Severity: Warning
Message: file_get_contents(https://...@gmail.com&api_key=61f08fa0b96a73de8c900d749fcb997acc09&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 197
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 197
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 271
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 1075
Function: getPubMedXML
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3195
Function: GetPubMedArticleOutput_2016
File: /var/www/html/application/controllers/Detail.php
Line: 597
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 511
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 317
Function: require_once
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Lipase conformational dynamics at carrier interfaces dictate biocatalytic performance, yet their structural adaptability and molecular underpinnings remain unclear. This study elucidates how reduced graphene oxide (rGO) surface hydrophobicity modulates lipase activation through spectroscopy and molecular dynamics simulations, unveiling enzyme-specific mechanisms. By tuning rGO reduction, we found that rGO-4 h optimally enhanced Candida antarctica lipase B (CALB) activity by 201.4 % through rigidity-driven stabilization, as its non-blocking lid improved structural integrity and substrate affinity rather than undergoing interfacial activation. Rhizomucor miehei lipase (RML) and Porcine phospholipase (PPL), which rely on lid-dependent activation, exhibited increased activity (122.3 % and 165.4 %, respectively) due to enhanced lid opening and hydrophobic interactions. Molecular dynamics simulations revealed that PPL's long lid required the highest flipping energy (-1112.9 kJ/mol), limiting activation. In contrast, RML's short lid had a lower energy barrier (-596.1 kJ/mol), facilitating lid flipping and interfacial activation. Spectroscopic analysis confirmed that moderate hydrophobicity preserved α-helix structures, whereas excessive reduction induced α-to-β transitions. Radial distribution function analysis indicated that increased solvent accessibility at the active site facilitated RML and PPL activation. For CALB, enhanced van der Waals (vdW) interactions (-207.3 kJ/mol) and reduced electrostatic repulsion within the active pocket strengthened substrate binding, shortening the catalytic serine-substrate distance (2.89 Å vs. 3.38 Å) and improving efficiency. These findings establish that rigidity-dependent enzymes benefit from structural stabilization, whereas lid-dependent lipases require hydrophobicity-tuned flexibility for optimal activation. This study provides a structure-function framework for designing advanced immobilization platforms, with applications in biocatalysis, pharmaceuticals, and biofuel production.
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http://dx.doi.org/10.1016/j.biortech.2025.133035 | DOI Listing |