Discovering new bioactive molecules from microbial sources

Summary 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...

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Veröffentlicht in:Microbial Biotechnology 2014-05, Vol.7 (3), p.209-220
Hauptverfasser: Monciardini, Paolo, Iorio, Marianna, Maffioli, Sonia, Sosio, Margherita, Donadio, Stefano
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container_end_page 220
container_issue 3
container_start_page 209
container_title Microbial Biotechnology
container_volume 7
creator Monciardini, Paolo
Iorio, Marianna
Maffioli, Sonia
Sosio, Margherita
Donadio, Stefano
description Summary 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. The concept of low hanging fruits in microbial product discovery, as determined by the explored microbial diversity and the sensitivity of the employed assays.
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subjects Actinobacteria - chemistry
Biological Products - isolation & purification
Biological Products - pharmacology
Case studies
Drug approval
Drug Evaluation, Preclinical - methods
Fungi - chemistry
Genomics
Minireviews
title Discovering new bioactive molecules from microbial sources
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