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14C-半乳糖在组织培养细胞中转化为氨基酸及其受锰的抑制作用。

Conversion of 14C-galactose into amino acids in tissue culture cells and its inhibition by manganese.

作者信息

Patschinsky T, Leveringhaus M, Werchau H, Reutter W

出版信息

Eur J Cell Biol. 1980 Apr;21(1):63-6.

PMID:6769675
Abstract

The incorporation of 14C-galactose into primary AGMK-cells was studied in the presence and absence of Mn2+. The transport of galactose into the cells is not influenced by Mn2+. 1 mM MnCl2 inhibits the incorporation of galactose into acid-precipitable material up to 50% after 6 hours incubation. In the absence of Mn2+ a substantial amount of galactose is converted to glucose, which is mainly metabolized into aspartic acid and serine. The conversion of galactose into glucose is inhibited by the addition of Mn2+. However, Mn2+ does not influence the activity of the UDP-galactose-4'-epimerase in vitro. Using the SDS-polyacrylamide electrophoresis the labelling of protein bands is similar with 14C-galactose or a 14C-amino acid mixture, respectively. In the presence of Mn2+ the incorporation of both galactose or amino acids is inhibited: With amino acids the inhibition is observed in all protein bands, whereas with galactose some bands remain unaffected. It is concluded that these are galactoproteins.

摘要

在有和没有Mn2+的情况下,研究了14C-半乳糖掺入原代AGMK细胞的情况。半乳糖进入细胞的转运不受Mn2+的影响。在孵育6小时后,1 mM MnCl2可将半乳糖掺入酸沉淀物质中的量抑制高达50%。在没有Mn2+的情况下,大量半乳糖转化为葡萄糖,葡萄糖主要代谢为天冬氨酸和丝氨酸。添加Mn2+可抑制半乳糖向葡萄糖的转化。然而,Mn2+在体外不影响UDP-半乳糖-4'-表异构酶的活性。使用SDS-聚丙烯酰胺电泳,分别用14C-半乳糖或14C-氨基酸混合物标记的蛋白带相似。在有Mn2+的情况下,半乳糖和氨基酸的掺入均受到抑制:对于氨基酸,在所有蛋白带中均观察到抑制作用,而对于半乳糖,一些条带不受影响。得出的结论是,这些是半乳糖蛋白。

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