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- W70746119 abstract "into other products. Glucoand galactocerebrosides, and ceramide trisaccharide, showed no activity (i.e. less than 300 cpm soluble in chloroform-methanol). Chloroform-methanolsoluble products were obtained with the following lipids: 4900 cpm with hematoside at 0.1 pmole per incubation mixture, and 7900 at 0.2 pmole; ceramide disaccharide, 720 cpm at 0.1 pmole, 1000 cpm at 0.25 pmole; Tay-Sachs ganglioside, 1300 cpm at 0.07 pmole. The optimum assay conditions for the enzyme system, as well as the nature of the chloroform-methanol-soluble products, remain to be determined. In summary, a UDP-galactose:glycolipid galactosyltransferase has been detected in a particulate preparation from chicken embryonic brain that catalyzed the synthesis of a monosialoganglioside from Tay-Sachs ganglioside. Whether or not the UDP-galactose:glycolipid galactosyltransferase is lacking in Tay-Sachs disease, and is thus responsible for the accumulation of large quantities of this “abnormal” ganglioside, is under investigation. The chicken brain preparation also appears to transfer N-acetylgalactosamine to certain lipids, such as hematoside." @default.
- W70746119 created "2016-06-24" @default.
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- W70746119 date "1965-10-01" @default.
- W70746119 modified "2023-10-18" @default.
- W70746119 title "The Amino Acid Sequence of Ribonuclease T1" @default.
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- W70746119 doi "https://doi.org/10.1016/s0021-9258(18)97162-0" @default.
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