McKeown M, Kahn M, Hanawalt P
J Bacteriol. 1976 May;126(2):814-22. doi: 10.1128/jb.126.2.814-822.1976.
A commonly used strain of Escherichia coli K-12 was shown to be deficient in the transport of a number of nucleosides, including thymidine. Thymidine incorporation was unaffected. Strain AB2497 exhibited a strikingly lower thymidine pulse-label incorporation at low (less than 1 mug/ml) thymidine concentrations than do many other strains. The deficiency appeared to be due to mutation in a single gene. This gene, which we designated nup (for nucleoside uptake), is located at 10 to 13 min on the E. coli linkage map. In nup+ strains, the transport of a given nucleoside was relatively insensitive to large excesses of other nucleosides but was competitively inhibited by the same nucleoside. Mutants deficient inthymidine kinase are deficient in thymidine uptake but normal in deoxyadenosine uptake. A two-step model for nucleoside transport is presented in which the first step, utilizing the nup gene product, is a nonspecific translocation of nucleoside to the interior of the cell. In the second step, the individual nucleosides are modified by cellular enzymes (e.g., nucleosides kinases) facilitate accumulation.
一种常用的大肠杆菌K - 12菌株被证明在多种核苷(包括胸苷)的转运方面存在缺陷。胸苷掺入不受影响。与许多其他菌株相比,AB2497菌株在低胸苷浓度(低于1微克/毫升)下的胸苷脉冲标记掺入显著降低。这种缺陷似乎是由于单个基因突变所致。我们将这个基因命名为nup(核苷摄取之意),它位于大肠杆菌连锁图谱上的10至13分钟处。在nup +菌株中,特定核苷的转运对大量其他核苷的过量存在相对不敏感,但会受到相同核苷的竞争性抑制。缺乏胸苷激酶的突变体在胸苷摄取方面存在缺陷,但在脱氧腺苷摄取方面正常。本文提出了一种核苷转运的两步模型,其中第一步利用nup基因产物,是核苷向细胞内部的非特异性转运。在第二步中,单个核苷被细胞内的酶(如核苷激酶)修饰以促进积累。