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Prescreening bacterial colonies for bioactive molecules with Janus plates, a SBS standard double-faced microbial culturing system

Despite the availability of many culture-based antibiotic screening methods, the lack of sensitive automated methods to identify functional molecules directly from microbial cells still limits the search for new biologically active compounds. The effectiveness of antibiotic detection is influenced b...

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Autores principales: Sánchez-Hidalgo, Marina, Pascual, Javier, de la Cruz, Mercedes, Martín, Jesús, Kath, Gary S., Sigmund, Janet M., Masurekar, Prakash, Vicente, Francisca, Genilloud, Olga, Bills, Gerald F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3397223/
https://www.ncbi.nlm.nih.gov/pubmed/22562433
http://dx.doi.org/10.1007/s10482-012-9746-7
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author Sánchez-Hidalgo, Marina
Pascual, Javier
de la Cruz, Mercedes
Martín, Jesús
Kath, Gary S.
Sigmund, Janet M.
Masurekar, Prakash
Vicente, Francisca
Genilloud, Olga
Bills, Gerald F.
author_facet Sánchez-Hidalgo, Marina
Pascual, Javier
de la Cruz, Mercedes
Martín, Jesús
Kath, Gary S.
Sigmund, Janet M.
Masurekar, Prakash
Vicente, Francisca
Genilloud, Olga
Bills, Gerald F.
author_sort Sánchez-Hidalgo, Marina
collection PubMed
description Despite the availability of many culture-based antibiotic screening methods, the lack of sensitive automated methods to identify functional molecules directly from microbial cells still limits the search for new biologically active compounds. The effectiveness of antibiotic detection is influenced by the solubility of the assayed compounds, indicator strain sensitivity, culture media and assay configuration. We describe a qualitative high throughput screening system for detecting cell-perturbing molecules from bacterial colonies employing two opposed agar layers sequentially formed in prototype Society for Biomolecular Screening (SBS) plates, named Janus plates. Direct assay of microbial colonies against target organisms in opposed agar layers overcomes some of the limitations of agar overlay methods. The system enables the rapid detection of extracellular cell-perturbing molecules, e.g., antibiotics, excreted directly from environmental isolates. The source bacterial colonies remain separate from the target organism. The growth layer is prepared and grown independently, so environmental strains can be grown for longer intervals, at temperatures and in media that favor their growth and metabolite expression, while the assay layer with pathogens, usually requiring nutrient-rich medium and elevated temperatures, are added later. Colonies to be tested can be precisely arrayed on the first agar surface, thus avoiding dispersion and disturbance of potential antibiotic-producing colonies by overlaying agar with the target strain. The rectangular SBS configuration facilitates factorial replication of dense microbial colony arrays for testing with multiple assays and assay conditions employing robotic colony pickers and pin tools. Opposed agar layers only slightly reduced the effectiveness for detecting growth inhibition from pure antibiotics compared to single-layer agar diffusion assays. The Janus plate enabled an automation-assisted workflow where a lone operator can effectively identify and accumulate bioactive soil bacterial strains within a few weeks. We also envisage the method’s utility for functional prescreening colonies of clones from genomic and metagenomic libraries or improved strains originating from mutagenized cells. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s10482-012-9746-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-33972232012-07-23 Prescreening bacterial colonies for bioactive molecules with Janus plates, a SBS standard double-faced microbial culturing system Sánchez-Hidalgo, Marina Pascual, Javier de la Cruz, Mercedes Martín, Jesús Kath, Gary S. Sigmund, Janet M. Masurekar, Prakash Vicente, Francisca Genilloud, Olga Bills, Gerald F. Antonie Van Leeuwenhoek Original Paper Despite the availability of many culture-based antibiotic screening methods, the lack of sensitive automated methods to identify functional molecules directly from microbial cells still limits the search for new biologically active compounds. The effectiveness of antibiotic detection is influenced by the solubility of the assayed compounds, indicator strain sensitivity, culture media and assay configuration. We describe a qualitative high throughput screening system for detecting cell-perturbing molecules from bacterial colonies employing two opposed agar layers sequentially formed in prototype Society for Biomolecular Screening (SBS) plates, named Janus plates. Direct assay of microbial colonies against target organisms in opposed agar layers overcomes some of the limitations of agar overlay methods. The system enables the rapid detection of extracellular cell-perturbing molecules, e.g., antibiotics, excreted directly from environmental isolates. The source bacterial colonies remain separate from the target organism. The growth layer is prepared and grown independently, so environmental strains can be grown for longer intervals, at temperatures and in media that favor their growth and metabolite expression, while the assay layer with pathogens, usually requiring nutrient-rich medium and elevated temperatures, are added later. Colonies to be tested can be precisely arrayed on the first agar surface, thus avoiding dispersion and disturbance of potential antibiotic-producing colonies by overlaying agar with the target strain. The rectangular SBS configuration facilitates factorial replication of dense microbial colony arrays for testing with multiple assays and assay conditions employing robotic colony pickers and pin tools. Opposed agar layers only slightly reduced the effectiveness for detecting growth inhibition from pure antibiotics compared to single-layer agar diffusion assays. The Janus plate enabled an automation-assisted workflow where a lone operator can effectively identify and accumulate bioactive soil bacterial strains within a few weeks. We also envisage the method’s utility for functional prescreening colonies of clones from genomic and metagenomic libraries or improved strains originating from mutagenized cells. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s10482-012-9746-7) contains supplementary material, which is available to authorized users. Springer Netherlands 2012-05-05 2012 /pmc/articles/PMC3397223/ /pubmed/22562433 http://dx.doi.org/10.1007/s10482-012-9746-7 Text en © The Author(s) 2012 https://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Original Paper
Sánchez-Hidalgo, Marina
Pascual, Javier
de la Cruz, Mercedes
Martín, Jesús
Kath, Gary S.
Sigmund, Janet M.
Masurekar, Prakash
Vicente, Francisca
Genilloud, Olga
Bills, Gerald F.
Prescreening bacterial colonies for bioactive molecules with Janus plates, a SBS standard double-faced microbial culturing system
title Prescreening bacterial colonies for bioactive molecules with Janus plates, a SBS standard double-faced microbial culturing system
title_full Prescreening bacterial colonies for bioactive molecules with Janus plates, a SBS standard double-faced microbial culturing system
title_fullStr Prescreening bacterial colonies for bioactive molecules with Janus plates, a SBS standard double-faced microbial culturing system
title_full_unstemmed Prescreening bacterial colonies for bioactive molecules with Janus plates, a SBS standard double-faced microbial culturing system
title_short Prescreening bacterial colonies for bioactive molecules with Janus plates, a SBS standard double-faced microbial culturing system
title_sort prescreening bacterial colonies for bioactive molecules with janus plates, a sbs standard double-faced microbial culturing system
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3397223/
https://www.ncbi.nlm.nih.gov/pubmed/22562433
http://dx.doi.org/10.1007/s10482-012-9746-7
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