耐过氧化氢的锰过氧化物酶对三苯甲烷类染料的脱色

[目的]从一株白腐菌Trametes sp.SQ01中获得一种新型的锰过氧化物酶,探讨该酶的底物特异性和对过氧化氢的耐性,以及其对三苯甲烷类染料的脱色能力.[方法]通过丙酮沉淀和DEAE-cellulose 52柱层析法纯化锰过氧化物酶.利用UV-2010紫外可见分光光度法研究锰过氧化物酶对过氧化氢的耐性,同时,用紫外可见分光光度计对三苯甲烷类染料脱色效果进行分析.[结果]通过两步纯化,获得了均一性的锰过氧化物酶.该酶的最适pH和温度分别是4.5和70℃,在pH 3.0-8.0时,酶活相对稳定.该酶在二价锰离子存在下能够氧化2,6-二甲氧基苯酚、愈创木酚、2,2＇-连氮-双-(3-乙基苯并噻唑啉磺酸)和过氧化氢等化合物,同时也能作用二价锰离子.在与这些底物反应中,最适底物为过氧化氢(Km为3.7 tmmol/L).该酶具有抗过氧化氢漂白能力,锰过氧化物酶与高浓度的过氧化氢(2.5 mmol/L)作用60 min后仍能保持70％的活性.在所测试的染料中,锰过氧化物酶对结晶紫的脱色率最高达到65.8％.二价锰离子和过氧化氢对锰过氧化物酶脱色能力的影响进行研究,与孔雀绿相比,锰离子和过氧化氢对活性艳蓝脱色的影响很小.[结论]Trametes sp.SQ01锰过氧化物酶对过氧化氢的耐受性,以及对三苯甲烷类染料的高效脱色能力表明该酶在染料脱色降解方面有着广阔的应用前景.     

野生型糙皮侧耳Pleurotus ostreatus JY2746对合成染料脱色性能的评价（英文）

随着我国印染工业的不断发展,人工合成染料给环境造成严重污染,现急需开发一种成本低廉、脱色效果显著的方法治理水污染问题。本研究发现糙皮侧耳的胞外粗酶液对5种合成染料均具有良好的脱色作用,其中对结晶紫、酸性品红和考马斯亮蓝G-250(浓度为40mg/L)的最高脱色率可分别达到100%、98.67%和92.5%。糙皮侧耳在液体发酵过程中主要产生3种酶类,即漆酶、锰过氧化物酶和木质素过氧化物酶,他们分别在第12天,第7天和第8天酶活达到最高,并且第12天产生的粗酶液对染料的脱色效果最好,根据酶活高峰形成时间与脱色率之间的关系,推测糙皮侧耳分泌的漆酶对染料起主要降解作用,而锰过氧化物酶和木质素过氧化物酶起辅助作用。本研究发现发酵粗酶液较纯化的酶类工艺简单,成本低廉,因此糙皮侧耳发酵液中提取的粗酶液在染料废水脱色处理方面具有潜在的应用价值。     

猴头菌和金针菇漆酶对不同染料的降解

利用漆酶（laccase）处理染料废水是近年来研究的热点。本研究以猴头菌Hericium erinaceus和金针菇Flammulina filiformis的发酵液为试验材料,通过硫酸铵沉淀、离子交换层析和超滤等方法,对发酵液中的漆酶进行了初步的分离纯化,然后分别研究了两种初提纯漆酶及其与小分子介体组成的漆酶介体系统（laccase-mediator system,LMS）对12种常用染料的降解效果。结果表明,猴头菌的初提纯漆酶对甲基红、铬黑T、孔雀绿和活性蓝R都具有很好的降解效果,反应24h后,降解率分别为79.6%、66.8%、80.3%和64.6%,且表现出时间依赖性,而对其他染料的降解效果不明显。当反应体系中加入介体2,2′-连氮基-双-(3-乙基苯并二氢噻唑啉-6-磺酸)二铵盐[2,2′-azinobis-(3-ethylbenzothiazoline-6-sulphate),ABTS]后,可增加猴头菌漆酶对考马斯亮蓝、结晶紫和孔雀绿的降解率,分别提高到33.7%、45.6%和94.2%。金针菇初提纯漆酶对孔雀绿、活性艳橙K-7R和活性红KD-8B都具有一定的降解效果,降解率分别为37.8%、39.9%和49%,也表现出了明显的时间依赖性。当反应体系中也加入ABTS后,金针菇漆酶对活性红KM-8B的降解率明显增加,由9.7%增加到58.2%。以上研究为猴头菌和金针菇漆酶在染料废水处理领域的应用提供了科学依据。     

三种白腐真菌脱色噻嗪染料亚甲基蓝

本研究通过含亚甲基蓝染料的固体培养基,从19株白腐真菌菌株中分离获得3个脱色能力较强的菌株,其在平板上的脱色圈大小分别为7.5cm、6.8cm和5.5cm。鉴定其为：云芝栓孔菌Trametes versicolor（ZT-197）,绒毛栓孔菌Trametes pubescens（ZT-230）和亚黑管孔菌Bjerkandera fumosa（ZT-307）。其中,ZT-230对染料亚甲基蓝的脱色能力最强,可以将染料浓度为50mg/L的100mL液体培养基在6d之内100%脱色,而ZT-197和ZT-307在接种第10天时的脱色率为98%和80%。同时测定了3株白腐真菌在降解染料过程中的漆酶、锰过氧化物酶和木素过氧化物酶3种酶活力的规律：ZT-197和ZT-230均可分泌Lac和MnP两种酶,ZT-307只分泌LiP。本研究说明绒毛栓孔菌ZT-197在印染废水治理方面具有较好的应用前景。     

胶质射脉革菌漆酶的复合诱导及其脱色性能

[目的]研究复合诱导对胶质射脉革菌BBEL0901产漆酶的影响及其粗酶液对染料的脱色性能。[方法]采用分光光度法测定漆酶活性及其染料脱色性能。[结果]甘草渣和Cu2+对BBEL0901产漆酶均有促进作用,于发酵的第6 d向含甘草渣的低氮培养基中添加Cu2+(0.5 mmol/L)对漆酶的协同诱导作用最显著,活性达325.1 U/m L,分别为Cu2+单独诱导、甘草渣单独诱导和未诱导的4倍、14.4倍和19.8倍。粗酶液对不同结构的染料均有较强的脱色能力,对三苯甲烷类染料的脱色效果最好,脱色率达80%以上。[结论]甘草渣与Cu2+对BBEL0901漆酶具有协同诱导作用,酶活最高可达325.1 U/m L,产业化潜力大,所得粗酶液在染料脱色方面具有良好的应用前景。     

疣孢漆斑菌Myrothecium verrucaria GH-01漆酶的纯化和酶学性质研究

疣孢漆斑菌具有生长周期短,分泌漆酶酶活高等特点。利用已分离得到的疣孢漆斑菌GH-01(Myrothecium verrucaria GH-01)发酵产生粗酶液。进而通过分级沉淀、透析和层析的方法对漆酶粗酶液进行纯化。SDS-PAGE和Native-PAGE结果表明纯化可获得具有漆酶活性的单体蛋白。酶学性质研究表明,该漆酶催化最适温度为40℃,在底物ABTS存在条件下的最适p H值为4.0,且在低温及碱性条件具有较好的稳定性。此外通过漆酶对4大类染料脱色能力的研究,发现该漆酶对偶氮类的橙黄Ⅰ和蒽醌类的茜素红脱色有较好的脱色效果,反应1 h脱色率达80%以上;对三苯甲烷类的碱性品红脱色能力较弱,脱色率只能达到20%左右;脱色率最差的是杂环类的亚甲基蓝。在含10 U漆酶的体系中,对50 mg/L的染料降解效果相对最佳。     

宏基因组来源耐Mn2+、热稳定细菌漆酶的分子克隆及酶学特性

【背景】漆酶和锰过氧化物酶(Manganese peroxidase,Mnp)是木质素降解的主要酶,二者有协同效应。Mnp活性依赖于Mn~(2+),而Mn~(2+)是大多数漆酶的抑制剂。【目的】获得耐Mn~(2+)的细菌漆酶用于木质素降解。【方法】构建许昌市某污水河污泥宏基因组文库,通过活性筛选获得细菌漆酶基因lac1542。使用大肠杆菌异源表达Lac1542,研究纯化后的重组蛋白酶学性质并进一步检测了含Lac1542复合酶系降解木质素能力。【结果】测序结果显示lac1542编码一个含513个氨基酸的蛋白。以ABTS为底物Lac1542最适反应pH为4.0,在pH 3.0-6.5范围内酶活性稳定。最适反应温度是75°C,在70°C以下酶活性稳定;100 mmol/L的Mn~(2+)仍能提高酶的活性。动力学参数研究发现,该酶的最适底物顺序为:ABTS丁香醛联氮儿茶酚2,6-DMP愈创木酚。Lac1542/Mnp复合酶系对木质素降解率为47.8%,比单独使用Mnp木质素降解率(22.4%)提高25.4%。Lac1542/Mnp/灰盖鬼伞过氧化物酶(Coprinus cinereus Peroxidase,CIP)复合酶系木质素降解高达71.5%,比Mnp/CIP酶系木质素降解率(48.9%)提高22.6%,加入Lac1542后的复合酶系能明显提高木质素的降解率。【结论】Lac1542的可溶性表达、耐受高浓度Mn~(2+)、热稳定性使得Lac1542可以替代一些经典的真菌漆酶应用于制浆、造纸、纤维素乙醇生产、染料脱色等工业。     

木质素降解菌株的分离及其降解玉米秸秆过程中产酶特点

【目的】筛选高效降解木质素的菌株,并研究其以玉米秸秆为底物时木素降解酶活性。【方法】本研究以愈创木酚培养基和苯胺蓝培养基从吉林省不同经纬度的自然朽木及腐朽玉米秸秆土壤样品中分离、筛选得到高效降解木质素的菌株,并对其形态学鉴定,通过ITS序列分析构建系统发育树,分析菌株的分类地位。通过秸秆固体发酵过程产生的胞外木质素酶的活性分析,选出高效秸秆降解菌。【结果】筛选出1株高效降解秸秆的真菌,对其进行形态学特征和ITS序列分析,命名为白囊耙齿菌W2(Irpex lacteus W2)。该菌株在4–8 d内产生的锰过氧化物酶(Manganese peroxidase)呈上升趋势,并且在8 d达到峰值86.31 U/mL,与黄孢原毛平革菌(Phanerochaete chrysosporium)的最高酶活力45.86 U/mL相比,高出了88.20%(P0.01);该菌株的漆酶(Laccase)活力8 d时达到20.60 U/mL,比对照高40.76%(P0.05)。【结论】本研究分离到一株具有较强降解秸秆能力的真菌,初步鉴定为Irpex lacteus W2,具有较强的降解秸秆能力,其降解秸秆过程中产生较高的锰过氧化物酶与漆酶活力。     

贝壳状革耳菌染料脱色作用的研究

利用比色法研究了贝壳状革耳菌产漆酶体系在不同情况下对两种不同类型合成染料的降解脱色,结果表明,染料在较低浓度（10mg/L)时,漆酶对其降解迅速而彻底,pH值,培养方式（静态培养,摇瓶培养）对降解作用都有较大的影响;通过在不同时间（0d,6d,18d)向产酶体系中加入染料证实了漆酶活性与染料脱色率呈正相关。     

藜芦醇和吐温80对白腐菌产木质素降解酶的影响及在偶氮染料脱色中的作用

担子菌PM2在限氮液体培养下,分泌木质素过氧化物酶和锰过氧化物酶;藜芦醇、吐温 80的补充,提高了该菌锰过氧化物酶的产生,获得的最大锰过氧化物酶Mnp酶活为254.2u/L、190.2 u/L,分别是对照的3.4倍和2.5倍。选择三种偶氮染料,在染料体系下,进一步分析藜芦醇、吐温 80对担子菌PM2产过氧化物酶及染料脱色的影响。结果表明,担子菌PM2分泌的锰过氧化物酶Mnp与染料脱色有关,脱色程度受其分子结构特征影响;吐温80的补充,更有利于染料的脱色降解,48h后三种染料均可达到80%以上的脱色率。     

Decolorization of azo and triphenylmethane dyes by Pycnoporus sanguineus producing laccase as the sole phenoloxidase

Partial decolorization of two azo dyes (orange G and amaranth) and complete decolorization of two triphenylmethane dyes (bromophenol blue and malachite green) was achieved by cultures in submerged liquid culture producing laccase as the sole phenoloxidase. Enzyme production could be correlated with dye decolorization, with sorption of dye to mycelia accounting for less than 3% of dye removal.     

红平菇产漆酶条件优化及对孔雀绿染料脱色的研究

采用LNAS(低氮天冬酰胺-琥珀酸)培养基添加方式,对红平菇Pleurotus djamor HP1进行培养,检测不同时间培养液对不同底物的氧化作用,进而得到光密度值的变化情况,作为漆酶的产生及活性测定的主要依据。结果表明:在含Cu2+的培养液中漆酶最大酶活为235.4 U/L。含Cu2+的培养液添加底物木屑后漆酶最大酶活为458.8 U/L。提取经优化筛选后的培养基培养出的漆酶粗酶液,对4种具有不同化学结构的染料进行了脱色试验。结果表明:三苯基甲烷类的孔雀绿在6 h时脱色率为87.5%,蒽醌类的SN4R在24 h时脱色率为49.4%,偶氮类的甲基橙在24 h时脱色率为45%,杂环类的中性红在24 h时脱色率为23.6%。因此,显示出红平菇漆酶对孔雀绿染料脱色具有较大的应用潜力,进而对废水处理具有更好的应用前景。     

一株新分离的云芝栓孔菌Z-1应用于木质素降解及染料脱色

木质素是一种非结晶性的复杂三维网状酚类高分子聚合物,被认为是木质纤维素生物质抗降解的天然屏障。探索并开发高效降解木质素的微生物资源已成为近些年来的研究焦点。本研究对新分离的一株具有潜在木质素降解能力的菌株Z-1开展了系列研究。首先通过形态学和系统发育分析将菌株Z-1鉴定为云芝栓孔菌Trametes versicolor。平板定性检测初步表明云芝栓孔菌T. versicolor Z-1具有较强的产过氧化物酶和漆酶能力。以木质素为唯一碳源时,T. versicolor Z-1对木质素的降解率和脱色率分别可达13.38%和26.43%。酶活检测分析表明该菌主要是通过分泌漆酶和锰过氧化物酶（manganese peroxidase,MnP）降解木质素。利用傅里叶变换红外光谱（fourier transform-infrared spectroscopy,FT-IR）、扫描电镜（scanning electron microscope,SEM）及气相色谱-质谱联用（gas chromatography-mass spectroscopy,GC-MS）对云芝栓孔菌T. versicolor Z-1降解后木质素残渣结构以及代谢物的鉴定分析结果证实了该菌对木质素的强降解能力,并表明该菌对木质素的降解途径包括酚醚键的断裂、芳香环侧链氧化裂解以及芳香环开环反应等。此外,该菌还对多种芳香类染料展现出了强的脱色能力,其中对刚果红、孔雀石绿和考马斯亮蓝R-250 3种染料的脱色率达到100%。本研究表明云芝栓孔菌T. versicolor Z-1具有应用于工业化木质素降解与芳香化合物类染料脱色的开发前景。     

刺芹侧耳产漆酶条件优化及对偶氮染料甲基橙的脱色

漆酶是一种含铜的单电子多酚氧化酶,能够催化氧化各种酚类及多种染料,在处理染料废水方面具有巨大的潜力。刺芹侧耳Pleurotus eryngii具有较强的产漆酶能力,但漆酶产量在较大程度上受环境条件限制。本文研究了氮源含量、pH、温度、金属离子等环境条件对刺芹侧耳产漆酶能力的影响,优化了其产漆酶条件,并用其粗酶液对典型偶氮类染料甲基橙进行脱色,结果表明,在氮源0.5%（W/W）、pH 5.5、温度28℃、添加5.0mmol/L Mg ²⁺的培养条件下,刺芹侧耳产漆酶能力最强,培养6d时,漆酶酶活可达78.0U/L。用优化培养的刺芹侧耳粗酶液对偶氮染料甲基橙进行脱色,28h后脱色率可达90%,脱色反应为准一级动力学反应,甲基橙并未完全矿化,而是生成小分子中间产物。     

Isolation of a malachite green-degrading Pseudomonas sp. MDB-1 strain and cloning of the tmr2 gene

The release of malachite green, a commonly used triphenylmethane dye, into the environment is causing increasing concern due to its toxicity, mutagenicity, and carcinogenicity. A bacterial strain that could degrade malachite green was isolated from the water of an aquatic hatchery. It was identified as a Pseudomonas sp. based on the morphological, physiological, and biochemical characteristics, as well as the analysis of 16S rRNA gene sequence and designated as MDB-1. This strain was capable of degrading both malachite green and leucomalachite green, as well as other triphenylmethane dyes including Crystal Violet and Basic Fuchsin. The gene tmr2, encoding the triphenylmethane reductase from MDB-1, was cloned, sequenced and effectively expressed in E. coli. These results highlight the potential of this bacterium for the bioremediation of aquatic environments contaminated by malachite green.     

Adsorption and decolorization of dyes using solid residues from Pleurotus ostreatus mushroom production

We investigated the use of solid residues from Pleurotus ostreatus mushroom production in adsorbing and decolorizing different dyes. The solid residue used in this study was composed of hemicellulose and cellulose (52.81 %), acid-insoluble lignin (25.42%), chitin (6.5%), and water extractives (14.82%). After incubating 14% (wt/vol) solid residue in distilled water for 4 h, laccase and manganese peroxidase (MnP) activities were 0.5 U/g and 12 mU/g, respectively. Enzymatic decolorization percentages were up to 100 for azure B (heterocyclic dye) and indigo carmine (indigoid dye), 74.5 for malachite green (MG) (triphenylmethane dye), and zero for xylidine (azoic dye). The optimum temperature for decolorization was in the range of 26 ∼ 36°C for all dyes. Data obtained on adsorption (enzymatic decolorization was prevented with sodium azide) at different dye concentrations and in a pH range of 3 ∼ 7 were used to plot Freundlich isotherms. The spent fungal substrate (SFS) displayed large differences in adsorption capacity, depending on the dye tested. The highest adsorption capacity was observed at pH 3 for MG, while xylidine was slightly adsorbed at pH 3 and 4 and not adsorbed at higher pH values. Laccase and MnP production were affected by the presence of the dyes. The highest enzyme levels were observed in the presence of MG, when laccase and MnP increased 1.39- and 2.13-fold, respectively. Decolorization and adsorption to SFS are both important processes in removing dyes from aqueous solutions. The application of this spent substrate for wastewater treatment will be able to take advantage of both of these dye removal processes. An important problem in bioremediation processes involving microorganisms is the amount of time required for their growth. In this report, we used the spent substrates from mushroom cultivation in wastewater treatment, thus solving the problem of waiting for microorganisms to grow.     

Bioprocess optimization of laccase production through solid substrate fermentation using Perenniporia tephropora-L168 and its application in bioremediation of triaryl-methane dye

Laccases are multi copper oxidases that can oxidize both phenolic and nonphenolic lignin related compounds. Consequently, there has been continuous demand for laccases for the oxidative degradation of phenolic dyes in effluents. In view of this, the present work was focused on laccase production by solid substrate fermentation using a newly isolated fungus Perenniporia tephropora-L168. To intensify the laccase production, the process parameters pH, nitrogen, inducer, and substrate: water ratio were optimized by using statistical model. A set of optimal conditions noted were pH 3, nitrogen 0.001 g/L; inducer 0.5% and substrate: water ratio (1:10), which yielded laccase 1,160 U/g. The crude laccase exhibited noteworthy potential to degrade a triaryl-methane dye especially Malachite green. Also, during bioremediation studies, the statistical process optimization could achieve 81% decolourization within 180 min. The laccase treatment brought chemical transformation in malachite green as evident from UV–Visible spectra, FTIR, HPLC while toxicity against bacteria and fungi was also reduced. During phytotoxicity study, effect of treated and untreated dye on germination of seed was analyzed. Interestingly, the germination index for Vigna aconitifolia and Vigna radiata was increased by two and fourfold, respectively. Overall, this work demonstrates optimized production of laccase using Perenniporia tephropora-L168 and its efficient bioremediation potential for triaryl-methane dye.     

Capacity of Irpex lacteus and Pleurotus ostreatus for decolorization of chemically different dyes

The rate and efficiency of decolorization of poly R-478- or Remazol Brilliant Blue R (RBBR)-containing agar plates (200 μg g⁻¹) were tested to evaluate the dye degradation activity in a total of 103 wood-rotting fungal strains. Best strains were able to completely decolorize plates within 10 days at 28 °C. Irpex lacteus and Pleurotus ostreatus were selected and used for degradation of six different groups of dyes (azo, diazo, anthraquinone-based, heterocyclic, triphenylmethane, phthalocyanine) on agar plates. Both fungi efficiently degraded dyes from all groups. Removal of RBBR, Bromophenol blue, Cu-phthalocyanine, Methyl red and Congo red was studied with I. lacteus also in liquid medium. Within 14 days, the following color reductions were attained: RBBR 93%, Bromophenol blue 100%, Cu-phthalocyanine 98%, Methyl red 56%, Congo red 58%. The ability of I. lacteus to degrade RBBR spiked into sterile soil was checked, the removal being 77% of the dye added within 6 weeks. The capacity of selected white rot fungal species to remove efficiently diverse synthetic dyes from water and soil environments is documented.     

Optimization of a culture medium for ligninolytic enzyme production and synthetic dye decolorization using response surface methodology

A Box-Wilson central composite design was applied to optimize copper, veratryl alcohol and l-asparagine concentrations for Trametes trogii (BAFC 212) ligninolytic enzyme production in submerged fermentation. Decolorization of different dyes (xylidine, malachite green, and anthraquinone blue) by the ligninolytic fluids from the cultures was compared. The addition of copper stimulated laccase and glyoxal oxidase production, but this response was influenced by the medium N-concentration, with improvement higher at low N-levels. The medium that supported the highest ligninolytic production (22.75 U/ml laccase, 0.34 U/ml manganese peroxidase, and 0.20 U/ml glyoxal oxidase) also showed the greatest ability to decolorize the dyes. Only glyoxal oxidase activity limited biodecoloration efficiency, suggesting the involvement of peroxidases in the process. The addition of 1-hydroxybenzotriazole (a known laccase mediator) to the ligninolytic fluids increased both their range and rate of decolorization. The cell-free supernatant did not decolorize xylidine, poly R-478, azure B, and malachite green as efficiently as the whole broth, but results were similar in the case of indigo carmine and remazol brilliant blue R. This indicates that the mycelial biomass may supply other intracellular or mycelial-bound enzymes, or factors necessary for the catalytic cycle of the enzymes. It also implies that this fungus implements different strategies to degrade dyes with diverse chemical structures.