Designing tailor-made steric matters to improve the immobilized ficin specificity for small versus large proteins

The development of strategies that can permit to adjust the size specificity of immobilized proteases by the generation of steric hindrances may enlarge its applicability. Using as a model ficin immobilized on glyoxyl agarose, two strategies were assayed to generate tailor made steric hindrances. First, ficin has been coimmobilized on supports coated with large proteins (hemoglobin or bovine serum albumin (BSA)). While coimmobilization of ficin with BSA presented no effect on the activity versus any of the assayed substrates, coimmobilization with hemoglobin permitted to improve the immobilized ficin specificity for casein versus hemoglobin, but still significant activity versus hemoglobin remained. Second, aldehyde-dextran has been employed to modify the immobilized ficin, trying to generate steric hindrances to avoid the entry of large proteins (hemoglobin) while enabling the entry of small ones (casein). This also increased the size specificity of ficin, but still did not suppress the activity versus hemoglobin. The combination of both strategies and the use of 37ºC during the proteolysis enabled to almost fully nullify the hydrolytic activity versus hemoglobin while preserving a high percentage of the activity versus casein. The modifications improved enzyme stability and the biocatalyst could be reused for 5 cycles without alteration of its properties.

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Publication Details

Journal
Journal of Biotechnology
Published
2024-09-10
DOI
https://doi.org/10.1016/j.jbiotec.2024.09.005
Citations
5
Primary Topic
Enzyme Catalysis and Immobilization
Type
article
Field-Weighted Citation Impact
1.17

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article

Designing tailor-made steric matters to improve the immobilized ficin specificity for small versus large proteins

Roberto Fernández‐Lafuente, Javier Rocha‐Martín, Roberto Morellon‐Sterling, Juan Manuel Bolivar et al.
5 citations
Journal of Biotechnology
Enzyme Catalysis and Immobilization
1.17
article

Designing tailor-made steric matters to improve the immobilized ficin specificity for small versus large proteins

Roberto Fernández‐Lafuente, Javier Rocha‐Martín, Roberto Morellon‐Sterling, Juan Manuel Bolivar, Pedro Abellanas-Pérez, El Hocine Siar
article en
5 citations

Abstract

The development of strategies that can permit to adjust the size specificity of immobilized proteases by the generation of steric hindrances may enlarge its applicability. Using as a model ficin immobilized on glyoxyl agarose, two strategies were assayed to generate tailor made steric hindrances. First, ficin has been coimmobilized on supports coated with large proteins (hemoglobin or bovine serum albumin (BSA)). While coimmobilization of ficin with BSA presented no effect on the activity versus any of the assayed substrates, coimmobilization with hemoglobin permitted to improve the immobilized ficin specificity for casein versus hemoglobin, but still significant activity versus hemoglobin remained. Second, aldehyde-dextran has been employed to modify the immobilized ficin, trying to generate steric hindrances to avoid the entry of large proteins (hemoglobin) while enabling the entry of small ones (casein). This also increased the size specificity of ficin, but still did not suppress the activity versus hemoglobin. The combination of both strategies and the use of 37ºC during the proteolysis enabled to almost fully nullify the hydrolytic activity versus hemoglobin while preserving a high percentage of the activity versus casein. The modifications improved enzyme stability and the biocatalyst could be reused for 5 cycles without alteration of its properties.

Journal of BiotechnologyVol. 395
Universidad Complutense de Madrid (ES), Consejo Superior de Investigaciones Científicas (ES), Institute of Agrifood Research and Technology (ES), Instituto de Investigación en Ciencias de la Alimentación (ES), Universidad Autónoma de Madrid (ES)
Ministerio de Ciencia e Innovación, Agencia Estatal de Investigación
Openalex Percentile: Top 22%
Enzyme Catalysis and Immobilization
1.17
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