lipase immobilization mode on ethyl acetate hydrolysis in a continuous solid-gas biocatalytic membrane reactor

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바이오화학분류
    • 바이오플라스틱
      1. 플라스틱
    • 바이오정밀화학
      1. 용매
      2. 화학제품
      3. 연료
    • 화장품용 기능성소재
      1. 계면활성제⁄증점제
    • 의료용 화학소재
      1. 식품첨가제
논문

Influence of lipase immobilization mode on ethyl acetate hydrolysis in a continuous solid-gas biocatalytic membrane reactor

학술지

Bioconjugate chemistry

저자명

Vitola, Giuseppe; Mazzei, Rosalinda; Poerio, Teresa; Barbieri, Giuseppe; Fontananova, Enrica; Bü ning, Dominic; Ulbricht, Mathias; Giorno, Lidietta

초록

<P>Solid-gas biocatalysis was performed in a specially designed continuous biocatalytic membrane reactor (BMR). In this work, lipase from <I>Candida rugosa</I> (LCR) and ethyl acetate in vapor phase were selected as model enzyme and substrate, respectively, to produce acetic acid and ethanol. LCR was immobilized on functionalized PVDF membranes by using two different kinds of chemical bond: electrostatic and covalent. Electrostatic immobilization of LCR was carried out using a membrane functionalized with amino groups, while covalent immobilization was carried out using membrane, with or without surface-immobilized polyacrylamide (PAAm) microgels, functionalized with aldehyde groups. These biocatalytic membranes were tested in a solid-gas BMR and compared in terms of enzyme specific activity, catalytic activity, and volumetric reaction rate. Results indicated that lipase covalently immobilized is more effective only when the immobilization is mediated by microgels, showing catalytic activity doubled with respect to the other system with covalently bound enzyme (4.4 vs 2.2 &mu;mol h<SUP>-1</SUP>). Enzyme immobilized by ionic bond, despite a lower catalytic activity (3.5 vs 4.4 &mu;mol h<SUP>-1</SUP>), showed the same specific activity (1.5 mmol·h<SUP>-1</SUP>·g<SUP>-1</SUP><SUB>ENZ</SUB>) of the system using microgels, due to a higher enzyme degree of freedom coupled with an analogously improved enzyme hydration. Using the optimized operating conditions regarding immobilized enzyme amount, ethyl acetate, and molar water flow rate, all three BMRs showed continuous catalytic activity for about 5 months. On the contrary, the free enzyme (in water/ethyl acetate emulsion) at 50 °C was completely inactive and at 30 °C (temperature optimum) has a specific activity 2 orders of magnitude lower (8.4 × 10<SUP>-2</SUP> mmol h<SUP>-1</SUP> g<SUP>-1</SUP>) than the solid-gas biocatalytic membrane reactor. To the best of our knowledge, this is the first example of solid-gas biocatalysis, working in the gaseous phase in which a biocatalytic membrane reactor, with the enzyme/substrate system lipase/ethyl acetate, was used.</P><BR>[FIG OMISSION]</BR>

발행연도

2019

발행기관

American Chemical Society

ISSN

1043-1802

ISSN

1520-4812

30

8

페이지

pp.2238-2246

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1 2023-12-11
2 2023-12-11

논문; 2019-12-31

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