Aflatoxin B (AFB) contamination of oils is a serious concern for the safety of edible oil consumers. Enzyme-assisted detoxification of AFB is an efficient and safe method for decontaminating oils, but pristine enzymes are unstable in oils and require modifications before use. Therefore, we designed a novel and magnetically separable laccase-carrying biocatalyst containing spent-mushroom-substrate (SMS)-derived biochar (BF). Laccase was immobilized on NH-activated magnetic biochar (BF-NH) through covalent crosslinking, which provided physicochemical stability to the immobilized enzyme. After 30 days of storage at 4 °C, the immobilized laccase (product named "BF-NH-Lac") retained ~95 % of its initial activity, while after five repeated cycles of ABTS oxidation, ~85 % activity retention was observed. BF-NH-Lac was investigated for the oxidative degradation of AFB, which exhibited superior performance compared to free laccase. Among many tested natural compounds as mediators, p-coumaric acid proved the most efficient in activating laccase for AFB degradation. BF-NH-Lac demonstrated >90 % removal of AFB within 5.0 h, while the observed degradation efficiency in corn oil and buffer was comparable. An insight into the adsorptive and degradative removal of AFB revealed that AFB removal was governed mainly by degradation. The coexistence of multi-mycotoxins did not significantly affect the AFB degradation capability of BF-NH-Lac. Investigation of the degradation products revealed the transformation of AFB into non-toxic AFQ while corn oil quality remained unaffected after BF-NH-Lac treatment. Hence, this study holds practical importance for the research, knowledge-base and industrial application of newly proposed immobilized enzyme products.

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http://dx.doi.org/10.1016/j.ijbiomac.2024.133115DOI Listing

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