4.7 Article

Poly(butylene adipate-co-terephthalate) biodegradation by Purpureocillium lilacinum strain BA1S

Journal

APPLIED MICROBIOLOGY AND BIOTECHNOLOGY
Volume 107, Issue 19, Pages 6057-6070

Publisher

SPRINGER
DOI: 10.1007/s00253-023-12704-z

Keywords

PBAT plastic; Lipolytic enzymes; Cutinase; Cytochrome P450; Carbon catabolite repression; Purpureocillium lilacinum

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In this study, four PBAT-degrading fungal strains were isolated and a prominent degradation rate was observed in Purpureocillium lilacinum strain BA1S. The lipolytic enzyme activities and cutinase gene of BA1S were induced in the presence of PBAT. Intracellular cytochrome P450 (CYP) monooxygenase and CreA-mediated carbon catabolite repression were also found to be involved in the degradation process.
Poly(butylene adipate-co-terephthalate) (PBAT), a promising biodegradable aliphatic-aromatic copolyester material, can be applied as an alternative material to reduce the adverse effects of conventional plastics. However, the degradation of PBAT plastics in soil is time-consuming, and effective PBAT-degrading microorganisms have rarely been reported. In this study, the biodegradation properties of PBAT by an elite fungal strain and related mechanisms were elucidated. Four PBAT-degrading fungal strains were isolated from farmland soils, and Purpureocillium lilacinum strain BA1S showed a prominent degradation rate. It decomposed approximately 15 wt.% of the PBAT films 30 days after inoculation. Scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), and Liquid chromatography mass spectrometry (LC-MS) were conducted to analyze the physicochemical properties and composition of the byproducts after biodegradation. In the presence of PBAT, the lipolytic enzyme activities of BA1S were remarkably induced, and its cutinase gene was also significantly upregulated. Of note, the utilization of PBAT in BA1S cells was closely correlated with intracellular cytochrome P450 (CYP) monooxygenase. Furthermore, CreA-mediated carbon catabolite repression was confirmed to be involved in regulating PBAT-degrading hydrolases and affected the degradation efficiency. This study provides new insight into the degradation of PBAT by elite fungal strains and increases knowledge on the mechanism, which can be applied to control the biodegradability of PBAT films in the future.

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