Hantke K
Lehrstuhl für Mikrobiologie II, Universität Tübingen, Federal Republic of Germany.
Arch Microbiol. 1988;149(4):344-9. doi: 10.1007/BF00411654.
The mutant, generated by a Mud1 insertion, formed long non-viable filaments in the presence of iron and air. Under anaerobic conditions normal growth in the presence of iron was observed. The mutation was mapped by P1 transductions at 48 min on the genetic map of Escherichia coli. By Southern blotting the insertion point was determined to be in nrdB, the structural gene for the ribonucleotide reductase subunit B2. The mutation could be complemented by the cloned nrdB gene. Up to now it was assumed that E. coli possesses only one enzyme for the synthesis of deoxyribonucleotides and only conditional lethal (temperature sensitive) mutants were isolated in nrdB. The insertion of Mud1 in nrdB should lead to a complete loss of the essential B2 subunit. Since the strain was able to grow under anaerobic conditions on minimal medium lacking deoxyribonucleotides and additional pathway for the synthesis of deoxyribonucleotides is postulated.
由Mud1插入产生的突变体在有铁和空气存在的情况下形成了不可存活的长丝。在厌氧条件下,观察到在有铁存在时的正常生长。通过P1转导将该突变定位在大肠杆菌遗传图谱上的48分钟处。通过Southern印迹法确定插入点位于nrdB,即核糖核苷酸还原酶亚基B2的结构基因中。该突变可以由克隆的nrdB基因互补。到目前为止,人们认为大肠杆菌仅拥有一种用于合成脱氧核糖核苷酸的酶,并且仅在nrdB中分离出条件致死(温度敏感)突变体。Mud1插入nrdB应该导致必需的B2亚基完全丧失。由于该菌株能够在缺乏脱氧核糖核苷酸的基本培养基上在厌氧条件下生长,因此推测存在脱氧核糖核苷酸合成的额外途径。