Alam K Y, Worland M J, Clark D P
Department of Microbiology, Southern Illinois University, Carbondale 62901.
Appl Biochem Biotechnol. 1990 Spring-Summer;24-25:843-55. doi: 10.1007/BF02920299.
Escherichia coli NAR30 can oxidize thiophenes, furans, and various other aromatic compounds as a result of successive mutations in three novel genes (thdA, C, and D). Some of the mutant genes involved in thiophene degradation have been cloned into pUC19. One of the resulting plasmids, pKA10, which carries a 3.8-kb chromosomal fragment from NAR30, conferred the ability to partially degrade furfuryl alcohol and thiophene methanol on a fadR atoC host strain. The location of the thd gene(s) on the plasmid pKA10 was found by insertion of a kanamycin resistance cassette. One such insertion into a BglII site inactivated the thd gene(s). Disappearance of two proteins correlated with loss of oxidation ability vs thiophenes and furans. Strains carrying the thdA mutation oxidize these substrates by an oxidase that can be coupled to methylene blue. However, degradation of thiophenes by NAR30 is incomplete, with no organic sulfur being released.
大肠杆菌NAR30能够氧化噻吩、呋喃及其他各种芳香族化合物,这是三个新基因(thdA、C和D)连续发生突变的结果。一些参与噻吩降解的突变基因已被克隆到pUC19中。由此产生的一个质粒pKA10携带了来自NAR30的一个3.8 kb染色体片段,赋予了fadR atoC宿主菌株部分降解糠醇和噻吩甲醇的能力。通过插入卡那霉素抗性盒确定了pKA10质粒上thd基因的位置。其中一次插入BglII位点使thd基因失活。两种蛋白质的消失与对噻吩和呋喃氧化能力的丧失相关。携带thdA突变的菌株通过一种可与亚甲蓝偶联的氧化酶氧化这些底物。然而,NAR30对噻吩的降解并不完全,没有释放出有机硫。