Characterization of Immobilized Endo-Polygalacturonase PGC-AN64 from Aspergillus niger HO32 with Potential Biotechnological Interest

This study focuses on the characterization and application of an immobilized purified endo-polygalacturonase PGC-AN64 from Aspergillus niger HO32 using sodium alginate (SA), and its combinations with guar gum (SA-Gu) or chitosan (SA-Ch) as supports. Immobilization efficiencies were 75%, 83%, and 77% for PGC-AN64-SA, PGC-AN64-SA-Ch, and PGC-AN64-SA-Gu, respectively. Immobilized enzymes showed enhanced thermostability and pH stability. At 80°C, the half-lives reached 8, 11, and 16 h, and residual activity at pH 5 after extended incubation (12–24 h) was maintained at approximately 56–58%, depending on the matrix. Reusability tests showed activity retention of ~50% for PGC-AN64-SA after 4 cycles, and ~64% and 51% for PGC-AN64-SA-Ch and PGC-AN64-SA-Gu, respectively, after 6 cycles. Orange juice clarification efficiency was reflected by transmittance values of 85.20±1.68% for free PGC-AN64, and ~84% for all immobilized forms. XRD, FTIR-ATR, and FE-SEM analyses confirmed structural changes upon immobilization. In addition, orange juice clarification resulted in a decrease in total soluble solids and color modifications: reduced a* values, and increased L* and b* values. These findings highlight that immobilizing PGC-AN64 on SA-based matrices improves enzyme stability, operational reusability, and retains orange juice clarification performance. The approach offers an efficient and safe enzymatic solution for agro-industrial applications, particularly in juice processing.

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Journal
Tropical Journal of Natural Product Research
Published
2025-05-31
DOI
https://doi.org/10.26538/tjnpr/v9i5.64
Primary Topic
Enzyme Production and Characterization
Type
article
Field-Weighted Citation Impact
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article

Characterization of Immobilized Endo-Polygalacturonase PGC-AN64 from Aspergillus niger HO32 with Potential Biotechnological Interest

Marilize Le Roes‐Hill, Houssam Abouloifa, Ennouamane Saalaoui, Bassem Jaouadi et al.
Tropical Journal of Natural Product Research
Enzyme Production and Characterization
article

Characterization of Immobilized Endo-Polygalacturonase PGC-AN64 from Aspergillus niger HO32 with Potential Biotechnological Interest

Marilize Le Roes‐Hill, Houssam Abouloifa, Ennouamane Saalaoui, Bassem Jaouadi, Nour Eddine Bentouhami, Sondes Mechri, Reda Bellaouchi, Loubna Firdaous, Abdelkarim Abousalham, Nabil Ghabbour, Abdeslam Asehraou, Sara Moumnassi, Ayoub Bekkouch, Meryem Yahyaou
article en

Abstract

This study focuses on the characterization and application of an immobilized purified endo-polygalacturonase PGC-AN64 from Aspergillus niger HO32 using sodium alginate (SA), and its combinations with guar gum (SA-Gu) or chitosan (SA-Ch) as supports. Immobilization efficiencies were 75%, 83%, and 77% for PGC-AN64-SA, PGC-AN64-SA-Ch, and PGC-AN64-SA-Gu, respectively. Immobilized enzymes showed enhanced thermostability and pH stability. At 80°C, the half-lives reached 8, 11, and 16 h, and residual activity at pH 5 after extended incubation (12–24 h) was maintained at approximately 56–58%, depending on the matrix. Reusability tests showed activity retention of ~50% for PGC-AN64-SA after 4 cycles, and ~64% and 51% for PGC-AN64-SA-Ch and PGC-AN64-SA-Gu, respectively, after 6 cycles. Orange juice clarification efficiency was reflected by transmittance values of 85.20±1.68% for free PGC-AN64, and ~84% for all immobilized forms. XRD, FTIR-ATR, and FE-SEM analyses confirmed structural changes upon immobilization. In addition, orange juice clarification resulted in a decrease in total soluble solids and color modifications: reduced a* values, and increased L* and b* values. These findings highlight that immobilizing PGC-AN64 on SA-based matrices improves enzyme stability, operational reusability, and retains orange juice clarification performance. The approach offers an efficient and safe enzymatic solution for agro-industrial applications, particularly in juice processing.

Tropical Journal of Natural Product Research
Université Claude Bernard Lyon 1 (FR), Centre National de la Recherche Scientifique (FR), Cape Peninsula University of Technology (ZA), Université Ibn-Tofail (MA), Institut Charles Viollette (FR), Institut de Chimie et Biochimie Moléculaires et Supramoléculaires (FR), Mohamed I University (MA), Centre of Biotechnology of Sfax (TN), Université Hassan II Mohammedia (MA), Université d'Artois (FR), Premier University (BD), Sidi Mohamed Ben Abdellah University (MA), University of Hassan II Casablanca (MA)
European Commission, Campus France
Zero hunger
Openalex Percentile: Top 86%
Enzyme Production and Characterization
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