Mahan Kristina M, Penrod Joseph T, Ju Kou-San, Al Kass Natascia, Tan Watumesa A, Truong Richard, Parales Juanito V, Parales Rebecca E
Department of Microbiology and Molecular Genetics, College of Biological Sciences, University of California, Davis, California, USA.
Department of Microbiology and Molecular Genetics, College of Biological Sciences, University of California, Davis, California, USA
Appl Environ Microbiol. 2015 Jan;81(1):309-19. doi: 10.1128/AEM.02772-14. Epub 2014 Oct 24.
Acidovorax sp. strain JS42 uses 2-nitrotoluene as a sole source of carbon and energy. The first enzyme of the degradation pathway, 2-nitrotoluene 2,3-dioxygenase, adds both atoms of molecular oxygen to 2-nitrotoluene, forming nitrite and 3-methylcatechol. All three mononitrotoluene isomers serve as substrates for 2-nitrotoluene dioxygenase, but strain JS42 is unable to grow on 3- or 4-nitrotoluene. Using both long- and short-term selections, we obtained spontaneous mutants of strain JS42 that grew on 3-nitrotoluene. All of the strains obtained by short-term selection had mutations in the gene encoding the α subunit of 2-nitrotoluene dioxygenase that changed isoleucine 204 at the active site to valine. Those strains obtained by long-term selections had mutations that changed the same residue to valine, alanine, or threonine or changed the alanine at position 405, which is just outside the active site, to glycine. All of these changes altered the regiospecificity of the enzymes with 3-nitrotoluene such that 4-methylcatechol was the primary product rather than 3-methylcatechol. Kinetic analyses indicated that the evolved enzymes had enhanced affinities for 3-nitrotoluene and were more catalytically efficient with 3-nitrotoluene than the wild-type enzyme. In contrast, the corresponding amino acid substitutions in the closely related enzyme nitrobenzene 1,2-dioxygenase were detrimental to enzyme activity. When cloned genes encoding the evolved dioxygenases were introduced into a JS42 mutant lacking a functional dioxygenase, the strains acquired the ability to grow on 3-nitrotoluene but with significantly longer doubling times than the evolved strains, suggesting that additional beneficial mutations occurred elsewhere in the genome.
食酸菌属菌株JS42以2-硝基甲苯作为唯一的碳源和能源。降解途径的第一种酶,即2-硝基甲苯2,3-双加氧酶,将分子氧的两个原子添加到2-硝基甲苯上,形成亚硝酸盐和3-甲基邻苯二酚。所有三种一硝基甲苯异构体都是2-硝基甲苯双加氧酶的底物,但菌株JS42不能在3-或4-硝基甲苯上生长。通过长期和短期筛选,我们获得了能在3-硝基甲苯上生长的JS42菌株的自发突变体。通过短期筛选获得的所有菌株在编码2-硝基甲苯双加氧酶α亚基的基因中发生了突变,这些突变将活性位点的异亮氨酸204变为缬氨酸。通过长期筛选获得的菌株发生的突变将相同的残基变为缬氨酸、丙氨酸或苏氨酸,或者将活性位点外的405位的丙氨酸变为甘氨酸。所有这些变化改变了酶对3-硝基甲苯的区域特异性,使得4-甲基邻苯二酚成为主要产物而非3-甲基邻苯二酚。动力学分析表明,进化后的酶对3-硝基甲苯的亲和力增强,并且与野生型酶相比,对3-硝基甲苯的催化效率更高。相比之下,在密切相关的酶硝基苯1,2-双加氧酶中相应的氨基酸取代对酶活性有害。当将编码进化后的双加氧酶的克隆基因导入缺乏功能性双加氧酶的JS42突变体中时,这些菌株获得了在3-硝基甲苯上生长的能力,但倍增时间比进化菌株长得多,这表明基因组的其他地方发生了额外的有益突变。