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>Adenosine metabolism in wild‐type and enzyme‐deficient variants of Chinese hamster ovary and Novikoff rat hepatoma cells
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Adenosine metabolism in wild‐type and enzyme‐deficient variants of Chinese hamster ovary and Novikoff rat hepatoma cells
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机译：Adenosine metabolism in wild‐type and enzyme‐deficient variants of Chinese hamster ovary and Novikoff rat hepatoma cells
AbstractVariants of Chinese hamster ovary and Novikoff rat hepatoma cells resistant to tubercidin and 2,5‐diaminopurine, or to both drugs, were isolated, and their ability to convert adenosine and various adenosine analogs to nucleotides was compared to that of wild‐type cells, both in intact cells and cell‐free extracts. Adenosine deamination, and thus its conversion to nucleotides via inosine‐hypoxanthine‐inosine monophosphate, was inhibited by pretreatment of the cells or cell extracts with 2‐deoxycoformycin. Cell‐free extracts of the tubercidin‐resistant variants, as well as of two adenosine‐resistant mutants of Chinese hamster ovary cells, phosphorylated adenosine, tubercidin, pyrazofurin, or tricyclic nucleoside in the presence of ATP at<1 of the rate of extracts of wild‐type cells. However, addition of phosphoribosyl pyrophosphate stimulated the conversion of adenosine to nucleotides 40‐fold. Similarly, intact adenosine kinase‐deficient cells failed to phosphorylate the adenosine analogs, but still converted adenosine to nucleotides at 5–10 the rate observed with wild‐type cells. Phosphorylation of adenosine and tubercidin in wild‐type cells was inhibited by substrate at concentration above 5–10 μM. In contrast, the rate of conversion of adenosine to nucleotides by adenosine kinase‐deficient cells increased linearly up to a concentration of 400 μM adenosine, with the consequence that, at this concentration, these cells took up adenosine almost as rapidly as wild‐type cells. Adenosine uptake by these kinase‐deficient cells was inhibited by adenine and 5′‐deoxyadenosine, and was largely abolished in mutants devoid also of adenine phosphoribosyltransferase. We conclude that adenosine is converted to nucleotides in adenosine kinase‐deficient cells via adenine. Indirect evidence implicates 5′‐methylthioadenosine phosphorylase as the enzyme respon
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