Title
Unlocking the Spatial Control of Secondary Metabolism Uncovers Hidden Natural Product Diversity in Nostoc punctiforme
Date Issued
21 June 2019
Access level
metadata only access
Resource Type
journal article
Author(s)
Dehm D.
Krumbholz J.
Baunach M.
Wiebach V.
Hinrichs K.
Guljamow A.
Jenke-Kodama H.
Süssmuth R.D.
Dittmann E.
Okinawa Institute of Science and Technology
Publisher(s)
American Chemical Society
Abstract
Filamentous cyanobacteria belong to the most prolific producers of structurally unique and biologically active natural products, yet the majority of biosynthetic gene clusters predicted for these multicellular collectives are currently orphan. Here, we present a systems analysis of secondary metabolite gene expression in the model strain Nostoc punctiforme PCC73102 using RNA-seq and fluorescence reporter analysis. Our data demonstrate that the majority of the cryptic gene clusters are not silent but are expressed with regular or sporadic pattern. Cultivation of N. punctiforme using high-density fermentation overrules the spatial control and leads to a pronounced upregulation of more than 50% of biosynthetic gene clusters. Our data suggest that a combination of autocrine factors, a high CO2 level, and high light account for the upregulation of individual pathways. Our overarching study not only sheds light on the strategies of filamentous cyanobacteria to share the enormous metabolic burden connected with the production of specialized molecules but provides an avenue for the genome-based discovery of natural products in multicellular cyanobacteria as exemplified by the discovery of highly unusual variants of the tricyclic peptide microviridin.
Start page
1271
End page
1279
Volume
14
Issue
6
Language
English
OCDE Knowledge area
BioquÃmica, BiologÃa molecular
BiologÃa
Scopus EID
2-s2.0-85066450834
PubMed ID
Source
ACS Chemical Biology
ISSN of the container
15548929
Sponsor(s)
We thank H. Goto and the OIST DNA sequencing section (Okinawa, Japan) for providing technical assistance and performing the RNA sequencing. The study was supported by a grant of the German Research Foundation (Di910/12-1) to E.D. and the DFG-funded Collaborative Research Centre ChemBioSys (SFB 1127) to E.D. Further support to R.D.S. came from RTG 2473 and the cluster of Excellence under Germanyś Excellence Strategy − EXC 2008/1 (UniSysCat) − 390540038″.
Sources of information:
Directorio de Producción CientÃfica
Scopus