Key Laboratory of Agricultural Environmental Microbiology, Ministry of Agriculture, College of Life Sciences, Nanjing Agricultural University, Nanjing, Jiangsu, People's Republic of China.
Jiangsu Provincial Key Lab for Organic Solid Waste Utilization, Nanjing Agricultural University, Nanjing, Jiangsu, People's Republic of China.
Appl Environ Microbiol. 2018 Aug 1;84(16). doi: 10.1128/AEM.00805-18. Print 2018 Aug 15.
Carbofuran, a broad-spectrum systemic insecticide, has been extensively used for approximately 50 years. Diverse carbofuran-degrading bacteria have been described, among which sphingomonads have exhibited an extraordinary ability to catabolize carbofuran; other bacteria can only convert carbofuran to carbofuran phenol, while all carbofuran-degrading sphingomonads can degrade both carbofuran and carbofuran phenol. However, the genetic basis of carbofuran catabolism in sphingomonads has not been well elucidated. In this work, we sequenced the draft genome of sp. strain CDS-1 that can transform both carbofuran and carbofuran phenol but fails to grow on them. On the basis of the hypothesis that the genes involved in carbofuran catabolism are highly conserved among carbofuran-degrading sphingomonads, two such genes, and , were predicted from the 84 open reading frames (ORFs) that share ≥95% nucleic acid similarities between strain CDS-1 and another sphingomonad sp. strain KN65.2 that is able to mineralize the benzene ring of carbofuran. The results of the gene knockout, genetic complementation, heterologous expression, and enzymatic experiments reveal that and are responsible for the conversion of carbofuran and carbofuran phenol, respectively, in strain CDS-1. CehA hydrolyzes carbofuran to carbofuran phenol. CfdC, a reduced flavin mononucleotide (FMNH)- or reduced flavin adenine dinucleotide (FADH)-dependent monooxygenase, hydroxylates carbofuran phenol at the benzene ring in the presence of NADH, FMN/FAD, and the reductase CfdX. It is worth noting that we found that carbaryl hydrolase CehA, which was previously demonstrated to have no activity toward carbofuran, can actually convert carbofuran to carbofuran phenol, albeit with very low activity. Due to the extensive use of carbofuran over the past 50 years, bacteria have evolved catabolic pathways to mineralize this insecticide, which plays an important role in eliminating carbofuran residue in the environment. This study revealed the genetic determinants of carbofuran degradation in sp. strain CDS-1. We speculate that the close homologues and are highly conserved among other carbofuran-degrading sphingomonads and play the same roles as those described here. These findings deepen our understanding of the microbial degradation mechanism of carbofuran and lay a foundation for the better use of microbes to remediate carbofuran contamination.
呋喃丹是一种广谱的内吸性杀虫剂,已经被广泛使用了大约 50 年。已经描述了多种能够降解呋喃丹的细菌,其中,鞘氨醇单胞菌表现出了非凡的分解呋喃丹的能力;其他细菌只能将呋喃丹转化为呋喃丹酚,而所有能够降解呋喃丹的鞘氨醇单胞菌都可以同时降解呋喃丹和呋喃丹酚。然而,鞘氨醇单胞菌中呋喃丹代谢的遗传基础尚未得到很好的阐明。在这项工作中,我们对能够同时转化呋喃丹和呋喃丹酚但不能在其上生长的 sp. 菌株 CDS-1 进行了基因组测序。基于这样的假设,即参与呋喃丹代谢的基因在能够降解呋喃丹的鞘氨醇单胞菌中高度保守,我们从菌株 CDS-1 与另一种能够矿化呋喃丹苯环的鞘氨醇单胞菌 sp. 菌株 KN65.2 之间共享≥95%核酸相似性的 84 个开放阅读框(ORFs)中预测了两个这样的基因, 和 。基因敲除、遗传互补、异源表达和酶实验的结果表明, 和 分别负责菌株 CDS-1 中呋喃丹和呋喃丹酚的转化。CehA 水解呋喃丹生成呋喃丹酚。CfdC 是一种依赖还原黄素单核苷酸(FMNH)或还原黄素腺嘌呤二核苷酸(FADH)的单加氧酶,在 NADH、FMN/FAD 和还原酶 CfdX 的存在下,将呋喃丹酚芳环羟基化。值得注意的是,我们发现以前被证明对呋喃丹没有活性的carbaryl 水解酶 CehA 实际上可以将呋喃丹转化为呋喃丹酚,尽管活性非常低。由于过去 50 年来呋喃丹的广泛使用,细菌已经进化出了矿化这种杀虫剂的代谢途径,这在消除环境中呋喃丹残留方面发挥了重要作用。本研究揭示了 sp. 菌株 CDS-1 中呋喃丹降解的遗传决定因素。我们推测,在其他能够降解呋喃丹的鞘氨醇单胞菌中,紧密同源的 和 高度保守,并且发挥着与这里描述的相同的作用。这些发现加深了我们对呋喃丹微生物降解机制的理解,为更好地利用微生物修复呋喃丹污染奠定了基础。