CO_2浓度升高对铜镉污染土壤粳稻稻米安全品质的影响

采用盆栽试验,在开顶式气室(OTC)内种植水稻,研究了5个粳稻品种在铜镉复合污染土壤上,CO2浓度升高对水稻吸收Cu、Cd和矿质元素Fe、Zn的影响,并对稻米中Cd的安全性进行了评价。结果表明:在2种复合污染水平土壤上,CO2浓度升高条件下,除千重浪2号稻米中Cu含量在高污染土壤处理下增加20.3%外,其他品种稻米Cu含量均有所降低,降低幅度为20.6%~30.2%、2.4%~12.3%;CO2浓度升高除降低了高污染土壤上元丰6号稻米中Cd含量外,均增加了其他品种在低、高污染土壤上的稻米Cd含量,增加幅度分别为3.7%~297.4%、31.7%~209.1%;2种污染水平土壤上,CO2浓度升高对不同品种稻米中Fe、Zn含量变化影响差异显著;CO2浓度升高下,元丰6号、勇丰金穗品种稻米中Cd含量超过食品卫生标准(Cd≤0.2 mg·kg-1);CO2浓度升高会增加5种稻米中Cd的标靶危害系数,其中,勇丰金穗和元丰6号稻米中Cd的THQ值1,表明CO2浓度升高下,其对人体健康已构成了潜在风险。     

菰和菖蒲对重金属的胁迫反应及其富集能力

通过盆栽实验研究了Cu—Zn—Ph-Cd复合污染条件下,菰和菖蒲的生长状况、生理特性及吸收和富集重金属的能力。结果表明,高浓度污染下菰和菖蒲不能存活;低、中浓度中菖蒲的生长受到抑制,菰各生长指标与对照相比差异不显著,表明菰对低、中浓度重金属的耐性强于菖蒲。随着污染浓度的增加,菰和菖蒲叶片叶绿索含量显著降低;菰叶绿素a／b值略有降低,菖蒲叶绿素a／b值显著降低;菰和菖蒲叶片脯氨酸含量、相对电导率显著升高,超氧化物歧化酶（SOD）、过氧化物酶（POD）活性在低浓度时升高,中浓度时降低。菰体内重金属含量为Zn〉Cu〉Pb〉Cd,菖蒲体内的含量为Cu〉Zn〉Pb〉Cd,且二者体内的重金属含量都随着污染浓度的增加而升高。菰和菖蒲对Cd的富集系数较大,地上部分（茎与叶）和地下部分（根与根状茎）均大于1;对Pb的富集系数较小,地上部分和地下部分均小于1。菰和菖蒲地下部分重金属含量均高于地上部分含量,二者根系对4种重金属都有较强的滞留效应,平均滞留率均大于50％。各处理中菰对重金属的吸收量均高于菖蒲。综合分析菰和菖蒲的生长、生理及富集重金属的能力,菰比菖蒲更适用于低、中浓度重金属污染水体的生态修复。     

CO2浓度升高对不同品种水稻镉吸收和根形态的影响

为了探讨CO2浓度升高下不同水稻品种荣优398 (RY)和粤杂889(YZ)吸收重金属Cd差异性的原因,利用水培试验研究了不同浓度Cd处理下两种水稻吸收Cd的差异及根形态的变化特征.结果表明:低Cd处理(5、10、20 μmol·L-1)显著增加水稻生物量;当Cd浓度高于50 μmol·L-1时,Cd胁迫效果开始显现,水稻生物量减少.CO2浓度升高显著增加了水稻的生物量,增加了YZ茎Cd含量而降低了RY茎Cd含量.在5～200 μmol·L-1的Cd浓度下,CO2浓度升高增加了YZ活性根在总根长中的比例,降低了RY活性根的比例.CO2浓度升高下不同水稻品种根形态的变化是导致其对Cd吸收差异性的原因之一.     

蚯蚓对土壤中铜、镉生物有效性的影响

以第四纪红黏土红壤和长江冲积物形成的高砂土为供试土壤、分别加入3个浓度的Cu^2 (100、200、400mg／kg)或Cd^2-(5.10、20mg/kg)模拟土壤污染．设置接种蚯蚓(Pheretima sp.)处理与不加蚯蚓对照．并种植黑麦草(Lolium multiflorum)、研究蚯蚓活动对土壤中Cu、Cd生物有效性的影响．以揭示蚯蚓在植物修复重金属污染土壤中的作用。结果表明：蚯蚓活动显著增加红黏中DTPA提取态Cu的含量、只有在浓度低于200mg／kgCu的处理中．才能增加CaCl2提取态Cu的含量．对H2O提取态Cu影响甚微;而对高砂土上Cu、Cd的各种形态影响均不显著;除红黏中浓度高于100mg／kgCu和10mg／kgCd处理外．蚯蚓活动显著提高了两种土壤上黑麦草地上部的生物量;接种蚯蚓后各种重金属处理中黑麦草对Cu的吸收量也显著增加,而Cd的吸收量变化不大。蚯蚓可能通过提高重金属的生物有效性而间接影响植物对重金属的修复效率。     

巨菌草对Cu、Cd污染土壤的修复潜力

通过田间小区试验,对比研究了土著植物金黄狗尾草、香根草、海州香薷、巨菌草分别与0.21%石灰联合对Cu、Cd复合污染土壤的修复效果。结果表明,石灰处理可以显著提高土壤pH,降低土壤有效态Cu、Cd含量。4种植物在与石灰联合后均有一定的生产潜力,且表现为巨菌草海州香薷香根草金黄狗尾草;修复潜力方面表现出与生产潜力相同的趋势。     

镉在土壤-香根草系统中的迁移及转化特征

以无植物组处理为对照,采用盆栽试验方式探讨不同Cd浓度胁迫条件下香根草根际土壤中重金属Cd的积累、迁移及转化特征。土壤Cd处理设4个浓度梯度,分别为0、2、20、80 mg/kg土壤干重。结果表明:(1)香根草可以显著降低土壤中生物有效态Cd和总Cd含量。(2)香根草各部分Cd积累量随处理浓度的增加和处理时间的延长而增加,90 d时80 mg/kg处理组地上部分和根的Cd积累量分别高达180.42 mg/kg和241.54 mg/kg。(3)各浓度Cd处理下,富集系数随着Cd处理浓度的增加而显著降低,随处理时间的延长而升高。(4)香根草地上部分Cd含量小于根部,各处理转移系数均小于1。随着处理时间的延长,中低浓度处理组的转移系数稍有降低,高浓度处理组的转移系数则显著上升。(5)种植香根草使其根际土中残渣态的Cd转化为生物有效态Cd,提高Cd清除效率。研究结果表明,香根草能够有效地吸收土壤中的Cd,降低土壤中总Cd含量,提高土壤安全性,可作为Cd污染地区植物修复的备选物种。     

重金属对土壤中小麦种子发芽与根伸长抑制的生态毒性

测定了4种土壤（红壤、草甸棕壤、暗棕壤和栗钙土）条件下,Cu,Zn,Pb和Cd单一污染对小麦种子发芽与根伸长抑制主及其复合污染效应（暗棕壤条件下）。结果表明,同一浓度下,重金属对小麦根伸长抑制率均明显大于对种子发芽抑制率,植物根对金属污染的生态毒性比种子发芽敏感,土壤有机质和土壤N含量与Cu,Zn,Pb和Cd污染对小麦根伸长抑制率显著负相关（R^2OR=0.91,R^2K-N=0.92),土壤PH和阳离子交换量与Cu,Zn,Pb和Cd污染对小麦根伸长抑制率的相关性不显著（R^2PH=0.62,R^2CEC=0.60),在单一污染对小麦根伸长为刺激作用浓度（较低浓度）或为抑制作用浓度下（较高浓度）,复合污染均表现为协同作用。^     

Cd污染及其与大气CO2浓度升高、N添加复合作用对大叶相思生长的影响

为了解Cd污染胁迫下树木对CO_2浓度升高、N添加及其复合作用的响应,应用开顶箱,探讨Cd及其与CO_2、N的复合作用对大叶相思(Acacia auriculiformis)基径、树高和生物量的影响。结果表明,Cd添加抑制大叶相思基径、树高和生物量的增长,并且具有时间滞后性;大气CO_2浓度升高、N添加及CO_2+N均有缓解Cd对植物生长抑制作用的趋势,其中, N添加更能促进大叶相思基径的生长,树高生长则对CO_2升高更为敏感;在Cd污染土壤中,N添加的缓解作用最显著。因此,氮肥管理是重金属污染土地修复初期促进植物修复的重要策略。     

伴矿景天-水稻轮作及磷修复剂对水稻锌镐吸收的影响

采用盆栽试验,将锌镉超积累植物伴矿景天与镉低积累水稻中香1号轮作种植于重金属污染土壤,并向土壤添加钙镁磷肥和磷矿粉,研究两种磷修复剂对伴矿景天和锡低积累水稻生长及地上部重金属积累性的影响.盆栽试验结果表明,在轻污染土壤上施用50g"kg-'磷矿粉时伴矿景天地上部的Zn,Cd吸收量分别达到每盆11.5和0.79 mg,效果好于施用4g·kg(-1)钙镁磷肥处理.在重金属污染土壤上种植伴矿景天使后茬水稻地上部Zn、Cd浓度上升,但钙镁磷肥的施用显著降低了水稻体内的Zn,Cd积累量.种植伴矿景天后添加钙镁磷肥稳定调控剂对土壤中水溶态及NH4 OAc提取态Zn、Cd的稳定效果明显优于磷矿粉,且在高污染土壤上效果更佳.田间试验结果显示,施用钙镁磷肥不仅可增加水稻产量,且可一定程度上降低水稻地上部的Zn、Cd吸收量.     

翦股颖和高羊茅对铜、铅吸收及耐受性

测定了高羊茅和翦股颖两种草坪植物在Cu、Pb污染下发芽率、叶绿素、净光合速率和SOD的变化,以及两种草对Cu、Pb的吸收.结果表明, 重金属污染对高羊茅种子的萌发产生显著影响.高浓度Pb污染以及Pb、Cu复合污染对高羊茅的叶绿素影响很大,Cu单独污染对高羊茅叶绿素的抑制作用较小.翦股颖的叶绿素变化不显著.在3个Pb处理及350 mg·kg^-1 Cu处理下,翦股颖的SOD活性均高于对照,而只有在700 mg·kg^-1Pb 和350 mg·kg^-1 Cu+1 100 mg·kg^-1 Pb处理下高羊茅的SOD活性才升高.高羊茅的净光合速率受Cu污染影响较小,而受Pb污染影响较大.在Cu、Pb单独污染条件下,翦股颖净光合速率均呈下降趋势.从生理角度来看,翦股颖对Cu、Pb污染的耐受性强于高羊茅,而高羊茅对Cu污染的耐受性强于Pb.高羊茅Cu吸收量大,但Cu吸收量不随污染浓度升高而升高.翦股颖对土壤Pb的吸收能力较强, 且Pb吸收量随污染浓度的增加而增加.翦股颖和高羊茅可分别用于Pb和Cu污染土壤的治理.     

Unambiguous through-bond sugar-to-base correlations for purines in 13C, 15N-labeled nucleic acids: The HsCsNb,HsCs(N)bCb,and HbNbCb experiments

Summary A set of three 3D (¹H, ¹³C, ¹⁵N) triple-resonance correlation experiments has been designed to provide H1-H8 intraresidue sugar-to-base correlations in purines in an unambiguous and efficient manner. Together, the H_sC_sN_b, H_sC_s(N)_bC_b, and H_bN_bC_b experiments correlate the H1 sugar proton to the H8 proton of the attached base by means of the {H1, C1, N9, C8, H8} heteronuclear scalar coupling network. The assignment strategy presented here allows for unambiguous H1-H8 intraresidue correlations, provided that no two purines have both the same H1 and C1 chemical shifts and the same C8 and N9 chemical shifts. These experiments have yielded H1-H8 intraresidue sugar-to-base correlations for all five guanosines in the [¹³C, ¹⁵N] isotopically labeled RNA duplex r(GGCGCUUGCGUC)₂.     

Crystal structure of the ternary FimC-FimF(t)-FimD(N) complex indicates conserved pilus chaperone-subunit complex recognition by the usher FimD

Type 1 pili, anchored to the outer membrane protein FimD, enable uropathogenic Escherichia coli to attach to host cells. During pilus biogenesis, the N-terminal periplasmic domain of FimD (FimD(N)) binds complexes between the chaperone FimC and pilus subunits via its partly disordered N-terminal segment, as recently shown for the FimC-FimH(P)-FimD(N) ternary complex. We report the structure of a new ternary complex (FimC-FimF(t)-FimD(N)) with the subunit FimF(t) instead of FimH(p). FimD(N) recognizes FimC-FimF(t) and FimC-FimH(P) very similarly, predominantly through hydrophobic interactions. The conserved binding mode at a "hot spot" on the chaperone surface could guide the design of pilus assembly inhibitors.     

μ- and μ4-η coordination of A2H2 (A = C, Si, Ge, Sn and Pb) ligands with transition metals

The heavier analogs of C₂H₂ have been studied at the B3LYP level for their μ and μ₄-η² coordination properties with the transition metals. Based on known alkyne compounds, transition metal fragments [W₂(μ-NH)(Cp)₂(Cl)₂] and [Fe₄(CO)₁₂] have been chosen. The SBKJC relativistic effective core potentials and their associated basis sets were used on W, Fe, Sn and Pb, and the 6-31G(d) basis set was used on all other elements. All the complexes of Si₂H₂, Ge₂H₂, Sn₂H₂ and Pb₂H₂ are found to be local minima. The trans-twist nature of the ligand A₂H₂ (A = Si-Pb) is large in μ-coordinated complexes of W, and it is very small in μ₄-η² coordinated complexes of Fe. The electronic structure of these complexes was investigated using fragment molecular orbital method (FMO).     

Introduction: A Close Look at the Vacuolar ATPase

The vacuolar ATPases (V-type ATPases) are a family of ATP-dependent ion pumps and found in two principal locations, in endomembranes and in plasma membranes. This family of ATPases is responsible for acidification of intracellulare compartments and, in certain cases, ion transport across the plasma membrane of eucaryotic cells. V-ATPases are composed of two distinct domains: a catalytic V₁ sector, in which ATP hydrolysis takes place, and the membrane-embedded sector, V₀, which functions in ion conduction. In the past decade impressive progress has been made in elucidating the properties structure, function and moleculare biology. These knowledge sheds light also on the evolution of V-ATPases and their related families of A-(A₁A₀-ATPase) and F-type (F₁F₀-ATPases)ATPases.     

Acetylcholinesterase/Butyrylcholinesterase inhibition activity of some new carbacylamidophosphate deriviatives

Eight newly synthesized carbacylamidophosphates with the general formula RC(O)NHP(O)Cl₂ with R = pCl–C₆H₄ 1a, pBr–C₆H₄ 2a, C₆H₅ 3a, and pMe–C₆H₄ 4a and RC(O)NHP(O)(NC₄H₈O)₂ R = pCl–C₆H₄ 1b, pBr–C₆H₄ 2b, C₆H₅ 3b, pMe–C₆H₄ 4b, were selected to compare the inhibition kinetic parameters, IC₅₀, K_i, k_p and K_D, on human erythrocyte acetylcholinesterase (hAChE) and bovine serum butyrylcholinesterase (BuChE), Also, the in vivo inhibition potency of compound 2a, 2b and 3a, were studied. The data demonstrates that compound 2a and compound 2b are the potent sensitive as AChE and BuChE inhibitors respectively, and the inhibition of hAChE is about 10-fold greater than that of BuChE.     

Earthworm effects on gaseous emissions during vermifiltration of pig fresh slurry

Treatment of liquid manure can result in the production of ammonia, nitrous oxide and methane. Earthworms mix and transform nitrogen and carbon without consuming additional energy. The objective of this paper is to analyse whether earthworms modify the emissions of NH₃, N₂O, CH₄ and CO₂ during vermifiltration of pig slurry.The experiment used mesocosms of around 50 L, made from a vermifilter treating the diluted manure of a swine house. Three levels of slurry were added to the mesocosms, with or without earthworms, during one month, in triplicate. Earthworm abundance and gas emissions were measured three and five times, respectively.There was a decrease in emissions of ammonia and nitrous oxide and a sink of methane in treatments with earthworms. We suggest that earthworm abundance can be used as a bioindicator of low energy input, and low greenhouse gas and ammonia output in systems using fresh slurry with water recycling.     

Antibacterial properties of recombinant human non-pancreatic secretory phospholipase A2

Human non-pancreatic secretory phospholipase A₂ (hnpsPLA₂) is a group IIA phospholipase A₂ which plays an important role in the innate immune response. This enzyme was found to exhibit bactericidal activity toward Gram-positive bacteria, but not Gram-negative ones. Though native hnpsPLA₂ is active over a broad pH range, it is only highly active at alkaline conditions with the optimum activity pH of about 8.5. In order to make it highly active at neutral pH, we have obtained two hnpsPLA₂ mutants, Glu89Lys and Arg100Glu that work better at neutral pH in a previous study. In the present study, we tested the bactericidal effects of the native hnpsPLA₂ and the two mutants. Both native hnpsPLA₂ and the two mutants exhibit bactericidal activity toward Gram-positive bacteria. Furthermore, they can also kill Escherichia coli, a Gram-negative bacterium. The two mutants showed better bactericidal activity for E. coli at neutral pH than the native enzyme, which is consistent with the enzyme activities. As hnpsPLA₂ is highly stable and biocompatible, it may provide a promising therapy for bacteria infection treatment or other bactericidal applications.     

Crystal structure of the archaeal A1Ao ATP synthase subunit B from Methanosarcina mazei Gö1: Implications of nucleotide-binding differences in the major A1Ao subunits A and B

The A1Ao ATP synthase from archaea represents a class of chimeric ATPases/synthases, whose function and general structural design share characteristics both with vacuolar V1Vo ATPases and with F1Fo ATP synthases. The primary sequences of the two large polypeptides A and B, from the catalytic part, are closely related to the eukaryotic V1Vo ATPases. The chimeric nature of the A1Ao ATP synthase from the archaeon Methanosarcina mazei G?1 was investigated in terms of nucleotide interaction. Here, we demonstrate the ability of the overexpressed A and B subunits to bind ADP and ATP by photoaffinity labeling. Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry was used to map the peptide of subunit B involved in nucleotide interaction. Nucleotide affinities in both subunits were determined by fluorescence correlation spectroscopy, indicating a weaker binding of nucleotide analogues to subunit B than to A. In addition, the nucleotide-free crystal structure of subunit B is presented at 1.5 A resolution, providing the first view of the so-called non-catalytic subunit of the A1Ao ATP synthase. Superposition of the A-ATP synthase non-catalytic B subunit and the F-ATP synthase non-catalytic alpha subunit provides new insights into the similarities and differences of these nucleotide-binding ATPase subunits in particular, and into nucleotide binding in general. The arrangement of subunit B within the intact A1Ao ATP synthase is presented.     

Assessing the Impact of Advected African Dust on Air Quality and Health in the Eastern United States

Large quantities of African dust are carried into the southeastern United States each summer with concentrations typically in the range of 10 to 100?µg m^?3. Because approximately one-third to one-half of the dust mass is in the size range under 2.5?µm diameter, the advection of African dust has implications for the EPA's newly implemented standard for PM_2.5 particulate matter and for the assessment of human health effects. It will be difficult to assess the impact of African dust events on air quality because they occur during the summer (maximum in July) when photochemical pollution events are frequent and intense in the eastern United States. Indeed, the presence of dust could affect the evolution of photochemical dust events. In order to assess the role of African dust in air quality in the United States, it will be necessary to develop a set of diagnostic indicators; it appears that dust mineralogy and elemental composition might be useful for this purpose. Various satellite products can be used to characterize the spatial coverage of dust events and, when coupled with meteorological tools, to predict impact regions.