2020
DOI: 10.1016/j.freeradbiomed.2020.01.010
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First evidence of ovothiol biosynthesis in marine diatoms

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Cited by 20 publications
(32 citation statements)
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“…We recently described the occurrence and distribution of OvoA in diatoms and we identified ovothiol B as the ovothiol form produced by the coastal centric diatom Skeletonema marinoi at micromolar concentrations, when grown under moderate light condition [23]. Our hypothesis is that ovothiol biosynthesis could have been evolved and conserved in diatoms to help them to defend from the oxidative stress enhanced by high light, thus contributing to the ecological success of these photosynthetic protists.…”
Section: Discussionmentioning
confidence: 91%
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“…We recently described the occurrence and distribution of OvoA in diatoms and we identified ovothiol B as the ovothiol form produced by the coastal centric diatom Skeletonema marinoi at micromolar concentrations, when grown under moderate light condition [23]. Our hypothesis is that ovothiol biosynthesis could have been evolved and conserved in diatoms to help them to defend from the oxidative stress enhanced by high light, thus contributing to the ecological success of these photosynthetic protists.…”
Section: Discussionmentioning
confidence: 91%
“…For ovoA, the expression levels of the transcript SmOvoA_2388 containing all the canonical domains of metazoan OvoAs [23] were examined. For nos genes, the expression of two different transcripts previously reported in S. marinoi [44] was analyzed.…”
Section: Reverse Transcription-quantitative Pcr (Rt-qpcr) Experimentsmentioning
confidence: 99%
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“…Considering this evidence, antioxidant compounds are able to inhibit immune system cells (lymphocytes) through apoptosis and then release proinflammatory cytokines (IL-1, IL-6 and TNFa) that are likely to prevent lymphopenia, hypoferremia and, thus lower the viral replication in patients suffering severe viral diseases [40]. Antioxidants such as vitamin E [41] are able to prevent the inhibition of the site of superoxide production (Site II), while the NF-kB-induced gene transcription can be inhibited by thiol groups [42] belonging to molecules that strongly interact with the antioxidant system [43,44]. Antioxidant therapy might further be related to the inhibition of virally induced cell death by antioxidants that scavenge peroxides, such as N-acetylcysteine and glutathione peroxidase [45].…”
Section: Which Consists Of Virus Adhesion Adsorption Entry and Invamentioning
confidence: 99%