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Discovering new bioactive molecules from microbial sources
There is an increased need for new drug leads to treat diseases in humans, animals and plants. A dramatic example is represented by the need for novel and more effective antibiotics to combat multidrug-resistant microbial pathogens. Natural products represent a major source of approved drugs and sti...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3992017/ https://www.ncbi.nlm.nih.gov/pubmed/24661414 http://dx.doi.org/10.1111/1751-7915.12123 |
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author | Monciardini, Paolo Iorio, Marianna Maffioli, Sonia Sosio, Margherita Donadio, Stefano |
author_facet | Monciardini, Paolo Iorio, Marianna Maffioli, Sonia Sosio, Margherita Donadio, Stefano |
author_sort | Monciardini, Paolo |
collection | PubMed |
description | There is an increased need for new drug leads to treat diseases in humans, animals and plants. A dramatic example is represented by the need for novel and more effective antibiotics to combat multidrug-resistant microbial pathogens. Natural products represent a major source of approved drugs and still play an important role in supplying chemical diversity, despite a decreased interest by large pharmaceutical companies. Novel approaches must be implemented to decrease the chances of rediscovering the tens of thousands of known natural products. In this review, we present an overview of natural product screening, focusing particularly on microbial products. Different approaches can be implemented to increase the probability of finding new bioactive molecules. We thus present the rationale and selected examples of the use of hypersensitive assays; of accessing unexplored microorganisms, including the metagenome; and of genome mining. We then focus our attention on the technology platform that we are currently using, consisting of approximately 70 000 microbial strains, mostly actinomycetes and filamentous fungi, and discuss about high-quality screening in the search for bioactive molecules. Finally, two case studies are discussed, including the spark that arose interest in the compound: in the case of orthoformimycin, the novel mechanism of action predicted a novel structural class; in the case of NAI-112, structural similarity pointed out to a possible in vivo activity. Both predictions were then experimentally confirmed. |
format | Online Article Text |
id | pubmed-3992017 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | John Wiley & Sons Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-39920172014-05-01 Discovering new bioactive molecules from microbial sources Monciardini, Paolo Iorio, Marianna Maffioli, Sonia Sosio, Margherita Donadio, Stefano Microb Biotechnol Minireviews There is an increased need for new drug leads to treat diseases in humans, animals and plants. A dramatic example is represented by the need for novel and more effective antibiotics to combat multidrug-resistant microbial pathogens. Natural products represent a major source of approved drugs and still play an important role in supplying chemical diversity, despite a decreased interest by large pharmaceutical companies. Novel approaches must be implemented to decrease the chances of rediscovering the tens of thousands of known natural products. In this review, we present an overview of natural product screening, focusing particularly on microbial products. Different approaches can be implemented to increase the probability of finding new bioactive molecules. We thus present the rationale and selected examples of the use of hypersensitive assays; of accessing unexplored microorganisms, including the metagenome; and of genome mining. We then focus our attention on the technology platform that we are currently using, consisting of approximately 70 000 microbial strains, mostly actinomycetes and filamentous fungi, and discuss about high-quality screening in the search for bioactive molecules. Finally, two case studies are discussed, including the spark that arose interest in the compound: in the case of orthoformimycin, the novel mechanism of action predicted a novel structural class; in the case of NAI-112, structural similarity pointed out to a possible in vivo activity. Both predictions were then experimentally confirmed. John Wiley & Sons Ltd 2014-05 2014-03-24 /pmc/articles/PMC3992017/ /pubmed/24661414 http://dx.doi.org/10.1111/1751-7915.12123 Text en © 2014 The Authors. Microbial Biotechnology published by John Wiley & Sons Ltd and Society for Applied Microbiology. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Minireviews Monciardini, Paolo Iorio, Marianna Maffioli, Sonia Sosio, Margherita Donadio, Stefano Discovering new bioactive molecules from microbial sources |
title | Discovering new bioactive molecules from microbial sources |
title_full | Discovering new bioactive molecules from microbial sources |
title_fullStr | Discovering new bioactive molecules from microbial sources |
title_full_unstemmed | Discovering new bioactive molecules from microbial sources |
title_short | Discovering new bioactive molecules from microbial sources |
title_sort | discovering new bioactive molecules from microbial sources |
topic | Minireviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3992017/ https://www.ncbi.nlm.nih.gov/pubmed/24661414 http://dx.doi.org/10.1111/1751-7915.12123 |
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