<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Harrison EH</submitter><funding>National Institutes of Health</funding><funding>NIH HHS</funding><pagination>1411</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9003029</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(7)</volume><pubmed_abstract>Naturally occurring retinoids (retinol, retinal, retinoic acid, retinyl esters) are a subclass of β-apocarotenoids, defined by the length of the polyene side chain. Provitamin A carotenoids are metabolically converted to retinal (β-apo-15-carotenal) by the enzyme β-carotene-15,15'-dioxygenase (BCO1) that catalyzes the oxidative cleavage of the central C=C double bond. A second enzyme β-carotene-9'-10'-dioxygenase cleaves the 9',10' bond to yield β-apo-10'-carotenal and β-ionone. Chemical oxidation of the other double bonds leads to the generation of other β-apocarotenals. Like retinal, some of these β-apocarotenals are metabolically oxidized to the corresponding β-apocarotenoic acids or reduced to the β-apocarotenols, which in turn are esterified to β-apocarotenyl esters. Other metabolic f</pubmed_abstract><journal>Nutrients</journal><pubmed_title>Carotenoids, β-Apocarotenoids, and Retinoids: The Long and the Short of It.</pubmed_title><pmcid>PMC9003029</pmcid><funding_grant_id>R01-DK055598, R01-DK10151, R01-HL04987</funding_grant_id><pubmed_authors>Harrison EH</pubmed_authors></additional><is_claimable>false</is_claimable><name>Carotenoids, β-Apocarotenoids, and Retinoids: The Long and the Short of It.</name><description>Naturally occurring retinoids (retinol, retinal, retinoic acid, retinyl esters) are a subclass of β-apocarotenoids, defined by the length of the polyene side chain. Provitamin A carotenoids are metabolically converted to retinal (β-apo-15-carotenal) by the enzyme β-carotene-15,15'-dioxygenase (BCO1) that catalyzes the oxidative cleavage of the central C=C double bond. A second enzyme β-carotene-9'-10'-dioxygenase cleaves the 9',10' bond to yield β-apo-10'-carotenal and β-ionone. Chemical oxidation of the other double bonds leads to the generation of other β-apocarotenals. Like retinal, some of these β-apocarotenals are metabolically oxidized to the corresponding β-apocarotenoic acids or reduced to the β-apocarotenols, which in turn are esterified to β-apocarotenyl esters. Other metabolic f</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Mar</publication><modification>2025-04-19T12:12:06.507Z</modification><creation>2024-10-19T06:51:33.354Z</creation></dates><accession>S-EPMC9003029</accession><cross_references><pubmed>35406024</pubmed><doi>10.3390/nu14071411</doi></cross_references></HashMap>