邻苯二甲酸二(2-乙基己基)酯酶促降解性的研究

从处理石化厂废水的活性污泥中分离出一株邻苯二甲酸酯降解菌FS1（Pseudomonas fluorescens FS1),测定了P.fluorescens FS1的邻苯二甲酸酯降解酸对邻苯二甲酸二（2－乙基已基）酯（DEHP）的降解特性。P.fluorescens FS1细胞中的颗粒部分、溶液部分对DEHP都具有降解作用，初步认为P.fluorescens FS1降解酶属胸内酶。P.fluorescens FS1降解酶对DEHP的最适酸度为pH6.5-8.0，温度为25－35℃，米氏常数Km为190.48nmol/mL。在好氧条件下，DEHP与P.fluorescens FS1降解酯酶作用，形成邻苯二甲酸单酯和邻苯二甲酸后，可进一步降解成苯甲酸、对羟基苯甲酸，最终转化为CO2与H2O。     

废水中硝基酚类化合物生物降解的研究进展

硝基酚是一类重要且常用的化工原料，一些硝基酚毒性大且难以生物降解，被美国环保局列入“优先控制污染物名单”。在自然环境条件下，硝基酚的生物降解速率缓慢，导致硝基酚在环境中长期滞留和积累。分析了人工强化条件下废水中硝基酚的生物降解性能，主要从具有降解硝基酚能力的微生物、硝基酚的厌氧生物降解性、硝基酚的好氧生物降解性和硝基酚的共基质代谢降解方面进行了较全面的综述，讨论了该研究当前仍存在的一些问题和研究展望。     

Photodegradation of new amino acid derivatives suitable for chelating agents in pulp bleaching applications

The purpose of this study was to evaluate photodegradabilities of the following new low-nitrogen chelating agents: N-bis[(carboxymethoxy)ethyl]glycine (compound 1), N-bis[(1,2-dicarboxyethoxy)ethyl]glycine (compound 2) and N-bis[(1,2-dicarboxyethoxy)ethyl]aspartic acid (compound 3). At first photodegradation of these chelating agents as uncomplexed Na-compound 1–3 and Cu(II) complexes were tested, both in lake and distilled water, by exposing them to near-UV region radiation at the range of 315–400 nm. Uncomplexed Na-compounds 2 and 3 were selected to sunlight exposure experiments carried out in lake and distilled water. Compound 3 was also tested in sunlight as Cu and Ca complexes in both solutions. Photodegradation of Na₆-compound 3 in distilled water was studied by exposing it to radiation at the wavelength of 253.7 nm. Photodegradation products were analysed by means of GC-MS (gas chromatography with mass selective detector).

The results demonstrated that compound 1 was quite photostable even as Cu complex while compounds 2 and 3 were found to be photodegradable. Over 90% reduction of compound 3 was achieved during one week and 80% reduction of compound 2 in two weeks' time when they were added as Na salt to lake water and exposed to sunlight. Compound 3 as Cu complex degraded totally in the sunlight in less than one week. In the case of compound 3, the degradation rate decreased depending on the counter cation in the order Cu > Na  Ca. The study demonstrated that photodegradation of Na₆-compound 3 does not result in total mineralization of the compound. A photodegradation pathway for Na₆-compound 3 is proposed.     

A new approach to graphical and numerical analysis of links between plant chemotaxonomy and secondary metabolism from HPLC data smoothed by a simplex mixture design

Summary. HPLC analysis of secondary metabolites represents an efficient tool for the studying of plant chemical diversity under different aspects: chemotaxonomy, metabolomics, adaptative responses to ecological factors, etc. Statistical analyses of HPLC databases, e.g. correlation analysis between HPLC peaks, can reliably provide information on the similarity/dissimilarity degrees between the chemical compounds. The similarities, corresponding to positive correlations, can be interpreted in terms of analogies between chemical structures, synchronic metabolisms or co-evolution of two compounds under certain environment conditions, etc. . In terms of metabolism, positive correlations can translate precursor-product relationships between compounds; negative correlations can be indicative of competitive processes between two compounds for a common precursor(s), enzyme(s) or substrate(s). Furthermore, the correlation analysis under a metabolic aspect can help to understand the biochemical origins of an observed polymorphism in a plant species. With the aim of showing this, we present a new approach based on a simplex mixture design, Scheffé matrix, which provides a correlation network making it possible to graphically visualise and to numerically model the metabolic trends between HPLC peaks. The principle of the approach consisted in mixing individual HPLC profiles representative of different phenotypes, then from a complete mixture set, a series of average profiles were calculated to provide a new database with a small variability. Several iterations of the mixture design provided a smoothed final database from which the relationships between the secondary metabolites were graphically and numerically analysed. These relationships were scale-dependent, namely either deterministic or systematic: the first consisted of a monotonic global trend covering the whole variation field of each metabolites’ pair; the second consisted of repetitive monotonic variations which gradually attenuated or intensified along a global trend. This new metabolomic approach was illustrated from 404 individual plants of Astragalus caprinus (Leguminoseae), belonging to four chemical phenotypes (chemotypes) on the basis of flavonoids analysed in their leaves. After smoothing, the relationships between flavonoids were numerically fitted using linear or polynomial models; therefore the co-response coefficients were easily interpreted in terms of metabolic affinities or competitions between flavonoids which would be responsible of the observed chemical polymorphism (the four chemotypes). The statistical validation of the approach was carried out by comparing Pearson correlations to Spearman correlations calculated from the smoothed and the crude HPLC database, respectively. Moreover, the signs of the smoothed relationships were finely supported by analogies and differences between the chemical structures of flavonoids, leading to fluent interpretation in relation to the pathway architecture.     

鼎湖山主要植被类型土壤微生物生物量研究

对鼎湖山国家级自然保护区3种主要植被类型：季风常绿阔叶林，针阔叶混交林和马尾松林土壤微生物生物量进行了研究。结果表明，土壤微生物生物量（mg.kg^-1）在季风常绿阔叶林、针阔叶混交林和马尾松林中分别为：822，588，530，季风常绿阔叶林显著高于针阔叶混交林和马尾松林（P〈0．01），而针阔叶混交林和马尾松林无显著差异（P〉0．05）；土壤中微生物量高的土壤中，有机碳含量也相应高，两者的比值可反应土壤碳的积累或损失，研究表明，鼎湖山3种主要植被类型土壤均处于碳积累过程；季风常绿阔叶林、针阔叶混交林和马尾松林土壤微生物碳周转量（t.hm^-2．a^-1）依次为：14．07，11．45，9，60，碳素的周转带动了其他营养元素的循环和能量的流动；土壤微生物代谢熵（mg.g^-1．h^-1）由低到高依次是季风常绿阔叶林（0．59）、针阔叶混交林（0．96）和马尾松林（1．33），表明土壤微生物对土壤碳的利用效率季风常绿阔叶林较高，马尾松林较低。     

光合细菌乳酸代谢机制的初步研究

分离获得4株能利用乳酸作为唯一碳源分别进行好氧生长和厌氧生长的光合细菌菌株，对其无细胞抽提液进行透析和乳酸转化为丙酮酸能力的测定．结果表明，这4株光合细菌在好氧和厌氧条件下对乳酸的代谢机制是不同的．对筛选获得的高乳酸转化能力的S1菌株的进一步研究表明，黑暗好氧条件下，S1菌株的乳酸代谢能力与生长呈正相关关系；而光照厌氧条件下，乳酸代谢酶的合成滞后于生长．图5表1参10     

同型乙酸菌研究进展及应用前景

同型乙酸菌是一类分布极广、形态差异极大的微生物类群.该类微生物利用厌氧乙酰辅酶A途径合成代谢中间体乙酰辅酶A,即可营自养生活亦可营异养生活;可利用多种物质作电子供体及电子受体,代谢能力强,底物范围广,能够生成多种代谢产物,如乙酸、乳酸、琥珀酸及甲酸;其独具特色的生理代谢特点,具有应用于工业生产的巨大潜力.本文就同型乙酸菌特有的代谢特点及应用前景作一综述.图2表1参18     

2014年海口市大气污染物演变特征及典型污染个例分析

主要分析了2014年海口市逐日的空气质量指数(AQI)和6种大气污染物的演变特征,同时,结合卫星遥感和轨迹模式等资料和方法对1次典型污染个例进行诊断.结果表明:海口市2014年的空气质量主要以优和良为主,6 d达到轻度污染级别,1 d达到中度污染(1月5日,AQI值为158).1月污染最为严重,其中,阶段1(1-6日)和阶段3(18-23日)AQI值偏高,阶段2(7-17日)和阶段4(24-31日)偏低.1月东亚地区天气形势演变对海口市AQI值具有动力影响.AQI偏高阶段,地面高压系统位于内蒙古东部,华南低层东北风场有利于污染物向海口市输送;而在AQI偏低阶段,地面高压系统东移出海,低层偏东风场不利于污染物的输送.后向轨迹聚类分析表明,1月海口市比率最大(39%)的气流主要经过大气污染相对严重的广东珠江三角洲(珠三角)地区,有利于污染物的区域传输.污染个例分析表明,海口市污染物浓度变化与气象要素有密切关系,10 m风速较小有助于近地面的污染物在区域内累积,水平风垂直切变偏弱对天气尺度扰动的发展和大气的垂直混合不利.卫星遥感和后向轨迹分析也表明,外源输送与海口市这次大气污染事件有直接关系.     

蜡状芽胞杆菌对芘的降解特性及降解酶研究

考察蜡状芽胞杆菌(Bacillus cereus)对水体中芘的降解特性,分析其代谢产物和降解酶的活性.结果表明,1 mg·L-1Mn2+、0.1 mg·L-1Fe3+和10 mg·L-1葡萄糖混合物对芘的降解有明显促进作用;1 g·L-1菌体在120 h内对2.5μmol·L-1芘的降解率达到61.4%.利用LC-MS/MS分析芘代谢产物,检测到1-萘酚、2-萘酚、9-羟基菲和1-羟基芘4种单羟基多环芳烃,表明芘在单加氧酶作用下开环降解,且B.cereus能有效分解利用4种代谢产物,其最高利用率分别为100%、90.3%、98.3%和52.7%.酶活力分析实验结果表明,B.cereus具有的水杨酸羟化酶,邻苯二酚1,2-双加氧酶和邻苯二酚2,3-双加氧酶在芘的降解中起关键作用,其酶活力经芘诱导后均有明显提高.结合产物分析及酶活测定,推断B.cereus对芘的降解途径以及降解过程是由单加氧酶和双加氧酶联合起作用.     

Synthesis,crystal structure,photodegradation kinetics and photocatalytic activity of novel photocatalyst ZnBiYO4

ZnBiYO4 was synthesized by a solid-state reaction method for the first time. The structural and photocatalytic properties of ZnBiYO4 were characterized by X-ray diffraction, scanning electron microscopy, X-ray photoelectron spectroscopy and UV–Vis diffuse reflectance.ZnBiYO4 crystallized with a tetragonal spinel structure with space group I41/A. The lattice parameters for ZnBiYO4 were a = b = 11.176479  and c = 10.014323 . The band gap of ZnBiYO4 was estimated to be 1.58 e V. The photocatalytic activity of ZnBiYO4 was assessed by photodegradation of methyl orange under visible light irradiation. The results showed that ZnBiYO4 had higher catalytic activity compared with N-doped Ti O2 under the same experimental conditions using visible light irradiation. The photocatalytic degradation of methyl orange with ZnBiYO4 or N-doped Ti O2 as catalyst followed first-order reaction kinetics, and the first-order rate constant was 0.01575 and 0.00416 min-1for ZnBiYO4 and N-doped Ti O2, respectively. After visible light irradiation for 220 min with ZnBiYO4 as catalyst, complete removal and mineralization of methyl orange were observed. The reduction of total organic carbon, formation of inorganic products, SO2-4and NO-3, and evolution of CO2 revealed the continuous mineralization of methyl orange during the photocatalytic process. The intermediate products were identified using liquid chromatography–mass spectrometry. The ZnBiYO4/(visible light) photocatalysis system was found to be suitable for textile industry wastewater treatment and could be used to solve other environmental chemical pollution problems.