微生物降解多氯联苯的研究进展

多氯联苯是一种持续性有机污染物,在自然环境中很难降解。在目前研究的降解方法中,微生物降解最具潜力。本文对多氯联苯微生物降解的研究进展进行了综述,包括厌氧还原脱氯,好氧氧化以及生物表面活性剂的作用,介绍了几种降解方法耦合应用的现状和前景,指出了应用中存在的问题和今后的发展方向。     

铜污染土壤的生物修复研究进展

随着工业化与农业化进程的加快,土壤重金属污染问题日益突出。铜(Cu)既是生命体生长发育的必需微量元素,也是重金属污染物之一。土壤中过量的Cu不仅会对植物产生毒害,而且能够通过食物链的富集作用,对人类健康造成严重威胁。生物修复技术作为治理重金属污染土壤的一种新型技术受到广泛关注。文中对生物修复的主要技术如植物修复、微生物修复、植物-微生物联合修复、动物修复等在治理Cu污染土壤方面的研究进展进行综述,以期为重金属污染土壤有效治理和可持续农业的发展提供理论依据。     

红树植物秋茄对PCBs污染沉积物的修复

通过盆栽试验,研究了红树植物秋茄(Kandelia candel)对污染沉积物中系列浓度的PCB47(2,2′,4,4′-tetrachlorobiphenyl)和PCB155( 2,2′,4,4′,6,6′, -hexachlorophenyl)的修复作用与累积机理.结果表明:(1)经过180d处理,栽种了秋茄的沉积物中PCB47的残留浓度为53.99～528.37μg·kg-1,PCB155的残留浓度为68.25～682.90μg·kg-1,分别比对照1(加二氯化汞)低10.40%～15.46% 和6.10%～11.94%;比对照2(无二氯化汞)低7.70%～12.85% 和5.28%～8.27%;(2)秋茄对沉积物中PCB47和PCB155均具有较强的吸收积累作用,并随沉积物中PCB47和PCB155含量的增加而增大,不同种类PCBs在秋茄体内不同部位的积累趋势相同,不论是PCB47还是PCB155的累积量均是根> 叶> 茎.秋茄叶片中多氯联苯来自根部传输和空气吸收两部分,较低浓度的处理中,主要来自空气吸收,较高浓度的处理中,主要来自根部传输;(3)秋茄根对PCBs的生物富集系数(BCFs) 随着沉积物中PCB47和PCB155含量的增加而减小.不同种类PCBs 以及植物不同部位间BCFs 差异较大, PCB47的生物富集系数大于PCB155, 秋茄不同部位对PCBs生物富集系数大小不同,无论是PCB47还是PCB155,生物富集系数均是根＞叶＞茎.总体看来,秋茄能积累与去除污染沉积物中的PCB47和PCB155,表明用红树植物秋茄修复PCBs污染沉积物是一种有效、可行的方法.     

生物修复的研究和应用现状及发展前景

综述了生物修复的研究和应用现状及发展前景。内容涉及生物修复的研究方法和手段、生物修复在土壤和水体中的应用、生物修复的发展前景等。     

生物修复的研究和应用现状及发展前景

综述了生物修复的研究和应用现状及发展前景。内容涉及生物修复的研究方法和手段、生物修复在土壤和水体中的应用、生物修复的发展前景等。     

土壤与水体有机污染的生物修复及其应用研究进展

系统论述了土壤、水有机污染物的主要来源、特点、有机污染生物修复的概念、应用范围、成功实例与研究进展等,特别是对于泄漏石油污染的生物成功降解方法、效果,土壤中易爆炸物如ＴＮＴ、废水中有机污染的有效降解等,评价了生物修复所具有突出优势,对有机、无机污染物降解过程中植物、微生物筛选、基因修饰、分子克隆与转基因植物方面近年来所取得的惊人成果与突破性进展,无疑正激励着人们开拓更大的应用范围。预计不久的将来,更多具有环境净化与生物修复功能的商业性综合技术与高效性工程生物将投入应用。     

重金属污染土壤的湿地生物修复技术

生物修复技术是近年来发展起来的一种有前途的污染治理技术,重金属的湿地植物稳定技术和植物萃取技术等植物修复技术是一研究热点;同时,针对微生物对重金属的生物积累、生物转化及生物修复作一分析,重金属的生物修复生理机制及其提高富集效率的条件作一综述,以期推动国内这一国际热点领域的研究。     

2020污染土壤的生物修复专刊序言

生物修复技术,作为可持续发展的重要方向,因其环境友好、高效且无二次污染并能从根本上解决土壤污染问题而受到关注,已经在土壤污染治理中得到了广泛的应用.为了梳理和凝练生物修复技术的发展状况,本专刊收录了该研究领域的16篇论文,分别从植物修复、微生物修复、联合修复、重金属吸收积累的相关分子机制、资源化再利用等方面,详细阐述生...     

我国污染土壤生物修复技术的发展及现状

本文简要回顾了近30年来我国污染土壤生物修复技术的发展过程,主要包括生物修复技术在我国的发展阶段、生物修复的4大类型及其所适用对象与范围、生物修复用菌株的筛选与特性研究、活性菌株(菌剂)在典型污染土壤中的应用及其效果等,并针对土壤污染和生物修复技术的发展现状,简要讨论了未来生物修复技术的发展。     

Aerobic degradation of polychlorinated biphenyls by Alcaligenes sp. JB1: metabolites and enzymes

In contrast to the degradation of penta-and hexachlorobiphenyls in chemostat cultures, the metabolism of PCBs by Alcaligenes sp. JB1 was shown to be restricted to PCBs with up to four chlorine substituents in resting-cell assays. Among these, the PCB congeners containing ortho chlorine substituents on both phenyl rings were found to be least degraded. Monochloro-benzoates and dichlorobenzoates were detected as metabolites. Resting cell assays with chlorobenzoates showed that JB1 could metabolize all three monochlorobenzoates and dichlorobenzoates containing only meta and para chlorine substituents, but not dichlorobenzoates possessing an ortho chlorine substituent. In enzyme activity assays, meta cleaving 2,3-dihydroxybiphenyl 1,2-dioxygenase and catechol 2,3-dioxygenase activities were constitutive, whereas benzoate dioxygenase and ortho cleaving catechol 1,2-dioxygenase activities were induced by their substrates. No activity was found for pyrocatechase II, the enzyme that is specific for chlorocatechols. The data suggest that complete mineralization of PCBs with three or more chlorine substituents by Alcaligenes sp. JB1 is unlikely.Abbreviations PCB polychlorinated biphenyls - CBA chlorobenzoate - D di - Tr tri - Te tetra - Pe penta- - H hexa     

The ability of different plant species to remove polycyclic aromatic hydrocarbons and polychlorinated biphenyls from incubation media

The ability of in vitro cultured cells of black nightshade, wheat, barley, soybean, tomato, mulberry and birch to grow in the presence of polycyclic aromatic hydrocarbons (PAHs) and polychlorinated biphenyls (PCBs) and to metabolise them was compared. No correlation was found between the resistance of the plants and removal of xenobiotics. Up to 20% of PCBs and over 90% of PAHs were removed by wheat cells from nutrient media in two weeks.     

On the inhibition of microsomal drug metabolism by polychlorinated biphenyls (PCB) and related phenolic compounds.

The in vitro metabolism of p-nitroanisole, aminopyrine, and aniline by rat liver microsomal monoxygenases were studied in the presence of different polychlorinated biphenyl (PCB) mixtures and some related hydroxybiphenyls. The tested PCB mixtures contained preferably dichloro- (di-CB), tetrachloro- (tetra-CB), or hexachlorobiphenyls (hexa-CB). All PCB were competitive inhibitors of only aminopyrine demethylation by normal microsomes (Ki 22-39 micron). In microsomes of PCB-pretreated rats the aminopyrine demethylation was inhibited noncompetitively by di-CB and hexa-CB whereas tetra-CB remained a competitive inhibitor (Ki 12 micron). Moreover, after PCB pretreatment all PCB were competitive inhibitors of p-nitroanisole demethylation. 2-OH-biphenyl and 4-OH-biphenyl caused competitive inhibition of aminopyrine demethylation and aniline hydroxylation but failed to inhibit p-nitroanisole metabolism by normal microsomes. Chlorinated 4-hydroxybiphenyls inhibited competitively the metabolism of both type I and type II substrates. However, after PCB pretreatment all phenolic compounds caused uncompetitive inhibition of aniline hydroxylation.     

Degradation of polychlorinated biphenyls by extracellular enzymes of Phanerochaete chrysosporium produced in a perforated plate bioreactor

The white rot fungus Phanerochaete chrysosporium was cultivated in a perforated plate bioreactor and the expression of activities of manganese-dependent peroxidase (MnP) and lignin peroxidase (LiP) was measured. Peak activities of the two enzymes were reached close to day 11 and therefore the cultivation was terminated on that day. Extracellular proteins were concentrated and both peroxidases separated by isoelectric focusing. Degradation of technical PCB mixtures containing low and highly chlorinated congeners (Delor 103 and Delor 106 as equivalents of Aroclor 1242 and Aroclor 1260, respectively) was performed using intact mycelium, crude extracellular liquid and enriched MnP and LiP. A decrease in PCB concentration caused by a 44-h treatment with mycelium (74% w/w for Delor 103 and 73% for Delor 106) or crude extracellular liquid (62% for Delor 103 and 58% for Delor 106) was observed. The degradation was not substrate-specific, because no significant differences between the respective degradation rates were observed with di-, tri-, tetra-, penta-, hexa-, hepta-, and octachlorinated congeners. In contrast, MnP and LiP isolated from the above-mentioned extracellular liquid did not catalyse any degradation.     

Strategies for bioremediation of polychlorinated biphenyls

Polychlorinated biphenyls (PCBs) are serious environmental pollutants that threaten both the natural ecosystem and human health. For remediation of environments contaminated with PCBs, several approaches that exploit the potential of microbes to degrade PCBs have been developed. These approaches include improvement of PCB solubilization and entry into the cell, pathway and enzyme engineering, and control of enzyme expression. In this mini-review, we briefly summarize these strategies and provide potentially useful knowledge for the further improvement of the bacterial breakdown of PCBs.     

Potential for phytoremediation of polychlorinated biphenyl-(PCB-)contaminated soil

Weathered soils contaminated with commercial-grade Aroclor 1260 from three sites in Canada were used to investigate the polychlorinated biphenyl (PCB) phytoextraction potential of nine plant species (Festuca arundinacea, Glycine max, Medicago sativa, Phalaris arundinacea, Lolium multiflorum, Carex normalis, and three varieties of Cucurbita pepo ssp. pepo) under controlled greenhouse conditions. The soils used varied in PCB concentration (90-4200 microg/g) and total organic content (0.06-2.02%). Greenhouse experiments controlled for PCB volatilization through the use of a vented enclosure and by isolating the contaminated soils with parafilm. After 8 wks, PCB concentrations of 47-6700 microg/g were observed in root tissues. Although PCB concentrations in shoot tissues were lower (< 1-470 microg/g), the absolute amounts of PCBs observed in shoot tissue were significant (1.7-290 microg) once shoot biomass was accounted for. Congener signatures indicated that tetra- to hexa-chlorobiphenyls contributed the largest proportions to shoot tissues, but hepta-to nona-chorobiphenyls were also present in measurable amounts. Overall, the results indicate that varieties of C. pepo were more effective at extracting PCBs from soil than other plants screened The evidence suggests that this was mainly due to root uptake of PCBs and tranlocation to the shoots, rather than volatilization of PCBs from soil. All plants screened showed signs of stress in the most highly contaminated soil (4200 microg/g), but not in the two lower PCB contaminated soils (250 and 90 microg/g, respectively). No detectable decreases in soil PCB concentrations were observed in these short-term greenhouse experiments, but the results suggest that this may be achievable through multiple plantings.     

Metabolism of polychlorinated biphenyls by Solanum nigrum hairy root clone SNC-9O and analysis of transformation products

The study investigates aspects of PCB metabolism by a hairy root culture of Solanum nigrum L. (clone SNC-9O) in vitro. Standard conditions were established for efficient, up to 72% PCB conversion (22 individual PCB congeners examined in commercial mixture Delor 103, 5 g fresh biomass in 100 ml media shaken with 5 mg PCB for 14 days). The conversion products formed from three monochlorobiphenyls were monohydroxychlorobiphenyls and dihydroxychlorobiphenyls, while six dichlorobiphenyls yielded different monohydroxydichlorobiphenyls. Efficiency of the transformation of individual PCB congeners was evaluated together with phytotoxic effect on the clone SNC-9O. Major metabolites of monochlorobiphenyls analysed after extraction from biomass were hydroxylated at the position 4, and 4′, respectively. This revised version was published online in June 2006 with corrections to the Cover Date.     

Genetic construction of PCB degraders

Genetic construction of recombinant strains with expanded degradative abilities may be useful for bioremedation of recalcitrant compounds, such as polychlorinated biphenyls (PCBs). Some degradative genes have been found either on conjugative plasmids or on transposons, which would facilitate their genetic transfer. The catabolic pathway for the total degradation of PCBs is encoded by two different sets of genes that are not normally found in the same organism. ThebphABCD genes normally reside on the chromosome and encode for the four enzymes involved in the production of benzoate and chlorobenzoates from the respective catabolism of biphenyl and chlorobiphenyls. The genes encoding for chlorobenzoate catabolism have been found on both plasmids and the chromosome, often in association with transposable elements. Ring fission of chlorobiphenyls and chlorobenzoates involves themeta-fission pathway (3-phenylcatechol 2,3-dioxygenase) and theortho-fission pathway (chlorocatechol 1,2-dioxygenase), respectively. As the catecholic intermediates of both pathways are frequently inhibitory to each other, incompatibilities result. Presently, all hybrid strains constructed by in vivo matings metabolize simple chlorobiphenyls through complementary pathways by comprising thebph, benzoate, and chlorocatechol genes of parental strains. No strains have yet been verified which are able to utilize PCBs having at least one chlorine on each ring as growth substrates. The possible incompatibilities of hybrid pathways are evaluated with respect to product toxicity, and the efficiency of both in vivo and in vitro genetic methods for the construction of recombinant strains able to degrade PCBs is discussed.     

Effect of chlorobenzoates on the degradation of polychlorinated biphenyls (PCB) by Pseudomonas stutzeri

Chlorobenzoic acids (CBA) are frequently dead-end products of partial aerobic biodegradation of polychlorinated biphenyls (PCB). When CBA produced from PCB accumulate in the growth medium, they can inhibit the bacterial growth and consequently, slow down PCB biodegradation. In this study, the effects of seven mono- and dichlorinated CBA on growth of Pseudomonas stutzeri on different substrates and on the PCB degradation by this strain in a liquid mineral medium were tested. 3-CBA was the strongest growth inhibitor for P. stutzeri growing on glucose, benzoate and biphenyl. It was found to inhibit heavily the elimination of some di- and trichlorinated biphenyls. In contrast, its influence on the elimination of more chlorinated congeners was much less significant.The authors are with the Department of Biochemical Technology, Faculty of Chemical Technology, Slovak Technical University, 812 37 Bratislava, Slovakia.