<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Suzuki N</submitter><funding>Moonshot Research and Development Program of the New Energy and Industrial Technology Development Organization, Japan</funding><funding>Japan Science and Technology Agency</funding><funding>New Energy and Industrial Technology Development Organization</funding><pagination>2324</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9782182</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>10(12)</volume><pubmed_abstract>Microbial degradation of natural rubber and synthetic poly(&lt;i>cis&lt;/i>-1,4-isoprene) is expected to become an alternative treatment system for waste from poly(&lt;i>cis&lt;/i>-1,4-isoprene) products including scrap tires. &lt;i>Nocardia farcinica&lt;/i> NBRC 15,532, a gram-positive rubber-degrading bacterium, can utilize poly(&lt;i>cis&lt;/i>-1,4-isoprene) as the sole source of carbon and energy to produce oligo-isoprene metabolites containing aldehyde and keto end groups. A homology-based search of the genome revealed a gene encoding a latex-clearing protein (Lcp). Gene disruption analysis indicated that this gene is essential for the utilization of poly(&lt;i>cis&lt;/i>-1,4-isoprene) in this strain. Further analysis of the genome sequence identified aldehyde dehydrogenase (ALDH) genes as potential candidates for oxidative degradation of oligo-isoprene aldehydes. Based on the enzymatic activity of the ALDH candidates, NF2_RS14000 and NF2_RS14385 may be involved in the degradation of oligo-isoprene aldehydes. Analysis of the reaction products revealed that these ALDHs oxidized tri- to penta-isoprene aldehydes, which were generated by the reaction of Lcp. Based on the inability of ALDH gene deletion mutants, we concluded that NF2_RS14000 is mainly involved in the utilization of poly(&lt;i>cis&lt;/i>-1,4-isoprene) and the oxidative degradation of oligo-isoprene aldehydes in &lt;i>Nocardia farcinica&lt;/i> NBRC 15,532.</pubmed_abstract><journal>Microorganisms</journal><pubmed_title>Characterization of Latex-Clearing Protein and Aldehyde Dehydrogenases Involved in the Utilization of poly(cis-1,4-isoprene) by Nocardia farcinica NBRC 15532</pubmed_title><pmcid>PMC9782182</pmcid><funding_grant_id>Moonshot Research and Development Program</funding_grant_id><funding_grant_id>JPMJMI19E6</funding_grant_id><pubmed_authors>Suda D</pubmed_authors><pubmed_authors>Kasai D</pubmed_authors><pubmed_authors>Anh TK</pubmed_authors><pubmed_authors>Suzuki N</pubmed_authors><pubmed_authors>Ngan NTT</pubmed_authors><pubmed_authors>Huong NL</pubmed_authors><pubmed_authors>Gibu N</pubmed_authors></additional><is_claimable>false</is_claimable><name>Characterization of Latex-Clearing Protein and Aldehyde Dehydrogenases Involved in the Utilization of poly(cis-1,4-isoprene) by Nocardia farcinica NBRC 15532</name><description>Microbial degradation of natural rubber and synthetic poly(&lt;i>cis&lt;/i>-1,4-isoprene) is expected to become an alternative treatment system for waste from poly(&lt;i>cis&lt;/i>-1,4-isoprene) products including scrap tires. &lt;i>Nocardia farcinica&lt;/i> NBRC 15,532, a gram-positive rubber-degrading bacterium, can utilize poly(&lt;i>cis&lt;/i>-1,4-isoprene) as the sole source of carbon and energy to produce oligo-isoprene metabolites containing aldehyde and keto end groups. A homology-based search of the genome revealed a gene encoding a latex-clearing protein (Lcp). Gene disruption analysis indicated that this gene is essential for the utilization of poly(&lt;i>cis&lt;/i>-1,4-isoprene) in this strain. Further analysis of the genome sequence identified aldehyde dehydrogenase (ALDH) genes as potential candidates for oxidative degradation of oligo-isoprene aldehydes. Based on the enzymatic activity of the ALDH candidates, NF2_RS14000 and NF2_RS14385 may be involved in the degradation of oligo-isoprene aldehydes. Analysis of the reaction products revealed that these ALDHs oxidized tri- to penta-isoprene aldehydes, which were generated by the reaction of Lcp. Based on the inability of ALDH gene deletion mutants, we concluded that NF2_RS14000 is mainly involved in the utilization of poly(&lt;i>cis&lt;/i>-1,4-isoprene) and the oxidative degradation of oligo-isoprene aldehydes in &lt;i>Nocardia farcinica&lt;/i> NBRC 15,532.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2026-06-22T03:19:16.553Z</modification><creation>2025-02-19T03:00:57.426Z</creation></dates><accession>S-EPMC9782182</accession><cross_references><pubmed>36557577</pubmed><doi>10.3390/microorganisms10122324</doi></cross_references></HashMap>