Department of Microbiology, College of Biological Sciences, University of California, Davis, CA 95616, USA.
Mol Microbiol. 2011 Oct;82(2):355-64. doi: 10.1111/j.1365-2958.2011.07817.x. Epub 2011 Sep 13.
Bacteria that assimilate synthetic nitroarene compounds represent unique evolutionary models, as their metabolic pathways are in the process of adaptation and optimization for the consumption of these toxic chemicals. We used Acidovorax sp. strain JS42, which is capable of growth on nitrobenzene and 2-nitrotoluene, in experiments to examine how a nitroarene degradation pathway evolves when its host strain is challenged with direct selective pressure to assimilate non-native substrates. Although the same enzyme that initiates the degradation of nitrobenzene and 2-nitrotoluene also oxidizes 4-nitrotoluene to 4-methylcatechol, which is a growth substrate for JS42, the strain is incapable of growth on 4-nitrotoluene. Using long-term laboratory evolution experiments, we obtained JS42 mutants that gained the ability to grow on 4-nitrotoluene via a new degradation pathway. The underlying basis for this new activity resulted from the accumulation of specific mutations in the gene encoding the dioxygenase that catalyses the initial oxidation of nitroarene substrates, but at positions distal to the active site and previously unknown to affect activity in this or related enzymes. We constructed additional mutant dioxygenases to identify the order of mutations that led to the improved enzymes. Biochemical analyses revealed a defined, step-wise pathway for the evolution of the improved dioxygenases.
能够以硝基苯和 2-硝基甲苯为生长基质的 Acidovorax sp. 菌株 JS42 被用于实验,以研究当宿主菌株受到直接选择压力以同化非天然基质时,硝基芳烃降解途径是如何进化的。尽管起始降解硝基苯和 2-硝基甲苯的同一种酶也能将 4-硝基甲苯氧化为 4-甲基儿茶酚,而 4-甲基儿茶酚是 JS42 的生长基质,但该菌株不能以 4-硝基甲苯为生长基质。通过长期的实验室进化实验,我们获得了能够通过新的降解途径生长在 4-硝基甲苯上的 JS42 突变体。这种新活性的潜在基础是编码双加氧酶的基因中特定突变的积累,该基因催化硝基芳烃底物的初始氧化,但位于活性位点的远端,以前未知的突变会影响该酶或相关酶的活性。我们构建了额外的突变双加氧酶,以确定导致改进酶的突变顺序。生化分析揭示了改进型双加氧酶进化的明确的、逐步的途径。