Covalent immobilization of glucoamylase on 3D-printed poly(lactic acid) carriers for starch hydrolysis in stirred tank reactor
| dc.contributor.author | de Lima Junior, David Spressão [UNESP] | |
| dc.contributor.author | Sessak, Ilana [UNESP] | |
| dc.contributor.author | Remonatto, Daniela | |
| dc.contributor.author | Galán, Julián Paul Martínez | |
| dc.contributor.author | Innocentini, Murilo Daniel de Mello | |
| dc.contributor.author | de Paula, Ariela Veloso [UNESP] | |
| dc.contributor.author | Bocchini, Daniela Alonso [UNESP] | |
| dc.contributor.institution | Universidade Estadual Paulista (UNESP) | |
| dc.contributor.institution | Science and Technology of São Paulo (IFSP) | |
| dc.contributor.institution | University of Antioquia (UdeA) | |
| dc.contributor.institution | University of Ribeirão Preto (UNAERP) | |
| dc.contributor.institution | University of Bath | |
| dc.date.accessioned | 2025-04-29T19:33:13Z | |
| dc.date.issued | 2025-07-01 | |
| dc.description.abstract | This study presents a novel 3D-printed poly(lactic acid) (PLA) carrier for the covalent immobilization of a commercial glucoamylase. Enzyme carriers were functionalized by aminolysis with ethylenediamine (EDA) and activated with glutaraldehyde. Since covalent immobilization using glutaraldehyde as activating agent involves the formation of imine bonds which are inherently unstable, the use of borohydride as a reducing agent to stabilize these imine bonds after the functionalization step was considered. The highest enzymatic activity (13.68 U g−1 carrier) was obtained when immobilization was performed at pH 10 using NaBH4 (immobilization yield of 32.80 % ± 0.51 %). Optimal activity conditions were pH 4.92 and 50 °C for the soluble enzyme and pH 5.5 and 50 °C for the immobilized enzyme. The operational stability of immobilized glucoamylase was evaluated for 10 consecutive reaction cycles (of 10 minutes each) and the enzyme maintained 65.19 % of its original activity at the end of the third cycle. Starch saccharification in a stirred tank reactor by immobilized glucoamylase reached 95 % conversion after 12 h and 74 % conversion after 12 h in the first reuse cycle. These findings demonstrate the potential of PLA for glucoamylase immobilization, offering promising prospects for efficient and sustainable starch hydrolysis in industrial enzymatic processes. | en |
| dc.description.affiliation | Institute of Chemistry São Paulo State University (UNESP), SP | |
| dc.description.affiliation | Federal Institute of Education Science and Technology of São Paulo (IFSP), SP | |
| dc.description.affiliation | School of Nutrition and Dietetics University of Antioquia (UdeA) | |
| dc.description.affiliation | Graduate Program in Chemical Engineering University of Ribeirão Preto (UNAERP), SP | |
| dc.description.affiliation | Centre for Regenerative Design and Engineering for a Net-Positive World (RENEW) University of Bath | |
| dc.description.affiliation | School of Pharmaceutical Sciences UNESP, SP | |
| dc.description.affiliationUnesp | Institute of Chemistry São Paulo State University (UNESP), SP | |
| dc.description.affiliationUnesp | School of Pharmaceutical Sciences UNESP, SP | |
| dc.description.sponsorship | Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) | |
| dc.description.sponsorship | Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) | |
| dc.description.sponsorship | Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) | |
| dc.description.sponsorshipId | CAPES: 1765/2023 | |
| dc.description.sponsorshipId | FAPESP: 2020/09592–1 | |
| dc.description.sponsorshipId | CNPq: 304399/2022–1 | |
| dc.description.sponsorshipId | CAPES: 88887.817466/2023–00 | |
| dc.format.extent | 52-62 | |
| dc.identifier | http://dx.doi.org/10.1016/j.procbio.2025.04.003 | |
| dc.identifier.citation | Process Biochemistry, v. 154, p. 52-62. | |
| dc.identifier.doi | 10.1016/j.procbio.2025.04.003 | |
| dc.identifier.issn | 1359-5113 | |
| dc.identifier.scopus | 2-s2.0-105002637741 | |
| dc.identifier.uri | https://hdl.handle.net/11449/303850 | |
| dc.language.iso | eng | |
| dc.relation.ispartof | Process Biochemistry | |
| dc.source | Scopus | |
| dc.subject | 3D printing | |
| dc.subject | Batch starch hydrolysis | |
| dc.subject | Covalent immobilization | |
| dc.subject | Enzymatic reactors | |
| dc.subject | Glucoamylase | |
| dc.subject | Poly(lactic acid) carriers | |
| dc.title | Covalent immobilization of glucoamylase on 3D-printed poly(lactic acid) carriers for starch hydrolysis in stirred tank reactor | en |
| dc.type | Artigo | pt |
| dspace.entity.type | Publication | |
| relation.isOrgUnitOfPublication | 95697b0b-8977-4af6-88d5-c29c80b5ee92 | |
| relation.isOrgUnitOfPublication | bc74a1ce-4c4c-4dad-8378-83962d76c4fd | |
| relation.isOrgUnitOfPublication.latestForDiscovery | 95697b0b-8977-4af6-88d5-c29c80b5ee92 | |
| unesp.author.orcid | 0000-0002-5340-4530[3] | |
| unesp.campus | Universidade Estadual Paulista (UNESP), Instituto de Química, Araraquara | pt |
| unesp.campus | Universidade Estadual Paulista (UNESP), Faculdade de Ciências Farmacêuticas, Araraquara | pt |

