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地表水中蓝藻次生代谢产物的生物转化动力学及产物

Biotransformation Dynamics and Products of Cyanobacterial Secondary Metabolites in Surface Waters.

作者信息

Wang Xuejian, Ingold Andrea, Janssen Elisabeth M-L

机构信息

Swiss Federal Institute of Aquatic Science and Technology, (EAWAG), Dübendorf 8600, Switzerland.

出版信息

Environ Sci Technol. 2025 Sep 30;59(38):20726-20737. doi: 10.1021/acs.est.5c09247. Epub 2025 Sep 19.

Abstract

Cyanobacteria produce toxic and bioactive secondary metabolites, posing risks to ecosystems and human health, yet their transformation pathways in surface waters remain unclear. We assessed biotransformation for 40 cyanopeptides including microcystins, anabaenopeptins and cyanopeptolins in surface waters and enriched biofilm suspensions. In surface waters, most cyanopeptides did not degrade significantly over the course of 7 days. A wide range of biodegradability across cyanopeptides was apparent in biofilm suspensions from three rivers. Increasing the biofilm density shortened the lag time and increased initial removal of cyanopeptides. Increasing the initial cyanopeptide concentration lengthened the lag time and decreased their initial removal, supporting inhibitory effects of cyanopeptides toward enzymes involved in their own transformation. Transformation kinetics and product analysis demonstrated a structure-reactivity relationship across and within cyanopeptide classes. Anabaenopeptins were hydrolyzed at the C-terminus when arginine, tyrosine and (iso)leucine were present, but not when phenylalanine or tryptophan was present. Microcystins showed tetrapeptide formation when adda linked to arginine but not when it linked to alanine, leucine, or tyrosine. Oxidation of tyrosine and deamination of arginine residues showed an interdependence across cyanopeptide classes. These novel insights into biotransformation products and pathways of a wide range of cyanopeptides facilitate assessment of exposure scenarios in surface waters and inform about kinetics and product formation in biological water treatment.

摘要

蓝藻细菌会产生有毒且具有生物活性的次生代谢产物,对生态系统和人类健康构成风险,但其在地表水中的转化途径仍不清楚。我们评估了地表水中以及富集生物膜悬浮液中40种蓝藻肽(包括微囊藻毒素、鱼腥藻肽和蓝藻肽毒素)的生物转化情况。在地表水中,大多数蓝藻肽在7天内没有明显降解。来自三条河流的生物膜悬浮液中,各种蓝藻肽的生物降解性差异明显。增加生物膜密度缩短了滞后期,并提高了蓝藻肽的初始去除率。提高蓝藻肽初始浓度延长了滞后期,并降低了其初始去除率,这支持了蓝藻肽对其自身转化相关酶的抑制作用。转化动力学和产物分析表明,不同蓝藻肽类别之间以及同一类别内存在结构 - 反应性关系。当存在精氨酸、酪氨酸和(异)亮氨酸时,鱼腥藻肽在C端被水解,但存在苯丙氨酸或色氨酸时则不会。当Adda与精氨酸相连时,微囊藻毒素会形成四肽,而与丙氨酸、亮氨酸或酪氨酸相连时则不会。酪氨酸的氧化和精氨酸残基的脱氨在不同蓝藻肽类别之间呈现出相互依存关系。这些关于多种蓝藻肽生物转化产物和途径的新见解有助于评估地表水中的暴露情况,并为生物水处理中的动力学和产物形成提供信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a41/12490008/2a4ff40805ef/es5c09247_0001.jpg

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