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2024 | Buch

SARP-Driven Activation of Antibiotic Biosynthetic Gene Clusters in Actinomycetes

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Über dieses Buch

Actinomycetes are a group of Gram-positive bacteria of which many representatives are prominent for being prolific producers of bioactive natural products including antibiotics, fungicides, antitumor agents, or immunosuppressants. SARP transcriptional regulators are widely distributed among actinomycetes, especially in streptomycetes and are known to activate antibiotic biosynthesis. The set of genes responsible for the production of natural products, including pathway specific transcriptional regulators such as SARPs, are typically located in contiguous regions of the genome known as "biosynthetic gene clusters" (BGCs). In this book, Oona Rössler reports on the activation of antibiotic BGCs in selected actinomycetes strains upon heterologous expression of the SARP-type regulator PapR2 from Streptomyces pristinaespiralis. Applying a bioinformatic screening for the abundance of SARP genes and SARP consensus sequences as part of BGCs, the author has selected actinomycetes candidate strains from the DSMZ strain collection for heterologous SARP expression. It is shown that overexpression of papR2 increased the production of predominantly unknown antimicrobial compounds in more than half of the selected actinomycetes strains, as observed by bioassays against different microbial test strains including bacteria and fungi.

Inhaltsverzeichnis

Frontmatter
Chapter 1. Introduction
Abstract
The discovery of bioactive molecules originating from microorganisms has been the greatest medical advancement in history. Over 70% of all antibiotics in clinical use are derived from natural products produced by the bacterial group of actinomycetes (Bérdy, 2012; Newman & Cragg, 2012). Paul Ehrlich introduced the first antibiotic in 1910, an arsenic-based synthetic drug called “salvarsan” to treat syphilis (Hutchings et al., 2019).
Oona Rössler
Chapter 2. Material and Methods
Abstract
To find DSMZ strains whose genomes have been sequenced and carry candidate BGCs for activation by PapR2, an advanced bioinformatic search for candidate genomes was conducted with all available genomes from the Integrated Microbial Genomes (IMG) facility of the Joint Genome Institute (JGI). BGCs that contain genes coding for SARP transcriptional regulators were identified with antiSMASH 6.0 and “relaxed” was set as strictness. The genomes were drawn from National Center for Biotechnology Information (NCBI, https://www.ncbi.nlm.nih.gov/).
Oona Rössler
Chapter 3. Results
Abstract
The aim of the work was to activate antibiotic biosynthetic gene cluster expression of prioritized genome-sequenced actinomycetes with the help of SARP-type regulators. PapR2 is a SARP-type regulator and pathway-specific activator of pristinamycin biosynthesis in S. pristinaespiralis. To achieve biosynthetic gene cluster activation with the help of PapR2, suitable overexpression constructs are a prerequisite.
Oona Rössler
Chapter 4. Discussion
Abstract
In this study, SARP-driven expression of BGCs of a selected number of genome-sequenced actinomycetes strains was successfully achieved. Overexpression of PapR2 resulted in increased production of bioactive compounds which were assessed with bioassays against different test strains including bacteria and fungi. Thus, it was verified that the targeted SARP-driven activation strategy is a valuable method to be applied to unlock the genetic potential of actinomycetes to produce novel natural products.
Oona Rössler
Backmatter
Metadaten
Titel
SARP-Driven Activation of Antibiotic Biosynthetic Gene Clusters in Actinomycetes
verfasst von
Oona Rössler
Copyright-Jahr
2024
Electronic ISBN
978-3-658-44552-2
Print ISBN
978-3-658-44551-5
DOI
https://doi.org/10.1007/978-3-658-44552-2

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