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Hormesis effects of phenol on growth and cellular metabolites of Chlorella sp. under different nutritional conditions using response surface methodology

The present study investigated the effects of different phenol concentrations (200 – 1000 mg L(−1)) towards Chlorella sp. under different culture conditions (light vs. dark) and NaNO(3) concentrations (0 – 0.1 g L(−1)) using central composite design. Phenol induced hormesis effects on the algal grow...

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Autores principales: Gomaa, Mohamed, El-Naeb, Eman H., Hifney, Awatief F., Adam, Mahmoud S., Fawzy, Mustafa A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10121499/
https://www.ncbi.nlm.nih.gov/pubmed/36928704
http://dx.doi.org/10.1007/s11356-023-26249-1
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author Gomaa, Mohamed
El-Naeb, Eman H.
Hifney, Awatief F.
Adam, Mahmoud S.
Fawzy, Mustafa A.
author_facet Gomaa, Mohamed
El-Naeb, Eman H.
Hifney, Awatief F.
Adam, Mahmoud S.
Fawzy, Mustafa A.
author_sort Gomaa, Mohamed
collection PubMed
description The present study investigated the effects of different phenol concentrations (200 – 1000 mg L(−1)) towards Chlorella sp. under different culture conditions (light vs. dark) and NaNO(3) concentrations (0 – 0.1 g L(−1)) using central composite design. Phenol induced hormesis effects on the algal growth and cellular metabolites. Nitrate was identified as a crucial factor for promoting the uptake of phenol by Chlorella cells, while light was a limiting factor for growth, but the phyco-toxicity of phenol was decreased in the dark. The pigment contents were generally increased in the treated cells to protect against the oxidative phenol stress. The incorporation of 200 mg L(−1) phenol and 0.05 g L(−1) NaNO(3) to the illuminated cells markedly promoted biomass and lipid contents to 0.22 g L(−1) and 26.26% w/w, which was 44 and 112% higher than the phenol-less control, respectively. Under the same conditions, the increase of phenol concentration to 600 mg L(−1), the protein contents were increased to 18.59% w/w. Conversely, the algal cells were able to accumulate more than 60% w/w of soluble carbohydrates under dark conditions at 600 mg L(−1) of phenol. Nitrate replete conditions stimulated lipid accumulation at the expense of protein biosynthesis. Furthermore, most of the treatments showed an increase of H(2)O(2) and malonaldehyde contents, especially for the illuminated cells. However, catalase activity tended to increase under dark conditions, especially at low phenol and nitrate concentrations. This study is valuable in indicating the effects of phenol on microalgae by exploiting response surface methodology, which can be applied as a powerful tool in growth monitoring and toxicity assessment. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11356-023-26249-1.
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spelling pubmed-101214992023-04-23 Hormesis effects of phenol on growth and cellular metabolites of Chlorella sp. under different nutritional conditions using response surface methodology Gomaa, Mohamed El-Naeb, Eman H. Hifney, Awatief F. Adam, Mahmoud S. Fawzy, Mustafa A. Environ Sci Pollut Res Int Research Article The present study investigated the effects of different phenol concentrations (200 – 1000 mg L(−1)) towards Chlorella sp. under different culture conditions (light vs. dark) and NaNO(3) concentrations (0 – 0.1 g L(−1)) using central composite design. Phenol induced hormesis effects on the algal growth and cellular metabolites. Nitrate was identified as a crucial factor for promoting the uptake of phenol by Chlorella cells, while light was a limiting factor for growth, but the phyco-toxicity of phenol was decreased in the dark. The pigment contents were generally increased in the treated cells to protect against the oxidative phenol stress. The incorporation of 200 mg L(−1) phenol and 0.05 g L(−1) NaNO(3) to the illuminated cells markedly promoted biomass and lipid contents to 0.22 g L(−1) and 26.26% w/w, which was 44 and 112% higher than the phenol-less control, respectively. Under the same conditions, the increase of phenol concentration to 600 mg L(−1), the protein contents were increased to 18.59% w/w. Conversely, the algal cells were able to accumulate more than 60% w/w of soluble carbohydrates under dark conditions at 600 mg L(−1) of phenol. Nitrate replete conditions stimulated lipid accumulation at the expense of protein biosynthesis. Furthermore, most of the treatments showed an increase of H(2)O(2) and malonaldehyde contents, especially for the illuminated cells. However, catalase activity tended to increase under dark conditions, especially at low phenol and nitrate concentrations. This study is valuable in indicating the effects of phenol on microalgae by exploiting response surface methodology, which can be applied as a powerful tool in growth monitoring and toxicity assessment. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11356-023-26249-1. Springer Berlin Heidelberg 2023-03-17 2023 /pmc/articles/PMC10121499/ /pubmed/36928704 http://dx.doi.org/10.1007/s11356-023-26249-1 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Gomaa, Mohamed
El-Naeb, Eman H.
Hifney, Awatief F.
Adam, Mahmoud S.
Fawzy, Mustafa A.
Hormesis effects of phenol on growth and cellular metabolites of Chlorella sp. under different nutritional conditions using response surface methodology
title Hormesis effects of phenol on growth and cellular metabolites of Chlorella sp. under different nutritional conditions using response surface methodology
title_full Hormesis effects of phenol on growth and cellular metabolites of Chlorella sp. under different nutritional conditions using response surface methodology
title_fullStr Hormesis effects of phenol on growth and cellular metabolites of Chlorella sp. under different nutritional conditions using response surface methodology
title_full_unstemmed Hormesis effects of phenol on growth and cellular metabolites of Chlorella sp. under different nutritional conditions using response surface methodology
title_short Hormesis effects of phenol on growth and cellular metabolites of Chlorella sp. under different nutritional conditions using response surface methodology
title_sort hormesis effects of phenol on growth and cellular metabolites of chlorella sp. under different nutritional conditions using response surface methodology
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10121499/
https://www.ncbi.nlm.nih.gov/pubmed/36928704
http://dx.doi.org/10.1007/s11356-023-26249-1
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