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. 2016 Oct 12;11(10):e0164468.
doi: 10.1371/journal.pone.0164468. eCollection 2016.

Metagenomic Analysis of the Sponge Discodermia Reveals the Production of the Cyanobacterial Natural Product Kasumigamide by 'Entotheonella'

Affiliations

Metagenomic Analysis of the Sponge Discodermia Reveals the Production of the Cyanobacterial Natural Product Kasumigamide by 'Entotheonella'

Yu Nakashima et al. PLoS One. .

Abstract

Sponge metagenomes are a useful platform to mine cryptic biosynthetic gene clusters responsible for production of natural products involved in the sponge-microbe association. Since numerous sponge-derived bioactive metabolites are biosynthesized by the symbiotic bacteria, this strategy may concurrently reveal sponge-symbiont produced compounds. Accordingly, a metagenomic analysis of the Japanese marine sponge Discodermia calyx has resulted in the identification of a hybrid type I polyketide synthase-nonribosomal peptide synthetase gene (kas). Bioinformatic analysis of the gene product suggested its involvement in the biosynthesis of kasumigamide, a tetrapeptide originally isolated from freshwater free-living cyanobacterium Microcystis aeruginosa NIES-87. Subsequent investigation of the sponge metabolic profile revealed the presence of kasumigamide in the sponge extract. The kasumigamide producing bacterium was identified as an 'Entotheonella' sp. Moreover, an in silico analysis of kas gene homologs uncovered the presence of kas family genes in two additional bacteria from different phyla. The production of kasumigamide by distantly related multiple bacterial strains implicates horizontal gene transfer and raises the potential for a wider distribution across other bacterial groups.

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Conflict of interest statement

The authors have declared that no competing interests exist.

Figures

Fig 1
Fig 1. Kasumigamide from the marine sponge Discodermia calyx.
(a) The marine sponge Discodermia calyx. (b) Structure of kasumigamide.
Fig 2
Fig 2. The biosynthetic gene cluster and proposed biosynthetic pathway to kasumigamide.
(a) ORFs encoded in the putative kasumigamide biosynthetic gene cluster, kasA-I. Double-headed arrows show the location of pDCYN1-2. The ORFs related to PKS-NRPS are highlighted in red. Putative transposases are colored in green. (b) The domain organization and proposed biosynthetic pathway to kasumigamide.
Fig 3
Fig 3. Symbiont bacteria bearing kas genes.
(a) Phase contrast image of D. calyx homogenate. A filamentous bacterium ‘Entotheonella’ sp. is designated as "F". A small filamentous bacterium with bright color is designated as "S". Scale bars was 20 μm. (b) PCR analysis of dissected cells with the kas-specific primers pair, DCKS10F/DCKS10R (S1 Table), using dissected cells ("F" or "S") as templates.
Fig 4
Fig 4. Comparative analysis of domain organizations of the putative kasumigamide biosynthetic gene clusters.
Each gene cluster derived from (a) D. acidovorans CCUG 274B (b) Herbaspirillum sp. CF444 (c) ‘Entotheonella’ sp. (d) M. aeruginosa NIES-87.
Fig 5
Fig 5. Substrate selectivity of A domains.
The relative adenylation activity was estimated by the malachite green phosphate assay. Error bars represent SEM (n = 3).

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