Abdulrashid N, Clark D P
J Bacteriol. 1987 Mar;169(3):1267-71. doi: 10.1128/jb.169.3.1267-1271.1987.
Successive mutations of Escherichia coli yielded a strain that was able to degrade a variety of heterocyclic oxygen- and sulfur-containing ring compounds. In particular, this strain could use both furan-2-carboxylic acid and thiophene-2-carboxylic acid as sole carbon and energy sources. Nitrogen-containing heterocyclic compounds were not degraded. This mutant was isolated by selecting first for oxidation of furan derivatives and then for thiophene degradation. Genetic analysis revealed that mutations in three novel genes, thdA (12 min), thdC (92 min), and thdD (98 min), were required for thiophene degradation. In addition, constitutively at both of the previously characterized fadR and atoC loci was required for efficient thiophene breakdown. The pathway of furan and thiophene degradation remains obscure, but the inability of our mutants to degrade 5-nitro- or 5-bromo-substituted furan derivatives suggests that hydroxylation at position 5 may be involved. Thiophene derivatives were toxic when they were present at concentrations of 0.1% or greater; however, addition of trace amounts of phenylalanine plus tyrosine greatly reduced this effect.
大肠杆菌的连续突变产生了一种能够降解多种含氧和含硫杂环化合物的菌株。特别地,该菌株能够将呋喃 - 2 - 羧酸和噻吩 - 2 - 羧酸都用作唯一的碳源和能源。含氮杂环化合物不能被降解。通过首先选择呋喃衍生物的氧化,然后选择噻吩降解来分离该突变体。遗传分析表明,噻吩降解需要三个新基因thdA(12分钟)、thdC(92分钟)和thdD(98分钟)发生突变。此外,高效的噻吩分解需要先前已鉴定的fadR和atoC位点都持续表达。呋喃和噻吩的降解途径仍然不清楚,但我们的突变体无法降解5 - 硝基或5 - 溴取代的呋喃衍生物,这表明5位的羟基化可能参与其中。当噻吩衍生物的浓度达到0.1%或更高时具有毒性;然而,添加微量的苯丙氨酸和酪氨酸可大大降低这种影响。