Dokument-ID Dokumenttyp Verfasser/Autoren Herausgeber Haupttitel Abstract Auflage Verlagsort Verlag Erscheinungsjahr Seitenzahl Schriftenreihe Titel Schriftenreihe Bandzahl ISBN Quelle der Hochschulschrift Konferenzname Quelle:Titel Quelle:Jahrgang Quelle:Heftnummer Quelle:Erste Seite Quelle:Letzte Seite URN DOI Abteilungen OPUS4-50788 Wissenschaftlicher Artikel Pancrace, Claire; Ishida, Keishi; Briand, Enora; Pichi, Douglas Gatte; Weiz, Annika R.; Guljarmow, Arthur; Scalvenzi, Thibault; Sassoon, Nathalie; Hertweck, Christian; Dittmann, Elke; Gugger, Muriel Unique Biosynthetic Pathway in Bloom-Forming Cyanobacterial Genus Microcystis Jointly Assembles Cytotoxic Aeruginoguanidines and Microguanidines The cyanobacterial genus Microcystis is known to produce an elaborate array of structurally unique and biologically active natural products, including hazardous cyanotoxins. Cytotoxic aeruginoguanidines represent a yet unexplored family of peptides featuring a trisubstituted benzene unit and farnesylated arginine derivatives. In this study, we aimed at assigning these compounds to a biosynthetic gene cluster by utilizing biosynthetic attributes deduced from public genomes of Microcystis and the sporadic distribution of the metabolite in axenic strains of the Pasteur Culture Collection of Cyanobacteria. By integrating genome mining with untargeted metabolomics using liquid chromatography with mass spectrometry, we linked aeruginoguanidine (AGD) to a nonribosomal peptide synthetase gene cluster and coassigned a significantly smaller product to this pathway, microguanidine (MGD), previously only reported from two Microcystis blooms. Further, a new intermediate class of compounds named microguanidine amides was uncovered, thereby further enlarging this compound family. The comparison of structurally divergent AGDs and MGDs reveals an outstanding versatility of this biosynthetic pathway and provides insights into the assembly of the two compound subfamilies. Strikingly, aeruginoguanidines and microguanidines were found to be as widespread as the hepatotoxic microcystins, but the occurrence of both toxin families appeared to be mutually exclusive. Washington American Chemical Society 2018 9 ACS chemical biology 14 1 67 75 10.1021/acschembio.8b00918 Institut für Biochemie und Biologie OPUS4-31452 Wissenschaftlicher Artikel Ziemert, Nadine; Ishida, Keishi; Weiz, Annika; Hertweck, Christian; Dittmann-Thünemann, Elke Exploiting the natural diversity of microviridin gene clusters for discovery of novel tricyclic depsipeptides Microviridins are ribosomally synthesized tricyclic depsipeptides produced by different genera of cyanobacteria. The prevalence of the microviridin gene clusters and the natural diversity of microviridin precursor sequences are currently unknown. Screening of laboratory strains and field samples of the bloom-forming freshwater cyanobacterium Microcystis via PCR revealed global occurrence of the microviridin pathway and an unexpected natural variety. We could detect 15 new variants of the precursor gene mdnA encoding microviridin backbones that differ in up to 4 amino acid positions from known isoforms of the peptide. The survey not only provides insights into the versatility of the biosynthetic enzymes in a closely related group of cyanobacteria, but also facilitates the discovery and characterization of cryptic microviridin variants. This is demonstrated for microviridin L in Microcystis aeruginosa strain NIES843 and heterologously produced variants. 2010 10.1128/AEM.02858-09 Institut für Biochemie und Biologie OPUS4-36498 Wissenschaftlicher Artikel Weiz, Annika R.; Ishida, Keishi; Makower, Katharina; Ziemert, Nadine; Hertweck, Christian; Dittmann-Thünemann, Elke Leader Peptide and a Membrane Protein Scaffold Guide the Biosynthesis of the Tricyclic Peptide Microviridin Microviridins are unique protease inhibitors from bloom-forming cyanobacteria that have both ecological and pharmacological relevance. Their peptide backbones are produced ribosomally, and ATP grasp ligases introduce omega-ester and omega-amide bonds to yield rare cage-like structures. Bioinformatic analysis of the microviridin biosynthesis gene cluster suggests a novel type of processing machinery, which could rationalize the challenging in vivo/in vitro reconstitution of the pathway. In this work, we report the establishment of a minimal expression system for microviridins. Through bioinformatics and mutational analysis of the MdnA leader peptide we identified and characterized a strictly conserved binding motif that is specific for microviridin ligases. Furthermore, we showed that the ABC transporter MdnE is crucial for cyclization and processing of microviridins and demonstrated that MdnE is essential for stability of the microviridin biosynthesis complex. Cambridge Cell Press 2011 9 Chemistry & biology 18 11 1413 1421 10.1016/j.chembiol.2011.09.011 Institut für Biochemie und Biologie OPUS4-38075 Wissenschaftlicher Artikel Gatte-Picchi, Douglas; Weiz, Annika; Ishida, Keishi; Hertweck, Christian; Dittmann-Thünemann, Elke Functional analysis of environmental DNA-derived microviridins provides new insights into the diversity of the tricyclic peptide family Microviridins represent a unique family of ribosomally synthesized cage-like depsipeptides from cyanobacteria with potent protease-inhibitory activities. The natural diversity of these peptides is largely unexplored. Here, we describe two methodologies that were developed to functionally characterize cryptic microviridin gene clusters from metagenomic DNA. Environmental samples were collected and enriched from cyanobacterial freshwater blooms of different geographical origins containing predominantly Microcystis sp. Microviridins were produced either directly from fosmid clones or after insertion of environmental DNA-derived gene cassettes into a minimal expression platform in Escherichia coli. Three novel microviridin variants were isolated and tested against different serine-type proteases. The comparison of the bioactivity profiles of the new congeners allows deduction of further structure-function relationships for microviridins. Moreover, this study provides new insights into microviridin processing and gene cluster organization. Washington American Society for Microbiology 2014 8 Applied and environmental microbiology 80 4 1380 1387 10.1128/AEM.03502-13 Institut für Biochemie und Biologie OPUS4-36563 Wissenschaftlicher Artikel Liaimer, Anton; Jenke-Kodama, Holger; Ishida, Keishi; Hinrichs, Katrin; Stangeland, Janne; Hertweck, Christian; Dittmann-Thünemann, Elke A polyketide interferes with cellular differentiation in the symbiotic cyanobacterium Nostoc punctiforme Nostoc punctiforme is a filamentous cyanobacterium capable of forming symbiotic associations with a wide range of plants. The strain exhibits extensive phenotypic characteristics and can differentiate three mutually exclusive cell types: nitrogen-fixing heterocysts, motile hormogonia and spore-like akinetes. Here, we provide evidence for a crucial role of an extracellular metabolite in balancing cellular differentiation. Insertional mutagenesis of a gene of the polyketide synthase gene cluster pks2 led to the accumulation of short filaments carrying mostly terminal heterocysts under diazotrophic conditions. The mutant has a strong tendency to form biofilms on solid surfaces as well as in liquid culture. The pks2-strain keeps forming hormogonia over the entire growth curve and shows an early onset of akinete formation. We could isolate two fractions of the wildtype supernatant that could restore the capability to form long filaments with intercalary heterocysts. Growth of the mutant cells in the neighbourhood of wild-type cells on plates led to a reciprocal influence and a partial reconstruction of wild-type and mutant phenotype respectively. We postulate that extracellular metabolites of Nostoc punctiforme act as life cycle governing factors (LCGFs) and that the ratio between distinct factors may guide the differentiation into different life stages. Malden Wiley-Blackwell 2011 9 Environmental microbiology reports 3 5 550 558 10.1111/j.1758-2229.2011.00258.x Institut für Biochemie und Biologie OPUS4-37943 Wissenschaftlicher Artikel Weiz, Annika R.; Ishida, Keishi; Quitterer, Felix; Meyer, Sabine; Kehr, Jan-Christoph; Mueller, Kristian M.; Groll, Michael; Hertweck, Christian; Dittmann-Thünemann, Elke Harnessing the evolvability of tricyclic microviridins to dissect protease-inhibitor interactions Understanding and controlling proteolysis is an important goal in therapeutic chemistry. Among the natural products specifically inhibiting proteases microviridins are particularly noteworthy. Microviridins are ribosomally produced and posttranslationally modified peptides that are processed into a unique, cagelike architecture. Here, we report a combined rational and random mutagenesis approach that provides fundamental insights into selectivity-conferring moieties of microviridins. The potent variant microviridin J was co-crystallized with trypsin, and for the first time the three-dimensional structure of microviridins was determined and the mode of inhibition revealed. Weinheim Wiley-VCH 2014 4 Angewandte Chemie : a journal of the Gesellschaft Deutscher Chemiker ; International edition 53 14 3735 3738 10.1002/anie.201309721 Institut für Biochemie und Biologie