<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>12(7)</volume><submitter>Jiang F</submitter><pubmed_abstract>Both natural ginsenoside F2 and unnatural ginsenoside 3&lt;i>β&lt;/i>,20&lt;i>S&lt;/i>-Di-&lt;i>O&lt;/i>-Glc-DM were reported to exhibit anti-tumor activity. Traditional approaches for producing them rely on direct extraction from &lt;i>Panax ginseng&lt;/i>, enzymatic catalysis or chemical synthesis, all of which result in low yield and high cost. Metabolic engineering of microbes has been recognized as a green and sustainable biotechnology to produce natural and unnatural products. Hence we engineered the complete biosynthetic pathways of F2 and 3&lt;i>β&lt;/i>,20&lt;i>S&lt;/i>-Di-&lt;i>O&lt;/i>-Glc-DM in &lt;i>Saccharomyces cerevisiae via&lt;/i> the CRISPR/Cas9 system. The titers of F2 and 3&lt;i>β&lt;/i>,20&lt;i>S&lt;/i>-Di-&lt;i>O&lt;/i>-Glc-DM were increased from 1.2 to 21.0 mg/L and from 82.0 to 346.1 mg/L at shake flask level, respectively, by mul</pubmed_abstract><journal>Acta pharmaceutica Sinica. B</journal><pagination>3167-3176</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9293705</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Metabolic engineering of yeasts for green and sustainable production of bioactive ginsenosides F2 and 3&lt;i>β&lt;/i>,20&lt;i>S&lt;/i>-Di-&lt;i>O&lt;/i>-Glc-DM.</pubmed_title><pmcid>PMC9293705</pmcid><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Gong T</pubmed_authors><pubmed_authors>Yang J</pubmed_authors><pubmed_authors>Zhu P</pubmed_authors><pubmed_authors>Jiang F</pubmed_authors><pubmed_authors>Chen J</pubmed_authors><pubmed_authors>Zhou C</pubmed_authors><pubmed_authors>Deng H</pubmed_authors><pubmed_authors>Chen T</pubmed_authors></additional><is_claimable>false</is_claimable><name>Metabolic engineering of yeasts for green and sustainable production of bioactive ginsenosides F2 and 3&lt;i>β&lt;/i>,20&lt;i>S&lt;/i>-Di-&lt;i>O&lt;/i>-Glc-DM.</name><description>Both natural ginsenoside F2 and unnatural ginsenoside 3&lt;i>β&lt;/i>,20&lt;i>S&lt;/i>-Di-&lt;i>O&lt;/i>-Glc-DM were reported to exhibit anti-tumor activity. Traditional approaches for producing them rely on direct extraction from &lt;i>Panax ginseng&lt;/i>, enzymatic catalysis or chemical synthesis, all of which result in low yield and high cost. Metabolic engineering of microbes has been recognized as a green and sustainable biotechnology to produce natural and unnatural products. Hence we engineered the complete biosynthetic pathways of F2 and 3&lt;i>β&lt;/i>,20&lt;i>S&lt;/i>-Di-&lt;i>O&lt;/i>-Glc-DM in &lt;i>Saccharomyces cerevisiae via&lt;/i> the CRISPR/Cas9 system. The titers of F2 and 3&lt;i>β&lt;/i>,20&lt;i>S&lt;/i>-Di-&lt;i>O&lt;/i>-Glc-DM were increased from 1.2 to 21.0 mg/L and from 82.0 to 346.1 mg/L at shake flask level, respectively, by mul</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jul</publication><modification>2025-04-19T09:24:58.095Z</modification><creation>2022-08-08T09:51:40.35Z</creation></dates><accession>S-EPMC9293705</accession><cross_references><pubmed>35865098</pubmed><doi>10.1016/j.apsb.2022.04.012</doi></cross_references></HashMap>