五氯酚对细菌反硝化过程的影响

Q3 Chemical Engineering
Bairen Yang, Aihui Chen
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引用次数: 9

摘要

摘要五氯酚(PCP)由于对生态环境和人类的不利影响,在世界上许多国家被禁止或限制使用。然而,PCP对反硝化微生物的潜在破坏作用值得更多的分析。本研究以反硝化副球菌为模型反硝化菌,研究了PCP对反硝化的影响。与对照组相比,10 μM和50 μM PCP的存在显著降低了反硝化效率,分别从98.5%降至87.2%和68.7%。机制研究表明,PCP诱导活性氧的产生,使糖酵解过程相关的重要酶活性降低,导致P.反硝化菌利用碳源(葡萄糖)的代谢和细胞的生长受到干扰,从而导致通过NAD+还原反硝化的电子供体(NADH)的产生受到严重抑制。进一步研究表明,PCP还降低了硝酸盐还原酶(NAR)的napA、亚硝酸盐还原酶的nirS、一氧化氮还原酶的norB和一氧化氮还原酶的nosZ等反硝化关键酶的基因表达;然而,只有NAR酶活性受到明显抑制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of pentachlorophenol on the bacterial denitrification process
Abstract The use of pentachlorophenol (PCP) was banned or restricted in many countries worldwide because of its adverse influences on the ecological environment and humans. However, the potential disrupting effects of PCP on denitrifying microorganisms have warranted more analysis. In this study, the impacts of PCP on denitrification were investigated by using Paracoccus denitrificans as a model denitrifying bacterium. Compared with the control, the presences of 10 and 50 μM of PCP were found to significantly decrease the denitrification efficiencies from 98.5 to 87.2% and 68.7%, respectively. The mechanism studies showed that PCP induced the generation of reactive oxygen species, which decreased the vital enzymes activities related to glycolysis process, causing the disturbance of the metabolism of P. denitrificans utilizing carbon source (glucose) and the growth of the cell, and subsequently the generation of electron donor (NADH) for denitrification via NAD+ reduction was severely depressed. Further studies indicated that PCP also decreased the genes expression of several key enzymes responsible for denitrification, such as napA of nitrate reductase (NAR), nirS of nitrite reductase, norB of nitric oxide reductase, and nosZ of nitrous oxide reductase; however, there was only the enzyme activity of NAR was remarkably inhibited.
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来源期刊
CiteScore
1.62
自引率
0.00%
发文量
0
审稿时长
1 months
期刊介绍: Chemical Speciation & Bioavailability ( CS&B) is a scholarly, peer-reviewed forum for insights on the chemical aspects of occurrence, distribution, transport, transformation, transfer, fate, and effects of substances in the environment and biota, and their impacts on the uptake of the substances by living organisms. Substances of interests include both beneficial and toxic ones, especially nutrients, heavy metals, persistent organic pollutants, and emerging contaminants, such as engineered nanomaterials, as well as pharmaceuticals and personal-care products as pollutants. It is the aim of this Journal to develop an international community of experienced colleagues to promote the research, discussion, review, and spread of information on chemical speciation and bioavailability, which is a topic of interest to researchers in many disciplines, including environmental, chemical, biological, food, medical, toxicology, and health sciences. Key themes in the scope of the Journal include, but are not limited to, the following “6Ms”: Methods for speciation analysis and the evaluation of bioavailability, especially the development, validation, and application of novel methods and techniques. Media that sustain the processes of release, distribution, transformation, and transfer of chemical speciation; of particular interest are emerging contaminants, such as engineered nanomaterials, pharmaceuticals, and personal-care products. Mobility of substance species in environment and biota, either spatially or temporally. Matters that influence the chemical speciation and bioavailability, mainly environmentally relevant conditions. Mechanisms that govern the transport, transformation, transfer, and fate of chemical speciation in the environment, and the biouptake of substances. Models for the simulation of chemical speciation and bioavailability, and for the prediction of toxicity. Chemical Speciation & Bioavailability is a fully open access journal. This means all submitted articles will, if accepted, be available for anyone to read, anywhere, at any time. immediately on publication. There are no charges for submission to this journal.
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