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Cyanobacterial peptides beyond microcystins - A review on co-occurrence, toxicity, and challenges for risk assessment

机译:微囊藻毒素以外的蓝细菌肽-关于共现,毒性和风险评估挑战的评论

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摘要

Cyanobacterial bloom events that produce natural toxins occur in freshwaters across the globe, yet the potential risk of many cyanobacterial metabolites remains mostly unknown. Only microcystins, one class of cyanopeptides, have been studied intensively and the wealth of evidence regarding exposure concentrations and toxicity led to their inclusion in risk management frameworks for water quality. However, cyanobacteria produce an incredible diversity of hundreds of cyanopeptides beyond the class of microcystins. The question arises, whether the other cyanopeptides are in fact of no human and ecological concern or whether these compounds merely received (too) little attention thus far. Current observations suggest that an assessment of their (eco)toxicological risk is indeed relevant: First, other cyanopeptides, including cyanopeptolins and anabaenopeptins, can occur just as frequently and at similar nanomolar concentrations as microcystins in surface waters. Second, cyanopeptolins, anabaenopeptins, aeruginosins and microginins inhibit proteases in the nanomolar range, in contrast to protein phosphatase inhibition by microcystins. Cyanopeptolins, aeruginosins, and aerucyclamide also show toxicity against grazers in the micromolar range comparable to microcystins. The key challenge for a comprehensive risk assessment of cyanopeptides remains their large structural diversity, lack of reference standards, and high analytical requirements for identification and quantification. One way forward would be a prevalence study to identify the priority candidates of tentatively abundant, persistent, and toxic cyanopeptides to make comprehensive risk assessments more manageable. (C) 2019 The Author(s). Published by Elsevier Ltd.
机译:产生天然毒素的蓝藻水华事件在全球的淡水中发生,但许多蓝藻代谢物的潜在风险仍然未知。仅对微囊藻毒素(一类氰肽)进行了深入研究,有关接触浓度和毒性的大量证据导致将其纳入水质风险管理框架。然而,除了微囊藻毒素之外,蓝细菌还产生了令人难以置信的多样性数百种氰肽。问题是,其他氰基肽实际上是否与人类和生态无关,还是到目前为止这些化合物是否仅受到(太)少的关注。当前的观察结果表明,对其(生态)毒理学风险的评估确实是相关的:首先,其他氰肽,包括氰肽素和阿那巴肽素,与地表水中的微囊藻毒素一样,其发生频率和纳摩尔浓度与之相同。其次,与微囊藻毒素抑制蛋白磷酸酶相反,氰基肽蛋白,anaabaenopeptins,铜绿素酶和微ginins抑制纳摩尔浓度的蛋白酶。氰肽肽,铜绿素和铜环酰胺还显示出与微囊藻毒素相当的微摩尔范围内对放牧者的毒性。对氰肽进行全面风险评估的主要挑战仍然是其巨大的结构多样性,缺乏参考标准以及对鉴定和定量的高分析要求。一种前进的方法是进行流行度研究,以确定暂定丰富,持久和有毒的氰基肽的优先候选者,以使综合风险评估更易于管理。 (C)2019作者。由Elsevier Ltd.发布

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