<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>9(4)</volume><submitter>Li S</submitter><funding>Jiangnan University</funding><pubmed_abstract>The diterpene &lt;i>ent&lt;/i>-copalol is an important precursor to the synthesis of andrographolide and is found only in green chiretta &lt;i>(Andrographis paniculata)&lt;/i>. &lt;i>De novo&lt;/i> biosynthesis of &lt;i>ent&lt;/i>-copalol has not been reported, because the catalytic activity of &lt;i>ent&lt;/i>-copalyl diphosphate synthase (CPS) is very low in microorganisms. In order to achieve the biosynthesis of &lt;i>ent&lt;/i>-copalol, &lt;i>Saccharomyces cerevisiae&lt;/i> was selected as the chassis strain, because its endogenous mevalonate pathway and dephosphorylases could provide natural promotion for the synthesis of &lt;i>ent&lt;/i>-copalol. The strain capable of synthesizing diterpene geranylgeranyl pyrophosphate was constructed by strengthening the mevalonate pathway genes and weakening the competing pathway. Five full-leng</pubmed_abstract><journal>Synthetic and systems biotechnology</journal><pagination>784-792</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11253141</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Screening of &lt;i>ent&lt;/i>-copalyl diphosphate synthase and metabolic engineering to achieve &lt;i>de novo&lt;/i> biosynthesis of &lt;i>ent&lt;/i>-copalol in &lt;i>Saccharomyces cerevisiae&lt;/i>.</pubmed_title><pmcid>PMC11253141</pmcid><pubmed_authors>Yin X</pubmed_authors><pubmed_authors>Li S</pubmed_authors><pubmed_authors>Lu J</pubmed_authors><pubmed_authors>Xu S</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Luo S</pubmed_authors><pubmed_authors>Gao S</pubmed_authors><pubmed_authors>Zhao X</pubmed_authors><pubmed_authors>Zhou J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Screening of &lt;i>ent&lt;/i>-copalyl diphosphate synthase and metabolic engineering to achieve &lt;i>de novo&lt;/i> biosynthesis of &lt;i>ent&lt;/i>-copalol in &lt;i>Saccharomyces cerevisiae&lt;/i>.</name><description>The diterpene &lt;i>ent&lt;/i>-copalol is an important precursor to the synthesis of andrographolide and is found only in green chiretta &lt;i>(Andrographis paniculata)&lt;/i>. &lt;i>De novo&lt;/i> biosynthesis of &lt;i>ent&lt;/i>-copalol has not been reported, because the catalytic activity of &lt;i>ent&lt;/i>-copalyl diphosphate synthase (CPS) is very low in microorganisms. In order to achieve the biosynthesis of &lt;i>ent&lt;/i>-copalol, &lt;i>Saccharomyces cerevisiae&lt;/i> was selected as the chassis strain, because its endogenous mevalonate pathway and dephosphorylases could provide natural promotion for the synthesis of &lt;i>ent&lt;/i>-copalol. The strain capable of synthesizing diterpene geranylgeranyl pyrophosphate was constructed by strengthening the mevalonate pathway genes and weakening the competing pathway. Five full-leng</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Dec</publication><modification>2026-07-15T05:13:05.56Z</modification><creation>2025-04-04T15:02:28.785Z</creation></dates><accession>S-EPMC11253141</accession><cross_references><pubmed>39021361</pubmed><doi>10.1016/j.synbio.2024.06.005</doi></cross_references></HashMap>