Roca Amalia, Rodríguez-Herva Jose J, Ramos Juan L
Department of Environmental Protection, Consejo Superior de Investigaciones Científicas, Estación Experimental del Zaidín, Granada, Spain.
J Bacteriol. 2009 May;191(10):3367-74. doi: 10.1128/JB.00076-09. Epub 2009 Mar 20.
Pseudomonas putida KT2440 exhibits redundant formaldehyde dehydrogenases and formate dehydrogenases that contribute to the detoxification of formaldehyde, a highly toxic compound. Physical and transcriptional analyses showed that the open reading frame (ORF) PP0328, encoding one of the formaldehyde dehydrogenases, is self-sufficient, whereas the other functional formaldehyde dehydrogenase gene (ORF PP3970) forms an operon with another gene of unknown function. Two formate dehydrogenase gene clusters (PP0489 to PP0492 and PP2183 to PP2186) were identified, and genes in these clusters were found to form operons. All four transcriptional promoters were mapped by primer extension and revealed the presence of noncanonical promoters expressed at basal level in the exponential growth phase and at a higher level in the stationary phase regardless of the presence of extracellular formaldehyde or formate. These promoters were characterized by a 5'-AG-CCA-C/A-CT-3' conserved region between -7 and -16. To determine the contribution of the different gene products to formaldehyde and formate mineralization, mutants with single and double mutations of formaldehyde dehydrogenases were generated, and the effect of the mutations on formaldehyde catabolism was tested by measuring (14)CO(2) evolution from (14)C-labeled formaldehyde. The results showed that both enzymes contributed to formaldehyde catabolism. A double mutant lacking these two enzymes still evolved CO(2) from formaldehyde, suggesting the presence of one or more still-unidentified formaldehyde dehydrogenases. Mutants with single and double mutations in the clusters for formate dehydrogenases were also generated, and all of them were able to metabolize [(14)C]formate to (14)CO(2), suggesting a redundancy of functions that was not limited to only the annotated genes. Single and double mutants deficient in formaldehyde dehydrogenases and formate dehydrogenases exhibited longer lag phases than did the parental strain when confronted with concentrations of formaldehyde close to the MICs. This suggests a role for the detoxification system in tolerance to sublethal concentrations of formaldehyde.
恶臭假单胞菌KT2440具有多种冗余的甲醛脱氢酶和甲酸脱氢酶,这些酶有助于对剧毒化合物甲醛进行解毒。物理和转录分析表明,编码其中一种甲醛脱氢酶的开放阅读框(ORF)PP0328是独立存在的,而另一个功能性甲醛脱氢酶基因(ORF PP3970)与另一个功能未知的基因形成一个操纵子。鉴定出了两个甲酸脱氢酶基因簇(PP0489至PP0492和PP2183至PP2186),并且发现这些簇中的基因形成操纵子。通过引物延伸对所有四个转录启动子进行了定位,结果表明存在非典型启动子,这些启动子在指数生长期以基础水平表达,在稳定期表达水平更高,无论细胞外是否存在甲醛或甲酸。这些启动子的特征是在-7至-16之间有一个5'-AG-CCA-C/A-CT-3'保守区域。为了确定不同基因产物对甲醛和甲酸矿化的贡献,构建了甲醛脱氢酶单突变和双突变的突变体,并通过测量来自14C标记甲醛的14CO2释放来测试这些突变对甲醛分解代谢的影响。结果表明这两种酶都对甲醛分解代谢有贡献。缺乏这两种酶的双突变体仍能从甲醛中释放CO2,这表明存在一种或多种尚未鉴定的甲醛脱氢酶。还构建了甲酸脱氢酶基因簇单突变和双突变的突变体,并且所有这些突变体都能够将[14C]甲酸代谢为14CO2,这表明功能冗余并不局限于仅注释的基因。当面对接近最低抑菌浓度的甲醛浓度时,缺乏甲醛脱氢酶和甲酸脱氢酶的单突变体和双突变体比亲本菌株表现出更长的延迟期。这表明解毒系统在耐受亚致死浓度甲醛方面发挥作用。