La3+,Ce3+对厌氧颗粒污泥在不同VFA底物中的产甲烷促进效应

采用静态实验研究了分别添加O.05mg·L^-1La^3＋和Ce^3＋对不同来源和保存状况条件下不同VFA底物的厌氧颗粒污泥产甲烷的影响。结果表明，乙酸为底物时加入Ce^3＋，丙酸加入La^3＋或Ce^3＋，乳酸加入La^3＋时都大大加快了反应初期污泥的产甲烷速率，且对比产甲烷活性SMA也有3％-8％的提高；O.05mg·L^-1La^3＋或Ce^3＋的加入使污泥利用丙酸的速度加快，对于厌氧反应器的恢复运行有一定的实际意义。甲酸为底物时，La^3＋，Ce^3＋的加入对污泥产甲烷曲线形状没有影响，对SMA则分别降低了9.21％和3.37％；乙酸添加La^3＋在反应初期明显降低了产甲烷速率，但SMA并未降低。厌氧颗粒污泥经长时间低温存放后，原来对其SMA有提高作用的稀土浓度此时可能会作用不明显甚至会降低SMA；低浓度稀土离子对污泥产甲烷活性产生抑制作用时，相同质量浓度下Ce^3＋比La^3＋对污泥的抑制作用小；驯化培养过程有利于污泥对稀土的适应。     

长链脂肪酸对厌氧颗粒污泥产甲烷活性的影响及其相互作用研究

采用间歇培养实验研究了辛酸、癸酸和月桂酸等三种长链脂肪酸对UASB反应器厌氧颗粒污泥产甲烷活性的毒性，以及癸酸对辛酸和月桂酸抑制作用的影响。结果表明，辛酸、癸酸和月桂酸对UASB反应器厌氧颗粒污泥的产甲烷活性有严重抑制，对厌氧颗粒污泥最大比产甲烷活性产生50%抑制的浓度(IC     

园林植物土壤酶活性和微生物活性对盐碱胁迫的响应

以园林植物石楠为试材,通过混合2种中性盐(NaCl和Na2SO4)和2种碱性盐(NaHCO3和Na2CO3)分别模拟不同强度的盐、碱胁迫条件,对园林植物(石楠)进行3年(2015—2017年)的胁迫处理,以期探讨盐碱胁迫对园林植物土壤酶活性和微生物的影响。结果表明:1)土壤中有机酸含量随着盐碱浓度的增加呈逐渐降低趋势。随胁迫强度增加,盐、碱胁迫均使土壤中Na⁺浓度大幅度上升,K⁺浓度大幅度下降,但碱胁迫下Na⁺浓度上升幅度和K⁺浓度下降幅度均大于盐胁迫。2)随着盐碱浓度的增加,土壤中氨基酸类、碳水化合物类、羧酸类、聚合物类、胺类、酚酸类碳源呈逐渐降低趋势,总体而言,碳水化合物和羧酸类碳源是盐碱胁迫下园林植物土壤微生物的主要碳源,其次为氨基酸类、酚酸类和聚合物类,胺类碳源的利用率最小。3)土壤微生物物种丰富度指数(H)、均匀度指数(E)和碳源利用丰富度指数(S)、土壤微生物量碳、微生物呼吸和微生物代谢熵随盐碱浓度的增加而增加。4)土壤糖苷酶、几丁质酶、亮氨酸氨基肽酶、碱性磷酸酶、酚氧化酶δ和过氧化物酶δ随盐碱浓度的增加呈逐渐降低趋势。5)交互作用分析显示,盐胁迫、碱胁迫、盐胁迫×碱胁迫对有机酸、Na⁺、K⁺、Na⁺/K⁺、物种丰富度指数(H)、碳源利用丰富度指数(S)、土壤微生物量碳、土壤微生物呼吸、土壤微生物代谢熵、糖苷酶和碱性磷酸酶具有显著的影响(P<0.05),其中碱胁迫对土壤酶活性和微生物群落多样性的影响高于盐胁迫,并且盐胁迫×碱胁迫的影响高于单独盐胁迫或碱胁迫.     

Structural Effects of N-Arylcarbamoylpyrazolines on Calcium Uptake in Rat Brain Synaptosomes

N-Arylcarbamoylpyrazolines with various substituents at the para position of the carbamoyl benzene ring inhibited ATP-dependent Ca²⁺-uptake in synaptosomes prepared from the rat brain. The activity of these compounds was evaluated as log(1/I₅₀), the reciprocal logarithm of half inhibitory concentration, I₅₀ (m ), from the concentration–response curve for the inhibition of Ca²⁺-uptake. Among the compounds tested, methyl 3-(4-chlorophenyl)-4-methyl-1-[N-(4-trifluoromethylphenyl)carbamoyl]-2-pyrazoline-4-carboxylate was the most potent, the I₅₀ value of which as 9·12×10⁻⁷ m . Variations in the activity in terms of log(1/I₅₀) were quantitatively analysed using a substituent parameter, showing that the higher the electron-withdrawing effect of the substituent, the higher was the activity. The substituent effects were similar to those on insecticidal activity against the Americal cockroach. The higher the inhibitory activity against Ca²⁺ uptake, the higher seemed to be the insecticidal activity. Methyl(4S) - 3 - (4 - chlorophenyl) - 4 - methyl - 1 - [N - (4 - chlorophenyl)carbamoyl] - 2 - pyrazoline -4-carboxylate had higher inhibitory activity against Ca²⁺-uptake and higher in-secticidal activity than the R-isomer, but the difference was greater in theCa²⁺-uptake system.     

Synthesis and Structure–Activity Relationships of Miticidal 4,5-Dihydropyrazole-5-thiones

A series of novel 4,5-dihydropyrazole-5-thiones (DHPs) was synthesised by treating the corresponding dihydropyrazolones with ‘Lawesson’s reagent and evaluated for miticidal activity against two-spotted spider mites (Tetranychus urticae Koch). Of these, 3-(4-chlorophenyl)-4,4-dimethyl-1-phenyl-4,5-dihydropyrazole-5-thione, 3-(4-chlorophenyl)-4-ethyl-4-methyl-1-phenyl-4,5-dihydropyrazole-5-thione, 3-(4-chlorophenyl)-1-phenyl-4,5-dihydropyrazole-5-thione-4-spirocyclopentane and 4,4-dimethyl-1-phenyl-3-(4-trifluoromethyl-phenyl)-4,5-dihydropyrazole-5-thione were highly active (pEC₅₀>4·0) and were more effective than the miticide dicofol (pEC₅₀=3·879), which has traditionally been used for the control of phytophagous mites. Structure–activity relationship (SAR) studies were performed on each position of the pyrazole ring of DHPs. The results indicated that the unsubstituted phenyl, 4-substituted phenyl and thioxo groups on the 1-, 3- and 5-positions of DHPs respectively were required for activity. Quantitative SAR studies using physicochemical parameters of substituents and the capacity factor k′ as a hydrophobicity index suggested that: (a) the activities of all types of DHPs examined were mainly dominated by hydrophobicity, (b) the bulkiness of 4-substituents of the 3-phenyl ring favoured the activity and (c) the log k′ optimum for all DHPs was 1·675, equivalent to a log P_ow value of c. 5·0.     

一种可降解黄原胶的鞘氨醇单胞菌的凝集活性

采用血凝测试及血凝活性糖抑制测试方法,测定了一种可降解黄原胶的鞘氨醇单胞菌XT-11Sphingom onassp.对红细胞的凝集活性及糖抑制专一性,同时进行了温度、pH及Ca2 对红细胞凝集活性影响的试验。结果表明:XT-11菌悬液能凝集家兔、家鸡两种红细胞,其凝集效价分别为26和24;菌悬液对兔红细胞的凝集作用可以被肝素所抑制;鞘氨醇单胞菌的凝集活性不依赖于Ca2 ,且在pH为6.0~10.0时较稳定,在温度为60℃时完全丧失凝集活性。这说明该菌含有能凝集红细胞的活性物质。     

甲基盐霉素对鲤白细胞吞噬活性和溶菌酶活力的影响

选用60 g左右健康正常的鲤540尾,随机平均分为6组,每组设3个重复。试验设6种处理,即基础饲料中分别添加甲基盐霉素0(对照组)、10、20、40、80、160 mg/kg。研究了甲基盐霉素对鲤白细胞吞噬活性和溶菌酶活性的影响。试验结果表明,饲料中添加10 mg/kg甲基盐霉素对鲤白细胞吞噬活性和溶菌酶活性影响不显著,而添加20~160 mg/kg甲基盐霉素对鲤白细胞吞噬活性和溶菌酶活性有一个从促进到抑制的转变,剂量越高,这个转变越快,并且随饲喂时间的延长,其抑制作用越来越强。     

转移因子与重组转移因子及其在疾病防治中的应用

转移因子是来自于免疫淋巴细胞的一类可透析小分子多肽,它能够将致敏淋巴细胞的免疫信息传递给未致敏的受体淋巴细胞。转移因子具有特异性和非特异性免疫活性,特异性转移因子具有转移特异性细胞免疫的能力,非特异性转移因子具有促进淋巴细胞活化增殖,增强其免疫活性,并可诱导靶细胞产生大量的细胞因子。重组转移因子是利用基因工程技术将编码具有免疫增强活性的转移因子基因,进行克隆和体外表达,表达产物经纯化制备而成,试验表明其具有增强细胞免疫活性的作用。转移因子和重组转移因子是一种具有免疫增强活性的新型高效安全的生物药品,在临床上用于疾病的防治,具有广阔的应用前景。     

乳铁多肽及其生物学活性的研究进展

乳铁多肽(乳铁素)是乳铁蛋白在酸性环境下经胃蛋白酶水解,产生的具有特殊生理功能的活性多肽。乳铁素不仅保持乳铁蛋白的活性,而且活性要比乳铁蛋白更强。乳铁素具有抑菌、杀菌、抗癌、抗病毒、免疫调节等多种乳铁蛋白所具有的活性。乳铁素的抗菌活性很强,但其抗病毒活性相对较弱。文章讨论了乳铁素成员中活性较强的牛乳铁素和人乳铁素,内容涵盖了目前乳铁素研究的重点领域,讨论了乳铁素的作用范围及其作用机制,探讨了乳铁素结构与活性之间的联系。