首页> 美国卫生研究院文献>International Journal of Environmental Research and Public Health >The Antialgal Mechanism of Luteolin-7-O-Glucuronide on Phaeocystis globosa by Metabolomics Analysis
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The Antialgal Mechanism of Luteolin-7-O-Glucuronide on Phaeocystis globosa by Metabolomics Analysis

机译:代谢组学分析木犀草素7-O-葡糖醛酸对球囊藻的抗藻机理

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摘要

Antialgal compounds from plants have been identified as promising candidates for controlling harmful algal blooms (HABs). In our previous study, luteolin-7-O-glucuronide was used as a promising algistatic agent to control Phaeocystis globosa (P. globose) blooms; however, its antialgal mechanism on P. globosa have not yet been elaborated in detail. In this study, a liquid chromatography linked to tandem mass spectrometry (LC-MS/MS)-based untargeted metabolomic approach was used to investigate changes in intracellular and extracellular metabolites of P. globosa after exposure to luteolin-7-O-glucuronide. Significant differences in intracellular metabolites profiles were observed between treated and untreated groups; nevertheless, metabolic statuses for extracellular metabolites were similar among these two groups. For intracellular metabolites, 20 identified metabolites showed significant difference. The contents of luteolin, gallic acid, betaine and three fatty acids were increased, while the contents of α-Ketoglutarate and acetyl-CoA involved in tricarboxylic acid cycle, glutamate, and 11 organic acids were decreased. Changes in those metabolites may be induced by the antialgal compound in response to stress. The results revealed that luteolin played a vital role in the antialgal mechanism of luteolin-7-O-glucuronide on P. globosa, because luteolin increased the most in the treatment groups and had strong antialgal activity on P. globosa. α-Ketoglutarate and acetyl-CoA were the most inhibited metabolites, indicating that the antialgal compound inhibited the growth through disturbed the tricarboxylic acid (TCA) cycle of algal cells. To summarize, our data provides insights into the antialgal mechanism of luteolin-7-O-glucuronide on P. globosa, which can be used to further control P. globosa blooms.
机译:来自植物的抗藻类化合物已被确认为控制有害藻类开花(HABs)的有前途的候选者。在我们以前的研究中,木犀草素-7-O-葡糖醛酸被用作一种有希望的止血剂,以控制球状Phaeocystis globosa(P. globose)的花开。然而,其对球状疟原虫的抗藻机理尚未详细阐明。在这项研究中,液相色谱联用基于串联质谱(LC-MS / MS)的非靶向代谢组学方法研究了暴露于木犀草素-7-O-葡糖醛酸中的球状疟原虫细胞内和细胞外代谢产物的变化。在治疗组和未治疗组之间观察到细胞内代谢物谱的显着差异。然而,两组的细胞外代谢物的代谢状态相似。对于细胞内代谢物,20种鉴定出的代谢物表现出显着差异。木犀草素,没食子酸,甜菜碱和三种脂肪酸的含量增加,而参与三羧酸循环,谷氨酸和11种有机酸的α-酮戊二酸和乙酰辅酶A的含量降低。抗藻化合物响应压力可能会诱导这些代谢物发生变化。结果表明,木犀草素在木犀草中木犀草素-7-O-葡糖醛酸的抗藻机理中起着至关重要的作用,因为木犀草素在治疗组中增加最多,并且对木犀草具有很强的抗藻活性。 α-酮戊二酸和乙酰辅酶A是最受抑制的代谢产物,表明抗藻类化合物通过干扰藻类细胞的三羧酸(TCA)周期来抑制生长。总而言之,我们的数据提供了木犀草中木犀草素-7-O-葡糖醛酸的抗藻机理的见解,可用于进一步控制球白杨的开花。

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