常用化学絮凝剂的环境效应与生态毒性研究进展

化学混凝法是国内外应用最为广泛的一种水处理方法,因此化学絮凝剂在使用过程中的生态安全性也越来越受到人们的关注.本文对常用的铝盐絮凝剂、铁盐絮凝剂和有机高分子絮凝剂在制备和使用过程中的生态安全性进行了分析,认为铝盐絮凝剂的长期使用会造成水中过高的铝离子残留,其在环境中的迁移转化会造成植物、动物、微生物和人的危害;铁盐絮凝剂在制备过程中可能会引入有害离子,并产生NO2有害气体,铁离子可以促进自由基的产生,导致细胞和组织的损害;聚丙烯酰胺在自然条件下可缓慢降解为剧毒的丙烯酰胺单体.基于国内外化学絮凝剂在生态安全性方面的研究现状,提出了今后絮凝剂应用和研究的方向.     

微生物降解磺胺甲恶唑的研究进展

抗生素是一类难降解、低浓度就有高生态毒性效应的化合物,近年来被归为新型环境污染物,其环境残留与去除备受关注。作为广泛使用的抗生素之一,磺胺甲恶唑在水土环境中的残留量不断增加,检出率也越来越高。研究表明,磺胺甲恶唑是少数几种可被微生物降解的抗生素之一,微生物降解法是最具潜力的残留磺胺甲恶唑去除手段。本文总结了磺胺甲恶唑在土壤、沉积物、活性污泥、混合菌群、酶等条件下的降解及已分离的具有降解能力的单菌株对磺胺甲恶唑的降解情况,包括其降解效率、降解条件等,归纳了目前磺胺甲恶唑微生物降解的主要分类,并讨论了影响磺胺甲恶唑降解的两个特有因素。指出从分子生物学及生物信息学角度研究其降解途径,降解菌、降解菌群的人工构建及其在含磺胺甲恶唑污水处理中的应用与效果评价等应为今后磺胺甲恶唑生物降解与应用研究的重点。     

好氧细菌对多环芳烃降解机制的研究进展

多环芳烃(PAHs)是指两个或两个以上的苯环以线性排列、弯接或簇聚方式构成的一类碳氢化合物。这类化合物广泛分布于环境中, 具有潜在的致畸性、致癌性和遗传毒性。在自然环境中, 好氧细菌对PAHs的生物降解是一种很重要的方式, 凸显其在清除环境PAHs污染物中具有广阔的应用前景。在过去二十多年中, 科学家们已经从基因水平上对好氧细菌降解PAHs的机制进行了深入的研究, 其中包括PAHs降解基因的多样性、与PAHs降解有关的基因以及细菌群体PAHs遗传适应机制等。在此, 就好氧细菌对多环芳烃降解机制的研究进展进行了综述和讨论。     

好氧细菌对多环芳烃降解机制的研究进展

多环芳烃(PAHs)是指两个或两个以上的苯环以线性排列、弯接或簇聚方式构成的一类碳氢化合物.这类化合物广泛分布于环境中,具有潜在的致畸性、致癌性和遗传毒性.在自然环境中,好氧细菌对PAHs的生物降解是一种很重要的方式,凸显其在清除环境PAHs污染物中具有广阔的应用前景.在过去二十多年中,科学家们已经从基因水平上对好氧细菌降解PAHs的机制进行了深入的研究,其中包括PAHs降解基因的多样性、与PAHs降解有关的基因以及细菌群体PAHs遗传适应机制等.在此,就好氧细菌对多环芳烃降解机制的研究进展进行了综述和讨论.     

绿色木霉纤维素酶系中C1酶的提纯与性质

从绿色木霉(Trichoderma viride) X2-85的麸曲抽提液中,分离出纤维素酶系中的C1酶,经纯化后,用聚丙烯酰胺凝腔电泳和超速离心鉴定,都为均一蛋白。在我们的实验条件下,它对羧甲基纤维素、3-葡萄糖苷及纤维二糖,都不表现活性。该酶能降解徽晶纤维紊、磷酸膨胀纤维素和脱脂棉,主要产物是纤维二糖。用Sephadex G一100凝胶过滤和SDS一聚丙烯酰胺凝胶电泳测定其分子量,分别为54,000和55,000。其沉降系数为4.18。     

油田含聚合物污水微生物处理初步研究

对油田日益增多的并且对环境造成潜在危害的而现有污水处理工艺难于处理的含聚合物污水进行微生物处理初步研究。结果表明,从油田污水污泥中分离得到的七株聚丙烯酰胺(PAM)降解菌在合适的营养条件下协同作用,对大港油田的含PAM的污水具有较好的处理效果。经过3d的处理,微生物菌群将补充了磷和氮的污水的COD降低了87.7%;经过18d的处理,微生物菌群将补充了磷的污水的COD由13499mg.L-1降低为283 mg.L-1,降低幅度达到了97.9%。因而这7株PAM降解菌对含PAM污水处理具有很好的应用前景。     

邻苯二甲酸酯在环境中的降解机制

邻苯二甲酸酯是一类普遍使用的有机化合物, 主要用做聚氯乙烯的增塑剂。目前在环境中已经大量存在, 由于其具有致癌、致畸和致突变性, 近来引起广泛的关注。研究表明, 邻苯二甲酸酯属于环境内分泌干扰物, 对人类健康和自然环境有非常大的危害。针对邻苯二甲酸酯类污染物在环境中的污染现状以及其降解机制进行了综述。研究显示: 邻苯二甲酸酯在地表水中的分布非常的广泛, 主要来源于工业废水、固体废弃物以及PVC 合成塑料; 邻苯二甲酸酯能够在环境中存在水解、光解、微生物降解及植物修复的可能性, 但其降解速率不尽相同, 其中生物降解是邻苯二甲酸酯在环境中分解的主要途径。     

聚丙烯酰胺凝胶固定核酸方法及其应用

固相核酸已被广泛用于DNA/cDNA微阵列、固相PCR及其它核酸与生物分子检测的传感技术中.和硬质玻璃载片相比,三维聚丙烯酰胺凝胶作为固定核酸的载体具有结合核酸容量高、利于反应的类似液相环境和较少的空间效应等优点.综述了丙烯酰胺凝胶作为固定核酸载体的发展历史.着重介绍了丙烯酰胺修饰核酸直接聚合固定的方法以及在DNA芯片、焦测序、固相PCR(克隆)、及全基因组测序等核酸分析中的应用.     

聚丙烯酰胺对坡地苹果园水土流失和土壤养分流失的影响

为了改善坡地苹果园的土壤环境,遏制水土流失和土壤养分流失,探寻聚丙烯酰胺适宜的干撒施用量,2010—2012年在陕北丘陵沟壑区的坡地苹果园,以不施聚丙烯酰胺为对照,分别撒施0.6、0.8、1.0、1.2、1.4和1.6 g·m^-2的聚丙烯酰胺,监测果园地表产流、土壤流失、养分流失和苹果植株生长状况.结果表明: 坡地果园的径流量和5—7月的产流次数均随聚丙烯酰胺撒施量的增加呈“V”型变化,其中撒施量为1.0 g·m^-2时最低,但果园侵蚀泥沙量则随聚丙烯酰胺撒施量的增加而降低.地表径流和侵蚀泥沙中的铵态氮、速效磷和速效钾的浓度均随聚丙烯酰胺撒施量的增加而降低;聚丙烯酰胺可显著降低地表径流中的硝态氮含量,对侵蚀泥沙中的硝态氮含量则无显著影响;侵蚀泥沙中的有机质、全氮、全磷和全钾含量均随聚丙烯酰胺撒施量的增加而降低.聚丙烯酰胺提高了苹果单果质量及产量,但对苹果植株生长及果实风味品质无显著影响.聚丙烯酰胺在坡地苹果园中的适宜撒施量应为1.0 g·m^-2.     

人工碳纳米材料在环境中的降解与转化研究进展

随着人工碳纳米材料的大量生产和使用,其潜在的生态风险已引起学术界的广泛关注.碳纳米材料在环境中的转化和降解直接影响它们在环境中的归趋及生态毒性,对该过程的研究是确定其环境可容纳量及进行生命周期评价的重要环节.本文概述了主要人工碳纳米材料(碳纳米管、富勒烯)在环境中的化学转化、微生物降解及光降解过程,总结了影响人工碳纳米材料降解的环境与结构因素及降解的机理,指出了现有研究的不足和未来研究的方向.     

Loss of tRNA 5-methyluridine methyltransferase and pseudouridine synthetase activities in 5-fluorouracil and 1-(tetrahydro-2-furanyl)-5-fluorouracil (ftorafur)-treated Escherichia coli

The degradation of human erythrocyte membrane proteins in relation to the identification of the monosaccharide transporter has been investigated in whole membrane preparations and membrane protein extracts by polyacrylamide gel electrophoresis in sodium n-dodecyl sulphate and iodine-125 labelling. Evidence is presented for the degradation of band 3 polypeptide to lower molecular weight material some of which appears in region 4.5 of the polyacrylamide gel electrophoresis profile. It is found that the degradation process is inhibited by phenylmethylsulphonyl fluoride and is only significant in membrane extracts in the absence of detergent (Triton X-100) and on prolonged incubation at 37 degrees C, conditions which do not prevail during the isolation of membrane protein extracts for reconstitution studies. Extracts of band 3 and band 4.5 have been prepared and reconstituted in bilayer lipid membranes. The permeabilities of the reconstituted systems to D-glucose have been investigated and it is found that only bilayers incorporating band 4.5 exhibited enhanced monosaccharide transport. A linear relationship between D-glucose transport and the concentration of protein in the aqueous phase bathing the bilayers suggests a partitioning of the protein into the bilayer. Reconstitution is stereospecific and inhibited by cytochalasin B.     

Energy consumption and environmental degradation nexus: A systematic review and meta-analysis of fossil fuel and renewable energy consumption

This study examines the energy consumption and environmental degradation nexus at a disaggregated (i.e., fossil fuel energy and renewable energy) level by investigating bibliometric indicators on a global scale. For this purpose, the study considers a number of studies published between 1980 and 2021 that were selected on the Web of Science (WoS) database based on relevant keywords. A bibliometric analysis was done through VOSviewer from a comparative perspective. Thus, 17,298 studies on fossil fuel energy consumption & environmental degradation and 62,002 studies on renewable energy consumption & environmental degradation were identified. Bibliometric indicators and network visualizations were used to present the results, which show: (i) the topic of disaggregated energy consumption and environmental degradation has been a problem since 1991; (ii) the number of renewable energy-related studies has exceeded the number of fossil fuel-related studies regarding environmental degradation; (iii) many of the studies in both disaggregated groups fall under the categories of energy fuels, environmental sciences, and green sustainable science technology, respectively; (iv) most of the studies have been published by Elsevier; (v) most of the researchers are from the United States of America (USA), whereas those from China and Pakistan have recently come to the fore. Hence, this study assesses the emerging trends in the literature on the energy consumption and environmental degradation nexus at a disaggregated level. Moreover, potential issues to be included by future studies are suggested.     

The relative rates of degradation of the plasma membrane glycoproteins from normal rat liver.

Rat liver plasma membranes, as fractionated by sodium dodecylsulfate/polyacrylamide gel electrophoresis, have been examined for the incorporation in their subunits of radioactive leucine, glucosamine and fucose. Specific spectra were obtained. In contrast to leucine, where the activity is distributed in many peaks all over the fractions, the glucosamine and fucose activities are found principally in the high molecular weight region. The relative rates of degradation of the glycoprotein components of the plasma membrane have been measured in normal liver using the double isotope technique. A marked heterogeneity of degradation was observed among the different subunits and a correlation between the rate of degradation and the size of the labelled subunits was found with glucosamine and fucose as well with leucine. This suggests a similar mode for the degradation of these membrane components.     

The relative rates of degradation of the plasma membrane glycoproteins from normal rat liver

Rat liver plasma membranes, as fractionated by sodium dodecylsulfate/polyacrylamide gel electrophoresis, have been examined for the incorporation in their subunits of radioactive leucine, glucosamine and fucose. Specific spectra were obtained. In contrast to leucine, where the activity is distributed in many peaks all over the fractions, the glucosamine and fucose activities are found principally in the high molecular weight region.The relative rates of degradation of the glycoprotein components of the plasma membrane have been measured in normal liver using the double isotope technique. A marked heterogeneity of degradation was observed among the different subunits and a correlation between the rate of degradation and the size of the labelled subunits was found with glucosamine and fucose as well as with leucine. This suggests a similar mode for the degradation of these membrane components.     

Isoforms of mammalian ubiquitin-activating enzyme.

Ubiquitin-activating enzyme, "E1," is the first enzyme in the pathway leading to formation of ubiquitin-protein conjugates and represents a potential target for regulation in the metabolic control of the conjugation reaction. Antiserum raised against human E1 recognizes two immunoreactive proteins in extracts from several human cell lines and animal tissues. We have characterized these two immunoreactive proteins in HeLa cells and present evidence that they are isoforms of E1. We have designated these isoforms as "E1(110 kDa)" and "E1(117 kDa)" to reflect their apparent molecular masses determined from SDS-polyacrylamide gel electrophoresis. These two immunoreactive proteins are immunologically similar, have nearly identical peptide maps, and comigrate with enzymatic activity characteristic of E1 in native polyacrylamide gel electrophoretic separations. Pulse-labeling experiments reveal that both isoforms are long-lived in vivo with degradation rates which are inconsistent with a proenzyme/enzyme model. Furthermore, their rates of degradation, which vary depending on the cell line studied, are kinetically distinguishable in contact-inhibited human lung fibroblasts. This work represents the first demonstration of E1 isoforms in a non-plant species and carries important implications for studies of the regulatory mechanisms controlling ubiquitin conjugation.     

Low molecular weight plasma proteins isolated from preparations of human immunoglobulin

Low molecular weight proteins co-purified with IgG constitute 0.22% of the total protein purified from human plasma by ion-exchange chromatography on DEAE-cellulose. We have found that these low molecular weight proteins were obtained free of immunoglobulin by ultrafiltration in 5 M guanidinium chloride. Electrophoresis and isoelectric focusing in polyacrylamide gels demonstrated that this fraction of low molecular weight proteins is remarkably heterogeneous. Chromatography of an Mr 6000 to 12 000 fraction on hydroxyapatite resolved fourteen discrete protein peaks. Three of the peaks contained proteins which appeared to be homogeneous on acid-urea polyacrylamide gels. Two of these proteins were similar in composition to B2 globulin and may represent degradation products of some larger protein. The third protein was found to have an amino-terminal sequence identical to C3a. This population of low molecular weight plasma proteins has previously been shown to contain the cystic fibrosis mucociliary inhibitor and is here shown to contain two proteins similar to B2 globulin, C3a and many proteins remaining to be characterized. The presence of these low molecular weight proteins in measurable concentrations may be insufficiently appreciated in studies using 'purified' immunoglobulins as biological or chemical probes.     

Enhanced degradation of gamma-irradiated lignocelluloses by a new xylanolytic Flavobacterium sp. isolated from soil

An extracellular chitosanase produced by Rhodotorula gracilis CFR-1 that catalyses a limited degradation of chitosan with no detectable generation of glucosamine or reducing groups was identified. Ultracentrifugation, polyacrylamide gel electrophoresis and gel permeation studies suggest that chitosan of average molecular mass 36000 Da was reduced by the enzymic catalysis to nearly one-fourth this size without further hydrolysis of the products. The enzyme, produced constitutively by this yeast, was partially purified and some of its properties were studied.     

P-bodies and mitochondria: Which place in RNA interference?

Micro-RNAs (miRNAs) are major actors of RNA interference (RNAi), a regulation pathway which leads to translational repression and/or degradation of specific mRNAs. They provide target specificity by incorporating into the RISC complex and guiding its binding to mRNA. Since the discovery of RNAi, many progresses have been made on the mechanism of action of the RISC complex and on the identification of target mRNAs. However, the regulation of RNAi has been poorly investigated so far. Recently, various studies have revealed physical and functional relationships between RNAi, P-bodies and mitochondria. This review intends to recapitulate these data and discuss their potential importance in cell metabolism.     

Horizontal two-dimensional electrophoresis of plasma butyrylcholinesterase

Genetic variants of human plasma butyrylcholinesterase have been characterized and are highly relevant to anesthesiology. They might also represent potential genetic markers for neuropsychiatric disorders. Two-dimensional electrophoresis with isoelectrofocusing in the first and polyacrylamide gel electrophoresis in the second dimension has proved to be a powerful tool in search for genetic variants. Butyrylcholinesterase is an oligomeric enzyme with considerable charge heterogeneity. Conventional two-dimensional electrophoresis proved unsuitable for this enzyme possibly due to its tendency to aggregate by hydrophobic interactions. The inversion of the sequence applying polyacrylamide gel electrophoresis in the first and isoelectric focusing in the second dimension circumvented this problem.     

Aerobic and Anaerobic Biodegradation of Aged Pentachlorophenol by Indigenous Microorganisms

Pentachlorophenol (PCP) use as a general biocide, particularly for treating wood, has led to widespread environmental contamination. Biodegradation has emerged as the main mechanism for PCP degradation in soil and groundwater and a key strategy for remediation. Examining the microbial biodegrading potential for PCP at a contaminated site is crucial in determining its fate. Hundreds of studies have been published on PCP microbial degradation, but few have described the biodegradation of PCP that has been in contact with soils for many years. The bioavailability of “aged” hydrophobic organics is a significant concern. PCP- and 2,3,4,6-tetrachlorophenol (2,3,4,6-TeCP)-contaminated soil samples from several depths at a former wood treatment site were placed under varying conditions in the laboratory to determine the anaerobic and aerobic potential for biodegradation of chlorophenols at the site. PCP biodegradation occurred in both anaerobic and aerobic soil samples. Rapid aerobic degradation occurred in samples spiked with 2- and 4-chlorophenol, but not with 3-chlorophenol. Reductive dechlorination of PCP in anaerobic samples resulted in the accumulation of 3-chlorophenol. In most anaerobic replicates, 3-chlorophenol was degraded with the appearance of detectable, but not quantifiable amounts of phenol. These results indicate excellent potential for remediation at the site using the indigenous microorganisms under both aerobic and anaerobic conditions. However, a fraction of the PCP was unavailable for degradation.