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金黄杆菌属菌株GLY-1106产生的两种二酮哌嗪对有害水华形成铜绿微囊藻的协同杀藻效应及机制

Synergistic algicidal effect and mechanism of two diketopiperazines produced by Chryseobacterium sp. strain GLY-1106 on the harmful bloom-forming Microcystis aeruginosa.

作者信息

Guo Xingliang, Liu Xianglong, Pan Jianliang, Yang Hong

机构信息

State Key Laboratory of Microbial metabolism, and School of Life Science &Biotechnology, Shanghai Jiao Tong University, Shanghai, 200240, P.R. China.

出版信息

Sci Rep. 2015 Oct 1;5:14720. doi: 10.1038/srep14720.

Abstract

A potent algicidal bacterium isolated from Lake Taihu, Chryseobacterium sp. strain GLY-1106, produces two algicidal compounds: 1106-A (cyclo(4-OH-Pro-Leu)) and 1106-B (cyclo(Pro-Leu)). Both diketopiperazines showed strong algicidal activities against Microcystis aeruginosa, the dominant bloom-forming cyanobacterium in Lake Taihu. Interestingly, these two algicidal compounds functioned synergistically. Compared with individual treatment, combined treatment with cyclo(4-OH-Pro-Leu) and cyclo(Pro-Leu) significantly enhanced algicidal activity, accelerated the increase in intracellular reactive oxygen species (ROS) levels in M. aeruginosa, and further decreased the activities of antioxidases, effective quantum yield and maximal electron transport rate of M. aeruginosa. The results also showed that the algicidal characteristics of cyclo(4-OH-Pro-Leu) are distinct from those of cyclo(Pro-Leu). Cyclo(4-OH-Pro-Leu) mainly interrupted the flux of electron transport in the cyanobacterial photosynthetic system, whereas cyclo(Pro-Leu) mainly inhibited the activity of cyanobacterial intracellular antioxidases. A possible algicidal mechanism for the synergism between cyclo(4-OH-Pro-Leu) and cyclo(Pro-Leu) is proposed, which is in accordance with their distinct algicidal characteristics in individual and combined treatment. These findings suggest that synergism between algicidal compounds might be used as an effective strategy for the future control of Microcystis blooms.

摘要

从太湖分离出的一种高效杀藻细菌,金黄杆菌属菌株GLY - 1106,产生两种杀藻化合物:1106 - A(环(4 - 羟基 - 脯氨酸 - 亮氨酸))和1106 - B(环(脯氨酸 - 亮氨酸))。这两种二酮哌嗪对铜绿微囊藻均表现出很强的杀藻活性,铜绿微囊藻是太湖中形成水华的优势蓝藻。有趣的是,这两种杀藻化合物具有协同作用。与单独处理相比,联合使用环(4 - 羟基 - 脯氨酸 - 亮氨酸)和环(脯氨酸 - 亮氨酸)显著增强了杀藻活性,加速了铜绿微囊藻细胞内活性氧(ROS)水平的升高,并进一步降低了铜绿微囊藻抗氧化酶的活性、有效量子产率和最大电子传递速率。结果还表明,环(4 - 羟基 - 脯氨酸 - 亮氨酸)的杀藻特性与环(脯氨酸 - 亮氨酸)不同。环(4 - 羟基 - 脯氨酸 - 亮氨酸)主要干扰蓝藻光合系统中的电子传递通量,而环(脯氨酸 - 亮氨酸)主要抑制蓝藻细胞内抗氧化酶的活性。提出了环(4 - 羟基 - 脯氨酸 - 亮氨酸)和环(脯氨酸 - 亮氨酸)之间协同作用的一种可能的杀藻机制,这与它们在单独处理和联合处理中的不同杀藻特性一致。这些发现表明,杀藻化合物之间的协同作用可能作为未来控制微囊藻水华的有效策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca50/4589682/2e38ab2e816b/srep14720-f1.jpg

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