Zhou Su, Yin Hua, Tang Shaoyu, Peng Hui, Yin Donggao, Yang Yixuan, Liu Zehua, Dang Zhi
Key Laboratory of Ministry of Education on Pollution Control and Ecosystem Restoration in Industry Clusters, School of Environment and Energy, South China University of Technology, Guangzhou 510006,Guangdong, China.
Key Laboratory of Ministry of Education on Pollution Control and Ecosystem Restoration in Industry Clusters, School of Environment and Energy, South China University of Technology, Guangzhou 510006,Guangdong, China.
Ecotoxicol Environ Saf. 2016 May;127:214-21. doi: 10.1016/j.ecoenv.2016.02.001. Epub 2016 Feb 8.
Proliferation of cyanobacteria in aquatic ecosystems has caused water security problems throughout the world. Our preliminary study has showed that Pseudomonas aeruginosa can inhibit the growth of cyanobacterium, Microcystis aeruginosa. In order to explore the inhibitory mechanism of P. aeruginosa on the cell growth and synthesis of intracellular substances of M. aeruginosa, concentrations of Chlorophyll-a, intracellular protein, carbohydrate, enzyme activities and ion metabolism of M. aeruginosa, were investigated. The results indicated that 83.84% algicidal efficiency of P. aeruginosa was achieved after treatment for 7 days. The strain inhibited the reproduction of M. aeruginosa by impeding the synthesis of intracellular protein and carbohydrate of cyanobacterium, and only a very small part of intracellular protein and carbohydrate was detected after exposure to P. aeruginosa for 5 days. P. aeruginosa caused the alteration of intracellular antioxidant enzyme activity of M. aeruginosa, such as catalase, peroxidase. The accumulation of malondialdehyde aggravated membrane injury after treatment for 3 days. P. aeruginosa also affected the ion metabolism of cyanobacteria. The release of Na(+) and Cl(-) was significantly enhanced while the uptake of K(+), Ca(2+), Mg(2+), NO3(-) and SO4(2)(-) decreased. Surface morphology and intracellular structure of cyanobacteria and bacterial cells changed dramatically over time as evidenced by electron microscope (SEM) and transmission electron microscope (TEM) analysis. These results revealed that the algicidal activity of P. aeruginosa was primarily due to the fermentation liquid of P. aeruginosa that impeded the synthesis of intracellular protein and carbohydrate, and damaged the cell membrane through membrane lipid peroxidation.
蓝藻在水生生态系统中的大量繁殖已在全球范围内引发了水安全问题。我们的初步研究表明,铜绿假单胞菌能够抑制蓝藻——铜绿微囊藻的生长。为了探究铜绿假单胞菌对铜绿微囊藻细胞生长及细胞内物质合成的抑制机制,我们对铜绿微囊藻的叶绿素a浓度、细胞内蛋白质、碳水化合物、酶活性及离子代谢进行了研究。结果表明,处理7天后,铜绿假单胞菌的杀藻效率达到了83.84%。该菌株通过阻碍蓝藻细胞内蛋白质和碳水化合物的合成来抑制铜绿微囊藻的繁殖,在暴露于铜绿假单胞菌5天后,仅检测到极少量的细胞内蛋白质和碳水化合物。铜绿假单胞菌导致了铜绿微囊藻细胞内抗氧化酶活性的改变,如过氧化氢酶、过氧化物酶。处理3天后,丙二醛的积累加剧了膜损伤。铜绿假单胞菌还影响了蓝藻的离子代谢。Na(+)和Cl(-)的释放显著增强,而K(+)、Ca(2+)、Mg(2+)、NO3(-)和SO4(2)(-)的吸收减少。电子显微镜(SEM)和透射电子显微镜(TEM)分析表明,随着时间的推移,蓝藻和细菌细胞的表面形态及细胞内结构发生了显著变化。这些结果表明,铜绿假单胞菌的杀藻活性主要归因于其发酵液,该发酵液阻碍了细胞内蛋白质和碳水化合物的合成,并通过膜脂过氧化作用破坏了细胞膜。