# From Waste to Biocatalyst: Cocoa Bean Shells as Immobilization Support and Substrate Source in Lipase-Catalyzed Hydrolysis

**Authors:** Luciana Lordelo Nascimento, Bruna Louise de Moura Pita, César de Almeida Rodrigues, Paulo Natan Alves dos Santos, Yslaine Andrade de Almeida, Larissa da Silveira Ferreira, Maira Lima de Oliveira, Lorena Santos de Almeida, Cleide Maria Faria Soares, Fabio de Souza Dias, Alini Tinoco Fricks

PMC · DOI: 10.3390/molecules30153207 · 2025-07-30

## TL;DR

This study shows how cocoa bean shells can be used as a sustainable support for enzymes to produce free fatty acids, turning waste into a useful biocatalyst.

## Contribution

The novelty lies in using cocoa bean shells as both a substrate and support for enzyme immobilization, enhancing sustainability and catalytic performance.

## Key findings

- The covalently immobilized enzyme on cocoa bean shells (ORG-CB) achieved 60.1% FFA conversion from CBS oil.
- ORG-CB retained over 50% activity after eight reuse cycles and showed enhanced thermal resistance.
- Immobilization chemistry and support composition significantly impact the performance of biocatalysts.

## Abstract

This study reports the development of a sustainable biocatalyst system for free fatty acid (FFA) production from cocoa bean shell (CBS) oil using Burkholderia cepacia lipase (BCL). CBS was explored as both a support material and a reaction substrate. Six immobilized systems were prepared using organic (CBS), inorganic (silica), and hybrid (CBS–silica) supports via physical adsorption or covalent binding. Among them, the covalently immobilized enzyme on CBS (ORG-CB) showed the most balanced performance, achieving a catalytic efficiency (Ke) of 0.063 mM−1·min−1 (18.6% of the free enzyme), broad pH–temperature tolerance, and over 50% activity retention after eight reuse cycles. Thermodynamic analysis confirmed enhanced thermal resistance for ORG-CB (Ed = 32.3 kJ mol−1; ΔH‡ = 29.7 kJ mol−1), while kinetic evaluation revealed that its thermal deactivation occurred faster than for the free enzyme under prolonged heating. In application trials, ORG-CB reached 60.1% FFA conversion from CBS oil, outperforming the free enzyme (49.9%). These findings validate CBS as a dual-function material for enzyme immobilization and valorization of agro-industrial waste. The results also reinforce the impact of immobilization chemistry and support composition on the operational and thermal performance of biocatalysts, contributing to the advancement of green chemistry strategies in enzyme-based processing.

## Linked entities

- **Chemicals:** FFA (PubChem CID 3371), silica (PubChem CID 24261)
- **Species:** Burkholderia cepacia (taxon 292)

## Full-text entities

- **Genes:** Lipase [NCBI Gene 18603448]
- **Chemicals:** CBS (-), FFA (MESH:D005230), oil (MESH:D009821), silica (MESH:D012822)
- **Species:** Bacillus sp. CL (species) [taxon 1196798]

## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12348176/full.md

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Source: https://tomesphere.com/paper/PMC12348176