<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ren L</submitter><funding>Lei Ren</funding><funding>Yangyan Wang</funding><funding>Yanyan Wang</funding><pagination>8141</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12428281</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>26(17)</volume><pubmed_abstract>Phthalic acid esters (PAEs), ubiquitously employed as a plasticizer, have been classified as priority environmental pollutants because of their persistence, bioaccumulation, and endocrine-disrupting properties. As a characterized PAE-degrading strain of marine origin, &lt;i>Mycolicibacterium phocaicum&lt;/i> RL-HY01 utilizes di-(2-ethylhexyl) phthalate (DEHP) as its sole carbon and energy source. Genome sequencing and RT-qPCR analysis revealed a previously uncharacterized hydrolase gene (&lt;i>dehpH&lt;/i>) in strain RL-HY01, which catalyzes ester bond cleavage in PAEs. Subsequently, recombinant expression of the cloned &lt;i>dehpH&lt;/i> gene from strain RL-HY01 was established in &lt;i>Escherichia coli&lt;/i> BL21(DE3). The purified recombinant DehpH exhibited optimal activity at 30 °C and pH 8.0. Its activity </pubmed_abstract><journal>International journal of molecular sciences</journal><pubmed_title>Identification and Characterization of a Novel Di-(2-ethylhexyl) Phthalate Hydrolase from a Marine Bacterial Strain &amp;lt;i&amp;gt;Mycolicibacterium phocaicum&amp;lt;/i&amp;gt; RL-HY01.</pubmed_title><pmcid>PMC12428281</pmcid><funding_grant_id>College of Coastal Agricultural Sciences Distinguished Young Program (BH2025JCQN003)</funding_grant_id><funding_grant_id>Special Innovation Projects of Universities in Guangdong Province (2023KTSCX043)</funding_grant_id><funding_grant_id>Non-funded Projects of Zhanjiang City (2024B01096)</funding_grant_id><funding_grant_id>the National Natural Science Foundation of China(31800109 and 32271702)</funding_grant_id><funding_grant_id>Program for Scientific Research start-up Funds of Guangdong Ocean University (060302052312)</funding_grant_id><funding_grant_id>Guangdong Engineering Technology Research Center of Tropical Crops High-efficient Production (C16064)</funding_grant_id><funding_grant_id>Graduate Education Innovation Program of Guangdong Ocean University (202402)</funding_grant_id><pubmed_authors>Shi M</pubmed_authors><pubmed_authors>Ren L</pubmed_authors><pubmed_authors>Zhou JL</pubmed_authors><pubmed_authors>Kuang C</pubmed_authors><pubmed_authors>Hu H</pubmed_authors><pubmed_authors>Xu D</pubmed_authors><pubmed_authors>Wang H</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Identification and Characterization of a Novel Di-(2-ethylhexyl) Phthalate Hydrolase from a Marine Bacterial Strain &amp;lt;i&amp;gt;Mycolicibacterium phocaicum&amp;lt;/i&amp;gt; RL-HY01.</name><description>Phthalic acid esters (PAEs), ubiquitously employed as a plasticizer, have been classified as priority environmental pollutants because of their persistence, bioaccumulation, and endocrine-disrupting properties. As a characterized PAE-degrading strain of marine origin, &lt;i>Mycolicibacterium phocaicum&lt;/i> RL-HY01 utilizes di-(2-ethylhexyl) phthalate (DEHP) as its sole carbon and energy source. Genome sequencing and RT-qPCR analysis revealed a previously uncharacterized hydrolase gene (&lt;i>dehpH&lt;/i>) in strain RL-HY01, which catalyzes ester bond cleavage in PAEs. Subsequently, recombinant expression of the cloned &lt;i>dehpH&lt;/i> gene from strain RL-HY01 was established in &lt;i>Escherichia coli&lt;/i> BL21(DE3). The purified recombinant DehpH exhibited optimal activity at 30 °C and pH 8.0. Its activity </description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Aug</publication><modification>2026-04-08T18:35:16.821Z</modification><creation>2026-04-08T09:57:05.097Z</creation></dates><accession>S-EPMC12428281</accession><cross_references><pubmed>40943065</pubmed><doi>10.3390/ijms26178141</doi></cross_references></HashMap>