Fig. 7From: Metagenomics-resolved genomics provides novel insights into chitin turnover, metabolic specialization, and niche partitioning in the octocoral microbiomeSecondary metabolite coding potential in each MAG obtained from microbial metagenomes of healthy and necrotic octocoral samples and seawater. a Distribution of secondary metabolite biosynthesis gene clusters (SM-BGCs) across the 66 MAGs of this study. Symbols above bars indicate the origin of each MAG (same as in Fig. 3). SM-BGC counts per compound class were obtained using antiSMASH v.5.0 with default detection strictness (and all extra features on). PKS, polyketide synthase; hglEKS, heterocyst glycolipid synthase-like PKS; NRPS, nonribosomal peptide synthetase cluster; TfuA related, TfuA-related ribosomal peptides. b Percentage of SM-BGCs, identified on the 66 MAGs, with a hit to SM-BGCs of known compounds present in the MIBiG database. Only 14 of the 163 SM-BGCs obtained in this study shared 60% or more similarity to SM-BGCs of known compounds, highlighting the high degree of novelty encoded in these MAGs. c Predicted compounds among the SM-BGCs identified in the MAGs. d Chemical structures of isocalide A and bicornutin A1, encoded in the octocoral-derived MAGs of JAAAOG01 EV04H_Bin1 (Ca. Inquilinaceae, Alphaproteobacteria) and DT-91 LS06H_Bin2 (Pseudomonadales, Gammaproteobacteria). Structures were drawn with ChemDraw v. 12.0.2Back to article page