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      Synthesis and properties of porous CLEAs lipase by the calcium carbonate template method and its application in biodiesel production

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      RSC Advances
      The Royal Society of Chemistry

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          Abstract

          In this work, porous cross-linked enzyme aggregates (p-CLEAs) were synthesized by the in situ co-precipitation method using CaCO 3 microparticles as templates. The preparation procedure involved the immobilization of crude lipase as CLEAs via precipitation with ammonium sulfate and entrapping these lipase molecules into the CaCO 3 templates, followed by DTT (dithiothreitol)-induced assembly of lipase molecules to form lipase microparticles (lipase molecules were assembled into microparticles internally using disulfide bonds within the lipase molecules as the molecular linkers and stimulated by dithiothreitol); finally, the removal of CaCO 3 templates was performed by EDTA to form pores in CLEAs. The scanning electron microscopy analysis of p-CLEAs showed a porous structure. p-CLEAs showed obvious improvement in thermal stability (after incubation at 65 °C, p-CLEAs lipase retained 86% relative activity, while free lipase retained only 33.67%) and pH stability (p-CLEAs relative activity was over 90% while for free lipase, the relative activity ranged from 72% to 89% from pH 6 to 9) than free lipase and could hold relatively high activity retention without activity loss at 4 °C for more than six months. The application of p-CLEAs in producing biodiesel showed a higher degree of conversion. The conversion of fatty acid methyl ester (FAME) was 89.7%; this value was higher by approximately 7.4% compared to that of the conventional CLEAs under the optimized conditions of a methanol–oil molar ratio of 6 : 1, with a p-CLEAs lipase dose of 20% and water content of 3% at 45 °C for 24 h. The FAME conversion remained greater than 70% even after reusing the p-CLEAs lipase for 8 reactions. The results demonstrated that the p-CLEAs lipase is suitable for applications in the preparation of biodiesel.

          Abstract

          Porous cross-linked enzyme aggregates (p-CLEAs) were synthesized. This p-CLEAs presented a complete structure with abundant channels, large specific surface and more efficient catalytic effect compared with conventional CLEAs.

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          Most cited references28

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          Enzyme Immobilization: An Overview on Methods, Support Material, and Applications of Immobilized Enzymes.

          Immobilized enzymes can be used in a wide range of processes. In recent years, a variety of new approaches have emerged for the immobilization of enzymes that have greater efficiency and wider usage. During the course of the last two decades, this area has rapidly expanded into a multidisciplinary field. This current study is a comprehensive review of a variety of literature produced on the different enzymes that have been immobilized on various supporting materials. These immobilized enzymes have a wide range of applications. These include applications in the sugar, fish, and wine industries, where they are used for removing organic compounds from waste water. This study also reviews their use in sophisticated biosensors for metabolite control and in situ measurements of environmental pollutants. Immobilized enzymes also find significant application in drug metabolism, biodiesel and antibiotic production, bioremediation, and the food industry. The widespread usage of immobilized enzymes is largely due to the fact that they are cheaper, environment friendly, and much easier to use when compared to equivalent technologies.
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            Parameters in preparation and characterization of cross linked enzyme aggregates (CLEAs)

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              Cross-linked enzyme aggregates (CLEAs) of Pencilluim notatum lipase enzyme with improved activity, stability and reusability characteristics

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                Author and article information

                Journal
                RSC Adv
                RSC Adv
                RA
                RSCACL
                RSC Advances
                The Royal Society of Chemistry
                2046-2069
                19 September 2019
                18 September 2019
                19 September 2019
                : 9
                : 51
                : 29665-29675
                Affiliations
                [a] Guangzhou Institute of Energy Conversion, Chinese Academy of Sciences Guangzhou 510640 China yanglm@ 123456ms.giec.ac.cn lvpm@ 123456ms.giec.ac.cn +86 20 87065195 +86 20 87057727 +86 20 87057760
                [b] Key Laboratory of Renewable Energy, Chinese Academy of Sciences Guangzhou 510640 China
                [c] Guangdong Key Laboratory of New and Renewable Energy Research and Development Guangzhou 510640 China
                [d] Collaborative Innovation Center of Biomass Energy Zhengzhou 450002 Henan Province China
                Author information
                https://orcid.org/0000-0001-5322-5770
                https://orcid.org/0000-0001-9449-8652
                Article
                c9ra04365a
                10.1039/c9ra04365a
                9071971
                35531534
                c5b24a3f-a332-4acf-8df0-a8b38f83903e
                This journal is © The Royal Society of Chemistry
                History
                : 11 June 2019
                : 27 August 2019
                Page count
                Pages: 11
                Funding
                Funded by: Natural Science Foundation of Guangdong Province, doi 10.13039/501100003453;
                Award ID: 2016A030308004
                Funded by: National Basic Research Program of China (973 Program), doi 10.13039/501100012166;
                Award ID: 2017YFD0601003
                Funded by: National Natural Science Foundation of China, doi 10.13039/501100001809;
                Award ID: 21506217
                Funded by: Chinese Academy of Sciences, doi 10.13039/501100002367;
                Award ID: Y707j91001
                Categories
                Chemistry
                Custom metadata
                Paginated Article

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