Complete Genome Sequence of Two Deep-Sea <i>Streptomyces</i> Isolates from Madeira Archipelago and Evaluation of Their Biosynthetic Potential

The deep-sea constitutes a true unexplored frontier and a potential source of innovative drug scaffolds. Here, we present the genome sequence of two novel marine actinobacterial strains, MA3_2.13 and S07_1.15, isolated from deep-sea samples (sediments and sponge) and collected at Madeira archipelago...

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Autores principales: Pedro Albuquerque, Inês Ribeiro, Sofia Correia, Ana Paula Mucha, Paula Tamagnini, Andreia Braga-Henriques, Maria de Fátima Carvalho, Marta V. Mendes
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Publicado: MDPI AG 2021
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Acceso en línea:https://doaj.org/article/fb37d6f97e9e4f1d852ab86880935bb7
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spelling oai:doaj.org-article:fb37d6f97e9e4f1d852ab86880935bb72021-11-25T18:12:52ZComplete Genome Sequence of Two Deep-Sea <i>Streptomyces</i> Isolates from Madeira Archipelago and Evaluation of Their Biosynthetic Potential10.3390/md191106211660-3397https://doaj.org/article/fb37d6f97e9e4f1d852ab86880935bb72021-11-01T00:00:00Zhttps://www.mdpi.com/1660-3397/19/11/621https://doaj.org/toc/1660-3397The deep-sea constitutes a true unexplored frontier and a potential source of innovative drug scaffolds. Here, we present the genome sequence of two novel marine actinobacterial strains, MA3_2.13 and S07_1.15, isolated from deep-sea samples (sediments and sponge) and collected at Madeira archipelago (NE Atlantic Ocean; Portugal). The de novo assembly of both genomes was achieved using a hybrid strategy that combines short-reads (Illumina) and long-reads (PacBio) sequencing data. Phylogenetic analyses showed that strain MA3_2.13 is a new species of the <i>Streptomyces</i> genus, whereas strain S07_1.15 is closely related to the type strain of <i>Streptomyces xinghaiensis</i>. In silico analysis revealed that the total length of predicted biosynthetic gene clusters (BGCs) accounted for a high percentage of the MA3_2.13 genome, with several potential new metabolites identified. Strain S07_1.15 had, with a few exceptions, a predicted metabolic profile similar to <i>S. xinghaiensis</i>. In this work, we implemented a straightforward approach for generating high-quality genomes of new bacterial isolates and analyse in silico their potential to produce novel NPs. The inclusion of these in silico dereplication steps allows to minimize the rediscovery rates of traditional natural products screening methodologies and expedite the drug discovery process.Pedro AlbuquerqueInês RibeiroSofia CorreiaAna Paula MuchaPaula TamagniniAndreia Braga-HenriquesMaria de Fátima CarvalhoMarta V. MendesMDPI AGarticle<i>Streptomyces</i>deep-sea actinobacteriade novo assemblygenome miningnatural productsBiology (General)QH301-705.5ENMarine Drugs, Vol 19, Iss 621, p 621 (2021)
institution DOAJ
collection DOAJ
language EN
topic <i>Streptomyces</i>
deep-sea actinobacteria
de novo assembly
genome mining
natural products
Biology (General)
QH301-705.5
spellingShingle <i>Streptomyces</i>
deep-sea actinobacteria
de novo assembly
genome mining
natural products
Biology (General)
QH301-705.5
Pedro Albuquerque
Inês Ribeiro
Sofia Correia
Ana Paula Mucha
Paula Tamagnini
Andreia Braga-Henriques
Maria de Fátima Carvalho
Marta V. Mendes
Complete Genome Sequence of Two Deep-Sea <i>Streptomyces</i> Isolates from Madeira Archipelago and Evaluation of Their Biosynthetic Potential
description The deep-sea constitutes a true unexplored frontier and a potential source of innovative drug scaffolds. Here, we present the genome sequence of two novel marine actinobacterial strains, MA3_2.13 and S07_1.15, isolated from deep-sea samples (sediments and sponge) and collected at Madeira archipelago (NE Atlantic Ocean; Portugal). The de novo assembly of both genomes was achieved using a hybrid strategy that combines short-reads (Illumina) and long-reads (PacBio) sequencing data. Phylogenetic analyses showed that strain MA3_2.13 is a new species of the <i>Streptomyces</i> genus, whereas strain S07_1.15 is closely related to the type strain of <i>Streptomyces xinghaiensis</i>. In silico analysis revealed that the total length of predicted biosynthetic gene clusters (BGCs) accounted for a high percentage of the MA3_2.13 genome, with several potential new metabolites identified. Strain S07_1.15 had, with a few exceptions, a predicted metabolic profile similar to <i>S. xinghaiensis</i>. In this work, we implemented a straightforward approach for generating high-quality genomes of new bacterial isolates and analyse in silico their potential to produce novel NPs. The inclusion of these in silico dereplication steps allows to minimize the rediscovery rates of traditional natural products screening methodologies and expedite the drug discovery process.
format article
author Pedro Albuquerque
Inês Ribeiro
Sofia Correia
Ana Paula Mucha
Paula Tamagnini
Andreia Braga-Henriques
Maria de Fátima Carvalho
Marta V. Mendes
author_facet Pedro Albuquerque
Inês Ribeiro
Sofia Correia
Ana Paula Mucha
Paula Tamagnini
Andreia Braga-Henriques
Maria de Fátima Carvalho
Marta V. Mendes
author_sort Pedro Albuquerque
title Complete Genome Sequence of Two Deep-Sea <i>Streptomyces</i> Isolates from Madeira Archipelago and Evaluation of Their Biosynthetic Potential
title_short Complete Genome Sequence of Two Deep-Sea <i>Streptomyces</i> Isolates from Madeira Archipelago and Evaluation of Their Biosynthetic Potential
title_full Complete Genome Sequence of Two Deep-Sea <i>Streptomyces</i> Isolates from Madeira Archipelago and Evaluation of Their Biosynthetic Potential
title_fullStr Complete Genome Sequence of Two Deep-Sea <i>Streptomyces</i> Isolates from Madeira Archipelago and Evaluation of Their Biosynthetic Potential
title_full_unstemmed Complete Genome Sequence of Two Deep-Sea <i>Streptomyces</i> Isolates from Madeira Archipelago and Evaluation of Their Biosynthetic Potential
title_sort complete genome sequence of two deep-sea <i>streptomyces</i> isolates from madeira archipelago and evaluation of their biosynthetic potential
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/fb37d6f97e9e4f1d852ab86880935bb7
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