4.6 Article

Actinomadura graeca sp. nov.: A novel producer of the macrocyclic antibiotic zelkovamycin

Journal

PLOS ONE
Volume 16, Issue 11, Pages -

Publisher

PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pone.0260413

Keywords

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Funding

  1. Biotechnology and Biological Sciences Research Council Doctoral Training Partnership, UK (BBSRC DTP) studentship
  2. Engineering and Physical Sciences Research Council, UK (EPSRC) [EP/L022494/1]
  3. University of Nottingham
  4. University of Malaya [FP022-2018A, H-50001-A000027]

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In this study, a novel Actinomadura species, Actinomadura graeca sp. nov., was discovered from a soil sample collected in Santorini, Greece. Whole-genome sequencing revealed a high genetic similarity with A. macra, leading to the proposal of a new species. The newly discovered strain was confirmed to produce the non-ribosomal peptide antibiotic zelkovamycin, with a unique biosynthetic gene cluster described.
As part of a screening programme for antibiotic-producing bacteria, a novel Actinomadura species was discovered from a soil sample collected in Santorini, Greece. Preliminary 16S rRNA gene sequence comparisons highlighted Actinomadura macra as the most similar characterised species. However, whole-genome sequencing revealed an average nucleotide identity (ANI) value of 89% with A. macra, the highest among related species. Further phenotypic and chemotaxonomic analyses confirmed that the isolate represents a previously uncharacterised species in the genus Actinomadura, for which the name Actinomadura graeca sp. nov. is proposed (type strain 32-07(T)). The G+C content of A. graeca 32-07 is 72.36%. The cell wall contains DL-diaminopimelic acid, intracellular sugars are glucose, ribose and galactose, the predominant menaquinone is MK-9(H-6), the major cellular lipid is phosphatidylinositol and fatty acids consist mainly of hexadecanoic acid. No mycolic acid was detected. Furthermore, A. graeca 32-07 has been confirmed as a novel producer of the non-ribosomal peptide antibiotic zelkovamycin and we report herein a provisional description of the unique biosynthetic gene cluster.

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