Literature DB >> 27787679

Real-time PCR detection of aldoxime dehydratase genes in nitrile-degrading microorganisms.

Tríona Marie Dooley-Cullinane1, Catherine O'Reilly2, Lee Coffey2.   

Abstract

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.

Entities:  

Keywords:  Aldoxime dehydratase; Aldoxime–nitrile pathway; Amidase; High-throughput; Nitrile hydratase; Real-time PCR

Mesh:

Substances:

Year:  2016        PMID: 27787679     DOI: 10.1007/s10482-016-0786-2

Source DB:  PubMed          Journal:  Antonie Van Leeuwenhoek        ISSN: 0003-6072            Impact factor:   2.271


  1 in total

1.  The use of clade-specific PCR assays to identify novel nitrilase genes from environmental isolates.

Authors:  Tríona-Marie Dooley-Cullinane; Catherine O'Reilly; Bilal Aslam; David P Weiner; David O'Neill; Erica Owens; Denise O'Meara; Lee Coffey
Journal:  Microbiologyopen       Date:  2018-12-30       Impact factor: 3.139

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.