Biocatalytic Functionalization and Degradation of Synthetic Polymers

A special issue of Polymers (ISSN 2073-4360).

Deadline for manuscript submissions: closed (10 January 2019)

Special Issue Editor


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Guest Editor
Department of Microbiology and Bioprocess Technology, Leipzig University, Johannisallee 23, 04103 Leipzig, Germany
Interests: enzyme technology; industrial biotechnology; biocatalytic modification of polymers; carbohydrate bioengineering

Special Issue Information

Dear Colleagues,

It has been demonstrated that synthetic polymers, such as polyethylene terephthalate and polyester polyurethanes, can be effectively modified and even completely degraded by microbial enzymes. The biocatalytic hydrolysis of these polymers is emerging as a new strategy to improve the recycling of post-consumer plastic waste. Enzymes can also be used to modify the surface properties of synthetic polymers for example to enhance the hydrophilicity of synthetic fibers or plastic films.

Contributions presenting progress in our understanding of the biocatalytic mechanism, structure-function relationships, and engineering of novel polyester hydrolases are welcome. Topics may also include innovative applications of these enzymes, for example for the functionalization of polymer surfaces. Original work reporting novel enzymes for the degradation of other recalcitrant synthetic polymers, such as polyethylene and polystyrene, will also be of interest.

Prof. Dr. Wolfgang Zimmermann
Guest Editor

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Keywords

  • Synthetic polymers
  • Biocatalysis
  • Polymer functionalization
  • Plastic recycling
  • Polyester hydrolases
  • Polyethylene terephthalate
  • Polyurethanes
  • Polyethylene
  • Polystyrene

Published Papers (1 paper)

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Research

15 pages, 2832 KiB  
Article
Enzymatic Degradation of Star Poly(ε-Caprolactone) with Different Central Units
by Catherine J. Blackwell, Karolina Haernvall, Georg M. Guebitz, Michael Groombridge, Denis Gonzales and Ezat Khosravi
Polymers 2018, 10(11), 1266; https://doi.org/10.3390/polym10111266 - 14 Nov 2018
Cited by 34 | Viewed by 5288
Abstract
Four-arm star poly(ε-caprolactone) with a central poly(ethylene glycol) PEG unit bridged with 2,2-bis(methyl) propionic acid, (PCL)2-b-PEG-b-(PCL)2, and six-arm star PCL homopolymer with a central dipentaerythritol units were hydrolysed using a lipase from Pseudomonas [...] Read more.
Four-arm star poly(ε-caprolactone) with a central poly(ethylene glycol) PEG unit bridged with 2,2-bis(methyl) propionic acid, (PCL)2-b-PEG-b-(PCL)2, and six-arm star PCL homopolymer with a central dipentaerythritol units were hydrolysed using a lipase from Pseudomonas cepacia and the Thermobifida cellulosilytica cutinase Thc_Cut1. For comparative analysis, Y-shaped copolymers containing methylated PEG bridged with bisMPA, MePEG-(PCL)2, and linear triblock copolymers PCL-b-PEG-b-PCL were also subjected to enzymatic hydrolysis. The hydrophilic nature of the polymers was determined using contact angle analysis, showing that a higher PEG content exhibited a lower contact angle and higher surface wettability. Enzymatic hydrolysis was monitored by % mass loss, scanning electron microscopy (SEM), and differential scanning calorimetry (DSC). A higher rate of mass loss was found for lipase catalysed hydrolysis of those polymers with the highest PEG content, leading to significant surface erosion and increase in crystallinity within the first two days. Liquid chromatography (LC) and size exclusion chromatography (SEC) of samples incubated with the cutinase showed a significant decrease in molecular weight, increase in dispersity, and release of ε-CL monomer units after 6 h of incubation. Full article
(This article belongs to the Special Issue Biocatalytic Functionalization and Degradation of Synthetic Polymers)
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