Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Free-Radical Chain Reaction and Polymerization of Alkenes02:35

Free-Radical Chain Reaction and Polymerization of Alkenes

7.7K
The conversion of alkenes to macromolecules called polymers is a reaction of high commercial importance. The structure of the polymer is defined by a repeating unit, while the terminal groups are considered insignificant. The average degree of polymerization represents the number of repeating units in the polymer molecule and is denoted by the subscript n.
7.7K
Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)00:53

Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)

1.9K
Acyclic diene metathesis polymerization or ADMET polymerization involves cross-metathesis of terminal dienes, such as 1,8-nonadiene, to give linear unsaturated polymer and ethylene. As ADMET is a reversible process, the formed ethylene gas must be removed from the reaction mixture to complete the polymerization process.
Similar to cross-metathesis, ADMET also involves the formation of metallacyclobutane intermediate by [2+2] cycloaddition of one of the double bonds of a terminal diene with...
1.9K
Polymer Classification: Architecture01:14

Polymer Classification: Architecture

2.7K
Polymers are classified as linear or branched on the basis of their chain architecture. The polymer chains in linear polymers have a long chain-like structure with minimal to no branching at all. Even if a polymer features large substituent groups on the monomer, which appear as branches to the skeleton, it is not considered a branched polymer. A branched polymer contains secondary polymer chains that arise from the main polymer chain. The branching occurs when the polymer growth shifts from...
2.7K
Radical Chain-Growth Polymerization: Mechanism01:09

Radical Chain-Growth Polymerization: Mechanism

2.5K
The radical chain-growth polymerization mechanism consists of three steps: initiation, propagation, and termination of polymerization. The polymerization initiates when a free radical generated from the radical initiator adds to the unsaturated bond in the monomer. The unpaired electron of the free radical and one π electron in the unsaturated bond creates a σ bond between the free radical and the monomer. As a result, the other π electron in the unsaturated bond converts this...
2.5K
Olefin Metathesis Polymerization: Overview01:13

Olefin Metathesis Polymerization: Overview

2.0K
Recently, the development of olefin metathesis polymerization advanced the field of polymer synthesis. Simply put, the reorganization of substituents on their double bonds between two olefins in the presence of a catalyst is known as the olefin metathesis reaction. The use of metathesis reaction for polymer synthesis is called olefin metathesis polymerization.
Ruthenium-based Grubbs catalyst is the most commonly used catalyst for olefin metathesis polymerization. Grubbs catalyst consists...
2.0K
Hydrolysis01:15

Hydrolysis

104.7K
Overview
Hydrolysis is a chemical reaction in which the addition of water breaks down a polymer into its simpler monomer units. For example, peptides break into amino acids, carbohydrates into simple sugars, and DNA into nucleotides. Enzymes often facilitate these processes.
Hydrolysis Reverses Dehydration Synthesis
Complex carbohydrates can be broken down by breaking the bonds between individual sugar units. The reaction breaks a glycosidic bond as water is added to the compound. The...
104.7K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

High-throughput assays for SAM-dependent methyltransferases: advances, challenges, and future perspectives.

Natural product reports·2026
Same author

Reprogramming of bacterial virulence by lysine acetylation.

Nature communications·2026
Same author

AcuB senses cellular energy charge to coordinate acetyl-CoA synthesis in bacteria.

Nature communications·2026
Same author

Fructan utilization by members of marine Gammaproteobacteria involves SusC/D-like proteins.

The ISME journal·2026
Same author

A genetically encoded L-rhamnose biosensor for monitoring marine polysaccharide depolymerization.

Applied microbiology and biotechnology·2026
Same author

Dynamic shift of internal electric field accelerates enzymatic polyethylene terephthalate depolymerization.

Communications chemistry·2026
Same journal

A Domino-Synthesized Dicoordinate Copper(I) Bis-imidazopyridine Complex Triggering Cuproptosis/Ferroptosis for Enhanced Cancer Immunotherapy.

Angewandte Chemie (International ed. in English)·2026
Same journal

Mirror-Symmetric Organic Two-Dimensional Crystals for Alternative Photon Transport Pathways.

Angewandte Chemie (International ed. in English)·2026
Same journal

Cobalt-Catalyzed Migratory E-Selective Asymmetric Aza-Nozaki-Hiyama-Kishi Coupling.

Angewandte Chemie (International ed. in English)·2026
Same journal

Facile Synthesis of α,ω-Dihydroxy Telechelic Macromonomers From Ethylene and α-Olefins for Recyclable Alternating Block Copolymers.

Angewandte Chemie (International ed. in English)·2026
Same journal

Multi-Atom Sub-Nanometer Assemblies on Interpenetrating Multi-Chambered N/C Nanospheres.

Angewandte Chemie (International ed. in English)·2026
Same journal

A Synergistic C<sub>2+</sub> Alcohols/Olefins-Intermediated Pathway Boosts CO<sub>2</sub> Hydrogenation to Aromatics.

Angewandte Chemie (International ed. in English)·2026
See all related articles

Related Experiment Video

Updated: Jun 12, 2025

Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers
08:12

Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers

Published on: December 16, 2022

3.2K

Chemo-Enzymatic Depolymerization of Functionalized Low-Molecular-Weight Polyethylene.

Thomas Oiffer1, Friedemann Leipold2, Philipp Süss2

  • 1Institute of Biochemistry, Dept. of Biotechnology and Enzyme Catalysis, University of Greifswald, Felix-Hausdorff Str. 4, 17487, Greifswald, Germany.

Angewandte Chemie (International Ed. in English)
|September 24, 2024
PubMed
Summary
This summary is machine-generated.

Researchers developed a novel enzyme cascade to depolymerize low-molecular-weight polyethylene (PE), a common plastic. This bio-based approach offers a promising new avenue for recycling challenging polyolefin waste.

Keywords:
Baeyer–Villiger oxidationEnzymatic degradationPE nanoparticlesPolyethyleneRhamnolipidsmCPBA

More Related Videos

Microwave-assisted Functionalization of Polyethylene glycol and On-resin Peptides for Use in Chain Polymerizations and Hydrogel Formation
15:33

Microwave-assisted Functionalization of Polyethylene glycol and On-resin Peptides for Use in Chain Polymerizations and Hydrogel Formation

Published on: October 29, 2013

28.9K
Designed for Molecular Recycling: A Lignin-Derived Semi-aromatic Biobased Polymer
10:22

Designed for Molecular Recycling: A Lignin-Derived Semi-aromatic Biobased Polymer

Published on: November 30, 2020

3.4K

Related Experiment Videos

Last Updated: Jun 12, 2025

Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers
08:12

Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers

Published on: December 16, 2022

3.2K
Microwave-assisted Functionalization of Polyethylene glycol and On-resin Peptides for Use in Chain Polymerizations and Hydrogel Formation
15:33

Microwave-assisted Functionalization of Polyethylene glycol and On-resin Peptides for Use in Chain Polymerizations and Hydrogel Formation

Published on: October 29, 2013

28.9K
Designed for Molecular Recycling: A Lignin-Derived Semi-aromatic Biobased Polymer
10:22

Designed for Molecular Recycling: A Lignin-Derived Semi-aromatic Biobased Polymer

Published on: November 30, 2020

3.4K

Area of Science:

  • Polymer Chemistry
  • Biocatalysis
  • Environmental Science

Background:

  • Polyethylene (PE) is a prevalent plastic contributing to global waste.
  • The inert nature of PE's carbon backbone hinders enzymatic degradation and biocatalytic recycling.
  • Developing effective recycling methods for PE waste remains a significant challenge.

Purpose of the Study:

  • To demonstrate the enzymatic depolymerization of low-molecular-weight polyethylene (LMW PE).
  • To explore a multi-enzyme cascade approach for breaking down PE waste.
  • To investigate a novel bio-based recycling strategy for polyolefins.

Main Methods:

  • Chemical pretreatment of LMW PE using m-chloroperoxybenzoic acid (mCPBA) and ultrasonication.
  • Enzymatic depolymerization employing a cascade of catalase-peroxidase, alcohol dehydrogenase, Baeyer Villiger monooxygenase, and lipase.
  • Analysis of polymer conversion using Gas Chromatography-Mass Spectrometry (GC-MS) and weight loss determination.
  • Characterization of LMWPE-nanoparticles using Atomic Force Microscopy (AFM).

Main Results:

  • Achieved approximately 27% polymer conversion in gram-scale experiments.
  • Formation of medium-sized functionalized molecules, including ω-hydroxycarboxylic acids and α,ω-carboxylic acids.
  • Enzymatic depolymerization led to a reduction in the size of mCPBA- and enzyme-treated LMWPE-nanoparticles.

Conclusions:

  • A multi-enzyme catalytic system, combined with chemical pretreatment, can depolymerize LMW PE.
  • This approach represents a novel starting point for developing bio-based recycling methods for polyolefin waste.
  • The study highlights the potential of enzymatic strategies for addressing plastic waste challenges.