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Utilization of allelochemicals to inhibit overgrowth of toxic cyanobacteria is considered to be an environmentally friendly approach. However, the regulatory role of the signaling molecule nitric oxide (NO) on cyanobacteria under allelopathic stress remains unanswered. Here we demonstrate that the effect of NO on the cyanobacterium Microcystis aeruginosa depends on allelopathic stress of pyrogallic acid (PA). The experimental results revealed that general stimulation of M. aeruginosa by PA occurred within the concentration range 0.4-0.8 mg/L. In parallel with increasing concentration of PA (1.6-16.0 mg/L), the growth of M. aeruginosa was observed to decrease. The effect of NO on M. aeruginosa was evaluated by addition of the NO scavenger hemoglobin. In the stimulation stage, intracellular NO was seen to decreased to modulate the level of reactive oxygen species (ROS) and to maintain redox homeostasis of the cells. In the inhibition stage, the physiological characteristics of M. aeruginosa were changed significantly. Additionally, the accumulation of S-nitrosothiol by M. aeruginosa indicated that the high concentrations of PA induced nitric oxidative stress in M. aeruginosa. This study provides a new thought to understand the role of NO in controlling harmful algal blooms through the allelopathic effect of aquatic macrophytes.
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http://dx.doi.org/10.1016/j.scitotenv.2022.159785 | DOI Listing |
Crit Rev Food Sci Nutr
September 2025
Department of Analytical and Food Chemistry, Faculty of Science, Universidade de Vigo, Nutrition and Bromatology Group, Ourense, Spain.
The discovery of flavonoid amination metabolism has raised research interest in this new biotransformation mechanism. studies have revealed that flavonoids with pyrogallol structures readily react with N-nucleophilic ammonia, where amination occurs at intermediate -OH position, such as the B ring C4'-OH of epigallocatechin gallate and myricetin, A ring C6-OH of baicalein. Flavonoids are also covalently bound with amino acid residue by Schiff base, Michael addition or Strecker degradation, which are further rearranged to generate -NH substituted products.
View Article and Find Full Text PDFMed Oncol
August 2025
Department of Botany and Microbiology, College of Science, King Saud University, Riyadh, 11451, 2455, Saudi Arabia.
Cancer is the abnormal and uncontrolled growth of cells that changes the structure of nearby cells or tissues. Cancer treatment strategies include surgery, chemotherapy, immunotherapy, and radiotherapy. Radiation therapy is one of the most frequently used cancer treatment modalities.
View Article and Find Full Text PDFACS Omega
August 2025
Departamento de Ciencias Naturales, Universidad Autónoma MetropolitanaCuajimalpa, Av. Vasco de Quiroga 4871, Colonia Santa Fe Cuajimalpa, Alcaldía Cuajimalpa de Morelos, Ciudad de México 05348, Mexico.
Numerous compounds have been studied in the search for a potential drug to interrupt the process of formation of the amyloid fibers. Human lysozyme is a good model for studying the formation of amyloid fibers. In this research, the effect of phenolic compounds (caffeic acid, l-tyrosine, pyrogallol, guaiacol, 6-(-toluidino)-2-naphthalenesulfonic, epicatechin, chrysin, quercetin) during the formation of amyloid fibers at physiological conditions (37 °C and pH 7.
View Article and Find Full Text PDFMolecules
July 2025
Department of Chemistry, University of Cyprus, 1 Panepistimiou Avenue, Aglantzia, 2109 Nicosia, Cyprus.
Methylglyoxal (MGO) is a highly reactive -dicarbonyl compound produced in foods and endogenously in humans and constitutes a predominant precursor of advanced glycation end products that contribute to the pathology of several diseases, including diabetes and neurodegenerative diseases. In this study, the efficiency of pyrogallol, gallic acid, ethyl, and propyl gallate in trapping MGO was investigated at pH 6.5 to 8.
View Article and Find Full Text PDFBiochemistry
September 2025
Laboratory of Molecular Design Graduate School of Pharmaceutical Sciences, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba 260-8675, Japan.
The emergence of drug-resistant viruses is a significant concern for the treatment of human immunodeficiency virus type-1 (HIV-1) infection, despite the availability of various drugs that block viral replication and propagation. Drugs that act upon unexploited targets of the viral replicative cycle may be able to circumvent resistance. The RNase H activity of HIV-1 reverse transcriptase is a viral enzymatic function for which no approved inhibitors are available.
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