Evidence map›Paper›PMID 39605696›Full record

ArticlebioRxiv : the preprint server for biology2024

Identification and characterization of substrate- and product-selective nylon hydrolases.

Erin E Drufva, John F Cahill, Patricia M B Saint-Vincent, Alexis N Williams, Vera Bocharova, Nikolas Capra, Flora Meilleur, Dana L Carper, Célestin Bourgery, Kaito Miyazaki and 17 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

27 authors.

Erin E DrufvaBiosciences Division, Oak Ridge National Laboratory, Oak Ridge, TN, USA 37830.
John F CahillBiosciences Division, Oak Ridge National Laboratory, Oak Ridge, TN, USA 37830.ORCID 0000-0002-9866-4010
Patricia M B Saint-VincentBiosciences Division, Oak Ridge National Laboratory, Oak Ridge, TN, USA 37830.ORCID 0000-0001-6360-8206
Alexis N WilliamsCenter for Nanophase Materials Sciences, Oak Ridge National Laboratory, Oak Ridge, TN, USA 37830.ORCID 0000-0002-5283-5822
Vera BocharovaChemical Sciences Division, Oak Ridge National Laboratory, Oak Ridge, TN, USA 37830.ORCID 0000-0003-4270-3866
Nikolas CapraNeutron Scattering Division, and Oak Ridge National Laboratory, Oak Ridge, TN, USA 37830.ORCID 0000-0002-2898-6479
Flora MeilleurNeutron Scattering Division, and Oak Ridge National Laboratory, Oak Ridge, TN, USA 37830.ORCID 0000-0001-9313-8989
Dana L CarperBiosciences Division, Oak Ridge National Laboratory, Oak Ridge, TN, USA 37830.ORCID 0000-0002-4758-8054
Célestin BourgeryBiosciences Division, Oak Ridge National Laboratory, Oak Ridge, TN, USA 37830.ORCID 0000-0002-7318-2218
Kaito MiyazakiDepartment of Science, Graduate School of Science and Engineering, Kagoshima University, 1-21-35 Korimoto, Kagoshima, 890-0065, Japan.
Maina YonemuraDepartment of Science, Graduate School of Science and Engineering, Kagoshima University, 1-21-35 Korimoto, Kagoshima, 890-0065, Japan.
Yuki ShiraishiDepartment of Science, Graduate School of Science and Engineering, Kagoshima University, 1-21-35 Korimoto, Kagoshima, 890-0065, Japan.
Jerry M ParksBiosciences Division, Oak Ridge National Laboratory, Oak Ridge, TN, USA 37830.ORCID 0000-0002-3103-9333
Muchu ZhouChemical Sciences Division, Oak Ridge National Laboratory, Oak Ridge, TN, USA 37830.ORCID 0000-0001-8265-0215
Isaiah T DishnerChemical Sciences Division, Oak Ridge National Laboratory, Oak Ridge, TN, USA 37830.ORCID 0000-0002-7333-9182
Jeffrey C FosterChemical Sciences Division, Oak Ridge National Laboratory, Oak Ridge, TN, USA 37830.ORCID 0000-0002-9097-8680
Stephen J KoehlerDepartment of Chemistry and Macromolecules Innovation Institute, Virginia Tech, Blacksburg, Virginia 24061, United States.
Hannah R ValentinoBiosciences Division, Oak Ridge National Laboratory, Oak Ridge, TN, USA 37830.ORCID 0009-0008-3117-3541
Ada SedovaBiosciences Division, Oak Ridge National Laboratory, Oak Ridge, TN, USA 37830.ORCID 0000-0002-8233-3057
Vilmos KerteszBiosciences Division, Oak Ridge National Laboratory, Oak Ridge, TN, USA 37830.ORCID 0000-0003-0186-5797
Delyana P VasilevaBiosciences Division, Oak Ridge National Laboratory, Oak Ridge, TN, USA 37830.ORCID 0000-0002-7919-7883
Leah H HochanadelBiosciences Division, Oak Ridge National Laboratory, Oak Ridge, TN, USA 37830.
C Adrian FiggDepartment of Chemistry and Macromolecules Innovation Institute, Virginia Tech, Blacksburg, Virginia 24061, United States.ORCID 0000-0003-3514-7750
Seiji NegoroDepartment of Applied Chemistry, Graduate School of Engineering, University of Hyogo, 2167 Shosha, Himeji, Hyogo 671-2280, Japan.ORCID 0000-0002-9132-6860
Dai-Ichiro KatoDepartment of Science, Graduate School of Science and Engineering, Kagoshima University, 1-21-35 Korimoto, Kagoshima, 890-0065, Japan.ORCID 0000-0002-8255-8790
Serena H ChenComputational Sciences and Engineering Division, Oak Ridge National Laboratory, Oak Ridge, TN, USA 37830.ORCID 0000-0002-6535-6812
Joshua K MichenerBiosciences Division, Oak Ridge National Laboratory, Oak Ridge, TN, USA 37830.ORCID 0000-0003-2302-8180

Funding

National HTX Center: Enabling Access to State-of-the-Art Crystallization CapabilitiesR24GM141256 · NIGMS · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI Sarah Elizabeth Johnson Bowman · 2021 to 2026
$6.3M
NIGMS NIH HHS R24 GM141256
6 · The paper itself

Abstract

Enzymes have evolved to rapidly and selectively hydrolyze diverse natural and anthropogenic polymers, but only a limited group of related enzymes have been shown to hydrolyze synthetic polyamides. In this work, we synthesized and characterized a panel of 95 diverse enzymes from the N-terminal nucleophile hydrolase superfamily with 30-50% pairwise amino acid identity. We found that nearly 40% of the enzymes had substantial nylon hydrolase activity, in many cases comparable to that of the best-characterized nylon hydrolase, NylC. There was no relationship between phylogeny and activity, nor any evidence of prior selection for nylon hydrolase activity. Several newly-identified hydrolases showed significant substrate selectivity, generating up to 20-fold higher product titers with Nylon 6,6 versus Nylon 6. Finally, we determined the crystal structure and oligomerization state of a Nylon 6,6-selective hydrolase to elucidate structural factors that could affect activity and selectivity. These new enzymes provide insights into the widespread potential for nylon hydrolase evolution and opportunities for analysis and engineering of improved hydrolases.

Identifiers

PMID39605696
PMCPMC11601465

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Registered trials

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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 OpenQuestion graph.