{"title":"人脑神经节苷脂的高碘酸盐氧化研究","authors":"G.A. Johnson , R.H. McCluer","doi":"10.1016/0926-6542(64)90128-3","DOIUrl":null,"url":null,"abstract":"<div><p></p><ul><li><span>1.</span><span><p>1. Four chromatographically homogenous gangliosides (FM, 1-G, 3-G, 4-G) and the ceramide-tetrose (asialoganglioside) were isolated and subjected to periodate oxidation.</p></span></li><li><span>2.</span><span><p>2. Periodate reduction was quantitatively determined with the mon-, di-, and trisialoganglioside (1-G, 3-G, 4-G) preparations.</p></span></li><li><span>3.</span><span><p>3. The periodate-resistant carbohydrate residues were determined in all five preparations.</p></span></li><li><span>4.</span><span><p>4. The results are consistent with the structure monosialoganglioside proposed by <span>Kuhn and Wiegandt</span>.</p></span></li><li><span>5.</span><span><p>5. The disialo- and trisialongangliosides (3-G and 4-G) isolated contained a sialic acid residue resistant to periodate oxiation. Ganglioside 4-G is apparently a previously unreported trisialogangliosides, since one of the galactose residues was subject to periodate oxidation.</p></span></li><li><span>6.</span><span><p>6. Structures for the ganglioside preparations are proposed.</p></span></li></ul></div>","PeriodicalId":100171,"journal":{"name":"Biochimica et Biophysica Acta (BBA) - Specialized Section on Lipids and Related Subjects","volume":"84 5","pages":"Pages 587-595"},"PeriodicalIF":0.0000,"publicationDate":"1964-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0926-6542(64)90128-3","citationCount":"11","resultStr":"{\"title\":\"Periodate oxidation studies of human brain gangliosides\",\"authors\":\"G.A. Johnson , R.H. McCluer\",\"doi\":\"10.1016/0926-6542(64)90128-3\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p></p><ul><li><span>1.</span><span><p>1. Four chromatographically homogenous gangliosides (FM, 1-G, 3-G, 4-G) and the ceramide-tetrose (asialoganglioside) were isolated and subjected to periodate oxidation.</p></span></li><li><span>2.</span><span><p>2. Periodate reduction was quantitatively determined with the mon-, di-, and trisialoganglioside (1-G, 3-G, 4-G) preparations.</p></span></li><li><span>3.</span><span><p>3. The periodate-resistant carbohydrate residues were determined in all five preparations.</p></span></li><li><span>4.</span><span><p>4. The results are consistent with the structure monosialoganglioside proposed by <span>Kuhn and Wiegandt</span>.</p></span></li><li><span>5.</span><span><p>5. The disialo- and trisialongangliosides (3-G and 4-G) isolated contained a sialic acid residue resistant to periodate oxiation. Ganglioside 4-G is apparently a previously unreported trisialogangliosides, since one of the galactose residues was subject to periodate oxidation.</p></span></li><li><span>6.</span><span><p>6. Structures for the ganglioside preparations are proposed.</p></span></li></ul></div>\",\"PeriodicalId\":100171,\"journal\":{\"name\":\"Biochimica et Biophysica Acta (BBA) - Specialized Section on Lipids and Related Subjects\",\"volume\":\"84 5\",\"pages\":\"Pages 587-595\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1964-10-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/0926-6542(64)90128-3\",\"citationCount\":\"11\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Biochimica et Biophysica Acta (BBA) - Specialized Section on Lipids and Related Subjects\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/0926654264901283\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biochimica et Biophysica Acta (BBA) - Specialized Section on Lipids and Related Subjects","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/0926654264901283","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Periodate oxidation studies of human brain gangliosides
1.
1. Four chromatographically homogenous gangliosides (FM, 1-G, 3-G, 4-G) and the ceramide-tetrose (asialoganglioside) were isolated and subjected to periodate oxidation.
2.
2. Periodate reduction was quantitatively determined with the mon-, di-, and trisialoganglioside (1-G, 3-G, 4-G) preparations.
3.
3. The periodate-resistant carbohydrate residues were determined in all five preparations.
4.
4. The results are consistent with the structure monosialoganglioside proposed by Kuhn and Wiegandt.
5.
5. The disialo- and trisialongangliosides (3-G and 4-G) isolated contained a sialic acid residue resistant to periodate oxiation. Ganglioside 4-G is apparently a previously unreported trisialogangliosides, since one of the galactose residues was subject to periodate oxidation.
6.
6. Structures for the ganglioside preparations are proposed.