Vassilia Partali , Karl Tangen , Synnøve Liaaen-Jensen
{"title":"类胡萝卜素在食物链中的研究——iii。贻贝类胡萝卜素的吸收和代谢转化","authors":"Vassilia Partali , Karl Tangen , Synnøve Liaaen-Jensen","doi":"10.1016/0305-0491(89)90272-1","DOIUrl":null,"url":null,"abstract":"<div><p></p><ul><li><span>1.</span><span><p>1. The quantitative carotenoid composition of <em>M. edulis</em> from two geographical localities at different seasons is reported.</p></span></li><li><span>2.</span><span><p>2. Twenty different carotenoids are structurally identified. Carotenoids with an acetylenic 3-hydroxy-7,8-didenhydro β-end group accumulate in <em>M. edulis</em>.</p></span></li><li><span>3.</span><span><p>3. Feeding experiments with algal unicultures are reported.</p></span></li><li><span>4.</span><span><p>4. Fucoxanthin, 19′-hexanoyloxyfucoxanthin, diadinoxanthin and peridinin were resorbed.</p></span></li><li><span>5.</span><span><p>5. Hydrolysis of carotenoid acetates, conversion of allenic to acetylenic end groups and conversion of 5,6-epoxides to 5,6-glycols were general metabolic reactions.</p></span></li><li><span>6.</span><span><p>6. Fucoxanthin provides isomytiloxanthin, confirmed by conversion of 19′-hexanoyloxyfucoxanthin to 19′-hexanoyloxyisomytiloxanthin.</p></span></li><li><span>7.</span><span><p>7. Fucoxanthin is converted to halocynthiaxanthin.</p></span></li><li><span>8.</span><span><p>8. The diacetylenic alloxanthin is a terminal metabolic product.</p></span></li><li><span>9.</span><span><p>9. Peridinin is converted to peridininol and pyrrhoxanthinol.</p></span></li><li><span>10.</span><span><p>10. Metabolic schemes are proposed.</p></span></li></ul></div>","PeriodicalId":100294,"journal":{"name":"Comparative Biochemistry and Physiology Part B: Comparative Biochemistry","volume":"92 2","pages":"Pages 239-246"},"PeriodicalIF":0.0000,"publicationDate":"1989-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0305-0491(89)90272-1","citationCount":"35","resultStr":"{\"title\":\"Carotenoids in food chain studies—III. Resorption and metabolic transformation of carotenoids in Mytilus edulis (Edible mussel)\",\"authors\":\"Vassilia Partali , Karl Tangen , Synnøve Liaaen-Jensen\",\"doi\":\"10.1016/0305-0491(89)90272-1\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p></p><ul><li><span>1.</span><span><p>1. The quantitative carotenoid composition of <em>M. edulis</em> from two geographical localities at different seasons is reported.</p></span></li><li><span>2.</span><span><p>2. Twenty different carotenoids are structurally identified. Carotenoids with an acetylenic 3-hydroxy-7,8-didenhydro β-end group accumulate in <em>M. edulis</em>.</p></span></li><li><span>3.</span><span><p>3. Feeding experiments with algal unicultures are reported.</p></span></li><li><span>4.</span><span><p>4. Fucoxanthin, 19′-hexanoyloxyfucoxanthin, diadinoxanthin and peridinin were resorbed.</p></span></li><li><span>5.</span><span><p>5. Hydrolysis of carotenoid acetates, conversion of allenic to acetylenic end groups and conversion of 5,6-epoxides to 5,6-glycols were general metabolic reactions.</p></span></li><li><span>6.</span><span><p>6. Fucoxanthin provides isomytiloxanthin, confirmed by conversion of 19′-hexanoyloxyfucoxanthin to 19′-hexanoyloxyisomytiloxanthin.</p></span></li><li><span>7.</span><span><p>7. Fucoxanthin is converted to halocynthiaxanthin.</p></span></li><li><span>8.</span><span><p>8. The diacetylenic alloxanthin is a terminal metabolic product.</p></span></li><li><span>9.</span><span><p>9. Peridinin is converted to peridininol and pyrrhoxanthinol.</p></span></li><li><span>10.</span><span><p>10. Metabolic schemes are proposed.</p></span></li></ul></div>\",\"PeriodicalId\":100294,\"journal\":{\"name\":\"Comparative Biochemistry and Physiology Part B: Comparative Biochemistry\",\"volume\":\"92 2\",\"pages\":\"Pages 239-246\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1989-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/0305-0491(89)90272-1\",\"citationCount\":\"35\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Comparative Biochemistry and Physiology Part B: Comparative Biochemistry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/0305049189902721\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Comparative Biochemistry and Physiology Part B: Comparative Biochemistry","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/0305049189902721","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Carotenoids in food chain studies—III. Resorption and metabolic transformation of carotenoids in Mytilus edulis (Edible mussel)
1.
1. The quantitative carotenoid composition of M. edulis from two geographical localities at different seasons is reported.
2.
2. Twenty different carotenoids are structurally identified. Carotenoids with an acetylenic 3-hydroxy-7,8-didenhydro β-end group accumulate in M. edulis.
3.
3. Feeding experiments with algal unicultures are reported.
4.
4. Fucoxanthin, 19′-hexanoyloxyfucoxanthin, diadinoxanthin and peridinin were resorbed.
5.
5. Hydrolysis of carotenoid acetates, conversion of allenic to acetylenic end groups and conversion of 5,6-epoxides to 5,6-glycols were general metabolic reactions.
6.
6. Fucoxanthin provides isomytiloxanthin, confirmed by conversion of 19′-hexanoyloxyfucoxanthin to 19′-hexanoyloxyisomytiloxanthin.
7.
7. Fucoxanthin is converted to halocynthiaxanthin.
8.
8. The diacetylenic alloxanthin is a terminal metabolic product.
9.
9. Peridinin is converted to peridininol and pyrrhoxanthinol.