五氯酚生物降解机理与外生菌根真菌对五氯酚可降解性

五氯酚是氯酚族中最具毒性和最难降解的有机污染物。不同种类的微生物由于其降解污染物的生化机制不同,使得五氯酚的降解途径多样化。文章通过综述好氧与厌氧微生物降解五氯酚的降解菌和降解途径,认为五氯酚首先通过脱氯转化为低氯代化合物后再开环,因此脱氯就成为五氯酚降解的关键步骤。参与脱氯的关键酶系主要包括过氧化物酶和酚氧化酶。外生菌根真菌可降解多种难降解有机污染物,并具有生成过氧化物酶和酚氧化酶的机制,因此外生菌根真菌具有降解五氯酚的潜力与优势。这些信息将为进一步开展五氯酚生物降解机理研究,应用微生物—植物复合系统修复污染土壤提供基础。     

持久性有机污染物(POPs)的生物降解与外生菌根真菌对POPs的降解作用

综述了持久性有机污染物(POPs)的生物降解途径,以及国内外在外生菌根真菌降解POPs方面的研究进展,阐述了其机制与优势.根据作用的微生物和环境条件的不同,POPs如PCBs、DDT等可以通过脱氯或开环等途径生物降解.外生菌根真菌能降解多种POPs,具有较大的潜力.图2表2参30     

烷基化多环芳烃的细菌降解研究进展

烷基化多环芳烃（alkylated polycyclic aromatic hydrocarbons, A-PAHs）是以多环芳烃（PAHs）为母环，具有烷基侧链的稠环芳香烃，是一类在环境中广泛存在的持久性有机污染物.微生物降解是其在环境中降解去除的主要途径，与真菌、藻类等相比，细菌降解A-PAHs得到更多的关注.本文对APAHs的污染现状及生态毒性，细菌降解甲基萘、甲基菲的研究进展进行了概述，以PAHs的降解酶和降解基因作为参考，总结了A-PAHs可能涉及的降解酶及降解基因.本文有助于了解环境中A-PAHs的生物降解研究现状，为寻找高效的A-PAHs降解方法及减轻其生态风险提供理论依据.     

氯乙酰胺类除草剂微生物降解研究进展

主要介绍了几种氯乙酰胺类除草剂的微生物降解机制和相关降解酶．目前没有一种纯菌培养物或混合菌群能完全矿化异丙甲草胺和甲草胺，它们只能被细菌和真菌共代谢．毒草胺能被纯菌或混合菌群完全矿化，且有几种不同的矿化途径．乙草胺是我国生产量和使用量最多的三大除草剂之一，然而关于其微生物降解方面的研究在国内外报道的非常少，因此关于乙草胺被微生物降解和矿化的研究工作还有待于进一步加强．参45     

微生物修复土壤多环芳烃污染的研究进展

多环芳烃是一类具有致癌、致畸、致突变性质的持久性有机污染物,主要来源于煤、石油等燃料的不完全燃烧,易吸附于固体颗粒表面和有机腐殖质,化学结构稳定,能长期存在于自然环境,给人类健康和生态环境带来很大的危害。中国土壤多环芳烃污染严重,因此急需寻求有效的修复方法进行治理。在众多的多环芳烃污染修复方法中,微生物修复因其低成本、高效、污染少等优点成为研究热点。科学家们从自然界中分离出了多种细菌、真菌等具有降解多环芳烃能力的微生物,并对多环芳烃的降解机理进行了探索,结果表明,微生物在代谢活动过程中能够产生酶来实现对土壤中多环芳烃的降解。细菌主要通过产生双加氧酶来催化多环芳烃的加氧反应,而真菌可以通过分泌木质素降解酶系或单加氧酶来氧化多环芳烃。两种途径均是首先通过降低多环芳烃的稳定性,使之容易被进一步降解。目前,微生物修复技术正逐步应用于PAHs污染土壤的实地修复,且已取得一定成效。文章简要介绍了降解多环芳烃的微生物,对多环芳烃的微生物降解机制进行了综述,讨论了影响微生物修复过程的因素,列举了常见的微生物修复相关技术,展望了今后的研究趋势。     

聚丁二酸丁二醇酯（PBS）在两种微生物环境中的降解性能

以西安花园土和昆明农田腐殖土浸提液作为降解介质,对聚丁二酸丁二醇酯（PBS）的降解行为和两种土壤中不同微生物对PBS的作用进行了研究.结果表明,PBS膜在昆明腐殖土中降解两个月后的质量损失达到42%,其降解效果大约是西安花园土的9倍.在花园土壤中,真菌对PBS的降解起着主要作用,而腐殖土中,放线菌对PBS的降解起着主要...     

有机废弃物降解过程酶作用及其调控机制的研究进展

有机废弃物处置不当造成的环境污染和资源浪费已引起广泛关注,生物降解可以有效地实现有机废弃物资源化利用。微生物分泌的酶能催化生物降解的矿化和腐殖化过程,提高有机物降解率。然而,以往研究主要集中于微生物作用,对有机废弃物降解过程酶作用及其调控机制的总结很少。该文从酶学和生物化学角度出发,论述了生物酶催化降解有机质、促进腐殖质合成和削减污染物毒性等作用过程。基于酶动力学和热力学特征,从微生物、酶的固定化、理化因子和添加剂4个方面阐述酶作用的调控机制。生物酶高效、环保、可控,是有机废弃物资源化利用的重要催化剂之一。未来应加强研究酶降解的途径与分子机制、微生物-酶-有机废弃物系统的新陈代谢、激活剂对酶作用的调控、酶的固定化技术以及降解酶的生产与应用,以推动有机废弃物资源化利用的进程。     

土壤和地下水中多环芳烃生物降解研究进展

多环芳烃是一类普遍存在于环境中的难降解的危险性"三致"有机污染物。受污染的土壤和地下水中的多环芳烃,生物降解是其归宿的主要途径。研究表明,对于土壤中低分子量多环芳烃类化合物,微生物一般以唯一碳源方式代谢;而大多数细菌和真菌对四环或四环以上的多环芳烃的降解作用一般以共代谢方式开始。文章重点论述了多环芳烃的来源、降解多环芳烃的微生物、生物降解机理、影响生物降解的因素以及生物修复方法。认为今后的研究方向是高分子量多环芳烃的降解机理与降解途径,基因工程技术在多环芳烃生物降解方面的应用,以及生物表面活性剂产生的机理及其在实际处理中的应用等。     

热活化过硫酸钠氧化去除水中邻苯二甲酸酯

邻苯二甲酸酯(PAEs)主要用作塑料产品制造和加工的增塑剂，是全球关注的新兴污染物之一.本研究以邻苯二甲酸(2-乙基己基)酯(DEHP)和邻苯二甲酸二丁酯(DBP)为目标污染物，研究了在不同污染物初始浓度、过硫酸钠活化温度及浓度、助溶剂添加量对过硫酸钠氧化去除水中邻苯二甲酸酯的影响及机理.结果表明，在实验条件下，邻苯二甲酸酯初始浓度与去除率呈反比，反应温度、过硫酸钠浓度和pH与邻苯二甲酸酯的去除率呈正比.在80℃，过硫酸钠浓度为84 mmol·L^-1，助溶剂的添加量为30%时，DBP的降解率达到了100%,DEHP的降解率达到了92.8%. GC/MS分析表明，在高温活化过硫酸钠的条件下，邻苯二甲酸和邻苯二甲酸酐是DBP降解的主要产物，脱烷基化和羟基化是DBP降解的主要机理.本研究为过硫酸钠去除环境介质中的邻苯二甲酸酯提供了理论和实践依据.     

杀草丹降解菌Bacillus sp. T2的筛选、鉴定及降解特性

为研发稻田除稗剂杀草丹污染环境的生物修复技术和探究杀草丹微生物降解代谢机制,通过微生物驯化与富集技术,从长期施用杀草丹水稻田土样中分离纯化一株能够以杀草丹为唯一碳源生长的高效降解菌株T2,在36 h内对0.4 mmol/L的杀草丹降解率达到98.3%以上.根据其形态、生理生化特征及16S rRNA基因序列相似性分析,将其初步鉴定为芽孢杆菌属(Bacillus sp.T2).通过GC-MS鉴定产物为对氯苄硫醇、对氯苯甲醛和对氯苯甲酸;依据产物鉴定结果推测菌株T2通过硫酯键水解的方式起始杀草丹的降解,首先将其转化为对氯苄硫醇,随后进一步被氧化为对氯苯甲醛和对氯苯甲酸,该降解途径可能是一种新的杀草丹微生物降解代谢途径.因此菌株Bacillus sp.T2对杀草丹具有非常高的降解效率,在污染环境的微生物修复方面具有很好的应用前景;本研究结果也为揭示土壤中杀草丹微生物降解代谢过程及机制提供了研究材料和理论依据.     

Fenton degradation of dialkylphthalates: products and mechanism

Contamination of wastewater by organic pollutants is a major worldwide issue. For instance plastic additives such as phthalates are found in wastewater. Efficient techniques are thus needed to clean wastewaters. The Fenton reaction involving H₂O₂ and Fe(II) salts can be used to treat polluted water. During the Fenton reaction pollutants are decomposed directly by hydroxyl radicals. In some cases toxic by-products are produced. Here dimethyl phthalate, diethyl phthalate, and dipropyl phthalate by-products formed during the Fenton reaction were studied. Fenton degradation of selected phthalates yielded numerous transformation products such as hydroxylated phthalates. The hydroxylation reaction occurred at the aromatic ring of phthalates and yielded mono- and dihydroxylated phthalates. For monohydroxylated phthalate, 3-hydroxy- and 4-hydroxydialkylphthalates are the main transformation products. In addition to hydroxylated derivatives, aliphatic chain degraded mono- and dihydroxylated phthalates were also detected.     

酞酸酯暴露及风险评价研究进展

酞酸酯的暴露及健康风险研究日趋深入。在综述了酞酸酯的物化性质、接触机会两方面特性,以及体内代谢、健康危害两方面的最新研究进展基础上,比较了其国内外相关标准现状,总结了酞酸酯暴露评估现状及健康风险研究现状,提出并分析了存在的问题,并对其今后的研究进行了展望。     

Phthalatkonzentrationen in Böden naturnaher Standorte des Sollings (Niedersachsen)

The phthalat concentrations in soil samples from the Solling (Ecological Research Project Solling) were measured. The samples were collected from a beech and a spruce forest and aTrisetum flavescens meadow. The distance from the tree trunks and the different horizons were taken into consideration as well. Dimethylphthalat, diethylphthalat, dibutylphthalat, butylbenzylphthalat, di-(2-ethylhexyl) phthalat and dioctylphthalat were determinated using GC/MS. From the six phthalates investigated, four were detected in the samples. Dimethyl and diethylphthalat were found at very low concentrations in only one sample. Dibutyl- and di-(2-ethylhexyl)phthalat were detected in eight of 21 samples. No phthalates were found in the samples from theTrisetum flavescens meadow. Two of the nine samples from the beech forest showed phthalates. In six of the nine samples from the spruce forest phthalates were detected. Phthalate concentrations in the spruce forest were always higher than those found in the beech forest.     

Environmental pollutants and type 2 diabetes: a review of human studies

The incidence of diabetes has increased dramatically in recent decades and become one of the leading health problems worldwide. Lifestyle and dietary changes alone cannot account for the dramatic rise of diabetes, while an increasing number of publications have reported the possible relationships between exposure to environmental pollutants and risk of diabetes. In the present review, our objective was to summarize the human studies on environmental pollutants, which includes persistent organic pollutants, pesticides (not on the Stockholm Convention list), bisphenol A, and phthalates, and the risk of diabetes. Currently published results suggest a positive relationship between certain persistent organic pollutants (dichlorodiphenyldichloroethene, dichlorodiphenyltrichloroethane, hexachlorobenzene, and polychlorinated biphenyls) and bisphenol A exposure and risk of diabetes. For pyrethroids, organophosphates, carbamates, and phthalates, there are insufficient studies to reach conclusions and therefore more studies, especially prospective studies, are needed along with in vivo and in vitro studies to understand the underlying mechanisms.     

Chemical characterization of Tan‐Sui River sediment in North Taiwan

Surface sediment samples from four downstream sites of Tan‐Sui River in Taipei metropolitan area were collected from 1997 to 1999. The semivolatile organic pollutants present in the sediments were screened by GC/MSD. Several target compounds including sixteen polycyclic aromatic hydrocarbons (PAHs), seven chlorobenzenes, two phthalates and the total amount of C8‐C32 aliphatic hydrocarbons were quantified. The concentration of the 16 PAHs ranges from 0.21 to 5.69 μg/g of which fluoranthene, pyrene and phenanthrene were the highest. The concentration of the total chlorobenzenes ranged from 0.04 to 5.85 μg/g. The concentration of bis(2‐ethylhexyl)phthalate ranges from 3.8 to 35.3 μg/g and that of the total C8‐C32 aliphatic hydrocarbons ranges from 0.94 to 10.6 μg/g. Some of these values are higher than similar sediment survey in Japan in the eighties. The concentration of bis(2‐ethylhexyl)phthalate is much higher than the no‐effect level (0.184 μg/g) set by McDonald. Some of the PAHs have already reached the level of biological effects. As compared with the sediment samples collected from Tou‐Chien River and Pu‐Ze River located at the west of Taiwan, the chlorobenzene concentrations of sediments in Tan‐Sui River are 5–6 times higher, the PAHs are 6–10 times higher and the phthalates are 11–20 times higher. Nonylphenol was also commonly found in the Tan‐Sui River sediment. There is a decreasing tendency of PAHs and phthalates concentration from surface to bottom for the core sample at Taipei Bridge site. Such tendency is less obvious for chlorobenzenes.     

中新世水杉叶片和白垩纪松型球果化石中的挥发性成分

采用气相色谱-质谱联用分析技术从中新世水杉叶片和白垩纪松型球果两种裸子植物化石中分别鉴定了51个和19个挥发性成分,类型涉及烷烃、烷烯、烷醇、长链脂肪酸及其酯、邻苯二甲酸酯、萜类和芳香族化合物.其中3种成分——松香烷型二萜、饱和十七碳脂肪酸和惹烯是裸子植物的生物标志分子.图1表2参22     

Determination of Phthalate Esters in Samples from the Marine Environment Using Gas Chromatography Mass Spectrometry

Phthalate esters have been extracted from water, sediment and biota samples using a single solvent system, dichloromethane, and clean up by alumina column chromato-graphy. Analysis for dimethyl, diethyl, di-iso-butyl, di-n-butyl, di-n-heptyl, di-(2-ethylhexyl) and di-n-nonyl phthalates was carried out by gas chromatography and mass spectrometry. Phthalate esters were quantified using multiple ion detection, focussed on m/z 163 and m/z 149.

The procedure was tested on samples of water, sediment, bivalves and fish from the estuary of the River Crouch. The method gave satisfactory sensitivity for the determination of phthalate ester levels above the commonly found blank values of 1 to 20 nanograms per gram of solid or litre of water.

Comparative samples of fish from the heavily industrialised Tees Bay area did not show greatly elevated levels of phthalate esters.     

Determination of Phthalate Esters in Samples from the Marine Environment Using Gas Chromatography Mass Spectrometry

Phthalate esters have been extracted from water, sediment and biota samples using a single solvent system, dichloromethane, and clean up by alumina column chromato-graphy. Analysis for dimethyl, diethyl, di-iso-butyl, di-n-butyl, di-n-heptyl, di-(2-ethylhexyl) and di-n-nonyl phthalates was carried out by gas chromatography and mass spectrometry. Phthalate esters were quantified using multiple ion detection, focussed on m/z 163 and m/z 149.

The procedure was tested on samples of water, sediment, bivalves and fish from the estuary of the River Crouch. The method gave satisfactory sensitivity for the determination of phthalate ester levels above the commonly found blank values of 1 to 20 nanograms per gram of solid or litre of water.

Comparative samples of fish from the heavily industrialised Tees Bay area did not show greatly elevated levels of phthalate esters.     

水环境中的微塑料及其生态效应

塑料在日常生活中无处不在,随意丢弃的塑料会在各种作用下最终进入江河、湖泊、近海、深海、以及大洋甚至极地地区。在外界条件(如高温、风化、紫外线)影响下,大型塑料结构的完整性易遭到破坏而被逐渐分解成微小的塑料碎片,当其粒径小于5 mm时即可被称为微塑料。塑料中的某些添加剂,如壬基苯酚、多溴联苯醚、邻苯二甲酸盐、双酚A等会在塑料降解为微塑料的过程中释放到水环境中,从而威胁到水生生态系统的安全。微塑料粒径小,易被浮游动物误食或沿着食物链传递,在生物体内累积转移,对机体产生不可逆转的毒害作用。此外,微塑料还能作为某些污染物富集的载体,产生较强的复合毒性。因此水环境正面临着微塑料污染的威胁,如何治理已成为全球性的环境问题。本文对水环境中微塑料的来源与分布、微塑料的迁移和转化以及微塑料对水环境的影响进行了综述,并对水环境中的微塑料污染问题提出了一些解决方案,期望能为微塑料及其在水环境中的生态效应研究提供理论基础和数据支持。     

The distribution of phthalate esters in indoor dust of Palermo (Italy)

In this work, phthalic acid esters (PAEs): dimethyl phthalate (DMP), diethyl phthalate (DEP), di-n-butyl phthalate, benzyl butyl phthalate, bis(2-ethylhexyl) phthalate, and di-n-octyl phthalate in indoor dust (used as passive sampler) were investigated. The settled dust samples were collected from thirteen indoor environments from Palermo city. A fast and simple method using Soxhlet and GC–MS analysis has been optimized to identify and quantify the phthalates. Total phthalates concentrations in indoor dusts ranged from 269 to 4,831 mg/kg d.w. (d.w. = dry weight). The data show a linear correlation between total PAEs concentration and a single compound content, with the exclusion of the two most volatile components (DMP and DEP) that are present in appreciable amounts only in two samples. These results suggest that most of the PAEs identified in the samples of settled dust originate from the same type of material. This evidence indicates that, in a specific indoor environment, generally is not present only one compound but a mixture having over time comparable percentages of PAEs. Consequently, for routine analyses of a specific indoor environment, only a smaller number of compounds could be determined to value the contamination of that environment. We also note differences in phthalate concentrations between buildings from different construction periods; the total concentration of PAEs was higher in ancient homes compared to those constructed later. This is due to a trend to reduce or remove certain hazardous compounds from building materials and consumer goods. A linear correlation between total PAEs concentration and age of the building was observed (R = 0.71).