Gerlach B A, Wiedemann B
Zentralbl Bakteriol Mikrobiol Hyg A. 1985 Aug;260(1):139-50. doi: 10.1016/s0176-6724(85)80110-3.
Plasmids of 31 E. coli strains coding for the TEM-1 beta-lactamase were analysed for the molecular basis of this enzyme. In transposition experiments we could demonstrate that only 50% of the plasmids were able to transpose their ampicillin-resistance gene. Two of the non-transposing structures were further examined. The 8.1 kb plasmid pBP738 contained Tn3 having suffered a point mutation within the transposase gene that could be complemented by an intact transposase. The 79 kb plasmid pBP749 carried a TEM-1 coding sequence, but the homology with Tn3 was limited to 1.18 kb.
对编码TEM-1β-内酰胺酶的31株大肠杆菌菌株的质粒进行了分析,以探究该酶的分子基础。在转座实验中,我们可以证明只有50%的质粒能够转座其氨苄青霉素抗性基因。对两个非转座结构进行了进一步研究。8.1 kb的质粒pBP738含有Tn3,其转座酶基因内发生了点突变,该突变可被完整的转座酶互补。79 kb的质粒pBP749携带TEM-1编码序列,但与Tn3的同源性仅限于1.18 kb。