<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Roman VA</submitter><funding>U.S. Department of Energy</funding><funding>U.S. Department of Energy (DOE)</funding><funding>DOD | Strategic Environmental Research and Development Program</funding><funding>DOD | USAF | AMC | Air Force Office of Scientific Research</funding><funding>DOD | Strategic Environmental Research and Development Program (SERDP)</funding><funding>DOD | USAF | AMC | Air Force Office of Scientific Research (AFOSR)</funding><pagination>e0169423</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11205760</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>90(5)</volume><pubmed_abstract>Given the multitude of extracellular enzymes at their disposal, many of which are designed to degrade nature's polymers (lignin, cutin, cellulose, etc.), fungi are adept at targeting synthetic polyesters with similar chemical composition. Microbial-influenced deterioration of xenobiotic polymeric surfaces is an area of interest for material scientists as these are important for the conservation of the underlying structural materials. Here, we describe the isolation and characterization of the &lt;i>Papiliotrema laurentii&lt;/i> 5307AH (&lt;i>P. laurentii&lt;/i>) cutinase, Plcut1. &lt;i>P. laurentii&lt;/i> is basidiomycete yeast with the ability to disperse Impranil-DLN (Impranil), a colloidal polyester polyurethane, in agar plates. To test whether the fungal factor involved in this clearing was a secreted e</pubmed_abstract><journal>Applied and environmental microbiology</journal><pubmed_title>Identification and recombinant expression of a cutinase from &lt;i>Papiliotrema laurentii&lt;/i> that hydrolyzes natural and synthetic polyesters.</pubmed_title><pmcid>PMC11205760</pmcid><funding_grant_id>DE-AC02-05CH11231</funding_grant_id><funding_grant_id>12RX14COR</funding_grant_id><funding_grant_id>WP-1381</funding_grant_id><pubmed_authors>Yan M</pubmed_authors><pubmed_authors>Grigoriev IV</pubmed_authors><pubmed_authors>Crable BR</pubmed_authors><pubmed_authors>Wagner DN</pubmed_authors><pubmed_authors>Biffinger J</pubmed_authors><pubmed_authors>Crookes-Goodson WJ</pubmed_authors><pubmed_authors>Kelley-Loughnane N</pubmed_authors><pubmed_authors>Haridas S</pubmed_authors><pubmed_authors>Ng V</pubmed_authors><pubmed_authors>Pangilinan J</pubmed_authors><pubmed_authors>Hung CS</pubmed_authors><pubmed_authors>Roman VA</pubmed_authors><pubmed_authors>Nadeau LJ</pubmed_authors><pubmed_authors>Gryganskyi A</pubmed_authors><pubmed_authors>Zelik S</pubmed_authors><pubmed_authors>Schratz L</pubmed_authors><pubmed_authors>Lipzen A</pubmed_authors><pubmed_authors>Cummings L</pubmed_authors><pubmed_authors>Barlow D</pubmed_authors><pubmed_authors>Stamps B</pubmed_authors><pubmed_authors>Na H</pubmed_authors><pubmed_authors>Varaljay VA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Identification and recombinant expression of a cutinase from &lt;i>Papiliotrema laurentii&lt;/i> that hydrolyzes natural and synthetic polyesters.</name><description>Given the multitude of extracellular enzymes at their disposal, many of which are designed to degrade nature's polymers (lignin, cutin, cellulose, etc.), fungi are adept at targeting synthetic polyesters with similar chemical composition. Microbial-influenced deterioration of xenobiotic polymeric surfaces is an area of interest for material scientists as these are important for the conservation of the underlying structural materials. Here, we describe the isolation and characterization of the &lt;i>Papiliotrema laurentii&lt;/i> 5307AH (&lt;i>P. laurentii&lt;/i>) cutinase, Plcut1. &lt;i>P. laurentii&lt;/i> is basidiomycete yeast with the ability to disperse Impranil-DLN (Impranil), a colloidal polyester polyurethane, in agar plates. To test whether the fungal factor involved in this clearing was a secreted e</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 May</publication><modification>2026-06-01T09:22:57.744Z</modification><creation>2025-04-05T17:57:31.069Z</creation></dates><accession>S-EPMC11205760</accession><cross_references><pubmed>38624219</pubmed><doi>10.1128/aem.01694-23</doi></cross_references></HashMap>