Dooley-Cullinane Tríona Marie, O'Reilly Catherine, Coffey Lee
Waterford Institute of Technology, Cork Rd, Waterford, Ireland.
Antonie Van Leeuwenhoek. 2017 Feb;110(2):271-279. doi: 10.1007/s10482-016-0786-2. Epub 2016 Oct 27.
Aldoxime dehydratase catalyses the conversion of aldoximes to their corresponding nitriles. Utilization of the aldoxime-nitrile metabolising enzyme pathway can facilitate the move towards a greener chemistry. In this work, a real-time PCR assay was developed for the detection of aldoxime dehydratase genes in aldoxime/nitrile metabolising microorganisms which have been purified from environmental sources. A conventional PCR assay was also designed allowing gene confirmation via sequencing. Aldoxime dehydratase genes were identified in 30 microorganisms across 11 genera including some not previously shown to harbour the gene. The assay displayed a limit of detection of 1 pg/μL DNA or 7 CFU/reaction. This real-time PCR assay should prove valuable in the high-throughput screening of micro-organisms for novel aldoxime dehydratase genes towards pharmaceutical and industrial applications.
醛肟脱水酶催化醛肟转化为相应的腈。利用醛肟-腈代谢酶途径有助于迈向更绿色的化学。在这项工作中,开发了一种实时PCR检测方法,用于检测从环境来源纯化的醛肟/腈代谢微生物中的醛肟脱水酶基因。还设计了一种常规PCR检测方法,通过测序进行基因确认。在11个属的30种微生物中鉴定出了醛肟脱水酶基因,其中包括一些以前未显示含有该基因的微生物。该检测方法的检测限为1 pg/μL DNA或7 CFU/反应。这种实时PCR检测方法在高通量筛选新型醛肟脱水酶基因的微生物以用于制药和工业应用方面应具有重要价值。