固定化白腐真菌处理含酚废水

研究了固定化白腐真菌在含酚废水处理中的应用,培养和固定了能有效降解含酚废水的白腐真菌,并用固定化的白腐真菌处理了各种条件(载体、浓度、pH和温度)下的含酚废水。利用静态实验,分析了去除效果的影响因素,并初步探讨了其降解机理。实验结果表明,白腐真菌去除酚类化合物的最佳条件为以木屑为载体、含酚废水浓度为250 mg/L以下、pH=6.5、温度为30℃,去除率可达89.97%。     

白腐菌处理染料废水的研究进展

白腐菌是一种可有效处理染料废水的丝状真菌，它可通过其分泌的特殊的降解酶系或其他机制将各种人工合成的染料彻底降解为CO2和H2O，同时，对脱色具有良好的作用。本文就白腐菌的生物学特性及其对染料的降解酶系，机理和白腐菌发酵的主要影响因子，白腐菌处理染料废水的有关研究及应用现状进行了综述。     

白腐菌处理染料废水的研究进展

白腐菌是一种可有效处理染料废水的丝状真菌 ,它可通过其分泌的特殊的降解酶系或其他机制将各种人工合成的染料彻底降解为CO2 和H2 O ,同时 ,对脱色具有良好的作用。本文就白腐菌的生物学特性及其对染料的降解酶系、机理和白腐菌发酵的主要影响因子、白腐菌处理染料废水的有关研究及应用现状进行了综述     

白腐菌应用于堆肥处理含木质素废物的研究

白腐菌对木质素具有较强的降解能力。通过在含大量木质素的模拟垃圾堆肥中采取添加白腐菌菌剂与不添加该菌剂2组实验对比，在相同堆肥处理条件下，接种菌剂的堆肥中木质素总量由27498．8mg降至15438mg，降解率达43．86％，远高于未接种菌剂的堆肥中木质素的降解率，表明白腐菌可有效用于含木质素废弃物的堆肥处理，并有望于加速堆肥腐熟，提高堆肥效率。     

白腐真菌生化降解酸性染料废水的效果研究

利用白腐真菌生化降解酸性染料废水,对其效果进行了研究,并进一步分析生化降解过程ＣＯＤ值出现振荡现象及不彻底的原因。     

白腐真菌降解经微电解预处理二硝基重氮酚废水的研究

利用自行培养、驯化的白腐真菌,对经过微电解预处理的二硝基重氮酚(DDNP)废水进行了生物降解试验.结果表明,经过微电解预处理后的DDNP废水(含CODCr467 mg/L)经生化处理108 h后,出水中CODCr在131 mg/L左右,达到国家二级排放标准;其中的苯胺类、硝基类的去除率达到99.9%以上,达到国家一级排放标准.对试验所获得的时间序列进行动力学研究结果证明,白腐真菌降解经微电解预处理后的DDNP废水的反应为准一级动力学反应.     

白腐菌应用于堆肥处理含木质素废物的研究

白腐菌对木质素具有较强的降解能力。通过在含大量木质素的模拟垃圾堆肥中采取添加白腐菌菌剂与不添加该菌剂2组实验对比,在相同堆肥处理条件下,接种菌剂的堆肥中木质素总量由274988mg降至15438mg,降解率达4386%,远高于未接种菌剂的堆肥中木质素的降解率,表明白腐菌可有效用于含木质素废弃物的堆肥处理,并有望于加速堆肥腐熟,提高堆肥效率。     

木质纤维素水提物促进白腐菌降解孔雀绿研究

对经白腐菌处理的木质纤维素水提物能否促进白腐菌对孔雀绿的降解及其反应机制进行了研究,并探讨了不同木质纤维素组分对白腐菌降解孔雀绿的影响.结果表明,经白腐菌处理不同时间的木质纤维素水提物均能促进白腐菌对孔雀绿的降解,该类物质的加入能缩短白腐菌生长周期及漆酶分泌周期;限氮培养基更有利于白腐菌对孔雀绿的脱色,半纤维素的加入对白腐菌降解孔雀绿的促进作用最为明显.     

改性膨润土处理酸性含铅废水

探讨了用改性膨润土处理蓄电池厂酸性含铅废水的新工艺。实验结果表明，此法成本低、效果好且简便易行，并根据实验结果，为某蓄电池厂设计了一个酸性含铅废水的处理方案。     

活性炭三维电极法对印染废水的处理研究

对三维电极方法处理印染废水进行了实验研究，初步探讨了活性炭三维电极法处理印染废水的机理，对影响处理效果的各种要素，如反应时间、槽电压和pH值等进行了条件实验，得出了活性炭三维电极法处理印染废水的最佳运行条件为：停留时间120～180min，槽电压25～30V，进水pH值6．5～75。结果表明，该反应器能有效地降低废水色度，有较高的COD去除效率，并能提高印染废水的可生化性。     

应用白腐真菌技术处理难降解有机物的研究进展

本文综述了白腐真菌的生物学特性及其在清洁生产、各种难降解有机物处理中的应用和应用基础研究方面的进展 ,探讨了白腐真菌应用的趋势。     

Removal of estrogenic activity of natural steroidal hormone estrone by ligninolytic enzymes from white rot fungi

Natural steroidal hormone estrone (E1) was treated with the white rot fungus Phanerochaete sordida YK-624 under ligninolytic condition with low-nitrogen and high-carbon culture medium. E1 decreased by 98% after 5 d of treatment and the activities of ligninolytic enzymes, manganese peroxidase (MnP) and laccase, were detected during treatment, which suggested that the disappearance of E1 is related to ligninolytic enzymes produced extracellularly by white rot fungus. Therefore, E1 was treated with MnP and laccase prepared from the culture of white rot fungi. HPLC analysis demonstrated that E1 disappeared completely in the reaction mixture after 1 h of treatment with either MnP or laccase. Using the yeast two-hybrid assay system, it was also confirmed that both enzymatic treatments completely removed the estrogenic activity of E1 after 2 h. These results strongly suggest that ligninolytic enzymes are effective in removing the estrogenic activity of E1.     

白腐真菌对染料脱色及降解过程机理和影响因素

许多白腐真菌对染料具有广谱的脱色和降解能力 ,其脱色及降解作用可能主要是由于其在次生代谢阶段产生的木质素过氧化酶LiPs和锰过氧化酶MnPs所致。培养条件对白腐真菌脱色及降解活性有较大的影响 ,在培养基中加入藜芦醇和二价锰等能够显著提高木质素过氧化酶的产生 ;富氮培养基会抑制LiPs的生成 ;硫脲、叠氮化物、氰化物等均能明显地抑制白腐真菌的脱色及降解活性 ;缓冲液的选择对维持稳定的 pH值和菌丝的形态有一定作用 ,从而影响其脱色效果 ;富氧环境是一切白腐真菌对染料进行脱色和降解的必要条件 ;适度的搅拌混合有利于反应时的物质之间传递 ;一般地 ,在培养时间达到 3天以后白腐真菌才能达到较高的脱色与降解活性。染料分子大小和结构及其基团的位置对脱色及降解效果有明显影响。使用特殊填料极大地提高处理系统中的生物量以克服真菌生长速度相对较慢、提高处理能力是该技术今后的研究重点。     

Chlorometabolite production by the ecologically important white rot fungus Bjerkandera adusta.

Two strains of the basidiomycete, Bjerkandera adusta (DAOM 215869 and BOS55) produce in static liquid culture, phenyl, veratryl, anisyl and chloroanisyl metabolites (CAM's) (alcohols, acids and aldehydes) as well as a series of compounds not previously known to be produced by Bjerkandera species: 1-phenyl, 1-anisyl, 1-(3-chloro-4-methoxy) and 1-(3,5-dichloro-4-methoxy) propan-1,2-diols, predominantly as erythro diastereomers with IR, 2S absolute configurations. 1-Anisyl-propan-1,2-diol and 1-(3,5-dichloro-4-methoxy)-propan-1,2-diol are new metabolites for which the names Bjerkanderol A and B, respectively, are proposed. Experiments with static liquid cultures supplied with 13C6- and 13C9-L-phenylalanine showed that all identified aromatic compounds (with the exception of phenol) can be derived from L-phenylalanine. For the aryl propane diols, the 13C label appeared only in the phenyl ring and the benzylic carbon, suggesting a stereoselective re-synthesis from a C7 and a C2-unit, likely aromatic aldehyde and decarboxylated pyruvate, respectively. Other compounds newly discovered to be derived from phenylalanine by this white rot fungus include phenylacetaldehyde and phenylpyruvic, phenylacetic, phenyllactic, mandelic and phenyl glyoxylic (benzoyl formic) acids. For both strains, cultures supplied with Na37Cl showed incorporation of 37Cl in all identified chlorometabolites. Veratryl alcohol and the CAM alcohols, which occur in both strains and can be derived from L-phenylalanine (all 13C-labelled), have reported important physiological functions in this white rot fungus. Possible mechanisms for their formation through the newly discovered compounds are discussed.     

Effect of Tween 80 and beta-cyclodextrin on degradation of decabromodiphenyl ether (BDE-209) by White rot fungi

The environmental safety of decabromodiphenyl ether (BDE-209), a widely used flame retardant, has been the topic of controversial discussions during the past several years. Degradation of BDE-209 into lower brominated diphenyl ether congeners, exhibiting a higher bioaccumulation potential, has been a critical issue. White rot fungi are known to degrade a wide variety of recalcitrant pollutants. In this work, white rot fungi were used to degrade BDE-209 in liquid culture medium, and the effects of Tween 80 and beta-cyclodextrin on BDE-209 degradation by white rot fungi were evaluated. On the basis of these results, it appears that BDE-209 could be degraded by white rot fungi, and Tween 80 and beta-cyclodextrin can both increase the biodegradation. The best result in Tween 80 experiments was obtained at a Tween 80 concentration of 500mgl(-1) within 10d, which showed 96.5% (w/w) BDE-209 transformed. Tween 80 at a high concentration will restrain the fungal growth and the degradation of BDE-209. However, beta-cyclodextrin had positive effects both on the BDE-209 degradation and the fungal growth.     

白腐真菌的广谱生物降解性研究进展

白腐真菌由于能够降解木质素而在地球的碳循环中发挥着不可或缺的作用.由胞外的过氧化物酶类和其他次级代谢产物组成的木质素降解系统除了能够降解木质素外,对众多的异生物质也具有广谱的生物降解性,赋予了白腐真菌巨大的环境工业应用潜力.对白腐真菌的木质素降解系统和其广谱的生物降解性进行了介绍与展望.     

Bioremediation of crude oil polluted soil by the white rot fungus, <Emphasis Type="Italic">Pleurotus tuberregium</Emphasis> (Fr.) Sing.

Bioremediation has become an attractive alternative to physicochemical methods of remediation of polluted sites. White rot fungi (WRF) are increasingly being investigated and used in bioremediation, because of their ability to degrade an extremely diverse range of very persistent or toxic environmental pollutants. The white rot fungus, Pleurotus tuberregium, was examined for its ability to ameliorate crude oil polluted soil. This was inferred from the ability of the polluted soil to support seed germination and seedling growth in Vigna unguiculata, at 0, 7 and 14 days post treatment. Results obtained from the present study showed that bioremediation of soil contaminated with crude oil was possible, especially when the fungus had been allowed to establish and fully colonize the substrate mixed with the soil. There were significant improvements in % germination, plant height and root elongation values of test plants, when seeds were planted 14 days post soil treatment. At 1 to 5% crude oil pollution, % germination values were comparable with the values in control plants in the 14 days treatment, and significantly higher than values obtained in the day 0 treatment. Also, at the highest level of crude oil pollution (15%), there was about 25% improvement in % germination value over the 0 day treatment. This trend of improvement in values was also observed for plant height, root elongation and biomass accumulation as well as decreased total hydrocarbon content.     

Ligninase-mediated transformation of 4,4′-dibromodiphenyl ether (BDE 15)

The structurally related hydroxylated polybrominated diphenyl ether (PBDE) like hydroxylated 4,4′-dibromodiphenyl ether widely occur in precipitation, surface water, and biotic media. The origins of hydroxylated PBDEs (OH-PBDEs) are of particular interest due to their greater toxic potencies than the corresponding PBDEs. We studied the transformation behavior and products of 4,4′-dibromodiphenyl ether (BDE 15) mediated by lignin peroxidase (LiP), an extracellular enzyme that is produced by certain white rot fungus and is widely present in the natural environment. We found that BDE 15 can be effectively transformed through the reaction mediated by LiP, and two different mono-OH-dibromodiphenyl ethers were identified by using gas chromatography–mass spectrometry (GC-MS) and GC-MS/MS. In particular, we compared the reaction behavior for systems variously containing natural organic matter (NOM) and/or veratryl alcohol (VA), a metabolite that certain fungus produces along with LiP in nature. It was found that the VA’s enhancement effect on LiP performance was impaired by the presence of NOM. The findings in this study provide useful information for better understanding the origins of OH-PBDEs found in the environment.     

Degradation of the antifouling compound Irgarol 1051 by manganese peroxidase from the white rot fungus Phanerochaete chrysosporium

Irgarol 1051 (2-methylthio-4-tert-butylamino-6-cyclopropylamino-s-triazine), a derivative of s-triazine herbicide, is an antifouling compound used as an alternative to organotins. The compound is highly persistent and is known to be biodegraded only by the white rot fungus, Phanerochaete chrysosporium. We used partially purified manganese peroxidase (MnP) prepared from P. chrysosporium to evaluate its capacity to degrade Irgarol 1051. MnP degraded Irgarol 1051 to two major products, one identified as M1 (identical to GS26575, 2-methylthio-4-tert-butylamino-6-amino-s-triazine) and the other not identified but with same mass spectrum as M1 and a different ultraviolet spectrum. This report clearly demonstrates that this ligninolytic enzyme is involved in the degradation of Irgarol 1051.