Cited by 247Marine Biology and Environmental ChemistryMicrobial Natural Products and BiosynthesisAquatic Ecosystems and Phytoplankton Dynamics

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Antialgal, antibacterial and antifungal activity of two metabolites produced and excreted by cyanobacteria during growth

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Volk, Rainer-B., Furkert, Franz H.·2006·Microbiological Research

DOI 10.1016/j.micres.2005.08.005

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Abstract

The antimicrobial activity of two cyanobacterial exometabolites, norharmane (9H-pyrido(3,4-b)indole) and 4,4'-dihydroxybiphenyl, was determined in suspension assays. Good anticyanobacterial activities (concentrations of 8-80 microg ml(-1)) and moderate antibacterial (16-160 microg ml(-1)) and antifungal (32-40 microg ml(-1)) activities were found for both compounds. The natural function as allelopathic chemicals and a possible applicability as antifouling agents or leads for the development of new antifouling chemicals are discussed.

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Cyanobacteria secondary metabolites—the cyanotoxins
Carmichael, W. W. (1992) · Journal of Applied Bacteriology · doi:10.1111/j.1365-2672.1992.tb01858.x · Cited by 1,457
Micro‐algal biotechnology
Rogers, L. J. (1988) · FEBS Letters · doi:10.1016/0014-5793(88)80268-0 · Cited by 1,289
Microalgal Biotechnology
Borowitzka, M. A., & Borowitzka, L. J. (2021) · Royal Society of Chemistry eBooks · doi:10.1039/9781839162473 · Cited by 568
Microalgae as sources of pharmaceuticals and other biologically active compounds
Borowitzka, M. A. (1995) · Journal of Applied Phycology · doi:10.1007/bf00003544 · Cited by 520
Structure and biosynthesis of toxins from blue-green algae (cyanobacteria)
RINEHART, K. L. J., Namikoshi, M., & Choi, B. W. (1994) · Journal of Applied Phycology · doi:10.1007/bf02186070 · Cited by 520
SAG ‐ Sammlung von Algenkulturen at the University of Göttingen Catalogue of Strains 1994
Schlösser, U. G. (1994) · Botanica Acta · doi:10.1111/j.1438-8677.1994.tb00784.x · Cited by 358
Exploitation of marine algae: biogenic compounds for potential antifouling applications
Bhadury, P., & Wright, P. (2004) · Planta · doi:10.1007/s00425-004-1307-5 · Cited by 327
The simple β-carboline alkaloids
Allen, J. R. F., & Holmstedt, B. R. (1980) · Phytochemistry · doi:10.1016/s0031-9422(00)83773-5 · Cited by 278
Exposure to β-carbolines norharman and harman
Pfau, W., & Skog, K. I. (2004) · Journal of Chromatography B · doi:10.1016/j.jchromb.2003.10.044 · Cited by 220
Bioactive natural products from blue-green algae
Patterson, G. M. L., Larsen, L. K., & Moore, R. E. (1994) · Journal of Applied Phycology · doi:10.1007/bf02186069 · Cited by 174

Show all 31 references

Research works printed but not linked: 1

Hasegawa, 1995, Inhibition of type A monoamine oxidase by N-methyl β-carbolinium ions, Biogen. Amines, 11, 295

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Self-citation

Authors: Volk, R.-B., & Furkert, F. H.
Affiliations: Christian-Albrechts-Universität zu Kiel (DE)
Corresponding author: Volk, Rainer-B.
Venue: Microbiological Research
Publisher: Elsevier BV
Published: 2006-02
Volume: 161
Issue: 2
Pages: 180-186
ISSN: 0944-5013 (ISSN-L)
DOI: 10.1016/j.micres.2005.08.005
OpenAlex: W2002556492
Cited by: 247
References: 31
Citations by year: 2026: 5 · 2025: 10 · 2024: 11 · 2023: 15 · 2022: 13 · 2021: 20 · 2020: 19 · 2019: 14 · 2018: 16 · 2017: 18 · 2016: 11 · 2015: 13 · 2014: 12 · 2013: 12 · 2012: 9
FWCI: 19.08
Type: journal article
Language: en
Open access: bronze
doi.org
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
www.elsevier.com/open-access/userlicense/1.0/ (vor, 2759 d)
Locations: Microbiological Research (publishedVersion)
PubMed (publishedVersion)
Topics: Physical Sciences › Engineering › Ocean Engineering › Marine Biology and Environmental Chemistry
Life Sciences › Immunology and Microbiology › Applied Microbiology and Biotechnology › Microbial Natural Products and Biosynthesis
Physical Sciences › Environmental Science › Environmental Chemistry › Aquatic Ecosystems and Phytoplankton Dynamics
Keywords: norharman, 4,4'-biphenol, antialgal activity, antibacterial activity, antifungal activity, allelopathy, antifouling agents, natural products
MeSH terms: Cyanobacteria, Anti-Bacterial Agents, Antifungal Agents, Biphenyl Compounds, Carbolines, Harmine, Microbial Sensitivity Tests

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Antialgal, antibacterial and antifungal activity of two metabolites produced and excreted by cyanobacteria during growth

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