大玉竹低聚糖硫酸酯抗HSV-2病毒活性的研究

从传统中药大玉竹中提取低聚糖Ｐｏｏｓ，用吡啶－氯磺酸法制备了它的硫酸酯衍生物Ｓ－Ｐｏｏｓ，产物经红外鉴定，证实Ｐｏｏｓ硫酸酯化后羟基连上硫酸基，硫含量为８．４７％，取代度（Ｄｓ）为０．６体外实验研究了Ｐｏｏｓ、Ｓ－Ｐｏｏｓ对非洲绿猴肾细胞（Ｖｅｒｏ）的细胞毒怀和抗单纯疱疹病毒２型（ＨＳＶ－２）活性。结果表明，Ｐｏｏｓ和Ｓ－Ｐｏｏｓ都无细胞毒性。Ｐｏｏｓ本身无抗病毒活性，对ＨＳＶ－２引起的细胞病变和     

转化血型用蕃茄α－D－半乳糖苷酶的分离、纯化及理化性质

成熟蕃茄匀浆后，经硫酸铵盐析，ＤＥＡＥ－ＳｅｐｈａｄｅｘＡ－５０离子交换层析，ＳｅｐａｄｅｘＧ－１００凝胶过滤和Ｍｅｌｉｂｉｏｓｅ－Ａｇａｒｏｓｅ亲和层析，获得了α－Ｄ－半乳糖苷酶（Ｃ．Ｅ．３．２．１．１１）。酶制剂经ＰＡＧＥ检测为一条带；ＳＤＳ－Ｇ－ＰＡＧＥ测得酶Ｍｒ为３４０００；比活力５２．９Ｕ／ｍｇ·；提纯倍数为５２９０１产率为４５％．酶专－催化以α－Ｄ－半乳糖为末端ａ－（１，３）连接的糖苷键，以ＰＮＰＧ（对硝基苯－α－Ｄ－半乳糖昔）为废物，酶催化反应的Ｋｍ＝０．１１ｍｍｏｌ／Ｌ，Ｖｍａｘ为６７μｍｏｌ·ｍｇ１－·ｍｉｎ－１．ｔ稳定范是０～３５℃；ＰＨ稳定范围是４．０～７．０．最适ｐＨ为５．１．半乳糖是酶的竞争性抑制剂；Ｃｕ２＋、Ｚｎ２＋、Ｍｎ２＋、Ｆｅ３＋、Ａｇ＋和ＥＤＴＡ对酶活性无影响．纯酶制剂可作为Ｂ型血向Ｏ型血转化的工具酶液．     

五氯酚及其钠盐中氯代二恶英类分析

采用ＨＰＬＣ和ＧＣ／ＭＳ的方法，对国产ＰＣＰ及其钠盐中的ＰＣＤＤｓ，ＰＣＤＦｓ进行了分析。测定了所有２，３，７，８－取代同系物。此外，还根据各ＣＤＤｓ，ＣＤＦｓ的毒性当量因于ＴＥＦｓ，计算了其毒性当量Ｉ－ＴＥＱｓ，分别为１４２，９２ｎｇ．ｇ＾－１。在前述基础上，仨算了由于ＰＣＰ及其钠盐的应用，引起的ＰＣＤＤｓ，ＰＣＤＦｓ环境输入。约为２４０ｋｇ／ａ。     

野生与养殖长吻血液及不同器官同工酶的比较

采用聚丙烯酰胺凝胶电泳（ＰＡＧＥ－Ｅｌｅｃｔｒｏｐｈｏｒｓｉｓ），对野生及养殖长吻Ｕａｉ心脏、肾脏、肌肉、肝脏四个器官及血液的ＬＤＨ（ＥＣ．１．１．１．２７）、ＰＯＤ（ＥＣ．１．１．１．１）、ＥＳＴ（ＥＣ．３．１．１．１）、ＭＤＨ（ＥＣ．１．１．１．３７）同工酶所获电泳图谱进行对比分析，发现以上各酶在不同组织器官中均表现出组织特异性；野生Ｕａｉ和养殖Ｕａｉ四种同工酶也存在差异；ＬＤＨ同工酶电泳带分     

转化血型用蕃茄α—D—半乳糖苷酶的分离,纯化及理化性质

成熟蕃茄匀浆后，经硫酸铵盐析，ＤＥＡＥ－ＳｅｐｈａｄｅｘＡ－５０离子交换层析，ＳｅｐａｄｅｘＧ－１００凝胶过滤和Ｍｅｌｉｂｉｏｓｅ－Ａｇａｒｏｓｅ亲和层析，获得了α－Ｄ－半乳糖苷酶（Ｃ．Ｅ．３．２．１．１１）。酶制剂经ＰＡＧＥ检测为一条带；ＳＤＳ－Ｇ－ＰＡＧＥ测得酶Ｍ，为３４０００；比活力５２．９Ｕ／ｍｇ．；提纯倍数为５２９０；产率为４５％。酶专一催化以α－Ｄ－半乳糖为末端ａ－（１，３）连接的糖苷     

进水PCP和CODCr质量浓度对厌氧反应器运行效能的影响

应用以氯酚驯化污泥接上流式厌氧消化反应器（ＵＡＤ）连续处理含五氯酚（ＰＣＰ）废水的试验结果表明，在一定的水力负荷下，试验反应器可稳定地处理ρ（ＣＯＤＣｒ）１２５０－１０００ｍｇ．Ｌ＾－１和ρ（ＰＣＲ）≤１８０ｍｇ．Ｌ＾－１的有毒有机废水，ＣＯＤＣｒ去除率大于９０％，ＰＣＰ去除率大于９９．５％，出水ρ（ＰＣＰ）小于０．５ｍｇ．Ｌ＾－１，维持试验反应器正常运行所必需的最低进水ρ（ＰＣＰ）有关，且进水ρ     

链霉菌碱性脂肪酶的研究

从杭州土壤中获得的一支链霉菌,通过ＵＶ、ＤＥＳ和Ｃｏ６０ － γ射线的５ 代诱变,选育成功了高产的Ｚ９４－ ２ 菌株,经过对Ｚ９４ －２ 的发酵研究,产碱性脂肪酶活力达５９６ ｕｍＬ,其最适培养基（λｕ Ｌ－１） 为：糊精１０、黄豆饼粉３０、尿素１０ 、Ｋ２ＨＰＯ４０ ．５、ＭｇＳＯ４·７Ｈ２Ｏ０ ．５、ＮａＣｌ１ 和ＡＥＯ９ ０．５ ,产酶的最适条件为：初始ｐＨ９．０～１０．０ ,２６℃培养４８ ｈ．对Ｚ９４－ ２ 与其他菌株的碱性脂肪酶的特性作了比较     

沈阳市农田土壤农药残留水平

对沈阳市农田（水田、旱田、菜田）土壤中农药残留调查表明，禾大壮、丁草胺、敌百虫、辛硫磷、阿特拉津、乐果、氧化乐果、溴氰菊酯、１６０５残留量测定结果均低于检出限。六六六残留几何平均水平为０．０１１ｍｇ／ｋｇ．ＤＤＴ为０．０３９ｍｇ／ｋｇ；旱田、水田六六六异构体的残留主要是β－ＢＨＣ，ＤＤＴ异构体的残留主要是ｐ，ｐ＇－ＤＤＥ．     

沈阳市农田土壤农药残留水平

对沈阳市农田（水田、旱田、菜田）土壤中农药残留调查表明，禾大壮、丁草胺、敌百虫、辛硫磷、阿特拉津、乐果、氧化乐果、溴氰菊酯、１６０５残留量测定结果均低于检出限。六六六残留几何平均水平为０．０１１ｍｇ／ｋｇ，ＤＤＴ为０．０３９ｍｇ／ｋｇ；旱田、水田六六六异构体的残留主要是β－ＢＨＣ，ＤＤＴ异构体的残留量主要是ｐ，ｐ＇－ＤＤＥ。     

轻度氧化处理纤维素生物降解性的初步研究

以纤维素为原料，通过二氧化氮和过碘酸化学氧化方法，在不同的低取代度条件下，有选择性地在纤维素葡萄糖残基的不同碳原子部位导入特定的取代基（羧基和二醛基），探讨不同的取代基对纤维素生物降解性能的影响．并将处理后所得的纤维素试验，通过土壤埋没，利用土壤中的微生物自然降解，然后测定分子量的变化，定量分析纤维素在不同取代基，不同程度化学处理后，其生物降解性能的变化。实验结果表明：（１）在纤维素葡萄糖残基Ｃ６     

Aqueous high‐temperature chemistry of arsenic‐containing compounds in water at 300°C

Arsenic compounds, and especially organo‐arsenic derivatives, are highly toxic and many have been manufactured as chemical warfare agents. This study was designed to provide background information relevant to the potential application of aquathermolysis techniques for the detoxification of such potent military warfare agents. Six arsenic‐containing compounds with structural features which mimic known agents were studied in neutral superheated water: 4‐aminophenylarsine oxide, 4‐arsanilic acid, 4‐nitrophenylarsonic acid, 5, 10‐dihydro‐10‐ethylphenarsazine, tetraphenylarsonium chloride hydrate, and (3‐cyanopropyl)dimethyl(2‐phenethyl)arsonium bromide. Most of these compounds were moderately susceptible to hydrolysis for 1h at 300°C. o‐ and p‐Aminosubsituted arsenic compounds were more reactive than compounds with an electron‐withdrawing group substituent. Aromatic C—As bonds were more resistant to cleavage than aliphatic C—As bonds.     

单取代苯衍生物的QSAR研究——分子表面积和活性基团表面积的应用

本文对３０种单取代苯衍生物的结构和毒性关系进行了研究，由于取代基的多样性和性质的各不相同，用量子化学计算所得电子性质参数，拓扑指数和某些经验参数作描述参数，均不能得到好的与毒性的相关性，为此，引入了与取代基相关的取代基活性基团表面积，再加上反映分子总体性质和形状分子表面积及三阶形状指数，所得回归方程较好反映了结构和毒性关系，这也说明了对于单取代苯衍生物，取代基在致毒作用中可能起重要作用。     

人工湿地植物生物质资源能源化利用潜力评估

通过测定不同人工湿地植物的纤维素组分和热值,并采用NaOH–酶解工艺研究不同人工湿地植物水解液组分,对在人工湿地技术体系中起重要作用的湿地植物能源化利用潜力进行系统评估.结果显示,15种人工湿地植物的纤维素含量在19.78%～36.9%之间,半纤维素含量在4.51%～19.67%之间,木质素含量在10.79%～20.47%之间,具有与玉米秸秆相当的热值,其热值在14.002～17.839 MJ/kg之间.在NaOH–酶解工艺条件下,不同人工湿地植物水解液中存在5种糖类组分,主要为葡萄糖和木糖.研究表明,人工湿地植物是一种较好的生物质资源,可通过生物质固体成型燃料技术、沼气技术和燃料乙醇技术加以利用,进而建立人工湿地植物生物质资源能源化藕联利用模式.图2表2参22     

Advances in the study of directed evolution for cellulases

If cellulose can be effectively hydrolyzed into glucose by cellulase, the production costs of hydrogen, ethanol or other chemicals from cellulosic materials will be greatly decreased, and economically viable production of biohydrogen and bioethanol will become feasible. Cellulose is degraded into glucoses by multi-component enzyme systems. Nowadays cellulases are widely used in brewing, food, bioenergy, fodder, textiles, paper, pharmaceuticals, environmental protection and other industries. However, existing cellulases have several problems that limit their wider applications, including the low turnover number for solid cellulosic materials, and low stability in adapting to various application conditions. For example, high temperature, low pH, and so on. Application of directed evolution technology may be one of the most effective ways for improving the characteristics of cellulases. This paper presents a brief review of the cellulose hydrolysis mechanism by cellulase, advances in cellulases (endoglucanase and β-glucosidase) improvement by directed evolution for several characteristics (for instance, thermal stability, pH adaptability and enzyme activity), limitations of directed evolution for cellulases, and the outlook for directed evolution for cellulase.     

部分离子液体及其混合物对发光菌的毒性作用

离子液体(ILs)因其环境安全和良好的非挥发性而得以广泛应用,尽管其理化性质与工程数据一直在不断扩充,但其可用的毒性及生态毒性数据很少.以青海弧菌Q67为指示生物,应用微板发光毒性测试方法,测定了C6H11BF4N(2S1)、C8H15ClN2(S2)、C8H15BF4N2(S3)、C9H14BF4N(S4)、C9H17BF4N2(S5)、C9H17BrN2(S6)、C11H13BF4N2(S7)、C11H13ClN2(S8)、C12H23BrN2(S9)、C14H27BF4N(2S10)、C14H27ClN(2S11)和C16H31ClN(2S12)等12种ILs对发光菌的发光抑制毒性.结果表明,4种ILs(S9、S10、S11、S12)具有高抑制毒性(pEC50>4.5),而另外8种毒性相对较小(pEC50<3.5).为研究混合ILs的联合毒性,根据单个ILs的剂量-效应关系,构建了两组混合物,即由S9、S10、S11和S12构成的高毒性组(简称H组)以及由S2、S3、S4、S5、S6和S8构成的低毒性组(简称L组)混合物.应用非线性模拟技术与剂量加和(DA)及独立作用(IA)模型对混合物毒性数据进行拟合与预测分析,结果表明,以等效应浓度比法设计的混合物,无论是对于H组的4个混合物还是L组的4个混合物,其联合毒性大小均可用DA模型准确预测.对于均匀试验设计浓度比法设计的混合物,H组的6个混合物的毒性可用DA模型有效预测,而L组的6个混合物由于剂量-效应曲线在低浓度区翘起,其混合物毒性用DA或用IA模型预测均有一定误差.     

Energetics,moult cycle and ecdysteroid titers in spider crab (Hyas araneus) larvae starved after the D0 threshold

Zoea I larvae of Hyas araneus L. (Decapoda: Brachyura: Majidae) were dredged in January 1986 from the German Bight and reared in the laboratory at constant 12°C, until they reached the transition of stages C/D₀ of the moult cycle (4 d after hatching). This developmental stage had previously been found to correspond with the point of reserve saturation (PRS) which allows autonomous (food-independent) development through the rest of the moult cycle and hence, was termed the D₀ threshold. One part of the larvae was continually fed (control), another group was starved from the D₀ threshold until moulting to the zoea II instar. In these two experimental groups, as well as in the two groups of zoea II larvae obtained from the different feeding conditions, the course of the moult cycle, biomass (dry weight, W; carbon, C; nitrogen, N; hydrogen, H; energy, E; the latter estimated from C), and ecdysteroid titers (measured with a radio-immuno-assay as ecdysone equivalents) were investigated. When the larvae reached the PRS, they had gained 90% in W, 72% in C, 32% in N, 53% in H, and 65% in E, since hatching, corresponding to an accumulation of 87% of final W and 62 to 69% of C, N, and H reached later, at the end of the mould cycle in the control. The period of starvation caused a 2.5-d delay of the moult cycle, mainly in late premoult, and significant losses of biomass and energy. Starved and fed larvae secreted similar amounts of moulting hormone per individual, but with a reduced rate in the starved group, thus causing developmental delay. Zoea II larvae moulting after starvation contained less than half of the control biomass and energy, and even less than a freshly hatched zoea I. Growth rate was only slightly enhanced in these zoea II larvae as compared to the fed control, but losses of biomass, mainly of lipids, were partly compensated by a 4-d prolongation of their moult cycle, chiefly (3 d) in stage C. Biomass curves were almost parallel in the two experimental groups of zoea II larvae, with significantly higher values in the control during all stages of the moult cycle. However, similar relative proportions (74 to 89%) of late premoult biomass and energy were reached at the D₀ threshold, regardless of different feeding history and initial or final values in a given group. The ecdysteroid titer curve of the zoea II which had moulted from starved zoea I was very similar to that in control larvae, but with a 3-d delay in the occurrence of premoult peak concentration (in both groups in stage D₁). Regulation and coordination of moult cycle, ecdysteroid titers, and growth in the larval development of decapod crustaceans are discussed, with special reference to the D₀ threshold.     

有机碳源物对淹水土壤中氮素转化的影响

八周淹水培养试验表明：木质素对土壤矿质氮影响不大，纤维素则影响强烈，而淀粉的影响比纤维素更为强烈持久．硫铵与纤维素或淀粉配施时，氮的固持作用大于矿化作用，在培养期间均没有释放出氮素．在八周时间内．氨基酸态氮趋向增加，表明是微生物对氮素的固持作用；氨基糖态氮占全氮比例很低而且变化不大；其它有机组分氮在短期内的变化没有明显的规律性．     

镉对桑蚕生长发育和蚕茧质量影响的研究

研究了土壤镉对桑叶含镉量［w（Cd）］、含水量［w（H2O）］的影响以及镉对蚕生长发育和蚕茧质量的影响结果表明：（1）桑叶w（Cd）与土壤w（Cd）呈极显著正相关（2）土壤w（Cd）＞22．3×10-6,则桑叶w（H20）＜75％，叶质开始变粗硬,（3）用w（Cd）＜3．66×10-6的添加Cd桑叶养蚕时，蚕能正常生长发育，蚕茧质量不受影响（4）当镉由土壤进入桑叶，用w（Cd）＜0．49×10-6的桑叶养蚕时，蚕的生长发育和蚕茧质量不受明显影响（5）当桑叶w（Cd）超过上述数值后，蚕的生长发育受阻，蚕茧质量明显下降。     

Formic acid fractionation towards highly efficient cellulose-derived PdAg bimetallic catalyst for H2 evolution

The present work, in which cellulose isolated from formic acid fractionation (FAC) is decorated with polyetherimide (PEI) to attain highly efficient cellulose-derived PdAgbimetallic catalyst (PdAg-PEI-FAC), has been investigated, and the catalyst properties are characterized by XRD, XPS, BET, ICP-AES and HAADF-STEM. The as-obtained Pd3.75Ag3.75-PEI-FAC exhibits excellent catalytic performance for H2 evo-lution from a sodium formate-free formic acid (FA) aqueous medium at ambient temperature and the turnover frequency (TOF) reaches a high value of 2875 h-1, which is superior to most of the previously reported Pd-based heterogeneous catalysts supported on a carbon matrix in the literature. The remarkable catalytic activities of PdAg-PEI-FAC result from high dispersion Pd and synergistic effects between the PdAg bimetallic system. Furthermore, the amide (-NH) group in PEI coated on cellulose acting as a proton scavenger efficiently improves the catalytic property of catalyst. In addition, the critical factors affecting H2 release, such as FA concentration, reaction temperature, PdAg compositions and support matrix type, are also evaluated. Based on the experimental results, the probable three-step mechanism of H2 evolution from FA over Pd3.75Ag3.75-PEI-FAC is proposed. In the end, the activation energy (Ea) of Pd3.75Ag3.75-PEI-FAC catalyst is calculated to 53.97 kJ mol-1, and this catalyst shows unique robustness and satisfactory re-usability with no loss of catalytic activity after five recycles. The findings in this work provide a novel routine from lignocellulose fractionation towards cellulose-derived catalyst for H2 evolution.