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. 2023 Sep 15;18(9):1959-1967.
doi: 10.1021/acschembio.3c00112. Epub 2023 Aug 21.

A Plastic Biosynthetic Pathway for the Production of Structurally Distinct Microbial Sunscreens

Affiliations

A Plastic Biosynthetic Pathway for the Production of Structurally Distinct Microbial Sunscreens

Sıla Arsın et al. ACS Chem Biol. .

Abstract

Mycosporine-like amino acids (MAAs) are small, colorless, and water-soluble secondary metabolites. They have high molar extinction coefficients and a unique UV radiation absorption mechanism that make them effective sunscreens. Here we report the discovery of two structurally distinct MAAs from the lichen symbiont strain Nostoc sp. UHCC 0926. We identified these MAAs as aplysiapalythine E (C23H38N2O15) and tricore B (C34H53N4O15) using a combination of high-resolution liquid chromatography-mass spectrometry (HR-LCMS) analysis and nuclear magnetic resonance (NMR) spectroscopy. We obtained a 8.3 Mb complete genome sequence of Nostoc sp. UHCC 0926 to gain insights into the genetic basis for the biosynthesis of these two structural distinct MAAs. We identified MAA biosynthetic genes encoded in three separate locations of the genome. The organization of biosynthetic enzymes in Nostoc sp. UHCC 0926 necessitates a branched biosynthetic pathway to produce two structurally distinct MAAs. We detected the presence of such discontiguous MAA biosynthetic gene clusters in 12% of the publicly available complete cyanobacterial genomes. Bioinformatic analysis of public MAA biosynthetic gene clusters suggests that they are subject to rapid evolutionary processes resulting in highly plastic biosynthetic pathways that are responsible for the chemical diversity in this family of microbial sunscreens.

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Conflict of interest statement

The authors declare no competing financial interest.

Figures

Figure 1
Figure 1
Chemical structures of the aplysiapalythine E (582 Da, λmax = 336 nm) and tricore B (756 Da, λmax = 312 nm) with a shoulder peak at 340 nm from the lichen symbiont Nostoc sp. UHCC 0926. 1H–1H COSY and 1H–13C HMBC correlations are given for each compound.
Figure 2
Figure 2
Proposed branched biosynthetic pathway for the synthesis of tricore B and aplysiapalythine E variants identified from Nostoc sp. UHCC 0926. The intermediate structures are numbered according to HR-LCMS data (Table S1). 4-Deoxygadusol synthesis is highlighted as it a shared biosynthetic intermediate for the biosynthesis of both the tricore B and aplysiapalythine E.
Figure 3
Figure 3
A maximum-likelihood phylogenomic tree of the complete cyanobacterial genomes that possess a MAA biosynthetic gene cluster. Tree was constructed using the sequences of 120 bacterial single-copy marker proteins with PROTGAMMAIGTR model with 1000 bootstraps. Cyanobacteria strains with discontiguous MAA biosynthetic gene clusters are marked with a red ribbon.
Figure 4
Figure 4
Distribution, domain architecture, and substrate variation including the Stachelhaus codes of the MysE enzymes found in MAA biosynthetic gene clusters of the analyzed cyanobacterial genomes. MysE enzymes are colored brighter alongside the MysF (dark green) and MysI (mustard yellow) to highlight the coclustering pattern.

References

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