Preparation of Magnetic Cross-Linked Amyloglucosidase Aggregates: Solving Some Activity Problems
The preparation of Cross-Linked Enzyme Aggregates (CLEAs) is a simple and cost-effective technique capable of generating insoluble biocatalysts with high volumetric activity and improved stability. The standard CLEA preparation consists of the aggregation of the enzyme and its further crosslinking,...
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description | The preparation of Cross-Linked Enzyme Aggregates (CLEAs) is a simple and cost-effective technique capable of generating insoluble biocatalysts with high volumetric activity and improved stability. The standard CLEA preparation consists of the aggregation of the enzyme and its further crosslinking, usually with glutaraldehyde. However, some enzymes have too low a content of surface lysine groups to permit effective crosslinking with glutaraldehyde, requiring co-aggregation with feeders rich in amino groups to aid the formation of CLEAs. The co-aggregation with magnetic particles makes their handling easier. In this work, CLEAs of a commercial amyloglucosidase (AMG) produced by Aspergillus niger were prepared by co-aggregation in the presence of polyethyleneimine (PEI) or starch with aminated magnetic nanoparticles (MNPs) or bovine serum albumin (BSA). First, CLEAs were prepared only with MNPs at different glutaraldehyde concentrations, yielding a recovered activity of around 20%. The addition of starch during the precipitation and crosslinking steps nearly doubled the recovered activity. Similar recovered activity (around 40%) was achieved when changing starch by PEI. Moreover, under the same conditions, AMG co-aggregated with BSA was also synthesized, yielding CLEAs with very similar recovered activity. Both CLEAs (co-aggregated with MNPs or BSA) were four times more stable than the soluble enzyme. These CLEAs were evaluated in the hydrolysis of starch at typical industrial conditions, achieving more than 95% starch-to-glucose conversion, measured as Dextrose Equivalent (DE). Moreover, both CLEAS could be reused for five cycles, maintaining a DE of around 90%. Although both CLEAs had good properties, magnetic CLEAs could be more attractive for industrial purposes because of their easy separation by an external magnetic field, avoiding the formation of clusters during the filtration or centrifugation recovery methods usually used. |
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The standard CLEA preparation consists of the aggregation of the enzyme and its further crosslinking, usually with glutaraldehyde. However, some enzymes have too low a content of surface lysine groups to permit effective crosslinking with glutaraldehyde, requiring co-aggregation with feeders rich in amino groups to aid the formation of CLEAs. The co-aggregation with magnetic particles makes their handling easier. In this work, CLEAs of a commercial amyloglucosidase (AMG) produced by Aspergillus niger were prepared by co-aggregation in the presence of polyethyleneimine (PEI) or starch with aminated magnetic nanoparticles (MNPs) or bovine serum albumin (BSA). First, CLEAs were prepared only with MNPs at different glutaraldehyde concentrations, yielding a recovered activity of around 20%. The addition of starch during the precipitation and crosslinking steps nearly doubled the recovered activity. Similar recovered activity (around 40%) was achieved when changing starch by PEI. Moreover, under the same conditions, AMG co-aggregated with BSA was also synthesized, yielding CLEAs with very similar recovered activity. Both CLEAs (co-aggregated with MNPs or BSA) were four times more stable than the soluble enzyme. These CLEAs were evaluated in the hydrolysis of starch at typical industrial conditions, achieving more than 95% starch-to-glucose conversion, measured as Dextrose Equivalent (DE). Moreover, both CLEAS could be reused for five cycles, maintaining a DE of around 90%. Although both CLEAs had good properties, magnetic CLEAs could be more attractive for industrial purposes because of their easy separation by an external magnetic field, avoiding the formation of clusters during the filtration or centrifugation recovery methods usually used.</description><identifier>ISSN: 2073-4344</identifier><identifier>EISSN: 2073-4344</identifier><identifier>DOI: 10.3390/catal8110496</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>Agglomeration ; Aggregates ; Catalysts ; Chemical reactions ; Crosslinking ; Dextrose ; Enzymes ; Ethanol ; Feeders ; Glucoamylase ; Glucose ; Glutaraldehyde ; Lysine ; Magnetic properties ; Nanoparticles ; Polyethylene glycol ; Polyethyleneimine ; Polymers ; Proteins ; Serum albumin</subject><ispartof>Catalysts, 2018-11, Vol.8 (11), p.496</ispartof><rights>2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). 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Although both CLEAs had good properties, magnetic CLEAs could be more attractive for industrial purposes because of their easy separation by an external magnetic field, avoiding the formation of clusters during the filtration or centrifugation recovery methods usually used.</description><subject>Agglomeration</subject><subject>Aggregates</subject><subject>Catalysts</subject><subject>Chemical reactions</subject><subject>Crosslinking</subject><subject>Dextrose</subject><subject>Enzymes</subject><subject>Ethanol</subject><subject>Feeders</subject><subject>Glucoamylase</subject><subject>Glucose</subject><subject>Glutaraldehyde</subject><subject>Lysine</subject><subject>Magnetic properties</subject><subject>Nanoparticles</subject><subject>Polyethylene glycol</subject><subject>Polyethyleneimine</subject><subject>Polymers</subject><subject>Proteins</subject><subject>Serum albumin</subject><issn>2073-4344</issn><issn>2073-4344</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNpNUE1LAzEUDKJgqb35AwJeXc3XbhJvpfgFFQvqeU2zb5fU3U1N0sL-e7fUQ99lHswwwwxC15Tcca7JvTXJtIpSInRxhiaMSJ4JLsT5yX-JZjFuyHiackXzCfpeBdiaYJLzPfY1fjNND8lZvAg-xmzp-h-o8LwbWt-0O-ujq0wEPG-aAI1JEB_wh2_3rm9G7EbCJrd3acCr4NctdPEKXdSmjTD7xyn6enr8XLxky_fn18V8mVlOaMoKyZgCLZkBa7WhBSiroVC0ZmOh2hYgJKyF5EWu-FoawSxQKm1dVZwLy_gU3Rx9t8H_7iCmcuN3oR8jS5YrJrUiuRxVt0eVPdQLUJfb4DoThpKS8jBjeToj_wMupmaI</recordid><startdate>20181101</startdate><enddate>20181101</enddate><creator>Amaral-Fonseca, Murilo</creator><creator>Kopp, Willian</creator><creator>Giordano, Raquel de Lima Camargo</creator><creator>Fernández-Lafuente, Roberto</creator><creator>Tardioli, Paulo Waldir</creator><general>MDPI AG</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>HCIFZ</scope><scope>JG9</scope><scope>KB.</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><orcidid>https://orcid.org/0000-0003-4976-7096</orcidid><orcidid>https://orcid.org/0000-0002-5011-9881</orcidid></search><sort><creationdate>20181101</creationdate><title>Preparation of Magnetic Cross-Linked Amyloglucosidase Aggregates: Solving Some Activity Problems</title><author>Amaral-Fonseca, Murilo ; Kopp, Willian ; Giordano, Raquel de Lima Camargo ; Fernández-Lafuente, Roberto ; Tardioli, Paulo Waldir</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c301t-67228e972aecc9a16e8c9e681f2049fc6e47eb4736583b7a42ce117cfdd334c23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Agglomeration</topic><topic>Aggregates</topic><topic>Catalysts</topic><topic>Chemical reactions</topic><topic>Crosslinking</topic><topic>Dextrose</topic><topic>Enzymes</topic><topic>Ethanol</topic><topic>Feeders</topic><topic>Glucoamylase</topic><topic>Glucose</topic><topic>Glutaraldehyde</topic><topic>Lysine</topic><topic>Magnetic properties</topic><topic>Nanoparticles</topic><topic>Polyethylene glycol</topic><topic>Polyethyleneimine</topic><topic>Polymers</topic><topic>Proteins</topic><topic>Serum albumin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Amaral-Fonseca, Murilo</creatorcontrib><creatorcontrib>Kopp, Willian</creatorcontrib><creatorcontrib>Giordano, Raquel de Lima Camargo</creatorcontrib><creatorcontrib>Fernández-Lafuente, Roberto</creatorcontrib><creatorcontrib>Tardioli, Paulo Waldir</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>SciTech Premium Collection</collection><collection>Materials Research Database</collection><collection>Materials Science Database</collection><collection>Materials Science Collection</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><jtitle>Catalysts</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Amaral-Fonseca, Murilo</au><au>Kopp, Willian</au><au>Giordano, Raquel de Lima Camargo</au><au>Fernández-Lafuente, Roberto</au><au>Tardioli, Paulo Waldir</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Preparation of Magnetic Cross-Linked Amyloglucosidase Aggregates: Solving Some Activity Problems</atitle><jtitle>Catalysts</jtitle><date>2018-11-01</date><risdate>2018</risdate><volume>8</volume><issue>11</issue><spage>496</spage><pages>496-</pages><issn>2073-4344</issn><eissn>2073-4344</eissn><abstract>The preparation of Cross-Linked Enzyme Aggregates (CLEAs) is a simple and cost-effective technique capable of generating insoluble biocatalysts with high volumetric activity and improved stability. The standard CLEA preparation consists of the aggregation of the enzyme and its further crosslinking, usually with glutaraldehyde. However, some enzymes have too low a content of surface lysine groups to permit effective crosslinking with glutaraldehyde, requiring co-aggregation with feeders rich in amino groups to aid the formation of CLEAs. The co-aggregation with magnetic particles makes their handling easier. In this work, CLEAs of a commercial amyloglucosidase (AMG) produced by Aspergillus niger were prepared by co-aggregation in the presence of polyethyleneimine (PEI) or starch with aminated magnetic nanoparticles (MNPs) or bovine serum albumin (BSA). First, CLEAs were prepared only with MNPs at different glutaraldehyde concentrations, yielding a recovered activity of around 20%. The addition of starch during the precipitation and crosslinking steps nearly doubled the recovered activity. Similar recovered activity (around 40%) was achieved when changing starch by PEI. Moreover, under the same conditions, AMG co-aggregated with BSA was also synthesized, yielding CLEAs with very similar recovered activity. Both CLEAs (co-aggregated with MNPs or BSA) were four times more stable than the soluble enzyme. These CLEAs were evaluated in the hydrolysis of starch at typical industrial conditions, achieving more than 95% starch-to-glucose conversion, measured as Dextrose Equivalent (DE). Moreover, both CLEAS could be reused for five cycles, maintaining a DE of around 90%. 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subjects | Agglomeration Aggregates Catalysts Chemical reactions Crosslinking Dextrose Enzymes Ethanol Feeders Glucoamylase Glucose Glutaraldehyde Lysine Magnetic properties Nanoparticles Polyethylene glycol Polyethyleneimine Polymers Proteins Serum albumin |
title | Preparation of Magnetic Cross-Linked Amyloglucosidase Aggregates: Solving Some Activity Problems |
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