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本文引用的文献

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Pseudomonas putida Strains Which Constitutively Overexpress Mercury Resistance for Biodetoxification of Organomercurial Pollutants.假单胞菌属菌株可组成性过表达汞抗性以进行有机汞污染物的生物解毒。
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Effect of salinity on mercury-methylating activity of sulfate-reducing bacteria in estuarine sediments.盐度对河口沉积物中硫酸盐还原菌汞甲基化活性的影响。
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Protein measurement with the Folin phenol reagent.使用福林酚试剂进行蛋白质测定。
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Long-Term Stability of Mercury-Reducing Microbial Biofilm Communities Analyzed by 16S-23S rDNA Interspacer Region Polymorphism.通过16S-23S rDNA间隔区多态性分析汞还原微生物生物膜群落的长期稳定性
Microb Ecol. 2001 Dec;42(4):624-634. doi: 10.1007/s00248-001-0028-6.
5
Bacterial community changes and enrichment of Burkholderia-like bacteria induced by chlorinated benzoates in a peat-forest soil-microcosm.泥炭森林土壤微宇宙中氯代苯甲酸诱导的细菌群落变化及类伯克霍尔德氏菌的富集
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6
An evaluation of terminal-restriction fragment length polymorphism (T-RFLP) analysis for the study of microbial community structure and dynamics.用于微生物群落结构与动态研究的末端限制性片段长度多态性(T-RFLP)分析评估。
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Effects of community composition and growth rate on aquifer biofilm bacteria and their susceptibility to betadine disinfection.群落组成和生长速率对含水层生物膜细菌及其对碘伏消毒敏感性的影响。
Environ Microbiol. 2001 Jan;3(1):43-52. doi: 10.1046/j.1462-2920.2001.00158.x.
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US to take temperature of mercury threat.美国将评估汞威胁的程度。
Nature. 2001 Jan 11;409(6817):124. doi: 10.1038/35051770.
9
Detection of small sequence differences using competitive PCR: molecular monitoring of genetically improved, mercury-reducing bacteria.使用竞争性聚合酶链反应检测小序列差异:对基因改良的汞还原细菌进行分子监测
Biotechniques. 2001 Jan;30(1):142-8. doi: 10.2144/01301rr02.
10
Development and dynamics of Pseudomonas sp. biofilms.假单胞菌属生物膜的形成与动态变化
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在不断变化的环境条件下,物种多样性可提高汞还原生物膜的效率。

Species diversity improves the efficiency of mercury-reducing biofilms under changing environmental conditions.

作者信息

Von Canstein Harald, Kelly Sven, Li Ying, Wagner-Döbler Irene

机构信息

Division of Microbiology. Division of Biochemical Engineering, German Research Centre for Biotechnology, D-38124 Braunschweig, Germany.

出版信息

Appl Environ Microbiol. 2002 Jun;68(6):2829-37. doi: 10.1128/AEM.68.6.2829-2837.2002.

DOI:10.1128/AEM.68.6.2829-2837.2002
PMID:12039739
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC123942/
Abstract

Six mercury-resistant environmental proteobacterial isolates and one genetically modified mercury-resistant Pseudomonas putida strain were analyzed for physiological traits of adaptive relevance in an environment of packed-bed bioreactors designed for the decontamination of mercury-polluted chlor-alkali wastewater. The strains displayed characteristic differences in each trait (i.e., biofilm formation capability, growth rate in mercury contaminated wastewaters, and mercury reduction efficiency). Subsequently, they were immobilized either as a monoculture or as a mixed culture on porous carrier material in packed-bed bioreactors through which different batches of filter-sterilized industrial chlor-alkali wastewater were pumped. In monospecies bioreactors, the mercury retention efficiency was sensitive to rapidly increasing mercury concentrations in the wastewater. Mixed culture biofilms displayed a high mercury retention efficiency that was not affected by rapid increases in mercury or continuously high mercury concentrations. The dynamic in the community composition of the mixed culture bioreactors was determined by ribosomal intergenic spacer polymorphism analysis. Mercury-mediated selective pressure decreased the number of prevalent strains. Microbial diversity was completely restored after easing of the selective pressure. Microbial diversity provides a reservoir of strains with complementary ecological niches that results in a superior bioreactor performance under changing environmental conditions.

摘要

对六株耐汞环境变形菌分离株和一株基因工程改造的耐汞恶臭假单胞菌菌株进行了分析,以研究它们在用于汞污染氯碱废水净化的填充床生物反应器环境中与适应性相关的生理特性。这些菌株在每个特性(即生物膜形成能力、在汞污染废水中的生长速率和汞还原效率)上都表现出特征差异。随后,将它们以单一培养物或混合培养物的形式固定在填充床生物反应器的多孔载体材料上,不同批次的过滤灭菌工业氯碱废水通过该反应器泵送。在单物种生物反应器中,汞保留效率对废水中汞浓度的快速增加很敏感。混合培养生物膜显示出高汞保留效率,不受汞的快速增加或持续高汞浓度的影响。通过核糖体基因间隔区多态性分析确定了混合培养生物反应器中群落组成的动态变化。汞介导的选择压力减少了优势菌株的数量。选择压力缓解后,微生物多样性完全恢复。微生物多样性提供了具有互补生态位的菌株库,这导致在不断变化的环境条件下生物反应器性能更优。