Plagemann P G, Wohlhueter R M
J Cell Physiol. 1983 Aug;116(2):236-46. doi: 10.1002/jcp.1041160216.
Variants 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 less than 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 microM. In contrast, the rate of conversion of adenosine to nucleotides by adenosine kinase-deficient cells increased linearly up to a concentration of 400 microM 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 responsible for the degradation of adenosine to adenine.
分离出了对杀结核菌素和2,5 - 二氨基嘌呤或对这两种药物均具有抗性的中国仓鼠卵巢细胞和诺维科夫大鼠肝癌细胞变体,并将它们在完整细胞和无细胞提取物中将腺苷及各种腺苷类似物转化为核苷酸的能力与野生型细胞进行了比较。用2 - 脱氧助间型霉素预处理细胞或细胞提取物可抑制腺苷脱氨作用,从而抑制其通过次黄苷 - 次黄嘌呤 - 次黄苷单磷酸转化为核苷酸。杀结核菌素抗性变体以及中国仓鼠卵巢细胞的两个腺苷抗性突变体的无细胞提取物,在ATP存在的情况下,将腺苷、杀结核菌素、吡唑呋喃或三环核苷磷酸化的速率不到野生型细胞提取物速率的1%。然而,添加磷酸核糖焦磷酸可使腺苷转化为核苷酸的速率提高40倍。同样,完整的腺苷激酶缺陷细胞无法将腺苷类似物磷酸化,但仍以野生型细胞观察到的速率的5 - 10%将腺苷转化为核苷酸。野生型细胞中腺苷和杀结核菌素的磷酸化受到浓度高于5 - 10微摩尔的底物的抑制。相比之下,腺苷激酶缺陷细胞将腺苷转化为核苷酸的速率在腺苷浓度高达400微摩尔时呈线性增加,结果是在该浓度下,这些细胞摄取腺苷的速度几乎与野生型细胞一样快。这些激酶缺陷细胞对腺苷的摄取受到腺嘌呤和5'-脱氧腺苷的抑制,并且在同时缺乏腺嘌呤磷酸核糖转移酶的突变体中基本消除。我们得出结论,腺苷在腺苷激酶缺陷细胞中通过腺嘌呤转化为核苷酸。间接证据表明5'-甲硫基腺苷磷酸化酶是负责将腺苷降解为腺嘌呤的酶。