4.6 Article

Taxogenomic and Comparative Genomic Analysis of the Genus Saccharomonospora Focused on the Identification of Biosynthetic Clusters PKS and NRPS

Journal

FRONTIERS IN MICROBIOLOGY
Volume 12, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fmicb.2021.603791

Keywords

actinobacteria; Saccharomonospora; biosynthetic gene clusters; secondary metabolites; polyketide synthase; non-ribosomal peptide synthetase; comparative genomic analysis; taxophylogenomic analysis

Categories

Funding

  1. FEDER/Spanish Ministry of Science and Innovation-State Research Agency [CGL2017-83385-P]
  2. National Council of Science and Technology [2018-000007-01EXTV-00289]
  3. Secretary for Research and Advanced Studies of the Autonomous University of the State of Mexico [5009/2020CIB]
  4. Junta de Andalucia, Spain [BIO-213, US-1263771]
  5. FEDER funds

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In this study, a comparative genomic analysis of the actinobacterial genus Saccharomonospora was conducted, revealing a high degree of novelty and diversity of biosynthetic gene clusters (BGCs) in members of this genus. The study supports a recent speciation event between Saccharomonospora halophila and Saccharomonospora iraqiensis.
Actinobacteria are prokaryotes with a large biotechnological interest due to their ability to produce secondary metabolites, produced by two main biosynthetic gene clusters (BGCs): polyketide synthase (PKS) and non-ribosomal peptide synthetase (NRPS). Most studies on bioactive products have been carried out on actinobacteria isolated from soil, freshwater or marine habitats, while very few have been focused on halophilic actinobacteria isolated from extreme environments. In this study we have carried out a comparative genomic analysis of the actinobacterial genus Saccharomonospora, which includes species isolated from soils, lake sediments, marine or hypersaline habitats. A total of 19 genome sequences of members of Saccharomonospora were retrieved and analyzed. We compared the 16S rRNA gene-based phylogeny of this genus with evolutionary relationships inferred using a phylogenomic approach obtaining almost identical topologies between both strategies. This method allowed us to unequivocally assign strains into species and to identify some taxonomic relationships that need to be revised. Our study supports a recent speciation event occurring between Saccharomonospora halophila and Saccharomonospora iraqiensis. Concerning the identification of BGCs, a total of 18 different types of BGCs were detected in the analyzed genomes of Saccharomonospora, including PKS, NRPS and hybrid clusters which might be able to synthetize 40 different putative products. In comparison to other genera of the Actinobacteria, members of the genus Saccharomonospora showed a high degree of novelty and diversity of BGCs.

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