indigo-carmine and indole-3-carboxylic-acid

indigo-carmine has been researched along with indole-3-carboxylic-acid* in 2 studies

Other Studies

2 other study(ies) available for indigo-carmine and indole-3-carboxylic-acid

ArticleYear
Engineering of a chromogenic enzyme screening system based on an auxiliary indole-3-carboxylic acid monooxygenase.
    MicrobiologyOpen, 2019, Volume: 8, Issue:8

    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.

    Topics: Aldehyde Dehydrogenase; Amidohydrolases; Chromogenic Compounds; Cloning, Molecular; Escherichia coli; Gene Expression; Genetic Testing; Genetics, Microbial; Indigo Carmine; Indoles; Mixed Function Oxygenases; Oxidation-Reduction; Rhodococcus

2019
Formation of indigo and related compounds from indolecarboxylic acids by aromatic acid-degrading bacteria: chromogenic reactions for cloning genes encoding dioxygenases that act on aromatic acids.
    Journal of bacteriology, 1995, Volume: 177, Issue:23

    The p-cumate-degrading strain Pseudomonas putida F1 and the m- and p-toluate-degrading strain P. putida mt-2 transform indole-2-carboxylate and indole-3-carboxylate to colored products identified here as indigo, indirubin, and isatin. A mechanism by which these products could be formed spontaneously following dioxygenase-catalyzed dihydroxylation of the indolecarboxylates is proposed. Indolecarboxylates were employed as chromogenic substrates for identifying recombinant bacteria carrying genes encoding p-cumate dioxygenase and toluate dioxygenase. Dioxygenase gene-carrying bacteria could be readily distinguished as dark green-blue colonies among other colorless recombinant Escherichia coli colonies on selective agar plates containing either indole-2-carboxylate or indole-3-carboxylate.

    Topics: Amino Acids; Carboxylic Acids; Chromogenic Compounds; Cloning, Molecular; Coloring Agents; Indigo Carmine; Indoles; Isatin; Oxygenases; Pseudomonas putida

1995