Hatch T P
J Bacteriol. 1976 Feb;125(2):706-12. doi: 10.1128/jb.125.2.706-712.1976.
The incorporation of [3H]thymidine into the deoxyribonucleic acid (DNA) of Chlamydia psittaci (strain 6BC) growing in thymidine kinase (adenosine 5'-triphosphate-thymidine 5'-phosphotransferase, EC 1.7.1.21)-containing L cells, L(TK+), and thymidine kinase-deficient L cells, LM(TK-), was examined by autoradiography. Label was detected over C. psittaci inclusions in L(TK+) but not LM(TK-) cells. No evidence for a chlamydia-specific thymidine kinase activity in either L(TK+) or LM(TK-) cells was obtained. Entry of [3H]thymidine into the DNA of C. psittaci growing in L(TK+) cells was quantitated by measuring label in purified C. psittaci. It was 265 times less efficient than entry into infected host cell DNA. It is concluded that low levels of exogenous thymidine are incorporated into the DNA of C. psittaci and that this incorporation is dependent on a fully competent host thymidine kinase activity. Evidence also is presented that L cells possess at least two thymidine kinase activities, both of which are capable of supplying thymidylate precursors for nuclear DNA synthesis.
通过放射自显影法检测了[3H]胸苷掺入在含有胸苷激酶(腺苷5'-三磷酸-胸苷5'-磷酸转移酶,EC 1.7.1.21)的L细胞(L(TK+))和胸苷激酶缺陷型L细胞(LM(TK-))中生长的鹦鹉热衣原体(菌株6BC)的脱氧核糖核酸(DNA)中的情况。在L(TK+)细胞的鹦鹉热衣原体包涵体上检测到了标记,但在LM(TK-)细胞中未检测到。在L(TK+)细胞或LM(TK-)细胞中均未获得衣原体特异性胸苷激酶活性的证据。通过测量纯化的鹦鹉热衣原体中的标记,对[3H]胸苷进入在L(TK+)细胞中生长的鹦鹉热衣原体DNA的情况进行了定量。其效率比进入受感染宿主细胞DNA低265倍。得出结论:低水平的外源性胸苷掺入鹦鹉热衣原体的DNA中,且这种掺入依赖于完全有功能的宿主胸苷激酶活性。还提供了证据表明L细胞具有至少两种胸苷激酶活性,这两种活性均能够为核DNA合成提供胸苷酸前体。