BiologybioRxiv

Ranked by formulaVerdict: Notable

Directed Evolution of Multimodal Plastic Degrading Enzymes

The inability to break down plastics is a major obstacle in the ongoing quest for sustainability.

By Petersson, Petersson

Score████░░░░░░4.4

Caveats

  • Preprint; not yet peer reviewed.

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Abstract

The inability to break down plastics is a major obstacle in the ongoing quest for sustainability. Advancements have been made in identifying enzymes that can break down certain polyesters; however, these enzymes are limited to the primary substrate and closely related plastic polymers. By increasing the catalytic promiscuity of polyester-degrading enzymes through directed evolution, a multimodal plastic degrading enzyme can be created. In order to achieve this, a polyesterase was first designed for secretion from the periplasm of E. coli. Through active site analysis, four sites were selected for amino acid randomization to create a >300,000 member mutant library. Next, a plate-based activity analysis system was developed to ensure efficient and reproducible screening of variants from the mutant library. Mutants with signs of activity on polyester- or polyurethane-containing agar were propagated and tested in liquid assays using a spectroscopic probe. A mutant was identified that retained polyesterase activity with newly developed polyurethane-degrading activity. Computational analysis indicated that these changes expanded the substrate pocket while retaining the positioning of the catalytic residues essential to the hydrolysis reaction. This provides the first demonstration of the directed evolution of a multimodal plastic degrading enzyme and serves as a model for further expanding polyesterase promiscuity to include multiple hydrolyzable plastics.

C. J. Petersson, E. J. Petersson

The editor's rubric

Heuristic review

Leverage3 / 5
A method or resource many groups across the field will adopt within a year.
24% of this desk’s rubric
Magnitude3 / 5
Large gain: roughly 2x, or a clear new state of the art on a hard, unsaturated problem.
16% of this desk’s rubric
Evidence3 / 5
Solid: multiple benchmarks or cohorts, ablations, fair baselines, released code or data.
20% of this desk’s rubric
Novelty3 / 5
A genuinely new approach to an open problem.
20% of this desk’s rubric
Trajectory3 / 5
A clear path to scale.
10% of this desk’s rubric
Stakes2 / 5
Benefits a professional community (practitioners, clinicians, engineers).
10% of this desk’s rubric

Editor’s rationale

Heuristic triage from title and abstract text only, not a reading of the paper. Cues found: breadth (many tasks); firsts (first); design (randomized); verification (independent replication); scale (efficient).

How the score was computed

rank-2026-10-18

Score████░░░░░░4.4

Score = 10 × (75% × adjusted merit / 10 + 15% × attention + 10% × freshness)

Desks place stronger verdicts first, then use this score to order work within the same verdict.

Merit
5.8 / 10
Weighted rubric, evidence-gated.
Adjusted merit
4.7 / 10
Shrunk toward the desk prior by editor confidence (40%).
Attention
0%
Citations, upvotes, points, mentions.
Freshness
88%
Half-life decay since publication.

No attention signals recorded yet.

The record

  • Reviewed by heuristic-v10 on Oct 29, 2026, 05:48 UTC. Paper type: empirical.
  • Categories: bioengineering
  • TOP, No.5 in the Biology edition of October 29, 2026.