Westfälische Wilhelms-Universität Münster, Institut für Molekulare Mikrobiologie und Biotechnologie, Münster, Germany.
Westfälische Wilhelms-Universität Münster, Institut für Molekulare Mikrobiologie und Biotechnologie, Münster, Germany
Appl Environ Microbiol. 2018 Jun 18;84(13). doi: 10.1128/AEM.00626-18. Print 2018 Jul 1.
The opportunistic pathogen strain PAO1 is able to use a variety of organic pollutants as growth substrates, including the anionic detergent sodium dodecyl sulfate (SDS) and long-chain alkanes. While the enzymes initiating SDS and alkane degradation are well known, the subsequent enzymatic steps for degradation of the derived primary long-chain alcohols have not yet been identified. By evaluating genes specifically induced during growth with SDS, a gene cluster encoding a putative alcohol dehydrogenase (PA0364/LaoA), a probable inner membrane protein (PA0365/LaoB), and a presumable aldehyde dehydrogenase (PA0366/LaoC) was identified and designated the Lao (ong-chain-lcohol/ldehyde-xidation) system. Growth experiments with deletion mutants with SDS, 1-dodecanol, and alkanes revealed that LaoA and LaoB are involved in the degradation of primary long-chain alcohols. Moreover, detection of 1-dodecanol oxidation in cell extracts by activity staining revealed an interdependency of LaoA and LaoB for efficient 1-dodecanol oxidation. An analysis yielded no well-characterized homologue proteins for LaoA and LaoB. Furthermore, a gene adjacent to the gene cluster encodes a putative transcriptional regulator (PA0367/LaoR). A deletion mutant exhibited constitutive expression of LaoA and LaoB, indicating that LaoR is a repressor for the expression of Taken together, these results showed that the proteins LaoA and LaoB constitute a novel oxidation system for long-chain alcohols derived from pollutants. The versatile and highly adaptive bacterium a is able to colonize a variety of habitats, including anthropogenic environments, where it is often challenged with toxic compounds. Its ability to degrade such compounds and to use them as growth substrates can significantly enhance spreading of this opportunistic pathogen in hygienic settings, such as clinics or water distribution systems. Thus, knowledge about the metabolism of can contribute to novel approaches for preventing its growth and reducing nosocomial infections. As the Lao system is important for the degradation of two different classes of pollutants, the identification of these novel enzymes can be a useful contribution for developing effective antibacterial strategies.
机会性病原体 PAO1 能够利用各种有机污染物作为生长基质,包括阴离子洗涤剂十二烷基硫酸钠(SDS)和长链烷烃。虽然启动 SDS 和烷烃降解的酶是众所周知的,但降解衍生的初级长链醇的后续酶步骤尚未确定。通过评估生长过程中特异性诱导的基因,鉴定并命名了一个基因簇,该基因簇编码一种假定的醇脱氢酶(PA0364/LaoA)、一种可能的内膜蛋白(PA0365/LaoB)和一种假定的醛脱氢酶(PA0366/LaoC),并将其命名为 Lao(长链醇/醛氧化)系统。用 SDS、1-十二烷醇和烷烃的缺失突变体进行生长实验表明,LaoA 和 LaoB 参与了初级长链醇的降解。此外,通过活性染色检测细胞提取物中的 1-十二烷醇氧化,发现 LaoA 和 LaoB 对于有效氧化 1-十二烷醇相互依赖。分析没有得到 LaoA 和 LaoB 的特征良好的同源蛋白。此外,基因簇旁边的一个基因编码一个假定的转录调节剂(PA0367/LaoR)。一个 缺失突变体表现出 LaoA 和 LaoB 的组成型表达,表明 LaoR 是 LaoA 和 LaoB 表达的阻遏物。综上所述,这些结果表明,LaoA 和 LaoB 蛋白构成了一种源自污染物的长链醇的新型氧化系统。这种多功能且适应性强的细菌能够在多种栖息地中定殖,包括人为环境,在这些环境中,它经常面临有毒化合物的挑战。它降解这些化合物并将其用作生长基质的能力可以显著增强这种机会性病原体在卫生环境中的传播,如诊所或水分配系统。因此,对 代谢的了解可以为预防其生长和减少医院感染提供新的方法。由于 Lao 系统对两种不同类别的污染物的降解很重要,因此鉴定这些新的酶可以为开发有效的抗菌策略做出有益的贡献。