The antialgal activity of a number of simple phenols was examined for their effect on the growth of 7 species of unicellular marine algae. The 3 knoiun algal phenols, 5-bromo-3,4-dihydroxybenzaldehyde; 2,3-dibromo-4,5-dihydroxybenzylalcohol, and 3,4-dihy-droxyphenylethylamine, were highly toxic as were other ortho dihydroxy compounds. Monohydroxy compounds were notably less toxic. Skeletonema costatum and Olisthodiscus sp. were the most sensitive organisms examined and Dunaliella tertiolecta was the most resistant. Possible ecological implications of these results are discussed.
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http://dx.doi.org/10.1111/j.1529-8817.1966.tb04609.x | DOI Listing |
BMC Microbiol
November 2024
Institute for Chemistry and Biology of the Marine Environment, University of Oldenburg, Oldenburg, Germany.
Background: Previous studies have identified structurally diverse N-acyl amino acid methyl esters (NAMEs) in culture extracts of Roseovarius tolerans EL-164 (Roseobacteraceae). NAMEs are structural analogues of the common signaling compounds N-acyl homoserine lactones (AHLs), but do not participate in AHL-mediated signaling. NAMEs show minor antialgal and antimicrobial activity, but whether this activity serves as the primary ecological role remains unclear.
View Article and Find Full Text PDFCarbohydr Polym
January 2025
School of Materials Science and Engineering, Hainan University, Haikou 570228, China. Electronic address:
Langmuir
July 2024
Key Laboratory of Green Catalysis and Reaction Engineering of Haikou, College of Chemistry and Chemical Engineering, Hainan University, Haikou 570228,People's Republic of China.
A series of 1,2,4-triazolo-quinazolinones and 1,2-benzisothiazolone derivatives (S1-S12) were successfully synthesized as environmentally friendly alternatives to copper-based antifouling paints using -alkylation, cyclocondensation, and one-pot three-component and amide coupling reactions. The monoclinic structure of single-crystal 1,2,4-triazolo-quinazolin-acetic acid (S8) was confirmed by single-crystal X-ray diffraction analysis. All the synthesized molecules were studied for their in silico molecular docking interactions with three target proteins, namely, RbmA, ToxR, and Bap.
View Article and Find Full Text PDFMar Drugs
June 2024
Jiangsu Key Laboratory of Marine Bioresources and Eco-Environment, Jiangsu Ocean University, Lianyungang 222005, China.
Ichthyotoxic red tide is a problem that the world is facing and needs to solve. The use of antialgal compounds from marine macroalgae to suppress ichthyotoxic red tide is considered a promising biological control method. Antialgal substances were screened and isolated from , , , , , , and sp.
View Article and Find Full Text PDFFront Microbiol
June 2024
Medical Science and Technology Innovation Center, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, China.
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