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1-脱氧甘露基野尻霉素对大鼠肝脏α-甘露糖苷酶的作用。

The effect of 1-deoxymannojirimycin on rat liver alpha-mannosidases.

作者信息

Bischoff J, Kornfeld R

出版信息

Biochem Biophys Res Commun. 1984 Nov 30;125(1):324-31. doi: 10.1016/s0006-291x(84)80371-x.

Abstract

The mannose analogue, 1-deoxymannojirimycin, has been tested for its effect on five alpha-mannosidase activities present in rat liver and shown to be a specific inhibitor of Golgi alpha-mannosidase I at low mumolar concentrations. Golgi alpha-mannosidases I and II were assayed in a highly purified Golgi membrane preparation. Endoplasmic reticulum alpha-mannosidase activity was measured in a rough endoplasmic reticulum detergent extract. A purified soluble alpha-mannosidase activity which we believe is derived from the endoplasmic reticulum during tissue homogenization was also tested. And finally, the lysosomal or acidic alpha-mannosidase was measured in a postnuclear supernatant fraction obtained from rat liver. The results presented here show that 1-deoxymannojirimycin inhibits only Golgi alpha-mannosidase I, which is consistent with its effect on oligosaccharide processing in vivo (Fuhrmann et al. Nature 1984 307:755-758).

摘要

已对甘露糖类似物1-脱氧甘露基野尻霉素对大鼠肝脏中存在的五种α-甘露糖苷酶活性的影响进行了测试,结果表明,在低微摩尔浓度下,它是高尔基体α-甘露糖苷酶I的特异性抑制剂。在高度纯化的高尔基体膜制剂中测定了高尔基体α-甘露糖苷酶I和II。在内质网去污剂提取物中测量内质网α-甘露糖苷酶活性。还测试了一种纯化的可溶性α-甘露糖苷酶活性,我们认为它是在组织匀浆过程中从内质网衍生而来的。最后,在从大鼠肝脏获得的核后上清液组分中测量溶酶体或酸性α-甘露糖苷酶。此处给出的结果表明,1-脱氧甘露基野尻霉素仅抑制高尔基体α-甘露糖苷酶I,这与其对体内寡糖加工的影响一致(Fuhrmann等人,《自然》,1984年,307:755 - 758)。

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