中国近海浮游植物生产的二甲基硫和二甲基硫丙酸的分布状况及其影响因素

于1994～1998年期间调查了浮游植物生产的生源气候气体二甲基硫(DMS)及其前身二甲基硫丙酸(DMSPp)在我国胶州湾、芝罘湾、东海的分布状况及其影响因素.结果表明,自然海区中二者浓度都存在明显的时空变化.地理分布规律是,高值出现在沿岸海区和陆架海区,低值出现在外海特别是贫营养海区.就不同季节而言,高值出现在春季或夏季,低值出现在秋季.DMS或DMSPp的分布在大尺度上主要受海流和水团的影响,而在小尺度上营养条件和生物因子则更重要.在近岸海区,硅藻是DMS和DMSPp的重要贡献者.研究海区硝酸盐与DMSPp的关系有两种情况:当硝酸盐浓度低于1μmol/L时,二者为正相关,硝酸盐浓度高于这个阈值时,二者为负相关.表明浮游植物细胞中二甲基硫丙酸作为渗透压调节物质其含量受到氮源可得性的调控.此外,研究结果还显示,生活污水入海、海水养殖等也对DMS和DMSPp的浓度分布有一定影响.     

三种典型赤潮藻产生与消耗二甲基硫化物的速率估算

采用抑制剂加入法估算了中肋骨条藻、棕囊藻和东海原甲藻在不同生长期内二甲基硫化物的产生与消耗速率.结果表明:颗粒态二甲基巯基丙酸(DMSPp)和颗粒态二甲亚砜(DMSOp)在3种藻类的不同生长期内均为净消耗,溶解态二甲基巯基丙酸(DMSPd)和溶解态二甲亚砜(DMSOd)的含量受藻类产生与细菌病毒消耗控制,在藻类不同生长期内存在不同的产生与消耗速率,而二甲基硫(DMS)在3种藻不同生长期内均为净产生.同一种藻在不同生长期内以及不同藻在相同生长期内二甲基硫化物的产生与消耗速率均存在较大差异,表明藻类的生理状态和种间差异均对二甲基硫化物的产生与消耗速率产生影响.     

海洋二甲基硫观测技术及其海-气通量分析研究进展

二甲基硫(DMS)海-气交换是全球硫循环的主要参与者,对全球气候变化产生重要影响。有关海洋DMS排放及其海-气交换过程研究已引起人们的广泛关注,并成为现今国际上的研究热点之一。从海洋DMS观测技术及海-气通量估算两方面进行了系统总结,并指出了它们的最新进展和发展趋势,具体包括:虽然遥感技术在获取DMS时空分布及大面数据方面具有独特优势,但气相色谱法是目前应用最为广泛的观测技术,而质谱也越来越受到研究者们的青睐;直接观测技术在提升分析性能的同时朝着自动化、智能化现场实时观测的方向发展;观测对象从单一DMS扩展至其前体、二甲基亚砜等其他物质,同时所获数据呈多元化趋势,准确度也逐渐提升;以滞膜模型为代表的模型估算和以涡旋相关法为代表的直接测量法是目前DMS海-气通量分析的主要方法,而多元化数据则促进了两种或两种以上通量分析方法的联合及对比;深入探究海洋环境因素对海-气交换过程的影响,进一步完善速率常数计算和通量估算方法,是获得适用性更广、准确度更高的DMS传输率常数及提高通量估算准确度的重要途径;将直接观测技术和遥感卫星观测技术相结合,开展时间、空间维度上的全球海域DMS大数据调查研究,并深入评估DMS对海洋环境及气候变化的影响将是未来研究的重要内容;基于大数据基础构建海洋DMS排放趋势模型,实现未来DMS排放的准确预测是DMS观测及其海-气通量分析研究的重要目标。     

微生物二甲基巯基丙酸内盐(DMSP)合成途径中关键酶的研究进展

二甲基巯基丙酸内盐(dimethylsulfoniopropionate,DMSP)是全球重要的有机硫化合物之一,参与全球硫循环、信号传递及气候调节。全球DMSP的产量每年高达10⁹ t。DMSP的主要生产者是海洋浮游植物及大型藻类,近年来发现一些海洋细菌也可以产生DMSP,是海洋中DMSP的一个重要来源。目前已报道的DMSP合成途径有3条：甲基化途径、转氨途径和脱羧途径,其中有5种DMSP合成关键酶被鉴定出来。根据近年来的研究成果,本文对DMSP合成过程中关键酶的研究进展进行综述,以期为进一步的研究提供思路。     

氮磷营养盐添加对二甲基巯基丙酸内盐合成与降解细菌及其功能基因的影响

【目的】二甲基巯基丙酸内盐(dimethylsulfoniopropionate,DMSP)是海洋中主要的有机硫化物之一,是海洋细菌硫的主要来源,海洋细菌将其分解成"冷室气体"二甲基硫(dimethylsulfide,DMS),对调节全球气候变化和驱动地球硫循环有重要作用。本研究通过中国东海水体的现场围隔实验模拟海水富营养化对DMSP、DMS产量以及DMSP合成基因(dsyB和mmtN)和降解基因(dddP和dmdA)及相关功能细菌的影响。【方法】通过流式细胞仪计数92个围隔海水样品中微微型浮游生物的数量,采用Illumina MiSeq测序技术对海水样品中细菌的16S rRNA基因进行高通量测序,利用荧光定量PCR技术定量测定16S rRNA基因、DMSP合成及降解基因的丰度。【结果】研究发现,同时添加硝酸盐(6.00μmol/L)和磷酸盐(0.375μmol/L)能促进叶绿素a、DMSP、DMS的浓度上升。对于DMSP合成基因,只加磷酸盐能促进dsyB及Phaeobacter等相应物种的富集,虽然同时添加硝酸盐和磷酸盐使dsyB富集,但相对只加磷酸盐却不利于dsyB积累;同时添加硝酸盐和磷酸盐也抑制Alteromonas的生长,进而抑制了mmtN的富集。对于DMSP降解基因,同时加入硝酸盐和磷酸盐促进了dddP及Thalassococcus、Thalassobius、Loktanella和Shimia等物种的富集,却抑制了SAR11、Sulfitobacter等的富集,从而导致dmdA无法被富集。【结论】氮限制能更好地促进DMSP合成基因的表达,从而迫使细菌增加DMSP的合成以应对氮营养条件不足的生存环境,并进而提高DMSP脱甲基化的比例为细菌提供更多能量;而在硝酸盐和磷酸盐充足情况下,细菌相对减少DMSP的合成且更倾向于裂解DMSP产生DMS来降低硫同化的比例。本研究结果强调了海水富营养化对细菌合成与降解DMSP过程的影响。     

围隔藻类水华演替过程中二甲基硫化物的含量动态

于2005年6月至7月,研究了海洋围隔不同藻类水华演替过程中二甲基硫化物的含量动态,并考察了相关环境参数对二甲基硫化物含量的影响。2个围隔实验组均出现未知藻水华-硅藻水华-甲藻水华的演替过程,这3次不同藻类水华分别对应了二甲基硫化物含量的3次高峰,表明藻类水华对二甲基硫化物含量有重要贡献。不同藻类水华的贡献有较大差异,甲藻水华的贡献最大,硅藻次之,未知藻类水华的贡献最小。实验结果还表明PO4^3-、NO2^-和NH4^＋主要通过影响藻类生长状态,进而影响DMSP和DMSO的含量;NO2^-和NH4^＋亦可能通过调节DMSP和DMSO在藻细胞内的生理功能,影响DMSP和DMSO的含量;PO4^3-、NO2^-和NH4^＋与DMS含量无显著相关。     

海洋微生物裂解二甲基巯基丙酸内盐(DMSP)的酶促催化机制

二甲基巯基丙酸内盐(dimethylsulfoniopropionate,DMSP)是全球硫循环和碳循环的重要载体物质。海洋浮游植物、大型藻类和临海被子植物是DMSP的主要生产者。每年DMSP的产量可以达到1×10~9吨。在北大西洋表面的某些区域,DMSP的产量可以达到碳固定总量的10%。微生物介导的DMSP的裂解是全球硫循环和碳循环的重要步骤。目前,8种参与裂解DMSP的DMSP裂解酶已被报道。在已发现的8种DMSP裂解酶中,3种DMSP裂解酶的催化机制得到了研究和阐明。本文根据国内外研究成果,主要对DMSP裂解过程的酶促催化机制的研究进展进行综述,认为在今后工作中需要继续发现新的DMSP裂解酶,并进一步揭示海洋微生物裂解DMSP的分子机制。     

用卫星数据计算北极二甲基硫的方法初探

本文主要研究的是利用可下载的卫星数据,计算北极2003~2006年格陵兰海区域(20°W~10°E,70°N~80°N)二甲基硫(DimethylSulfur,简称DMS)浓度的值,并探究其与海冰浓度(ICE)的相关性.通过对庞大的全球卫星数据的处理,提取出格陵兰海的叶绿素浓度(CHL)和ICE的数据,运用MATLAB软件将提取到的点数据转化为网格数据,利用温度差值法计算混合层深度(MLD),再根据Simo公式编程计算DMS的值.为了使结论更具有普遍性,划分70°N~75°N、75°N~80°N和70°N~80°N三个子区域来进行分析.使用SPSS软件,对ICE和DMS进行相关性检验,并回归分析得出表达式.得出在2003~2006年的格陵兰海区域,DMS和ICE具有相关性,呈负相关,相关系数在-0.57~0.45之间.本文对卫星数据的处理方法、DMS的计算方法以及统计上的耦合回归研究对生物地理化学研究者有一定的参考价值.     

颗石藻类群及其生态功能介绍

颗石藻(coccolithophore)是一类在全球海洋中广泛分布的海洋微型浮游植物, 它们在海洋浮游植物功能群落中是一类极其重要的钙化生物类群, 也是海洋中生源无机碳的重要来源, 并且在海洋的碳循环过程中起到重要的作用。颗石藻由于快速增殖而发生水华的过程中能够释放大量的具有挥发性的二甲基硫(DMS)和丙烯酸(acrylic acid), 它们是影响气候变化, 特别是引起区域性环境效应(温室效应)的关键性物质。     

二甲基精氨酸二甲基氨基水解酶与内皮功能异常

非对称二甲基精氨酸（asymmetric dimethylarginine,ADMA）是一氧化氮合酶（NOS）的内源性竞争性抑制物,竞争性抑制NOS使NO含量减少,引起一系列血管异常效应。二甲基精氨酸Z-甲基氨基水解酶（dimethylarginine dimethylaminohydrolase,DDAH）是主导ADMA代谢的催化酶。DDAH减少或活性降低会使ADMA在体内积累,导致内皮功能异常。本文介绍了DDAH引起内皮功能异常的机制,并对有关影响DDAH活性或表达的药物研究作一概述。     

Structure and function of S-adenosylhomocysteine hydrolase

In mammals, S-adenosylhomocysteine hydrolase (AdoHcyase) is the only known enzyme to catalyze the breakdown of S-adenosylhomocysteine (AdoHcy) to homocysteine and adenosine. AdoHcy is the product of all adenosylmethionine (AdoMet)-dependent biological transmethylations. These reactions have a wide range of products, and are common in all facets of biometabolism. As a product inhibitor, elevated levels of AdoHcy suppress AdoMet-dependent transmethylations. Thus, AdoHcyase is a regulator of biological transmethylation in general. The three-dimensional structure of AdoHcyase complexed with reduced nicotinamide adenine dinucleotide phosphate (NADH) and the inhibitor (1′R, 2′S, 3′R)-9-(2′,3′-dihyroxycyclopenten-1-yl)adenine (DHCeA) was solved by a combination of the crystallographic direct methods program, SnB, to determine the selenium atom substructure and by treating the multiwavelength anomalous diffraction data as a special case of multiple isomorphous replacement. The enzyme architecture resembles that observed for NAD-dependent dehydrogenases, with the catalytic domain and the cofactor binding domain each containing a modified Rossmann fold. The two domains form a deep active site cleft containing the cofactor and bound inhibitor molecule. A comparison of the inhibitor complex of the human enzyme and the structure of the rat enzyme, solved without inhibitor, suggests that a 17° rigid body movement of the catalytic domain occurs upon inhibitor/substrate binding.     

Land,livestock, and livelihoods: Changing dynamics of gender,caste, and ethnicity in a Nepalese Village

Over the past 10 years, Ghusel VDC, Lalitpur District has moved from primarily subsistence agriculture into the wider cash economy aided by the Small Farmers' Development Program (SFDP), which provides credit to farmers mainly for the purchase of buffalo for milk production, and by the National Dairy Corporation, which supports local dairy cooperatives. Analysis reveals that buffalo-keeping and milk sales are increasing the well-being of many households, while at the same time creating new inequalities in gender roles and responsibilities, greater inequities between Brahmin and Tamang residents in Ghusel, and placing pressures on the ecosystem for increased supplies of fodder and fuelwood. Evidence suggests that there is critical, need for attention to the social, and particularly gender-based, implications of maintaining livestock for milk sales and to the ecological underpinnings of this livelihood system.     

Tuning of electronic properties of one-dimensional cyano-bridged Cu-Ni, Cu-Pd, and Cu-Pt bimetallic assemblies by stereochemistry of ligands

Preparations, XPS and electronic spectroscopy, and magnetism of seven new one-dimensional cyano-bridged coordination polymers, chiral [Cu(RR-chxn)₂][Pd(CN)₄] · 2H₂O (1), [Cu(trans-chxn)₂][M(CN)₄] · 2H₂O (2, 4, and 6 for M = Pd, Ni, and Pt), and [Cu(cis-chxn)₂][M(CN)₄] · 2H₂O (3, 5, and 7 for M = Pd, Ni, and Pt) (RR-chxn = cyclohexane-(1R,2R)-diamine, trans-chxn = racemic trans-cyclohexane-(1,2)-diamine, and cis-chxn = racemic cis-cyclohexane-(1,2)-diamine) have been reported in view of tuning of their electronic properties by stereochemistry of chxn ligands and metal-substitution. Comparison of Cu 2p_1/2 and 2p_3/2 peaks of XPS and broad d-d bands around 18 000 cm⁻¹ of electronic spectra are described systematically for 1-7. Variable-temperature magnetic measurement shows that complexes 1-7 indicate weak antiferromagnetic interactions via cyano-bridges. Because of semi-coordination coupled with pseudo Jahn-Teller elongation and electrostatic interaction for 1, the axial Cu-N coordination bond distances of 2.330(7) and 3.092(8) Å are considerably longer than those of equatorial ones in the range from 2.016(6) to 2.030(6) Å. The former bond distances of 1 are intermediate values among the related Ni (2.324(6) and 3.120(8) Å) and Pt (2.34(1) and 3.09(1) Å) complexes.     

Influence of Fluoride on Rat Kidney Antioxidant System: Effects of Methionine and Vitamin E

The aim of the study has been to determine and compare the influence upon the kidney antioxidative system, exercised by administration of vitamin E, and vitamin E in combination with methionine, under conditions of oxidative stress induced by sodium fluoride. The experiment was carried out on Wistar FL rats (adult males) that, for 35 days, were administered water, NaF, NaF with vitamin E, or vitamin E with methionine (doses: 10 mg NaF/kg of body mass/24 h, 3 mg vitamin E per 10 μl per rat for 24 h, 2 mg methionine per rat for 24 h). The influence of administered sodium fluoride and antioxidants upon the antioxidative system in kidney was examined by analyzing the concentration of malondialdehyde (MDA) and the activity of the most important antioxidative enzymes (SOD, total and both its isoenzymes, GPX, GST, GR, and CAT). The studies carried out confirmed the disadvantageous effect of the administered dose of NaF upon the antixodiative system in rats (increase in the concentration MDA, decrease activity of all antioxidative enzymes). The administration of vitamin E increased the activity of studied enzymes with the exception of glutathione reductase GR; it also reduced the procesess of lipid peroxidation. It has been found that combined doses of vitamin E and methionine were most effective in inhibiting lipid peroxidation processes. The results confirmed the antioxidative properties of methionine.     

Gamma-glutamylcysteine protects ergothioneine-deficient Mycobacterium tuberculosis mutants against oxidative and nitrosative stress

Mycobacterium tuberculosis (M.tb.), the causative agent of tuberculosis (TB), cannot synthesize GSH, but synthesizes two major low molecular weight thiols namely mycothiol (MSH) and ergothioneine (ERG). Gamma-glutamylcysteine (GGC), an intermediate in GSH synthesis, has been implicated in the protection of lactic acid bacteria from oxidative stress in the absence of GSH. In mycobacteria, GGC is an intermediate in ERG biosynthesis, and its formation is catalysed by EgtA (GshA). GGC is subsequently used by EgtB in the formation of hercynine-sulphoxide-GGC. In this study, M.tb. mutants harbouring unmarked, in-frame deletions in each of the fives genes involved in ERG biosynthesis (egtA, egtB, egtC, egtD and egtE) or a marked deletion of the mshA gene (required for MSH biosynthesis) were generated. Liquid chromatography tandem mass spectrometry analyses (LC-MS) revealed that the production of GGC was elevated in the MSH-deficient and the ERG-deficient mutants. The ERG-deficient ΔegtB mutant which accumulated GGC was more resistant to oxidative and nitrosative stress than the ERG-deficient, GGC-deficient ΔegtA mutant. This implicates GGC in the detoxification of reactive oxygen and nitrogen species in M.tb.     

Reorientation of Microfibrils and Microtubules at the Outer Epidermal Wall of Maize Coleoptiles During Auxin-Mediated Growth

Auxin-mediated elongation growth of isolated subapical coleoptile segments of maize (Zea mays L.) is controlled by the extensibility of the outer cell wall of the outer epidermis (Kutschera et al., 1987). Here we investigate the hypothesis that auxin controls the extensibility of this wall by changing the orientation of newly deposited microfibrils through a corresponding change in the orientation of cortical microtubules. On the basis of electron micrographs it is shown that cessation of growth after removal of the endogenous source of auxin is correlated with a relative increase of longitudinally orientated microfibrils and microtubules at the inner wall surface. Conversely, reinduction of growth by exogenous auxin is correlated with a relative increase of transversely orientated microfibrils and microtubules at the inner wall surface. These changes can be detected 30–60 min after the removal and addition of auxin, respectively. The functional significance of directional changes of newly desposited wall microfibrils for the control of elongation growth is discussed.     

眶额叶微量注射谷氨酸和γ-氨基丁酸对胃运动的影响及其机制探讨

目的:研究眶额叶(OFC)的谷氨酸(Glu)和γ-氨基丁酸(GABA)含量变化对胃运动的影响及其调节神经机制。方法:实验采用了大鼠眶额叶微量注射给药,结合核团损毁的方法,以记录胃内压,统计胃收缩幅度作为胃运动变化的指标。结果:①OFC注射Glu可显著降低胃收缩幅度,损毁杏仁核后可反转该效应,胃收缩幅度显著增强;损毁蓝斑核后,Glu的作用无显著性变化。②OFC注射GABA可显著增强胃的收缩幅度,损毁蓝斑核后消除该效应;损毁杏仁核后,胃收缩幅度进一步增强。结论:外源性增加OFC区Glu含量导致的抑胃效应可能是通过增强了杏仁核的经常性抑胃作用而引起的;而增加OFC区GABA的含量引起的胃运动增强与蓝斑核密切相关。     

Highly flexible O,O′,N ligands and their Fe, Ni, Cu and Zn complexes

Three new chiral ligands bearing an O,O′,N donor set (O_methoxyO_hydroxyN_pyridine) were synthesised and coordinated to Fe^III, Fe^II, Ni^II, Cu^II and Zn^II to yield complexes with the general formula [M(OON)Cl_x]_y. While the pyridine N and the hydroxy O atoms coordinate strongly to all applied metal ions, the methoxy donor seems not to be involved in coordination, although some evidence for a weak interaction between O_Me and the Zn^II were found in NMR spectra. In the bidentate O′,N coordination mode the new ligands exhibit several coordination geometries as analysed in the solid compounds by XRD, EXAFS and EPR and in solution by UV-Vis absorption, cyclic voltammetry, EXAFS, EPR or NMR spectroscopy.     

邻苯二甲酸二丁酯对翡翠贻贝抗氧化酶及脂质过氧化水平的影响

实验室条件下,研究了不同浓度邻苯二甲酸二丁酯(DBP)长期胁迫(15 d)对翡翠贻贝内脏团和外套膜抗氧化酶(超氧化物歧化酶SOD、过氧化氢酶CAT)及脂质过氧化(LPO)水平(以MDA含量表示)的影响,以及受胁迫翡翠贻贝在清洁海水中恢复阶段上述生化指标的变化特征.结果表明:胁迫阶段,0.5和2.5 mg.L-1DBP下翡翠贻贝内脏团SOD活性表现为先抑制后逐渐恢复,12.5和62.5 mg.L-1下则持续受到显著抑制;不同浓度组CAT活性均明显被抑制.LPO水平明显升高.外套膜中,2.5 mg.L-1下SOD活性受到持续诱导,其他浓度组则先被抑制,后随曝露时间延长逐渐被诱导;各浓度组CAT的变化波动较大,没有明显规律;而LPO水平明显升高.净化恢复阶段,12.5和62.5 mg.L-1DBP胁迫下的内脏团SOD和CAT活性恢复较慢,其LPO水平随时间延长逐渐恢复至对照组水平;外套膜中SOD活性呈持续升高趋势,CAT活性和LPO水平则随时间延长恢复到对照组水平.     

Cu(II) and Zn(II) ions alter the dynamics and distribution of Mn(II) in cultured chick glial cells

Previous studies revealed that Mn(II) is accumulated in cultured glial cells to concentrations far above those present in whole brain or in culture medium. The data indicated that Mn(II) moves across the plasma membrane into the cytoplasm by facilitated diffusion or counter-ion transport with Ca(II), then into mitochondria by active transport. The fact that 1–10 M Mn(II) ions activate brain glutamine synthetase makes important the regulation of Mn(II) transport in the CNS. Since Cu(II) and Zn(II) caused significant changes in the accumulation of Mn(II) by glia, the mechanisms by which these ions alter the uptake and efflux of Mn(II) ions has been investigated systematically under chemically defined conditions. The kinetics of [⁵⁴MN]-Mn(II) uptake and efflux were determined and compared under four different sets of conditions: no adducts, Cu(II) or Zn(II) added externally, and with cells preloaded with Cu(II) or Zn(II) in the presence and absence of external added metal ions. Zn(II) ions inhibit the initial velocity of Mn(II) uptake, increase total Mn(II) accumulated, but do not alter the rate or extent Mn(II) efflux. Cu(II) ions increase both the initial velocity and the net Mn(II) accumulated by glia, with little effect on rate or extent of Mn(II) efflux. These results predict that increases in Cu(II) or Zn(II) levels may also increase the steady-state levels of Mn(II) in the cytoplasmic fraction of glial cells, which may in turn alter the activity of Mn(II)-sensitive enzymes in this cell compartment.