Correlation of Ligninolytic Enzymes from the Newly-Found Species Trametes versicolor U97 with RBBR Decolorization and DDT Degradation

Thirty strains of fungi collected from nature were investigated for their ability to grow on agar medium contaminated with Remazol Brilliant Blue R (RBBR) and 1,1,1-trichloro-2,2-bis(4-chlorophenyl)ethane (DDT). The results showed that strain U97, later identified as Trametes versicolor, was the most active decomposer. This fungus decolorized 85?% of RBBR in 6?h and degraded 71?% of DDT in 30?days. In RBBR decolorization, high-performance liquid chromatography analysis revealed that two peaks were identified as metabolic products. Among inducers for ligninolytic enzymes, only veratryl alcohol improved RBBR decolorization and DDT degradation by 93?% and 77?%, respectively. A partial least squares method using Minitab 15 showed that lignin peroxidase exhibited a positive correlation to the abilities of T. versicolor U97 to decolorize RBBR and degrade DDT. A multivariate linear equation, with the same values of ligninolytic activity during RBBR decolorization and DDT degradation, revealed that 1?% RBBR decolorization represented 1.16?% DDT degradation. Screening with agar or liquid medium and improvement of the mathematical modeling could have practical importance in the exploitation of T. versicolor U97 for the removal of DDT on a commercial scale.     

Oxidative transformation of natural and synthetic phenolic mixtures by Trametes versicolor laccase

The efficiency of Trametes versicolor laccase in the transformation of phenols (caffeic acid, catechol, hydroxytyrosol, methylcatechol, protocatechuic acid, syringic acid, m-tyrosol, 3-hydroxybenzoic acid, 3-hydroxyphenylacetic acid, 2,6-dihydroxybenzoic acid, 4-hydroxybenzaldehyde) usually present in waste water, such as that derived from an olive oil factory, was investigated. According to their response to 24 h laccase action the 11 phenolic compounds were classified in three groups: reactive (88-100% transformation), intermediate reactive (transformation lower than 50%), and recalcitrant (not transformed at all). The enzyme was able to transform the 11 substrates even when they were present in a mixture and also toward a phenolic extract from a Moroccan olive oil mill waste water (OMW) sample. The disappearance of protocatechuic, 3-hydroxyphenylacetic, and 2,6-dihydroxybenzoic acids, and 4-hydroxybenzaldehyde was enhanced whereas that of caffeic acid and m-tyrosol was depressed when the phenols were present in the mixture. A reduction of enzyme activity occurred in single and/or complex phenolic mixtures after enzymatic oxidation. No correspondence between phenol transformation and disappearance of enzymatic activity was, however, observed. The overall results suggest that laccases are effective in the transformation of simple and complex phenolic mixtures.     

Kinetic and Thermodynamic Studies of Chlorinated Organic Compound Degradation by Siderite-Activated Peroxide and Persulfate

The efficacy of two oxidant systems, iron-activated hydrogen peroxide (H₂O₂) and iron-activated hydrogen peroxide coupled with persulfate (S₂O₈ ^2?), was investigated for treatment of two chlorinated organic compounds, trichloroethene (TCE) and 1,2-dichloroethane (DCA). Batch tests were conducted at multiple temperatures (10–50 °C) to investigate degradation kinetics and reaction thermodynamics. The influence of an inorganic salt, dihydrogen phosphate ion (H₂PO₄ ^?), on oxidative degradation was also examined. The degradation of TCE was promoted in both systems, with greater degradation observed for higher temperatures. The inhibition effect of H₂PO₄ ^? on the degradation of TCE increased with increasing temperature for the iron-activated H₂O₂ system but decreased for the iron-activated hydrogen peroxide-persulfate system. DCA degradation was limited in the iron-activated hydrogen peroxide system. Conversely, significant DCA degradation (87% in 48 h at 20 °C) occurred in the iron-activated hydrogen peroxide-persulfate system, indicating the crucial role of sulfate radical (SO₄ ^??) from persulfate on the oxidative degradation of DCA. The activation energy values varied from 37.7 to 72.9 kJ/mol, depending on the different reactants. Overall, the binary hydrogen peroxide-persulfate oxidant system exhibited better performance than hydrogen peroxide alone for TCE and DCA degradation.     

地膜降解物对土壤微生物群落结构和多样性的影响

[目的]研究降解地膜残余组分对土壤微生物群落结构和多样性的影响,为环境友好型地膜研发过程中选择对土壤环境有最小负效应的聚乙烯分子量和降解模式提供理论参考。[方法]以L9(34)设计试验,采用PCR-DGGE检测技术分析混入地膜粉末的土壤在3a后的土壤微生物群落结构。[结果]土壤自身性质是影响土壤微生物群落结构和多样性变化的主要因素。就聚乙烯因素而言,Mn=2 000(数均分子量,下同)和线性低密度聚乙烯(LLDPE)在以大残留量处理的土壤中的微生物群落结构较之对照处理有明显变化;混入小分子量聚乙烯、大分子量大残留量聚乙烯的土壤中微生物群落多样性丰富。不同处理的土壤微生物复杂系数分别增加了18.7%和2.6%。[结论]不同处理间土壤微生物群落结构和多样性有明显差异,且各处理组土壤微生物的数量与相应对照组相比,多表现出增加的趋势。     

复合菌剂对小麦秸秆降解速率、土壤酶和土壤 微生物类群的影响

秸秆在农业上的有效利用日益受到关注。针对秸秆还田后腐解难的问题,本文选择7株纤维素降解菌种进行复配:拟茎点霉B3、茎点霉YY11、绿色木霉、里氏木霉、根霉、黑曲霉、蜂房芽孢杆菌。最终采用两种复配液体菌剂A(B3、YY11、绿色木霉和蜂房芽孢杆菌)、C(上述7个菌种),同时制作与液体菌剂A、C分别对应的固体菌剂B、D。探讨了复合菌剂对秸秆降解速率的促进作用和对土壤质量的提升效果。结果表明,4种菌剂均可促进小麦秸秆降解,改善土壤生物学特性,增加土壤养分,改良玉米农艺学性状。综合评价各个指标,菌剂B(B3、YY11、绿色木霉、蜂房芽孢杆菌;固体剂型)的表现最好,且玉米总产量比市售秸秆腐熟剂处理高20.72%。总之,本研究表明小麦秸秆还田后和联合菌剂使用能明显提高土壤降解功能,并且为实现经济可持续的农业管理方式提供了一种有应用前景的秸秆腐熟剂组合方式。     

Kinetic and Equilibrium Sorption Studies of Ceftriaxone and Paracetamol by Surfactant-Modified Zeolite

An organo-zeolite was prepared by loading hexadecyltrimethylammonium (HDTMA) onto clinoptilolite and was used to remove ceftriaxone sodium and paracetamol in aqueous solutions. Batch experiments were conducted to perform kinetics and sorption isotherms at 25 °C and 100 rpm. The results indicate that the equilibration times were 24 h for ceftriaxone sodium and 9 h for paracetamol. Furthermore, sorption capacities were 0.7288 and 0.0058 mg/g, respectively. The data were treatment with different models including pseudo first order, second order, and Elovich, the results suggested a chemical adsorption mechanism, and the adsorption equilibrium data for the two drugs show that they follow a linear trend, indicating a partitioning mechanism. Physicochemical properties such as solubility, log Kow, and pka play an important role in the adsorption process. Finally, the values obtained for zero charge point (ZPC) for zeolitic materials were 6.90, 6.94, and 6.90 for natural zeolite (ZN), sodium zeolite (ZNa), and zeolite modified surface at 30 mM HDTMA (ZMS-30), respectively.     

The Production of Ligninolytic Enzymes by Marine-Derived Basidiomycetes and Their Biotechnological Potential in the Biodegradation of Recalcitrant Pollutants and the Treatment of Textile Effluents

Filamentous fungi derived from marine environments are well known as a potential genetic resource for various biotechnological applications. Although terrestrial fungi have been reported to be highly efficient in the remediation of xenobiotic pollutants, fungi isolated from the marine environment may possess biological advantages over terrestrial fungi because of their adaptations to high salinity and pH extremes. The present study describes the production of ligninolytic enzymes under saline and non-saline conditions and the decolorization of Remazol Brilliant Blue R (RBBR) dye by three basidiomycetes recovered from marine sponges (Tinctoporellus sp. CBMAI 1061, Marasmiellus sp. CBMAI 1062, and Peniophora sp. CBMAI 1063). Ligninolytic enzymes were primarily produced by these fungi in a salt-free malt extract and malt extract formulated with artificial seawater (saline condition). CuSO₄ and wheat bran were the best inducers of lignin peroxidase and manganese peroxidase activity. RBBR was decolorized up to 100% by the three fungi, and Tinctoporellus sp. CBMAI 1061 was the most efficient. Our results revealed the biotechnological potential of marine-derived basidiomycetes for dye decolorization and the treatment of colored effluent as well as for the degradation of other organopollutants by ligninolytic enzymes in non-saline and saline conditions that resemble the marine environment.     

灰棕紫泥土脲酶动力学及反应条件研究

以底物浓度、pH、温度、培养时间作为处理,采用靛酚蓝比色法测定灰棕紫泥土脲酶动力学参数和反应条件。结果表明,灰棕紫泥土脲酶酶促反应V0与[S]的关系呈二次线性关系,[S]为11.67%时,V0达极大值;Km值在中性、35℃环境下较小,Vmax值在中性环境下较大,与温度呈二次正相关;脲酶酶促反应最适pH值为6.9、最适培养时间为24h、最适底物浓度为10%、最适温度为45℃。     

兽药磺胺间甲氧嘧啶对土壤呼吸及酶活性的影响

为评价兽药污染对土壤生态环境造成的潜在环境风险,采用室内培养的方法,研究了兽药抗生素磺胺间甲氧嘧啶对黄潮土土壤微生物呼吸及土壤酶活性的影响。结果表明,磺胺间甲氧嘧啶可显著影响土壤呼吸强度,抑制率和激活率分别可达72%和254%,药物对土壤酶活性的影响小于其对土壤呼吸强度的影响。在添加磺胺间甲氧嘧啶的前11 d,其对脲酶活性的影响主要以抑制作用为主;药物对蔗糖酶活性的影响较为明显,最大抑制和激活率可分别达到18%和30%;磺胺间甲氧嘧啶作用于过氧化氢酶和磷酸酶主要表现为激活效应,最大激活率分别为17%和25%。在试验浓度范围内,土壤微生物呼吸及酶活性的抑制率或激活率呈现一定的波动性。     

超声波活化风化煤对土壤砷形态及土壤酶活性的影响

通过土培盆栽试验研究了不同超声波活化风化煤添加量0g/kg,10g/kg,20g/kg,40g/kg,60g/kg对不同浓度砷污染土壤中砷形态及土壤酶活性的影响,结果表明:活化风化煤添加量40~60g/kg,能够最有效地降低土壤中As的可移动性,增加土壤中的残渣态砷,从而降低了土壤中As的生物毒性;添加活化风化煤60g/kg条件下,污染土壤中土壤蔗糖酶活性最高,风化煤添加量40g/kg时,缓解砷抑制土壤脲酶活性的效果最好。所以活化风化煤能够有效改善砷污染土壤质量,降低生物毒性,减轻对植物的毒害作用。     

沼渣有机无机复混肥对土壤养分含量和酶活性的影响

通过盆栽试验研究了不同沼渣有机无机复混肥对土壤养分及酶活性的影响。结果表明:与无机肥处理相比,沼渣有机无机复混肥处理土壤有机质、全氮和有效磷含量分别提高了12.4%~26.3%、0.1%~10.3%、10.1%~30.1%,且以秸秆沼渣有机无机复混肥效果较好。有机肥处理对提高土壤过氧化氢酶活性效果显著,而沼渣有机无机复混肥处理对提高土壤脲酶活性效果较好。     

石墨烯施用后对土壤酶活性及土壤微生物群落的影响

将不同浓度的纯石墨烯和氧化石墨烯(0、100、1 000 mg/kg)分别加入潮土和红壤两种土壤中,培养56天后测定潮土和红壤中的脲酶、过氧化氢酶活性,微生物功能及遗传多样性变化。结果表明,培养0、7、14、56天后,100和1 000 mg/kg浓度的石墨烯和氧化石墨烯对红壤和潮土的脲酶和过氧化氢酶活性没有显著的影响。两种浓度的石墨烯和氧化石墨烯对红壤和潮土微生物的AWCD指数没有显著的影响,且两种土壤之间未表现出差异。对添加0、200和1 000 mg/kg氧化石墨烯的潮土进行DGGE测试分析,处理组与对照组相比增加了3个条带,测序分析认为这3个条带与鞘氨醇单细胞菌属和未被培养的细菌类似,可见氧化石墨烯对土壤中微生物有一定的影响,能引起耐受菌数量的增加。     

蚯蚓对As污染土壤酶活性及其P养分的影响

从湖南石门县的As矿区附近采集不同程度As污染的农田土壤,分别设置添加秸秆、接种蚯蚓等处理,研究蚯蚓对As污染土壤酶活性及其P养分供给的影响。结果发现,高浓度As土壤的脱氢酶活性显著低于中、低浓度As土壤,而酸性磷酸酶活性及有效P含量则与之相反。蚯蚓+20g秸秆处理在50d时脱氢酶活性最高,而酸性磷酸酶活性则是秸秆处理在100d时最高,且接种蚯蚓和施用秸秆有利于土壤P素的释放。结果表明在施用秸秆条件下接种蚯蚓有利于改善As污染土壤的养分供给,从而改善根际营养。     

番茄工厂化育苗木糖渣基质与肥料配比研究

研究了以木糖渣为主料配合粉煤灰、煤渣与尿素、磷酸二氢钾、烘干鸡粪配成的不同基质对番茄幼苗生长的影响。结果表明：以６０％的木糖渣、３０％的煤灰、１０％的煤渣,每７２孔穴盘加尿素５ｇ,磷酸二氢钾５ｇ,鸡粪２０ｇ的配方做基质可代替蛭石、草炭用于蔬菜工厂化育苗降低蔬菜工厂化育苗成本。     

不同添加浓度DEHP在黑土中的降解特点及对酶活性的影响

[目的]本研究以邻苯二甲酸二-(2-乙基己基)酯(DEHP)为目标化合物,采用室内培养试验的方法,对不同浓度梯度的DEHP在黑土中的降解过程和对土壤酶活性影响进行了研究.[方法]在DEHP降解试验中,使添加到黑土中的 DEHP 浓度分别为0 mg kg-1、5 mg kg-1、10mg kg-1、20 mg kg-1、...     

麦田不同灌水处理对土壤酶活性时空分布的影响

以石麦15为材料,利用田间定位试验系统地研究了不同灌水处理(春季不灌水W0;春季灌拔节水75mm,W1;春季灌起身水、孕穗水和灌浆水共225mm,W3)碱性磷酸酶、脲酶、蔗糖酶活性等在0-200cm土层的垂直分布、动态变化。结果表明,随着春季灌水量减少,冬小麦生育中、后期0-80cm土层碱性磷酸酶和蔗糖酶活性呈现下降趋势,80cm以下土层的碱性磷酸酶和蔗糖酶活性呈增加的趋势;0-40cm土层的脲酶活性呈现降低的变化趋势,40-120cm土层呈现增强的趋势。籽粒产量以W3W1W0,最终的水分利用效率(WUE)则以W1处理最高。冬小麦春季适当亏缺灌溉使生长中、后期深土层的土壤酶活性增强,部分地补偿了因浅层土壤酶活性下降所导致的养分供应不足,这可能是实现节水高产的一个重要的原因。     

碳氮源对复合木质素降解菌木质素降解能力及相关酶活的影响

白腐真菌所具有的降解木质素能力源于其所产生的酶系统,碳源和氮源是其降解木质素和产酶的一个极为重要的影响因素。通过室内小麦秸秆固态发酵试验,研究了不同的碳、氮源对两株侧耳属真菌Tf1（P.pulmonarius）和JG1（P.cornucopiae）产酶活力、木质素降解和粗蛋白含量的影响。结果表明,Lip和MnP是参与复合木质素降解菌Tf1＋JG1降解小麦秸秆重要的木质素降解酶。以葡萄糖为碳源,酒石酸铵为氮源能显著提高复合木质素降解菌对木质素的降解能力,发酵9 d后小麦秸秆的失重率为14.87%,木质素含量为8.68%,木质素降解率为22.95%;粗蛋白含量为7.28%,比未发酵麦秸提高了36.84%（P〈0.05）;Lip和MnP活力分别为629.11 U.g-1和622.22 U.g-1。     

磷化铝对土壤微生物数量和酶活性的影响

为明确磷化铝对土壤微生物数量和酶活性的影响,采用室内培养的方法,研究了经0.1、1mg.g-1和10mg.g-13个浓度磷化铝熏蒸处理后,供试土壤中微生物数量和土壤酶活性的变化。结果表明,磷化铝处理土壤后,各个浓度的磷化铝对土壤细菌、真菌和放线菌数量具有抑制作用,浓度越高,抑制作用越强,但一段时间后低浓度（0.1mg.g-1）处理对土壤微生物数量的影响恢复至对照水平。磷化铝对土壤脲酶表现为抑制作用,并随浓度升高而增强;低浓度处理对土壤中的蔗糖酶活性抑制作用不明显,而高浓度（10mg.g-1）处理表现为强烈的抑制作用;各浓度处理初期对土壤过氧化氢酶表现为抑制或激活作用,但到第30d,恢复至对照水平。这说明,施入常规剂量的磷化铝对土壤微生物数量和土壤酶活性会产生一定的影响,在经过一定时间后均可恢复至对照水平。     

Equilibrium and Kinetic Studies on Biosorption of Heavy Metals by Leaf Powder of Paper Mulberry (Broussonetia papyrifera)

Paper mulberry (Broussonetia papyrifera) leaf powder was used to remove heavy metal ions from aqueous solutions. The specific uptakes of Cu (II), Pb (II), and Cd (II) by the leaf powder were 43.40?±?0.2, 43.9?±?0.5, and 30.65?±?0.9 mg g^?1, respectively, when 500 mg L^?1 of the metal solutions were used. The data fitted well to the Langmuir isotherm. The process followed the pseudo-second-order kinetic equation and intraparticle diffusion played an important role in the adsorption process. On the basis of the calculated thermodynamic parameters such as standard enthalpy (??H°), entropy (??S°) and free energy change (??G°), it was inferred that the sorption process was endothermic and spontaneous in nature. The surface properties of the leaf powder (revealed by scanning electron microscopic observations) were suitable for the metal adsorption process. Energy dispersive X-ray fluorescence analysis confirmed the sequestration of the metal ions by the leaf powder. Fourier transform infrared spectroscopy implicated that different functional groups on the leaf powder were involved in the metal adsorption process. The results obtained from this study implicated that the B. papyrifera leaf powder was a good choice as a metal adsorbent. This abundantly available natural and eco-friendly biosorbent could be effectively used to develop a technology in the future.     

一株产常温葡甘聚糖酶的芽孢杆菌的分离、鉴定及产酶发酵条件的研究

以魔芋生粉为唯一碳源的筛选培养基,从魔芋废渣中分离筛选出一株可以降解魔芋生粉的细菌菌株,编号为LS-6。根据16SrDNA序列和生理生化特性,将该菌株鉴定为枯草芽孢杆菌Bacillus subtilis。胞内外葡甘露聚糖酶酶活分析结果表明,LS-6产生的葡甘聚糖酶为胞外酶。LS-6产生葡甘聚糖酶的最佳培养基组分和条件是：1%魔芋生粉,0.5%酵母粉,0.5%NaCl,培养基初始pH为6.0,最佳发酵条件是25℃,摇床转速200r/min,培养48h。酶解产物的高效液相色谱分析结果表明,LS-6粗酶液的酶解产物主要为葡萄糖和甘露糖。LS-6的分离为进一步克隆常温葡甘聚糖酶基因和产酶工程菌的构建奠定了基础。