Degradation of Microcystins in a Gravity-Driven Ultra-Low Pressure

Total Page:16

File Type:pdf, Size:1020Kb

Degradation of Microcystins in a Gravity-Driven Ultra-Low Pressure Zurich Open Repository and Archive University of Zurich Main Library Strickhofstrasse 39 CH-8057 Zurich www.zora.uzh.ch Year: 2014 Structural characterization, bioactivity and biodegradation of cyanobacterial toxins Kohler, Esther Posted at the Zurich Open Repository and Archive, University of Zurich ZORA URL: https://doi.org/10.5167/uzh-105523 Dissertation Published Version Originally published at: Kohler, Esther. Structural characterization, bioactivity and biodegradation of cyanobacterial toxins. 2014, University of Zurich, Faculty of Science. STRUCTURAL CHARACTERIZATION, BIOACTIVITY AND BIODEGRADATION OF CYANOBACTERIAL TOXINS Dissertation zur Erlangung der naturwissenschaftlichen Doktorwürde (Dr. sc. nat.) vorgelegt der Mathematisch-naturwissenschaftlichen Fakultät der Universität Zürich von Esther Kohler von Schwaderloch AG Promotionskomitee Prof. Dr. Jakob Pernthaler (Vorsitz) Prof. Dr. Leo Eberl PD Dr. Judith F. Blom Zürich, 2015 Meiner Familie GLOSSARY Adda (2S,3S,8S,9S)-3-amino-9-methoxy-2,6,8-trimethyl-10-phenyldeca-4,6-dienoic acid AG 828A Aeruginosin 828A Ahp 3-amino-6-hydroxy-2-piperidone BMAA β-methyl-amino-L-alanine Choi 2-carboxy-6-hydroxyoctahydroindole CP 1020 Cyanopeptolin 1020 DNA Deoxyribonucleic acid DOPA Dihydroxyphenylalanine GC-MS Gas chromatography-mass spectrometry GDM Gravity-driven membrane filtration GSH Glutathione GST Glutathione-s-transferase (H)PLA (Hydroxyl)phenyllactic acid HPLC High-performance liquid chromatography IC50 Half maximal inhibitory concentration i.p. Intraperitoneal (injection) LC50 Median lethal concentration LC-ESI-MS Liquid chromatography coupled to electrospray ionization mass spectrometry LC-MS Liquid chromatography-mass spectrometry LPS Lipopolysaccharid MC Microcystin Mdha Methyl-dehydroalanine NRPS Nonribosomal peptide synthase OATPs Organic anion transport proteins PKS Polyketide synthase ROS Reactive oxygen species SAR Structure-activity relationship VTG Vitellogenin WHO World health organisation TABLE OF CONTENTS SUMMARY ..................................................................................................................................................... 1 ZUSAMMENFASSUNG ....................................................................................................................................... 3 PREFACE ........................................................................................................................................................ 6 INTRODUCTION ............................................................................................................................................... 7 1. CYANOBACTERIA – ECOLOGY AND ENVIRONMENTAL IMPACT .................................................................... 7 2. CYANOBACTERIAL SECONDARY METABOLITES .......................................................................................... 8 3. CYANOBACTERIAL PEPTIDES .................................................................................................................. 9 3.1. MICROCYSTINS – THE BEST STUDIED CYANOTOXINS ......................................................................... 9 3.2. MICROCYSTINS IN DRINKING WATER ........................................................................................... 11 3.3. AERUGINOSINS ......................................................................................................................... 12 3.4. CYANOPEPTOLINS ..................................................................................................................... 13 4. THE ECOLOGICAL ROLE OF CYANOBACTERIAL PEPTIDES .......................................................................... 14 4.1. MICROCYSTINS AS GRAZER DEFENCE ........................................................................................... 15 4.2. MICROCYSTIN-DEFICIENT STRAINS............................................................................................... 15 5. AIMS OF THE THESIS ......................................................................................................................... 17 CHAPTER 1 - DRINKING WATER ................................................................................................................... 20 MANUSCRIPT I ...................................................................................................................................... 20 CHAPTER 2 - STRUCTURE ELUCIDATION AND ENZYMATIC CHARACTERIZATION .................................................... 21 MANUSCRIPT II ..................................................................................................................................... 21 CHAPTER 3 - EFFECTS ON THE AQUATIC MODEL ORGANISMS ZEBRAFISH AND DAPHNIA MAGNA ......................... 22 MANUSCRIPT III .................................................................................................................................... 22 MANUSCRIPT IV ................................................................................................................................... 23 DISCUSSION ................................................................................................................................................. 54 6. TOXICOLOGICAL AND ECOTOXICOLOGICAL RELEVANCE OF CYANOBACTERIAL PEPTIDES ............................... 54 6.1. REMOVAL OF MICROCYSTINS FROM DRINKING WATER .................................................................. 56 6.2. SERINE PROTEASE INHIBITORS ..................................................................................................... 59 7. POSSIBLE FUNCTIONS OF CYANOBACTERIAL PEPTIDES ............................................................................ 60 7.1. GRAZER DEFENCE ..................................................................................................................... 61 7.2. ALLELOCHEMICALS .................................................................................................................... 62 7.3. PARASITE-DEFENCE MECHANISM ................................................................................................ 62 8. CONCLUSION .................................................................................................................................... 63 REFERENCES ................................................................................................................................................. 64 CURRICULUM VITAE ...................................................................................................................................... 74 ACKNOWLEDGEMENTS ................................................................................................................................... 76 SUMMARY Recurrent mass developments of cyanobacteria, so-called blooms, have become a matter of public concern as they are more and more frequently found in waters intended as recreational areas and drinking water. Many of the cyanobacterial species are known to produce toxins that have a variety of adverse effects, such as acute diarrhoea, skin irritation, liver damage, neurotoxicity, and even fatali- ties in humans a well as in domestic and wild animals. Yet, cyanobacterial impact on aquatic ecosystems can only be estimated, as knowledge about the effects of cyanobacterial bioactive compounds on aquatic organisms is rather limited. This thesis focused on three major topics: removal strategies for already known potentially toxic cyanobacterial peptides were evaluated; the chemical structure of a novel cyanobacterial toxin was elucidated; and, further studies included detailed characterizations of largely undescribed or novel toxins in order to evaluate their potential risk for humans and aquatic eco- systems in future. Drinking water purification in terms of the elimination of cyanobacterial toxins is of major im- portance. Particularly in developing countries, simple and inexpensive purification systems are required. Gravity-driven membrane (GDM) ultrafiltration was shown to be an effective tool for the removal of pathogens and suspended solids by retention. We evaluated the biodegradation potential of the bacte- rial biofilm forming on the GDM ultrafiltration membrane for a cyanotoxin, microcystin. Successful elim- ination of microcystins in a GDM system required a maturation process of the biofilm, e.g. enrichment of bacteria capable of degrading microcystins. Phylogenetic analysis of the microbial communities form- ing the biofilm on the GDM ultrafiltration membrane gave first hints about potential new microcystin degraders. Microcystins have long been considered as the most toxic and therefore most important cya- nobacterial peptide class. Moreover, the investment of high amounts of resources into the production of microcystins suggests a very distinct and important function of these peptides for Microcystis, Ana- baena and Planktothrix. Compounds being able to compensate the lack of microcystins were hypothe- sized. A screening of six Planktothrix strains with and without the ability to produce microcystins re- vealed the presence of a distinct peptide group, i.e. chlorinated and sulfated aeruginosins, in strains that lack microcystins. Structure elucidation of one representative of the chlorinated and sulfated aeru- ginosins, aeruginosin 828A, was conducted. Subsequent toxicological and enzymatic characterization revealed the discovery of a new cyanobacterial toxin. The toxicity of aeruginosin 828A towards the freshwater crustacean Thamnocephalus platyurus
Recommended publications
  • Algal Toxic Compounds and Their Aeroterrestrial, Airborne and Other Extremophilic Producers with Attention to Soil and Plant Contamination: a Review
    toxins Review Algal Toxic Compounds and Their Aeroterrestrial, Airborne and other Extremophilic Producers with Attention to Soil and Plant Contamination: A Review Georg G¨аrtner 1, Maya Stoyneva-G¨аrtner 2 and Blagoy Uzunov 2,* 1 Institut für Botanik der Universität Innsbruck, Sternwartestrasse 15, 6020 Innsbruck, Austria; [email protected] 2 Department of Botany, Faculty of Biology, Sofia University “St. Kliment Ohridski”, 8 blvd. Dragan Tsankov, 1164 Sofia, Bulgaria; mstoyneva@uni-sofia.bg * Correspondence: buzunov@uni-sofia.bg Abstract: The review summarizes the available knowledge on toxins and their producers from rather disparate algal assemblages of aeroterrestrial, airborne and other versatile extreme environments (hot springs, deserts, ice, snow, caves, etc.) and on phycotoxins as contaminants of emergent concern in soil and plants. There is a growing body of evidence that algal toxins and their producers occur in all general types of extreme habitats, and cyanobacteria/cyanoprokaryotes dominate in most of them. Altogether, 55 toxigenic algal genera (47 cyanoprokaryotes) were enlisted, and our analysis showed that besides the “standard” toxins, routinely known from different waterbodies (microcystins, nodularins, anatoxins, saxitoxins, cylindrospermopsins, BMAA, etc.), they can produce some specific toxic compounds. Whether the toxic biomolecules are related with the harsh conditions on which algae have to thrive and what is their functional role may be answered by future studies. Therefore, we outline the gaps in knowledge and provide ideas for further research, considering, from one side, Citation: G¨аrtner, G.; the health risk from phycotoxins on the background of the global warming and eutrophication and, ¨а Stoyneva-G rtner, M.; Uzunov, B.
    [Show full text]
  • Investigations on the Impact of Toxic Cyanobacteria on Fish : As
    INVESTIGATIONS ON THE IMPACT OF TOXIC CYANOBACTERIA ON FISH - AS EXEMPLIFIED BY THE COREGONIDS IN LAKE AMMERSEE - DISSERTATION Zur Erlangung des akademischen Grades des Doktors der Naturwissenschaften an der Universität Konstanz Fachbereich Biologie Vorgelegt von BERNHARD ERNST Tag der mündlichen Prüfung: 05. Nov. 2008 Referent: Prof. Dr. Daniel Dietrich Referent: Prof. Dr. Karl-Otto Rothhaupt Referent: Prof. Dr. Alexander Bürkle 2 »Erst seit gestern und nur für einen Tag auf diesem Planeten weilend, können wir nur hoffen, einen Blick auf das Wissen zu erhaschen, das wir vermutlich nie erlangen werden« Horace-Bénédict de Saussure (1740-1799) Pionier der modernen Alpenforschung & Wegbereiter des Alpinismus 3 ZUSAMMENFASSUNG Giftige Cyanobakterien beeinträchtigen Organismen verschiedenster Entwicklungsstufen und trophischer Ebenen. Besonders bedroht sind aquatische Organismen, weil sie von Cyanobakterien sehr vielfältig beeinflussbar sind und ihnen zudem oft nur sehr begrenzt ausweichen können. Zu den toxinreichsten Cyanobakterien gehören Arten der Gattung Planktothrix. Hierzu zählt auch die Burgunderblutalge Planktothrix rubescens, eine Cyanobakterienart die über die letzten Jahrzehnte im Besonderen in den Seen der Voralpenregionen zunehmend an Bedeutung gewonnen hat. An einigen dieser Voralpenseen treten seit dem Erstarken von P. rubescens existenzielle, fischereiwirtschaftliche Probleme auf, die wesentlich auf markante Wachstumseinbrüche bei den Coregonenbeständen (Coregonus sp.; i.e. Renken, Felchen, etc.) zurückzuführen sind. So auch
    [Show full text]
  • Mass-Spectrometry Based Metabolomics to Decipher Strain Specific Microcystis Cyanopeptide Profiles
    MASS-SPECTROMETRY BASED METABOLOMICS TO DECIPHER STRAIN SPECIFIC MICROCYSTIS CYANOPEPTIDE PROFILES by Kimberlynn Pearl McDonald A thesis submitted to the Faculty of Graduate and Postdoctoral Affairs in partial fulfillment of the requirements for the degree of Master of Science in Chemistry with Specialization in Chemical and Environmental Toxicology Carleton University Ottawa, Ontario © 2020, Kimberlynn Pearl McDonald i. Abstract Over the last one hundred years, ecosystem changes have occurred as a result of human population growth, pollution, increased temperatures, and habitat degradation. A visible change is the increase in frequency and magnitude of toxic cyanobacterial blooms. Cyanobacterial blooms release mixtures of biologically active compounds into freshwater that negatively impact human and ecosystem health as well as having socioeconomic consequences. The factors that influence cyanobacterial growth and toxin production are broadly understood. However, cyanobacteria are a prolific source of structurally diverse and strain specific mixtures of biologically active compounds. Currently, the chemistry, toxicology, environmental concentrations, and risks posed to human and ecosystem health by most cyanobacterial secondary metabolites are unknown. Advances in mass spectrometry and metabolomic techniques can aid in comprehension of complex metabolomes. Here, the use of untargeted and semi-targeted mass spectrometry-based metabolomics is used to decipher the non-ribosomal peptide natural products (cyanopeptides) from five Microcystis strains. Cyanopeptides are grouped based on shared structural features, such as the incorporation of non-proteogenic amino acids or partial amino acid sequences that generate diagnostic product ions with the MS/MS of metabolites within the same cyanopeptide group. Global natural product society (GNPS) molecular networking and diagnostic fragmentation filtering (DFF) techniques utilize the similarity in product ion spectra to visualize all variants in the different cyanopeptide groups and the production by Microcystis strains.
    [Show full text]
  • Skin,Mucosal and Blood-Brain Barrier Kinetics
    FACULTY OF PHARMACEUTICAL SCIENCES DRUG Quality & Registration (DRUQUAR) Lab SKIN, MUCOSAL AND BLOOD-BRAIN BARRIER KINETICS OF MODEL CYCLIC DEPSIPEPTIDES: THE MYCOTOXINS BEAUVERICIN AND ENNIATINS Thesis submitted to obtain the degree of Doctor in Pharmaceutical Sciences Lien TAEVERNIER Promoter Prof. Dr. Bart DE SPIEGELEER FACULTY OF PHARMACEUTICAL SCIENCES Drug Quality & Registration (DruQuaR) Lab SKIN, MUCOSAL AND BLOOD-BRAIN BARRIER KINETICS OF MODEL CYCLIC DEPSIPEPTIDES: THE MYCOTOXINS BEAUVERICIN AND ENNIATINS Lien TAEVERNIER Master of Science in Drug Development Promoter Prof. Dr. Bart DE SPIEGELEER 2016 Thesis submitted to obtain the degree of Doctor in Pharmaceutical Sciences COPYRIGHT COPYRIGHT The author and the promotor give the authorization to consult and to copy parts of this thesis for personal use only. Any other use is limited by the Laws of Copyright, especially the obligation to refer to the source whenever results from this thesis are cited. Ghent, 9th of September 2016 The promoter The author Prof. Dr. Bart De Spiegeleer Lien Taevernier 3 ACKNOWLEDGEMENTS ACKNOWLEDGEMENTS I never could have achieved this work on my own, therefore I wish to thank some very important people and address a few words to them. I consider myself fortunate to know you and I was honoured to be able to work together with you and learn a great deal from all of you. First of all, a special thank you to my promoter Prof. Dr. Bart De Spiegeleer. I am grateful that you gave me the opportunity to pursue my Ph.D. at DruQuaR. Your door was always open for me, even if it did not consider work.
    [Show full text]
  • Hepatotoxic Cyanobacterial Blooms in Louisiana's Estuaries
    Louisiana State University LSU Digital Commons LSU Master's Theses Graduate School 2010 Hepatotoxic Cyanobacterial Blooms in Louisiana's Estuaries: Analysis of Risk to Blue Crab (Callinectes sapidus) Following Exposure to Microcystins Ana Cristina Garcia Louisiana State University and Agricultural and Mechanical College, [email protected] Follow this and additional works at: https://digitalcommons.lsu.edu/gradschool_theses Part of the Oceanography and Atmospheric Sciences and Meteorology Commons Recommended Citation Garcia, Ana Cristina, "Hepatotoxic Cyanobacterial Blooms in Louisiana's Estuaries: Analysis of Risk to Blue Crab (Callinectes sapidus) Following Exposure to Microcystins" (2010). LSU Master's Theses. 1132. https://digitalcommons.lsu.edu/gradschool_theses/1132 This Thesis is brought to you for free and open access by the Graduate School at LSU Digital Commons. It has been accepted for inclusion in LSU Master's Theses by an authorized graduate school editor of LSU Digital Commons. For more information, please contact [email protected]. HEPATOTOXIC CYANOBACTERIAL BLOOMS IN LOUISIANA’S ESTUARIES: ANALYSIS OF RISK TO BLUE CRAB (CALLINECTES SAPIDUS) FOLLOWING EXPOSURE TO MICROCYSTINS A Thesis Submitted to the Graduate Faculty of the Louisiana State University and Agricultural and Mechanical College in partial fulfillment of the requirements for the degree of Master of Science in The Department of Oceanography and Coastal Sciences By Ana Cristina Garcia B.S. Louisiana State University, 2006 May 2010 ACKNOWLEDGEMENTS I would like to thank my major advisor Dr. Sibel Bargu. My experience at LSU as a graduate student has been invaluable under her guidance and support. Thanks to Dr. Bargu I have been provided with endless opportunities to explore the field of oceanography and limnology, for which I am forever grateful.
    [Show full text]
  • Bioassay Methods to Identify the Presence of Cyanotoxins in Drinking Water Supplies and Their Removal Strategies
    Available online a t www.pelagiaresearchlibrary.com Pelagia Research Library European Journal of Experimental Biology, 2012, 2 (2):321-336 ISSN: 2248 –9215 CODEN (USA): EJEBAU Bioassay methods to identify the presence of cyanotoxins in drinking water supplies and their removal strategies Monica Agrawal 1, Sulekha Yadav 1,2 , Chanda Patel 1,2 , Neelima Raipuria 1 and Manish K. Agrawal 2* 1M. H. College of Home Science and Science for Women, Napier Town, Jabalpur, India 2Daksh Laboratories, 1370, Home Science College Road, Napier Town, Jabalpur, India ______________________________________________________________________________ ABSTRACT A diversified group of toxins produced by freshwater cyanobacteria pose threat to human health as they frequently occur in drinking water sources. Though numerous qualitative as well as quantitative chemical analytical methods are now available, relatively simple low cost methods that are able to evaluate the potential health hazard and allow management decisions to be taken, are more useful to agencies that monitor drinking water supplies. Given that there is no single method that can provide adequate monitoring for all freshwater cyanotoxins in the increasing range of sample types, bioassays that can detect the toxic effects and safe levels of cyanobacterial toxins in drinking water supplies are discussed. Methods for removal of cyanobacterial cells as well as dissolved toxins in drinking waters prior to supply are also discussed. Key Words: Freshwater cyanobacteria, toxins, microcystins, bioassay, removal of toxins, waterworks. ______________________________________________________________________________ INTRODUCTION Most, though not all, cyanobacterial blooms and scums produce secondary metabolites that are toxic to aquatic animals, fishes, cattle and even human [1, 2, 3]. The most frequently found toxin producing cyanobacterial species in freshwaters are Microcystis, Anabaena, Nodularia, Planktothrix, Aphanizomenon, Cylindrospermopsin and Lyngbya etc.
    [Show full text]
  • Distribution and Conservation of Known Secondary Metabolite Biosynthesis Gene Clusters in the Genomes of Geographically Diverse Microcystis Aeruginosa Strains
    SPECIAL ISSUE CSIRO PUBLISHING Marine and Freshwater Research https://doi.org/10.1071/MF18406 Distribution and conservation of known secondary metabolite biosynthesis gene clusters in the genomes of geographically diverse Microcystis aeruginosa strains Leanne A. PearsonA,B, Nicholas D. CrosbieA and Brett A. NeilanB,C AApplied Research, Melbourne Water Corporation, 990 La Trobe Street, Docklands, Vic. 3008, Australia. BSchool of Environmental and Life Sciences, SR233, Social Sciences Building, The University of Newcastle, University Drive, Callaghan, NSW 2308, Australia. CCorresponding author. Email: [email protected] Abstract. The cyanobacterium Microcystis aeruginosa has been linked to toxic blooms worldwide. In addition to producing hepatotoxic microcystins, many strains are capable of synthesising a variety of biologically active compounds, including protease and phosphatase inhibitors, which may affect aquatic ecosystems and pose a risk to their use. This study explored the distribution, composition and conservation of known secondary metabolite (SM) biosynthesis gene clusters in the genomes of 27 M. aeruginosa strains isolated from six different Ko¨ppen–Geiger climates. Our analysis identified gene clusters with significant homology to nine SM biosynthesis gene clusters spanning four different compound classes: non-ribosomal peptides, hybrid polyketide–non-ribosomal peptides, cyanobactins and microviridins. The aeruginosin, microviridin, cyanopeptolin and microcystin biosynthesis gene clusters were the most frequently
    [Show full text]
  • Extraction and Preservation Protocol of Anti-Cancer Agents from Marine World Chemical Sciences Journal, Vol
    Chemical Sciences REVIEW Journal, Vol. 2012: CSJ-38 Extraction and Preservation Protocol of Anti-Cancer Agents from Marine World Chemical Sciences Journal, Vol. 2012: CSJ-38 1 Extraction and Preservation Protocol of Anti-Cancer Agents from Marine World B Dhorajiya, M Malani, B Dholakiya* Department of Applied Chemistry, SV National Institute of Technology, Ichhanath, Surat, Gujarat, India. *Correspondence to: Bharat Dholakiya, [email protected] Accepted: October 22, 2011; Published: May 3, 2012 Abstract Marine source plays an important role in the form of pharmaceutical care and for the discovery of new molecular structures (i.e. targets). Marine organisms are a source of new therapeutics, especially for oncology, as a tremendous chemical diversity is found in marine bacteria, fungus, cyanobacteria, seaweeds, mangroves, microalgae and other halophytes. Several marine-derived compounds are currently extracted and synthesized by chemical processes for cancer treatment. By studying various papers related to marine source for new therapeutics for cancer treatment instead of other chemical enriched sources, the marine sources are largely unexplored for anti- cancer lead compounds. Hence this paper reviews results on the aspect with a view to provide basic information about the methods to produce extracts from marine organisms that are unique and different from that used by marine natural products chemists previously, yields both organic solvents and water soluble material for anti-cancer screening purpose. Chemists synthesize these compounds and their analogues in the laboratory for studying their activity towards various cancer cell lines. Keywords: Marine anti-cancer agents; marine microbes; fungi; algae; bacteria; cyanobacteria; anti-cancer screening. 1. Introduction Cancer is a class of diseases in which a cell, or a group of cells represents uncontrolled growth (i.e.
    [Show full text]
  • 2.06 the Natural Products Chemistry of Cyanobacteria Kevin Tidgewell, Benjamin R
    2.06 The Natural Products Chemistry of Cyanobacteria Kevin Tidgewell, Benjamin R. Clark, and William H. Gerwick, University of California San Diego, La Jolla, CA, USA ª 2010 Elsevier Ltd. All rights reserved. 2.06.1 Introduction 142 2.06.2 Trends in the Structures of Cyanobacterial Natural Products 143 2.06.2.1 Taxonomy 143 2.06.2.2 Molecular Weight 144 2.06.2.3 Structural Classes 146 2.06.2.4 Amino Acids 147 2.06.2.5 Other Trends 150 2.06.3 Fatty Acid Derivatives from Cyanobacteria 150 2.06.4 Terpenes 153 2.06.4.1 Tolypodiol 153 2.06.4.2 Noscomin/Comnostins 154 2.06.4.3 Tasihalide 154 2.06.5 Saccharides and Glycosides 154 2.06.5.1 Iminotetrasaccharide 156 2.06.5.2 Cyclodextrin 157 2.06.6 Peptides 158 2.06.6.1 Lyngbyatoxins 159 2.06.6.2 Aeruginosins 159 2.06.6.3 Cyanopeptolins 161 2.06.6.4 Cyclamides 163 2.06.6.5 Anatoxin-a(s) 165 2.06.7 Polyketides 165 2.06.7.1 Biosynthesis of Polyketides 165 2.06.7.2 Oscillatoxin/Aplysiatoxin 166 2.06.7.3 Acutiphycin 166 2.06.7.4 Scytophycin/Tolytoxin/Swinholide 166 2.06.7.5 Nakienone 168 2.06.7.6 Nostocyclophanes 168 2.06.7.7 Caylobolide 168 2.06.7.8 Oscillariolide/Phormidolide 169 2.06.7.9 Borophycin 169 2.06.8 Lipopeptides 169 2.06.8.1 Ketide-Extended Amino Acids (Peptoketides) 169 2.06.8.1.1 Dolastatin 10 169 2.06.8.1.2 Barbamide 171 2.06.8.2 Simple Ketopeptides 171 2.06.8.2.1 Hectochlorin 171 2.06.8.2.2 Antanapeptin A 172 2.06.8.2.3 Makalika ester 173 2.06.8.2.4 Microcystin LR 174 2.06.8.3 Complex Ketopeptides 175 2.06.8.3.1 Jamaicamide A 175 2.06.8.3.2 Mirabimide E 176 2.06.8.3.3 Madangolide 178
    [Show full text]
  • Global Metabolomic Characterizations of Microcystis Spp. Highlights Clonal Diversity in Natural Bloom-Forming Populations and Expands Metabolite
    fmicb-10-00791 April 16, 2019 Time: 11:24 # 1 ORIGINAL RESEARCH published: 16 April 2019 doi: 10.3389/fmicb.2019.00791 Global Metabolomic Characterizations of Microcystis spp. Highlights Clonal Diversity in Natural Bloom-Forming Populations and Expands Metabolite Edited by: Structural Diversity Fabrice Martin-Laurent, Institut National de la Recherche Séverine Le Manach, Charlotte Duval, Arul Marie, Chakib Djediat, Arnaud Catherine, Agronomique (INRA), France Marc Edery, Cécile Bernard and Benjamin Marie* Reviewed by: UMR 7245 MNHN/CNRS Molécules de Communication et Adaptation des Micro-organismes, Muséum National d’Histoire Ernani Pinto, Naturelle, Paris, France University of São Paulo, Brazil Marie-Virginie Salvia, Université de Perpignan Via Domitia, Cyanobacteria are photosynthetic prokaryotes capable of synthesizing a large variety France of secondary metabolites that exhibit significant bioactivity or toxicity. Microcystis Steven Wilhelm, The University of Tennessee, constitutes one of the most common cyanobacterial genera, forming the intensive Knoxville, United States blooms that nowadays arise in freshwater ecosystems worldwide. Species in this genus *Correspondence: can produce numerous cyanotoxins (i.e., toxic cyanobacterial metabolites), which can Benjamin Marie [email protected] be harmful to human health and aquatic organisms. To better understand variations in cyanotoxin production between clones of Microcystis species, we investigated the Specialty section: diversity of 24 strains isolated from the same blooms or from different populations This article was submitted to Microbiotechnology, Ecotoxicology in various geographical areas. Strains were compared by genotyping with 16S- and Bioremediation, ITS fragment sequencing and metabolite chemotyping using LC ESI-qTOF mass a section of the journal spectrometry. While genotyping can help to discriminate among different species, the Frontiers in Microbiology global metabolome analysis revealed clearly discriminating molecular profiles among Received: 11 September 2018 Accepted: 27 March 2019 strains.
    [Show full text]
  • Natural Product Biosyntheses in Cyanobacteria: a Treasure Trove of Unique Enzymes
    Natural product biosyntheses in cyanobacteria: A treasure trove of unique enzymes Jan-Christoph Kehr, Douglas Gatte Picchi and Elke Dittmann* Review Open Access Address: Beilstein J. Org. Chem. 2011, 7, 1622–1635. University of Potsdam, Institute for Biochemistry and Biology, doi:10.3762/bjoc.7.191 Karl-Liebknecht-Str. 24/25, 14476 Potsdam-Golm, Germany Received: 22 July 2011 Email: Accepted: 19 September 2011 Jan-Christoph Kehr - [email protected]; Douglas Gatte Picchi - Published: 05 December 2011 [email protected]; Elke Dittmann* - [email protected] This article is part of the Thematic Series "Biosynthesis and function of * Corresponding author secondary metabolites". Keywords: Guest Editor: J. S. Dickschat cyanobacteria; natural products; NRPS; PKS; ribosomal peptides © 2011 Kehr et al; licensee Beilstein-Institut. License and terms: see end of document. Abstract Cyanobacteria are prolific producers of natural products. Investigations into the biochemistry responsible for the formation of these compounds have revealed fascinating mechanisms that are not, or only rarely, found in other microorganisms. In this article, we survey the biosynthetic pathways of cyanobacteria isolated from freshwater, marine and terrestrial habitats. We especially empha- size modular nonribosomal peptide synthetase (NRPS) and polyketide synthase (PKS) pathways and highlight the unique enzyme mechanisms that were elucidated or can be anticipated for the individual products. We further include ribosomal natural products and UV-absorbing pigments from cyanobacteria. Mechanistic insights obtained from the biochemical studies of cyanobacterial pathways can inspire the development of concepts for the design of bioactive compounds by synthetic-biology approaches in the future. Introduction The role of cyanobacteria in natural product research Cyanobacteria flourish in diverse ecosystems and play an enor- [2] (Figure 1).
    [Show full text]
  • Article 0103 - 5053 $6.00+0.00
    http://dx.doi.org/10.5935/0103-5053.20160191 J. Braz. Chem. Soc., Vol. 28, No. 4, 521-528, 2017. Printed in Brazil - ©2017 Sociedade Brasileira de Química Article 0103 - 5053 $6.00+0.00 MALDI Imaging Mass Spectrometry of Fresh Water Cyanobacteria: Spatial Distribution of Toxins and Other Metabolites Beatriz B. Sandonato,a Vanessa G. Santos,b Milena F. Luizete,a João L. Bronzel Jr.,a Marcos N. Eberlinb and Humberto M. S. Milagre*,a aInstituto de Química, Universidade Estadual Paulista “Júlio de Mesquita Filho” (UNESP), 14800-060 Araraquara-SP, Brazil bLaboratório Thomson de Espectrometria de Massas, Instituto de Química, Universidade Estadual de Campinas (UNICAMP), 13084-971 Campinas-SP, Brazil Cyanobacteria are among the most ancient forms of life, yet they are known to synthesize highly sophisticated defense molecules, such as the highly hepatotoxic cyclic peptides microcystins and nodularins produced by the genera Microcystis, Anabaena and Nodularia. These metabolites are released by cyanobacteria to water environments causing episodes of fatalities among animals and humans. To better understand the releasing of these metabolites, imaging mass spectrometry (IMS) using matrix-assisted laser desorption ionization-time of flight (MALDI-TOF) was herein applied to determine the spatial distribution of such toxins directly on agar-based cultures. Other key metabolites such as aeruginosin 602 and the siderophore anachelin were also mapped in mixed cyanobacterial cultures, showing the great potential of IMS to spatially monitor the biochemical
    [Show full text]