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. 2020 Jul 21;10(46):27369-27376.
doi: 10.1039/d0ra05311b.

Investigating the biosynthesis of Sch-642305 in the fungus Phomopsis sp. CMU-LMA

Affiliations

Investigating the biosynthesis of Sch-642305 in the fungus Phomopsis sp. CMU-LMA

Francesco Trenti et al. RSC Adv. .

Abstract

Sch-642305 is an unusual bicyclic 10-membered macrolide produced by the filamentous fungus Phomopsis sp. CMU-LMA for which no biosynthetic evidence exists. Here, we generate a draft genome sequence of the producing organism and discover the biosynthetic gene cluster responsible for formation of Sch-642305. Targeted gene disruptions together with reconstitution of the pathway in the heterologous host Aspergillus oryzae dissect key chemical steps and shed light on a series of oxidoreductions occuring in the pathway.

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Conflict of interest statement

There are no conflicts to declare.

Figures

Scheme 1
Scheme 1. A) Incorporation of labelled acetates and 18O2 into SCH 1 and brefeldin A 5; (B) sch biosynthetic gene cluster and comparison to the bref BGC and PVSCH BGC; (C) hypothetical biosynthetic route to SCH 1 proposed by Snider and Zhou on the basis of the fungal metabolite mutolide 3 (a) and on the basis of benquoine 4 (b). Incorporation of labelled sodium [1-13C]-acetate and 18O2 is displayed for 3.
Fig. 1
Fig. 1. Secondary metabolites concomitantly isolated with SCH 1. Compounds in blue were previously isolated from Phomopsis sp. CMU-LMA but not observed in this study.
Fig. 2
Fig. 2. Targeted gene disruption in Phomopsis sp. CMU-LMA. ELSD chromatograms of KO mutants for: (A) schPKS; (B) schR7; (C) schR3; (D) schR2; (E) schR5. ** = unrelated to SCH 1 biosynthesis. X-axis in minutes throughout.
Scheme 2
Scheme 2. Proposed biosynthesis of SCH 1 and route to shunt metabolites (green). Compounds in black were isolated in this study, compounds in blue were previously isolated from Phomopsis sp. CMU-LMA. Compounds in grey were not observed but suggested as plausible intermediates on the pathway to 1.
Fig. 3
Fig. 3. (A) Biotransformation of SCH 1 by A. oryzae NSAR1. ES+ traces of fed 1 to A. oryzae, a standard of 1 and WT control; (B) heterologous expression of the full sch BGC. Diode array detector (DAD) traces of pathway expression and WT control; (C) heterologous expression of the full sch BGC and comparison to fed 1 to A. oryzae. ES+ traces of fed 1 (top) and full sch BGC (bottom).
Fig. 4
Fig. 4. DAD chromatograms of fungal extracts from the heterologous expression of early biosynthetic genes in A. oryzae NSAR1. Top, co-expression of schPKS, schR1, schR2, schR3, schR7; middle, co-expression of schPKS, schR1, schR2; bottom, NSAR1 WT.

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