利用乙二胺四乙酸淋洗修复重金属污染的土壤及其动力学

通过室内模拟试验,采用振荡淋洗的方法研究了乙二胺四乙酸(EDTA)浓度、pH、淋洗时间对重金属去除效果的影响.利用一级反应动力学模型对试验数据进行拟合,并测定了EDTA处理前后土壤中重金属形态的变化.结果表明,EDTA溶液在浓度为0.1 mol·L^-1、pH 7、淋洗时间1 d的条件下能达到对污染土壤重金属的最大去除率,去除率分别为Cd 89.14%、Pb 34.78%、Cu 14.96%、Zn 45.14%.模型拟合结果表明,Cd的质量转移系数最大,其次是Zn、Pb和Cu.说明在土壤淋洗过程中,Cd和Zn最先达到质量转移的平衡状态,然后是Pb和Cu.形态分级结果表明,EDTA能有效地去除交换态、碳酸盐结合态和氧化物结合态重金属,而对有机态和残余态部分重金属作用效果不明显.     

外施Ca2+、ABA及H3PO4对盐碱胁迫的缓解效应

分别对300mmol·L^-1NaCl和100mmol·L^-1Na₂CO₃盐碱胁迫下的羊草苗进行以不同方式施加Ca²⁺、ABA和H₃PO₄等缓解胁迫处理.结果表明,外施Ca²⁺、ABA和H₃PO₄明显缓解了盐碱对羊草生长的抑制作用.叶面喷施效果好于根部处理;施用Ca(NO₃)₂效果好于施用CaCl₂效果;混合施用CaCl₂和ABA的效果比单独施用ABA或CaCl₂的效果好.     

柠檬酸、草酸和乙酸对污泥中镉、铅、铜和锌的去除效果

研究了柠檬酸、草酸和乙酸对污泥中Cd、Pb、Cu和Zn等重金属的去除效果,并分析了污泥中重金属的形态变化和生物有效性.结果表明,随着反应时间和酸浓度的增加,污泥中重金属（Cu除外）的去除率也相应增加.污泥加入柠檬酸溶液反应7 h即可去除污泥中52.0%的Pb和74.2％的Zn, 24 h后可去除76.0%的Pb和92.5%的Zn,草酸和乙酸对重金属的去除率较低.柠檬酸去除的Pb和Zn主要以稳定态存在,并导致污泥中不稳定态重金属的比例上升,其中可交换态重金属浓度有不同程度的增加.虽然有机酸对Cd和Cu的去除率较低,但反应后可交换态Cd和Cu的浓度仍有小幅增加.     

鄂尔多斯地区公路沿线土壤重金属形态与生物有效性

采用TessierA连续提取法对鄂尔多斯地区公路沿线土壤重金属（Pb、Zn、Cu、Ni、Cr）化学形态进行了测定。同时对土壤pH值、重金属含量和公路绿化植物重金属（Cd、Hg、Pb、Cu、Zn、Ni、Cr、As和Se）含量进行了分析，对该区域重金属的生物有效性与潜在生态风险进行预测。结果表明：土壤重金属有效态占总量百分比的大小序列为Zn〉Pb〉Ni、Cr〉Cu，与重金属元素在绿化植物中含量大小序列Zn〉Cu〉Ni、Cr、As、Pb〉Cd〉Hg并非完全趋于一致。不同公路段土壤重金属与其不同形态存在较大的变幅。公路沿线表层土壤中重金属的有效态占其总量为G109（东胜-准格尔段）15．7％～46．1％，G210（达拉特-东胜段）8．0％-40．9％，G109（东胜-鄂托克段）9．1％～33．9％，而且以有机态和Fe—Mn氧化结合态的比例较大，为各元素有效态的主要形态特征。Cu在不同植物不同器官中的含量较高，可能在鄂尔多斯地区特定环境条件下随植物的蒸腾拉力、水分和营养盐运移的生理生态作用下使其在植物体中富集。土壤重金属Zn的有效态含量较高，而残渣态含量低，须特别注意其对区域生态系统的潜在影响。     

海口城市土壤重金属污染特征与生态风险评估

对海口城市土壤重金属含量、空间分布特征与赋存形态进行了研究,并评估了其生态风险。结果表明,海口城市土壤重金属Hg、As、Cd、Cu、Cr、Ni、Pb、Zn的平均含量分别为0.073、3.82、0.25、26.7、92.4、52.5、29.1和84.1 mg·kg-1。与海口土壤背景值相比,海口城市土壤明显富集重金属Hg、As、Cd、Cu、Cr、Ni、Pb和Zn,受到一定程度重金属污染。Cr、Ni、Cu、Cd和Zn元素主要在郊区富集,Pb主要在路边绿化带中富集,Hg主要在生活区富集。海口城市土壤中Zn、As、Cr、Cu和Ni以残渣态为主,Hg主要以强有机态和残渣态存在,Pb主要以铁锰氧化态和残渣态存在,而Cd则主要以生物可利用态为主。生态风险评价结果显示,海口城市土壤重金属综合生态风险属于微弱水平,但Cd和Hg污染应引起重视。     

刺楸年轮中重金属含量动态变化及富集特性

为探索刺楸对受污染土壤重金属的富集和修复效应, 以南京栖霞山的乡土树种刺楸及其根际周边土壤为研究对象, 截取其根基部年轮盘及根际土壤样本, 采用ICP-AES法测定年轮及土壤样本中重金属(Cu、Cd、Cr、Mn、Ni、Pb、Zn)元素含量。结果表明: 栖霞山样地中的土壤受Mn、Pb和Zn污染最为严重, 存在Cu、Cd、Mn、Pb、Zn元素的高度复合污染, Cd、Cr、Cu、Ni、Zn在土壤和年轮中存在相关性, Mn和Pb则没有表现出明显的相关性; 刺楸修复受Cd、Mn、Pb、Zn污染的土壤效果并不显著, 更适用于Cr、Cu、Ni污染的土壤修复; 鉴于Cu元素含量变化特征, 刺楸也可以作为反映当地污染历史的记录载体; 刺楸年轮中的重金属元素之间存在交互作用, 其中Cd与Zn元素含量高度相关(r=0.984, p<0.01), 在刺楸年轮吸收重金属元素的过程中, Cu与Cd、Cr、Mn、Zn元素具有协同作用, Mn元素对其他元素有一定的拮抗作用。     

上海市小羽藓属植物重金属含量及其与环境的关系

应用原子吸收法对上海市13个样点的小羽藓植物体及相应土壤样品中的Cu、Pb、Cd、Zn、Cr 5种重金属元素含量进行了测定.通过对植物体内含量的聚类分析,将13个样点按重金属污染程度的轻重分为3个组：1)污染严重点,包括桂林公园、复兴公园、光启公园3个样点,均位于市区交通繁忙地带,其小羽藓体内重金属含量分别为：Cu 35.25～50.36 mg·kg^-1、Pb 55.50～65.00 mg·kg^-1、Cd 1.68～2.30 mg·kg^-1、Zn 829.63～1140.13 mg·kg^-1、Cr 7.41～16.41 mg·kg^-1;2)污染点,包括长风公园、古钟园、中山公园、和平公园、上海师范大学徐汇校区5个样点,均位于市区近郊,小羽藓体内重金属含量分别为：Cu 18.51～62.50 mg·kg^-1、Pb 14.38～34.25 mg·kg^-1、Cd 0.81～1.40 mg·kg^-1、Zn 354.25～671.75 mg·kg^-1、Cr 3.62～25.08 mg·kg^-1;3)相对清洁点,包括佘山、大观园、罗泾、植物园、崇明东平国家森林公园5个样点,位于上海市远郊,小羽藓体内重金属含量分别为：Cu 11.13～16.41 mg·kg^-1、Pb 4.63～27.25 mg·kg^-1、Cd 0.93～1.28 mg·kg^-1、Zn 489.25～1 086.75 mg·kg^-1、Cr 1.53～7.62 mg·kg^-1.结果表明,小羽藓属苔藓植物可作为监测上海地区环境重金属污染的良好指示植物.苔藓植物体内重金属含量水平与土壤重金属含量存在一定的相关性,而且也受其他因素的影响.     

公路绿化植物油松(Pinus tabulaeformis)和小叶杨(Populus simonii)对重金属元素的吸收与积累

对内蒙古西部公路绿化植物油松（Pinus tabulaeformis）、小叶杨（Populus simonii）及其根际土壤中重金属元素（Cd、Hg、Pb、Cu、Zn、Ni、Cr）和类金属元素（As和Se）含量以及根际土壤重金属（Cu、Zn、Pb、Ni和Cr）形态、土壤pH值进行了测定。对比分析了公路沿线不同绿化植物及其不同器官对重金属元素的吸收与积累特征。结果表明：绿化植物根际土壤对重金属元素的吸附及污染程度以Cd为最高。随原子序数的递增,小叶杨和油松两种植物的根部和茎叶两种营养器官中重金属的含量均表现出“N”字形变动趋势。而且重金属元素在不同植物不同器官中的含量具有Zn〉Cu〉Ni,Cr,As,Pb〉Cd〉Hg的基本规律。小叶杨茎叶对重金属元素Cr、Ni和Pb的富集能力较根部为强,油松茎叶对重金属元素Cr、Ni、Cu和Pb的富集能力较根部为强。绿化植物根际土壤重金属元素有效态占总量百分比的大小序列为Zn〉Pb〉Ni、Cr〉Cu,与重金属元素在不同植物不同器官中的含量大小序列Zn〉Cu〉Ni、Cr、As、Pb〉Cd〉Hg并非趋于一致。公路绿化植物对根际土壤中重金属元素的吸收和积累与重金属元素有效态所占的比例有关。     

临安市雷竹林土壤重金属污染特征及生态风险评价

为了解临安市雷竹林土壤重金属污染特征,采集并测定了160个土壤样品的Hg、As、Cu、Pb、Zn、Cd、Cr、Ni、Co、Mn等重金属含量,采用单因子污染指数和内梅罗综合污染指数对雷竹林土壤重金属污染程度进行分析,并应用Hankanson潜在生态风险指数法对雷竹林土壤重金属潜在生态风险进行评价.结果表明:雷竹林土壤重金属Hg、As、Cu、Pb、Zn、Cd、Cr、Ni、Co、Mn的平均含量分别为0.16、7.41、34.36、87.98、103.98、0.26、59.12、29.56、11.44、350.26mg·kg-1,Pb、Cd、Zn和Cu平均值超过浙江省土壤背景值,分别是对应背景值的2.89、1.70、1.12、1.12倍.经单因子污染指数评价,不同重金属元素的平均污染程度大小依次为Pb＞Cd＞Cu=Zn＞Hg＞As＞Ni＞Co＞Cr＞Mn,其中Pb有中度污染,Cd、Cu和Zn有轻度污染.经内梅罗综合污染指数评价,160个样点都受到不同程度的重金属污染,轻度污染、中度污染和重度污染水平所占比率分别为55.6％、29.4％和15.0％.各重金属单因子潜在生态风险指数平均值评价结果显示,只有Cd污染达到中等生态风险,其他重金属均为轻微生态风险,而局部采样点Cd和Hg单因子潜在生态风险指数最大值分别达到256.82和187.33,存在很强生态风险.重金属综合因子潜在生态风险指数评价结果表明,临安市雷竹林土壤整体上存在轻微生态风险.     

柠檬酸、草酸和乙酸对污泥中镉、铅、铜和锌的去除效果

研究了柠檬酸、草酸和乙酸对污泥中Cd、Pb、Cu和Zn等重金属的去除效果,并分析了污泥中重金属的形态变化和生物有效性.结果表明,随着反应时间和酸浓度的增加,污泥中重金属（Cu除外）的去除率也相应增加.污泥加入柠檬酸溶液反应7h即可去除污泥中52.0%的Pb和74.2%的Zn,24h后可去除76.0%的Pb和92.5%的Zn,草酸和乙酸对重金属的去除率较低.柠檬酸去除的Pb和Zn主要以稳定态存在,并导致污泥中不稳定态重金属的比例上升,其中可交换态重金属浓度有不同程度的增加.虽然有机酸对Cd和Cu的去除率较低,但反应后可交换态Cd和Cu的浓度仍有小幅增加.     

Phytoavailability assessment of heavy metals in soils by single extractions and accumulation by Phaseolus vulgaris

In Western Europe, policy makers are currently moving towards a more integrated risk-based approach of soil contamination assessment. As part of this approach, selective single extraction procedures have been proposed to add complementary insights regarding heavy metal behaviour and phytoavailability in soils and sediments. However, there is currently a wide range of such procedures available in literature, hampering standardisation and harmonisation of phytoavailability research of heavy metals. The current study examines shoot accumulation of Cd, Cu, Ni, Pb and Zn by the test plant Phaseolus vulgaris in 21 soils, differing in soil composition and level of contamination. On these soils, 12 different commonly used extraction procedures have been compared: soil solution extraction by Rhizon soil moisture samplers, 0.01 M CaCl₂, 0.1 M NaNO₃, 1 M NH₄NO₃, 1 M NH₄NOAc, 1 M MgCl₂, 0.11 M HOAc, 0.5 M HNO₃, 0.1 M HCl, DTPA–TEA–CaCl₂, EDTA-NH₄OAc and aqua regia. The plant species used in this study has previously been proposed as a test plant in a bioassay for assessing heavy metal induced oxidative stress in contaminated soils [Van Assche, F., Clijsters, H., 1990. A biological test system for the evaluation of the phytotoxicity of metal-contaminated soils. Environ. Pollut., 66, 157–172]. Cadmium shoot accumulation correlated best with soil solution concentrations, unbuffered nitrate solutions and the dilute CaCl₂ extraction procedure. The same was observed for Zn, yet for this element NH₄OAc and MgCl₂ also provided significant interactions. The best prediction for Ni was observed in the cluster containing CaCl₂ and NH₄NO₃. For Cd, Zn and Ni, the pseudo-total content and the aggressive chelate based and/or acidic extractants did not correlate well with shoot accumulation. Cu and Pb uptake on the other hand was found to correlate significantly (p = 0.01) with total content as well as with all aggressive extraction procedures over the range of soils used in this experiment. In general, the 0.01 M CaCl₂ extraction procedure proved to be the most versatile as it provided a good indication of phytoavailability for all five metals under evaluation.     

黑曲霉生产β-葡萄糖苷酶发酵条件的研究产

经多项式回归分析,研究了不同浓度N源、C源、无机盐等对酶产量的影响,确定出最佳培养基配方为:麸皮4.9%,(NH₄)_2>SO₄0.4%,KH₂PO₄0.29%,CaCl₂0.05%,MgSO₄·7H₂O0.04%,FeSO₄·7H₂O 5mg·L^-1,ZnCl₂1.4mg·L^-1,0.2%油酸钠。并对培养温度、时间、培养基初始pH、通气量、接种量、接种方式等培养条件进行优化,使黑曲霉生产β葡萄糖苷酶的产量由17U·ml^-1增至21.3U·ml^-1.     

不同保鲜剂对非洲菊切花的保鲜效应

探讨不同保鲜剂对非洲菊切花的瓶插寿命、观赏品质以及生理生化指标的影响。结果表明,在供试7组保鲜剂中,以处理7(T₇):20g/L Suc+200mg/L 8-HQC+150mg/L CA+75 mg/L KH₂PO₄·3H₂O+1g/L CaCl₂的保鲜效果最佳,可显著延长非洲菊切花瓶插寿命;T₇处理有利于减缓花瓣组织pH上升、花青素含量下降及花瓣细胞膜相对透性的上升,从而延长瓶插寿命。     

Avian Microchromosomes; As Shown by Prefixation Treatment with Colchicine, Squashing, and Haematoxylin Staining

Small pieces of bird tissue from developing feathers, embryos, embryonic gonads and adult testes are treated before fixation in a 0.25% solution of colchicine diluted with an equal volume of hypotonic Pannett and Compton solution containing KCI, 0.336 gm; CaCl₂, 0.160 gm; Na₂HP0₄. 12H₂O, 0.172 gm; and NaH₂PO₄. 4H₂O, 0.0172 gm per 1000 ml of double distilled water, for 20-30 min at 37° C. This material is subsequently centrifuged at 1000 rev/min for 1-3 min, fixed with acetic alcohol (1:3) and stained with either Gomori's haematoxylin or by Feulgen's procedure. Preparations are frozen in the freezing chamber of a refrigerator for the separation of the cover slips, then mounted in euparal after dehydration in alcohols. With this technique, unclumped and clear preparations of both macrochromosomes and microchromosomes are obtained regularly.     

Thermogravimetric study of starch derivatives with amine/ammonium ion-exchanging groups in oxidative environment

The amine/ammonium materials were prepared by cross-linking of starch (S) with epichlorohydrin (E→SE) in the presence of ammonia (A→SEA) or choline (C→SEC–HO⁻) or with 1,3-bis-(3-chloro-2-hydroxypropyl)imidazolium hydrogensulphate (BCHIHS→SHI–HO⁻) and transfered into the acid/salt forms with HCl (SEA–HCl, SEC–Cl⁻, or SHI–Cl⁻), H₂SO₄ (SEA–H₂SO₄, SEC–HSO₄⁻, or SHI–HSO₄⁻), and H₃PO₄ (SEA–H₃PO₄, SEC–H₂PO₄⁻, or SHI–H₂PO₄⁻) and analyzed with thermogravimetry (TG) under dynamic and isothermal conditions in nitrogen or oxygen environment. According to the values of thermooxidation maxima (TM) calculated from the maximal difference of measured residues on the dynamic TG curves run in nitrogen and oxygen environments the order of decreasing thermooxidation resistance is: S>SEA–H₃PO₄>SHI–H₂PO₄⁻>SHI–HSO₄⁻>SEA–H₂SO₄>SEC–HSO₄⁻>SEC–HO⁻>SEA–HCl>HCl–Cl⁻> SEC–Cl⁻>SHI–HO⁻>SEA>SEC–H₂PO₄⁻>SE. The first-order rate constants calculated by the linear regression method (regression coefficient R>0.95) represented the initial rate constants for residue formation (k_r's) and gasification (k_g's). All the derivatives had greater values of rate constants than S and the k_g's were about 1000 times greater than k_r's. The values obtained in nitrogen were smaller than those calculated from runs in oxygen environment with the exception of S. Most of the salt forms had greater values of k_g's in oxygen environment. The activation energies (E's) were usually greater in nitrogen than in oxygen as well as for residue formation than for gasification. The SHI–HO⁻ sample had high k_g's and low E_g's in oxygen environment while for SHI–H₂SO₄⁻ the opposite was true. This we consider as two extremes for labile and resistant samples for gasification.     

HNO3/H3PO4–NANO2 mediated oxidation of cellulose — preparation and characterization of bioabsorbable oxidized celluloses in high yields and with different levels of oxidation

The reaction of cellulose with a mixture of HNO₃/H₃PO₄–NaNO₂ (2:1:1.4, v/v/%w) at room temperature for different time intervals has been investigated to produce oxidized cellulose (OC), a biocompatible and bioresorbable polymer. The results revealed an increase in carboxyl content of OC with increasing reaction time, corresponding to about 8.0, 13.4, 17.4 and 18.4% carboxyl content after 12, 24, 36, and 48 h, respectively. The yield of OC ranged between 75 and 81%. The use of different ratios of HNO₃ and H₃PO₄, (11:1, 4:1, 2:1, 1:1, 1:2, and 1:4; v/v), in the reaction had no significant effect on the carboxyl content and yield of the OC products. All products, as produced, were low crystallinity (27–35%) fibrous materials. The length of fibers decreased with increasing reaction time. After ball milling for 24 h, the length of fibers further decreased and products converted into a fine powder consisting of small fibers and aggregated non-fibrous particles. The degrees of polymerization (DP) of the OC products produced after 12, 24, and 48 h of reaction duration were 81, 63, and 53, respectively. After ball milling for 24 h, the corresponding values changed to 57, 51 and 46. However, no significant change in the crystallinity of the products was noted after ball milling. The TGA results showed the OC products to be less thermally stable than cellulose. The degradation temperature appears to decrease with increasing carboxyl content. In conclusion, the results show that the low crystallinity OC products can be successfully prepared in high yields and with different levels of carboxyl content from cellulose by treatment with a mixture of HNO₃/H₃PO₄–NaNO₂.     

典型矿冶区周边土壤微生物功能特征及影响因素

土壤微生物对重金属污染胁迫敏感,但在实际野外环境中,土壤微生物群落生态效应通常是污染胁迫和环境因素综合作用的结果。为探究重金属污染土壤中微生物群落生态效应发生变化的主控因素,本研究以湖南省某典型矿冶区周边不同土地利用类型土壤为研究对象,以土壤碳氮循环过程主要的微生物功能指标土壤微生物生物量碳(MBC)、基础呼吸(BR)、诱导呼吸(SIR)和硝化潜势(PNR)为生态效应终点,进行采样调查分析。结果表明: 土地利用类型对MBC、BR和SIR影响均不显著;研究区土壤微生物功能的主要影响因子包括CaCl₂提取态Pb(CaCl₂-Pb)含量与土壤有机质(SOM)含量。多元回归分析结果表明,在CaCl₂-Pb含量为0.004～13.14 mg·kg^-1及SOM含量为0.24%～4.34%的条件下,土壤CaCl₂-Pb和SOM含量可以共同解释土壤中BR、SIR和PNR总变异的39.8%～58.3%;中等含量下(SOM在1.70%～2.36%,CaCl₂-Pb在0.004～12.98 mg·kg^-1),土壤CaCl₂-Pb和SOM含量与BR、SIR和PNR的变化能够建立显著的暴露-效应关系,可以作为测定终点定量评价重金属污染对微生物群落功能的生态效应。     

Improved Procedures in Fungal Cytology Utilizing Giemsa

To study nuclear events in fructifications of the Basidiomycetes, material was fixed 24 hr in a saturated aqueous solution of HgCl₂ containing 1% glacial acetic acid, and embedded in Aquax (G. T. Gurr Ltd.). Following a 4 hr hydrolysis at 20 C in 60% H₃PO₄, sections were stained for 30 min in a mixture of 4 ml Giemsa R66 (G T. Gurr Ltd.) and 100 ml phosphate buffer at pH 6.5. Differentiation was carried out in sodium cacodylate-HCl buffer at pH 5.8 when required. Preparations were dehydrated in an acetone-xylene series prior to mounting in Euparal. The use of paraffin wax as the embedding medium and HCl as the hydrolysing agent yielded preparations of an inferior quality.     

Handling Germinated Pollen on Millipore Membrane During the Feulgen and Autoradiographic Procedures

To prevent loss of pollen during the Feulgen's procedure, the pollen was grown on an autoclaved membrane filter (Millipore AA WP 025 00) in contact with a sterilized medium containing agar 0.5-1%, sucrose according to the genus (Malus 0.3-0.5 M; Persica and Tulipa 0.4 M), and H₃BO₃, 0.01%. To fix the germinated pollen of most species, the membrane was placed for 2 hr to overnight at 2-4 C on filter paper wet with the following mixture: OsO₄, 1 gm; CrO₃, 1.66 gm; and distilled water, 233 ml. To fix Persica pollen, 10% of glacial acetic acid had to be added to the fixative. Washing with distilled water and bleaching with a mixture of 3% H₂O₂ and sat. aq. ammonium oxalate, 1:1, were performed also on filter paper. Similarly, the preparation was processed for Feulgen staining by use of pieces of filter paper wet with the required fluids. Hydrolysis preceding the Schiff's reagent was performed at room temperature with 5 N HCl for 18 min. The differentiation after the Schiff's action was with 2% K₂S₂O₅ buffered to pH 2.3 with 9 ml of phosphate buffer (KH₂PO₄, 1.4 gm; conc. HCl, 0.35 ml and distilled water to make 100 ml). The stained pollen was floated off the membrane with a drop of glacial acetic acid to a gelatinized or an albumenized slide, and squashed. When the coverslip is removed the preparation may be either dehydrated and mounted or coated with autoradiographic film.     

Comparative characterization of a recombinant Volvariella volvacea endoglucanase I (EG1) with its truncated catalytic core (EG1-CM), and their impact on the bio-treatment of cellulose-based fabrics

Recombinant Volvariella volvacea endoglucanase 1 (EG1) and its catalytic module (EG1-CM) were obtained by expression in Pichia pastoris, purified by two-step chromatography, and the catalytic activities and binding capacities were compared. EG1 and EG1-CM exhibited very similar specific activities towards the soluble substrates carboxymethyl cellulose, lichenan and mannan, and insoluble H₃PO₄ acid-swollen cellulose, whereas the specific activities of EG1-CM towards the insoluble substrates -cellulose, Avicel and filter paper were approximately 58, 43 and 38%, respectively compared to EG1. No increase in reducing sugar release was detected in the reaction mixture supernatants after 50 h exposure of filter paper, Avicel or -cellulose to EG1-CM, whereas increases in the total reducing sugar equivalents (i.e. reducing sugar released into solution together with new reducing ends generated in the cellulosic substrates) in reaction mixtures were observed after 1 h. In reaction mixtures containing EG1, soluble reducing sugar equivalents were detected in supernatants after 3 h incubation with the insoluble cellulosic substrates. EG1-CM did not adsorb to Avicel, and the binding capacities of EG1-CM towards filter paper and H₃PO₄ acid-swollen cellulose were 27.9–33.3% and 29.6–60.6%, respectively of values obtained with EG1 within the range of total added protein. In enzymatic deinking experiments, the ink removal rate in EG1-CM-treated samples was only slightly higher (8%), than that of untreated controls, whereas that of the EG1-treated samples was 100% higher. Bio-stoning of denim with EG1-CM resulted in increases of 48% and 40% in weight loss and indigo dye removal, respectively compared with untreated controls. These increases were considerably lower than the corresponding values of 219% and 133% obtained when samples were treated with EG1.