Effects of the antimalarial lumefantrine on Lemna minor, Raphidocelis subcapitata and Chlorella vulgaris

2021 ◽  
Vol 85 ◽  
pp. 103635
Author(s):  
Mathias Ahii Chia ◽  
Ilu Ameh ◽  
Jerry Tersoo Agee ◽  
Regina Anya Otogo ◽  
Ahmad Fatima Shaba ◽  
...  
2021 ◽  
Author(s):  
Denglong Lu ◽  
Zhihua Ma ◽  
Jianglin Peng ◽  
Yibo Zhang ◽  
Shan Liu ◽  
...  

Abstract Two model algae Chlorella vulgaris (C. vulgaris) and Raphidocelis subcapitata (R. subcapitata) were generally used to test chemicals with antimicrobial properties during registration process. However, it has been reported that significant sensitivity difference in two algae when exposure to antibiotics. Furthermore, the selection of an appropriate test species play a vital role in evaluate of environmental hazards and risks of compounds. Since the balance between oxidative stress and antioxidant is a crucial factor on alga growth. This experiment is performed to investigate the working of oxidative stress and mechanism of antioxidant defense system of algae under antibiotic stress. A series of concentration of Tylosin (TYN), a macrolide antibiotic, were used to test in this study. Oxidative stress biomarkers (Malondialdehyde (MDA)), non-enzymatic antioxidants (Reduced glutathione (GSH)), antioxidant enzymes (Superoxide dismutase (SOD), Catalase (CAT), Glutathione Peroxidase (GP), Glutathione S-transferase (GST)) and photosynthetic pigments were measured to investigate antioxidant defense system. R. subcapitata was significantly inhibited with increasing concentration of TYN, whereas no effects on C. vulgaris. The contents of MDA increased significantly when species were inhibited, and thus, activating the antioxidant system, companying with the significantly increasing of SOD and CAT.


2020 ◽  
Vol 219 ◽  
pp. 105376 ◽  
Author(s):  
Jiahua Guo ◽  
Jianglin Peng ◽  
Yuan Lei ◽  
Mirella Kanerva ◽  
Qi Li ◽  
...  

2019 ◽  
Vol 9 (18) ◽  
pp. 3804 ◽  
Author(s):  
Ana Margarida Castro ◽  
Verónica Nogueira ◽  
Isabel Lopes ◽  
Teresa Rocha-Santos ◽  
Ruth Pereira

The textile industry has an important role in the economic development of several countries; however, it consumes large amounts of water and generates huge quantities of wastewater. These effluents are of great environmental concern due to their complex chemical content, known by their toxicity and low biodegradability, which can cause harmful effects to the aquatic environment. In the present study, bioassays with aquatic species were employed to evaluate the toxicity of effluent samples collected before and after the treatments performed by the textile company. The toxic effects were investigated using four organisms, namely Aliivibrio fischeri, Raphidocelis subcapitata, Daphnia magna and Lemna minor, to represent different trophic levels. The ecotoxicological data confirmed that the raw textile effluent was very toxic, with A. fischeri being the most sensitive organism. While the toxicity of the effluent collected after the treatment performed by the textile company was clearly reduced, we still recorded sublethal toxicity to D. magna. These results highlight the importance of the bioassays for continuous monitoring of the toxicity of the treated effluents to prevent adverse effects on the environment. Further, results suggest that ecotoxicological data should be required in parallel with chemical data to better evaluate the safety of environmental discharges of wastewaters.


Author(s):  
S. Edith Taylor ◽  
Patrick Echlin ◽  
May McKoon ◽  
Thomas L. Hayes

Low temperature x-ray microanalysis (LTXM) of solid biological materials has been documented for Lemna minor L. root tips. This discussion will be limited to a demonstration of LTXM for measuring relative elemental distributions of P,S,Cl and K species within whole cells of tobacco leaves.Mature Wisconsin-38 tobacco was grown in the greenhouse at the University of California, Berkeley and picked daily from the mid-stalk position (leaf #9). The tissue was excised from the right of the mid rib and rapidly frozen in liquid nitrogen slush. It was then placed into an Amray biochamber and maintained at 103K. Fracture faces of the tissue were prepared and carbon-coated in the biochamber. The prepared sample was transferred from the biochamber to the Amray 1000A SEM equipped with a cold stage to maintain low temperatures at 103K. Analyses were performed using a tungsten source with accelerating voltages of 17.5 to 20 KV and beam currents from 1-2nA.


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