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    • 26. 发明授权
    • Heparan sulfate 2-0-sulfotransferase
    • 硫酸肝素2-0-磺基转移酶
    • US5817487A
    • 1998-10-06
    • US685659
    • 1996-07-24
    • Masashi KobayashiHiroko HabuchiOsami HabuchiKoji Kimata
    • Masashi KobayashiHiroko HabuchiOsami HabuchiKoji Kimata
    • C12N9/10C12R1/91C12P19/00C12P11/00C12P19/26
    • C12N9/13
    • Heparan sulfate 2-O-sulfotransferase having the following properties is obtained from, for example, CHO cells: (i) action: sulfate group is transferred from a sulfate group donor selectively to the hydroxyl group at C-2 position of iduronic acid residue of a sulfate group acceptor; (ii) substrate specificity: sulfate group is transferred to heparan sulfate or CDSNS-heparin, but sulfate group is not transferred to chondroitin, chondroitin sulfate, dermatan sulfate, and keratan sulfate; (iii) optimum reaction pH: about pH 5 to 6.5; (iv) optimum ionic strength: about 50 to 200 mM when sodium chloride is used; and (v) inhibition and activation: the activity of the enzyme is increased by protamine, the activity of the enzyme is inhibited by adenosine-3',5'-diphosphate, and the activity of the enzyme is scarcely affected by dithiothreitol at 10 mM or less.
    • 具有以下性质的硫酸肝素2-O-磺基转移酶由例如CHO细胞获得:(i)作用:硫酸根基团从硫酸基供体选择性地转移到丙二酸残基C-2位的羟基 硫酸酯基受体; (ii)底物特异性:硫酸盐转移到硫酸乙酰肝素或CDSNS-肝素,但硫酸根不转移到软骨素,硫酸软骨素,硫酸皮肤素和硫酸角质素; (iii)最佳反应pH:约pH5至6.5; (iv)最佳离子强度:当使用氯化钠时为约50至200mM; 和(v)抑制和活化:酶的活性由鱼精蛋白增加,酶的活性受到腺苷-3',5'-二磷酸的抑制,酶的活性几乎不受二硫苏糖醇在10mM 或更少。