Aug 2026· Journal of Hazardous Materials· Vol 515, pp.
143252
· 0 citations· 48 references
Medicine
TL;DR
A theoretical basis for using substrate pre-activation and evolved biocatalysis to treat PET-contaminated alkaline industrial effluents is provided, providing a theoretical basis for using substrate pre-activation and evolved biocatalysis to treat PET-contaminated alkaline industrial effluents.
Abstract
Polyethylene terephthalate (PET) is a hazardous environmental contaminant that contributes to both plastic and microplastic pollution, with its biodegradation severely limited by the kinetic stability of ester bonds-particularly in alkaline industrial wastewater (pH 9-11) where most known biocatalysts are inactive. To overcome this, evolutionary engineering was employed to construct a whole-cell biocatalyst for alkaline environments. Through UV-LiCl mutagenesis and adaptive laboratory evolution, an alkaline-adapted Comamonas testosteroni strain F6 was developed, thriving at pH 10 with PET as sole carbon source. Strain F6 increased weight loss from 2.4% to 6.1% in 3 days and accelerated terephthalic acid release versus the wild-type under neutral conditions. This improvement arises from a synergistic mechanism: alkaline conditions chemically pre-activate ester bonds, and the released monomers fuel microbial growth and enzyme secretion, establishing a self-reinforcing degradation cycle. This feedback-driven process caused severe surface erosion, reducing fiber diameter from 20.2 to 18.1 μm. The system operates at mild pH 10 and 37 °C with a self-moderating effect that partially neutralizes alkalinity, contrasting with harsh chemical hydrolysis (pH >13, high temperature). This work provides a theoretical basis for using substrate pre-activation and evolved biocatalysis to treat PET-contaminated alkaline industrial effluents.
Integrating thermolabile enzymes into industrial melt processing remains a key challenge for achieving programmable self-degradable plastics. Here, we demonstrate a process-compatible stabilization strategy for bio-based polyesters using immobilized Alcalase. Two approaches were compared: adsorption onto zeolite (Z-En)...
J. Seo, In-Woo Nam, Hyojung Kim et al.· Polymers· 0 citations
Polybutylene adipate terephthalate (PBAT) is prone to incomplete degradation, leading to environmental pollution and carbon resource waste. Biodegradation and valorization of waste plastics are essential for addressing plastic pollution and promoting a circular economy. Enzymatic degradation offers advantages, but free...
Jiali Liu, Jie Yang, Xin Wang et al.· Bioresource Technology· 0 citations
Herein, a highly rigid monomer, 2-(2-hydroxyethyl)-1,3-dioxoisoindoline-5-carboxylic acid (HTI), was readily prepared from biosourced malic acid. A series of PET copolyesters were fabricated through an in situ chemical upcycling strategy, in which HTI units were inserted into the backbones of the PET waste via a depo...
In the context of a bio-based circular economy, replacing fossil raw materials with renewable alternatives has become a major trend. Platform chemicals such as itaconic acid and 2.5-furandicarboxylic acid can now be produced from sugars or lignocellulose and used to synthesize fully bio-based polyesters e.g. poly(e...
Daniel Sandvoß, J. S. Gutmann, M. Dornbusch· Journal of Coatings Technolo...· 0 citations
Abstract In this study, a hybrid biocatalyst was developed via rapid in-situ biomineralization of laccase within a cobalt(II)-malonate framework (Lac@MOF). The novelty lies in using malonic acid as a biocompatible linker, enabling rapid enzyme encapsulation under mild conditions. Structural integrity was confirmed thro...
Biocatalytic ester synthesis often encounters bottlenecks like vast substrate polarity differences and reliance on toxic solvents or activated acyl donors, severely limiting industrial expansion. To address this, a novel catalytic deep eutectic solvent (CDES) system composed of cyclohexanone, stearic acid, and N-methyl...