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A Droplet Microfluidics Based Platform for Mining Metagenomic Libraries for Natural Compounds
Historically, microbes from the environment have been a reliable source for novel bio-active compounds. Cloning and expression of metagenomic DNA in heterologous strains of bacteria has broadened the range of potential compounds accessible. However, such metagenomic libraries have been under-exploit...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6189830/ https://www.ncbi.nlm.nih.gov/pubmed/30400422 http://dx.doi.org/10.3390/mi8080230 |
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author | Theodorou, Elias Scanga, Randall Twardowski, Mariusz Snyder, Michael P. Brouzes, Eric |
author_facet | Theodorou, Elias Scanga, Randall Twardowski, Mariusz Snyder, Michael P. Brouzes, Eric |
author_sort | Theodorou, Elias |
collection | PubMed |
description | Historically, microbes from the environment have been a reliable source for novel bio-active compounds. Cloning and expression of metagenomic DNA in heterologous strains of bacteria has broadened the range of potential compounds accessible. However, such metagenomic libraries have been under-exploited for applications in mammalian cells because of a lack of integrated methods. We present an innovative platform to systematically mine natural resources for pro-apoptotic compounds that relies on the combination of bacterial delivery and droplet microfluidics. Using the violacein operon from C. violaceum as a model, we demonstrate that E. coli modified to be invasive can serve as an efficient delivery vehicle of natural compounds. This approach permits the seamless screening of metagenomic libraries with mammalian cell assays and alleviates the need for laborious extraction of natural compounds. In addition, we leverage the unique properties of droplet microfluidics to amplify bacterial clones and perform clonal screening at high-throughput in place of one-compound-per-well assays in multi-well format. We also use droplet microfluidics to establish a cell aggregate strategy that overcomes the issue of background apoptosis. Altogether, this work forms the foundation of a versatile platform to efficiently mine the metagenome for compounds with therapeutic potential. |
format | Online Article Text |
id | pubmed-6189830 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-61898302018-11-01 A Droplet Microfluidics Based Platform for Mining Metagenomic Libraries for Natural Compounds Theodorou, Elias Scanga, Randall Twardowski, Mariusz Snyder, Michael P. Brouzes, Eric Micromachines (Basel) Article Historically, microbes from the environment have been a reliable source for novel bio-active compounds. Cloning and expression of metagenomic DNA in heterologous strains of bacteria has broadened the range of potential compounds accessible. However, such metagenomic libraries have been under-exploited for applications in mammalian cells because of a lack of integrated methods. We present an innovative platform to systematically mine natural resources for pro-apoptotic compounds that relies on the combination of bacterial delivery and droplet microfluidics. Using the violacein operon from C. violaceum as a model, we demonstrate that E. coli modified to be invasive can serve as an efficient delivery vehicle of natural compounds. This approach permits the seamless screening of metagenomic libraries with mammalian cell assays and alleviates the need for laborious extraction of natural compounds. In addition, we leverage the unique properties of droplet microfluidics to amplify bacterial clones and perform clonal screening at high-throughput in place of one-compound-per-well assays in multi-well format. We also use droplet microfluidics to establish a cell aggregate strategy that overcomes the issue of background apoptosis. Altogether, this work forms the foundation of a versatile platform to efficiently mine the metagenome for compounds with therapeutic potential. MDPI 2017-07-25 /pmc/articles/PMC6189830/ /pubmed/30400422 http://dx.doi.org/10.3390/mi8080230 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Theodorou, Elias Scanga, Randall Twardowski, Mariusz Snyder, Michael P. Brouzes, Eric A Droplet Microfluidics Based Platform for Mining Metagenomic Libraries for Natural Compounds |
title | A Droplet Microfluidics Based Platform for Mining Metagenomic Libraries for Natural Compounds |
title_full | A Droplet Microfluidics Based Platform for Mining Metagenomic Libraries for Natural Compounds |
title_fullStr | A Droplet Microfluidics Based Platform for Mining Metagenomic Libraries for Natural Compounds |
title_full_unstemmed | A Droplet Microfluidics Based Platform for Mining Metagenomic Libraries for Natural Compounds |
title_short | A Droplet Microfluidics Based Platform for Mining Metagenomic Libraries for Natural Compounds |
title_sort | droplet microfluidics based platform for mining metagenomic libraries for natural compounds |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6189830/ https://www.ncbi.nlm.nih.gov/pubmed/30400422 http://dx.doi.org/10.3390/mi8080230 |
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