Correlation Engine 2.0
Clear Search sequence regions


  • ALDHs (1)
  • amides (1)
  • escherichia coli (2)
  • function (2)
  • gene (1)
  • indigo (3)
  • indoles (2)
  • indoxyl (3)
  • oxygenases (2)
  • rhodococcus (2)
  • Sizes of these terms reflect their relevance to your search.

    Here, we present a proof-of-principle for a new high-throughput functional screening of metagenomic libraries for the selection of enzymes with different activities, predetermined by the substrate being used. By this approach, a total of 21 enzyme-coding genes were selected, including members of xanthine dehydrogenase, aldehyde dehydrogenase (ALDH), and amidohydrolase families. The screening system is based on a pro-chromogenic substrate, which is transformed by the target enzyme to indole-3-carboxylic acid. The later compound is converted to indoxyl by a newly identified indole-3-carboxylate monooxygenase (Icm). Due to the spontaneous oxidation of indoxyl to indigo, the target enzyme-producing colonies turn blue. Two types of pro-chromogenic substrates have been tested. Indole-3-carboxaldehydes and the amides of indole-3-carboxylic acid have been applied as substrates for screening of the ALDHs and amidohydrolases, respectively. Both plate assays described here are rapid, convenient, easy to perform, and adaptable for the screening of a large number of samples both in Escherichia coli and Rhodococcus sp. In addition, the fine-tuning of the pro-chromogenic substrate allows screening enzymes with the desired substrate specificity. © 2019 The Authors. MicrobiologyOpen published by John Wiley & Sons Ltd.

    Citation

    Vida Časaitė, Mikas Sadauskas, Justas Vaitekūnas, Renata Gasparavičiūtė, Rita Meškienė, Izabelė Skikaitė, Mantas Sakalauskas, Jevgenija Jakubovska, Daiva Tauraitė, Rolandas Meškys. Engineering of a chromogenic enzyme screening system based on an auxiliary indole-3-carboxylic acid monooxygenase. MicrobiologyOpen. 2019 Aug;8(8):e00795

    Expand section icon Mesh Tags

    Expand section icon Substances


    PMID: 30666828

    View Full Text