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Cyanobacterial and microalgal bioactive compounds – the role of secondary metabolites in allelopathic interactions Cover

Cyanobacterial and microalgal bioactive compounds – the role of secondary metabolites in allelopathic interactions

By: Adam Żak and  Alicja Kosakowska  
Open Access
|Mar 2016

Figures & Tables

Bioactive properties of selected cyanobacterial compounds

SpeciesCompoundActivityTargetReferences
Dichotrix bauerianaBauerines A-CantiviralHSV-2 (Herpes Simplex Virus)Larsen et al. (1994)
Microcystis ichtyoblabeIchtyopeptin A, BantiviralInfluenza A virusZainuddin et al. (2007)
Nostoc ellipsosporumCyanovirin-NantiviralHIV-1 (Human Immunodeficiency Virus)Boyd et al. (1997) Dey et al. (2000)
Scytonema variumScytovirinantiviralHIV-1Bokesh et al. (2003)
Spirulina platensisCalcium spirulanantiviralHSV-1, HIV-1, Maesles virus, Mumps virus, Influenza virus, Polio virus, Coxsackie virusHayashi et al. (1996)
Anabaena minutissimaMinutissamide A,Dcytotoxic (anticancer)HT-29 (Human colon cancer cell line)Kang et al. (2011)
Calothrix sp.Calothrixin Acytotoxic (anticancer)Human T-lymphocyte cell line (Jurkat)Chen et al. (2003)
Lyngbya majusculaHomodolastatin 16cytotoxic (anticancer)Oesophageal and cervical cancer cell linesDavies-Coleman et al. (2003)
Lyngbya sp.Curacin Acytotoxic (anticancer)MCF-7 (Breast Cancer Cells)Verdier-Pinard et al. (1998)
Microcystis aeruginosaAeruginoguanidine 98-A, 98Ccytotoxic (anticancer)P388 leukemia cell lineIshida et al. (2002)
Moorea producensApratoxin H, Apratoxin A sulfoxidecytotoxic (anticancer)NCI-H460 (Human lung cancer cells)Thornburg et al. (2013)
Nostoc communeComnostin Bcytotoxic (anticancer)KB ( cervical adenocarcinoma cells) and Caco-2 (heterogeneous human epithelial colorectal adenocarcinoma cells)Jaki et al. (2000)
Nostoc spCryptophycin 8cytotoxic (anticancer)TSU-prostate, LNCaP-prostate, H116-colon, MX-1 breast, cell linesLiang et al. (2005)
Symploca sp.Symplostatin 3cytotoxic (anticancer)Human Tumor Cell LinesLuesch et al. (2002)

Selected identified bioactive compounds produced by cyanobacteria and microalgae and their allelopathic influence on target organisms

Group/speciesCompoundTarget organismMode of actionEffectReferences
Cyanobacteria
Nostoc insulare4,4’-dihydroxybiphenylcyanobacteriaunknowngrowth inhibitionVolk (2005) Volk and Furket (2006)
Nostoc linckiacyanobacterin LU-1 (phenolic compound)phytoplanktonunknowngrowth inhibition, photosynthesis inhibition, oxygen evolutionGromov et al. 1991
Nostoc spongiaeformenostocine Aphytoplanktonformation of ROSgrowth inhibitionHirata et al. (2003)
Nostoc spp .LMW bacteriocinphytoplanktonunknowncell deathFlores and Wolk (1986)
nostocyclamidphytoplanktonunknowngrowth inhibitionJüttner et al. (2001)
Scytonema hofmannicyanobacterinmicroalgaeunknownphotosynthesis inhibition at PSII, cell deathMason et al. (1982) Gleason and Paulson (1984) Abarzua et al. (1999)
Microalgae
Chlorella vulgarischlorellinphytoplanktonunknowngrowth retardant (autoinhibition)Pratt and Fong (1940) cited in Legrand et al. (2003)
Coolia monotiscooliatoxinphytoplanktonmembrane damagephotosynthesis inhibition, lysisDonner et al. (2000)
Haslea ostreariamarenninmicroalgaeunknowngrowth inhibitionPouvreau et al. (2007)
Karenia mikimotoigymnodiminephytoplanktonmembrane damagelysis, cell deathYasumoto et al. (1990) Uchida et al. (1995)
Prorocentrum limaokadaic acidphytoplanktonmodify physiological functiongrowth inhibition, protein phosphatase inhibitionSugg and Dolah (1999)
Prymnesium parvumprymnesinphytoplanktonmembrane damagelysis, cell deathIgarashi et al. (1998) Fistarol et al. (2003)
DOI: https://doi.org/10.1515/ohs-2016-0013 | Journal eISSN: 1897-3191 | Journal ISSN: 1730-413X
Language: English
Page range: 131 - 143
Submitted on: Jun 9, 2015
Accepted on: Jul 27, 2015
Published on: Mar 10, 2016
Published by: University of Gdańsk
In partnership with: Paradigm Publishing Services
Publication frequency: 4 issues per year

© 2016 Adam Żak, Alicja Kosakowska, published by University of Gdańsk
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.