Evidence map›Paper›PMID 42360106›Full record

ArticleAngewandte Chemie (International ed. in English)2026

Environmental Identification of Novel Enzymes for Polyurethane and Polyamide Degradation.

Malthe Kjær Bendtsen, Andreas Møllebjerg, Samuel Peña-Díaz, Rosie Graham, Nicolai Claus Petersen, Bjørk Nolsøe Isaksen, Mathias Carstensen, Martin B Johansen, Andreas Sommerfeldt, Allan R Petersen and 8 more

Abstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors.

Malthe Kjær BendtsenEnZync Center for Enzymatic Deconstruction of Thermoset Plastics, Aarhus, Denmark.ORCID 0009-0002-8505-9994
Andreas MøllebjergEnZync Center for Enzymatic Deconstruction of Thermoset Plastics, Aarhus, Denmark.ORCID 0000-0001-6633-6939
Samuel Peña-DíazEnZync Center for Enzymatic Deconstruction of Thermoset Plastics, Aarhus, Denmark.
Rosie GrahamEnZync Center for Enzymatic Deconstruction of Thermoset Plastics, Aarhus, Denmark.
Nicolai Claus PetersenEnZync Center for Enzymatic Deconstruction of Thermoset Plastics, Aarhus, Denmark.
Bjørk Nolsøe IsaksenEnZync Center for Enzymatic Deconstruction of Thermoset Plastics, Aarhus, Denmark.
Mathias CarstensenEnZync Center for Enzymatic Deconstruction of Thermoset Plastics, Aarhus, Denmark.
Martin B JohansenEnZync Center for Enzymatic Deconstruction of Thermoset Plastics, Aarhus, Denmark.
Andreas SommerfeldtEnZync Center for Enzymatic Deconstruction of Thermoset Plastics, Aarhus, Denmark.
Allan R PetersenEnZync Center for Enzymatic Deconstruction of Thermoset Plastics, Aarhus, Denmark.
Iddi Khamisi ChumaDepartment of Biological Sciences, Pwani University, Kilifi, Kenya.
Cecilie RybergInterdisciplinary Nanoscience Center (iNANO), Aarhus University, Aarhus, Denmark.
Thomas Rea WittenbornThe FACS Core Facility, Aarhus University, Aarhus, Denmark.
Virginia GichuruDepartment of Biological Sciences, Pwani University, Kilifi, Kenya.
Huabing WangThe First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Carsten ScaveniusDepartment of Molecular Biology and Genetics, Aarhus University, Aarhus, Denmark.
Alexander SandahlEnZync Center for Enzymatic Deconstruction of Thermoset Plastics, Aarhus, Denmark.
Daniel E OtzenEnZync Center for Enzymatic Deconstruction of Thermoset Plastics, Aarhus, Denmark.ORCID 0000-0002-2918-8989

Funding

Novo Nordisk Foundation NNF22OC0072891
6 · The paper itself

Abstract

Better enzymes are needed to develop sustainable methods to recycle plastics with C-X heterobonds such as polyurethane (PUR) and nylon, for which no industrial-scale solutions exist. Current methods rely largely on sequence mining based on a small number of known enzymes. Here, we expand the pool of PURases and nylonases by bioprospecting legacy plastic waste with fluorophore plastic mimics combined with fluorescence-assisted cell sorting (FACS). We identify 29 plastic-degrading bacteria, from which 12 enzymes are identified by mass spectrometry and homology searches. Compared to existing enzymes, these enzymes show higher thermostability and hydrolytic activities against different high-molecular weight PUR polymers and nylon textiles compared to previously described wildtype enzymes. To our knowledge, this is the first reported example of enzymes capable of hydrolyzing longer chains of untreated PUR and nylon as well as crosslinked PUR. This study significantly increases the number of known PURases and nylonases and provides starting points for optimization campaigns through protein engineering and for in silico discovery.

Indexed as

NylonsPolyurethanesBacteriaHydrolysisNylonsPolyurethanesbiocatalysisenzymesnylonasepolymersurethanase

Identifiers

PMID42360106
PMCPMC13502555

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.