Response of Scenedesmus Incrassatulus to Salt Stress as Affected by Methyl Jasmonate

Exposure of the freshwater green alga Scenedesmus incrassatulus Bohl, strain R-83 to salt stress (175 mM NaCl) resulted in a reduction of its growth and ¹⁴CO₂ fixation and in an increase of accumulation of free proline and malondialdehyde (MDA). The accumulation of proline in the light was higher than in dark. NaCl significantly inhibited the Fe-induced release of organic chelators from the cells. Exogenously supplied 10^–4M methyl jasmonate (JA-Me) did not considerably change the ¹⁴CO₂ fixation, but increased proline and MDA accumulation in the cells and moderately inhibited the release of chelators from cells. JA-Me supplied simultaneously with NaCl helps the algae to counteract the salt stress.     

长白山阔叶红松林生态系统碳动态及其对气候变化的响应

应用基于干物质生产理论的过程模型（Sim-CYCLE）估算了1982—2003年间长白山阔叶红松林生态系统总第一生产力（GPP）、净第一生产力（NPP）、净生态系统生产力（NEP）及其季节动态变化以及碳储量（WE）、植物碳储量（WP）和土壤碳储量（WS）,并分析了这些指标在当前气候情景和碳平衡情况时的差异及其对未来气候变化情景的响应.结果表明：在当前气候情景下, 长白山阔叶红松林GPP、NPP和NEP分别为14.9、8.7和2.7 Mg C·hm^-2·a^-1,三者分别比实测值减少2.8 Mg C·hm^-2·a^-1、增加1.4 Mg C·hm^-2·a^-1和增加0.2 Mg C·hm^-2·a^-1;长白山阔叶红松林6—8月的NEP占全年总量的90%以上,其中,7月最高（1.23 Mg C·hm^-2·month^-1）;研究区WE、WP和WS分别为550.8、183.8和367.0Mg C·hm^-2,其与实测值均具有较高的一致性.从当前气候情景下到达碳平衡前,长白山阔叶红松林碳储量均有不同程度的增加,GPP和NPP分别为17.7和7.3 Mg C·hm^-2·a^-1,表明研究区碳“汇”的作用随着碳储量的增加逐渐减弱;温度增加2 ℃时,不利于长白山阔叶红松林GPP、NPP和NEP的增长,CO²浓度倍增则可有利地促进三者的增长,CO²浓度倍增、温度增加2 ℃对GPP、NPP和NEP增幅的影响与单纯CO₂浓度倍增的影响相似,气候变化情景对长白山阔叶红松林碳储量的影响规律与对生产力幅度的影响相同,这可能是生态系统生产力影响碳积累所致.     

Mn/Fe superoxide dismutase interaction fingerprints and prediction of oligomerization and metal cofactor from sequence

Fe- and Mn-containing superoxide dismutase (sod) enzymes are closely related and similar in both amino acid sequence and structure, but differ in their mode of oligomerization and in their specificity for the Fe or Mn cofactor. The goal of the present work is to identify and analyze the sequence and structure characteristics that ensure the cofactor specificities and the oligomerization modes. For that purpose, 374 sod sequences and 17 sod crystal structures were collected and aligned. These alignments were searched for residues and inter-residue interactions that are conserved within the whole sod family, or alternatively, that are specific to a given sod subfamily sharing common characteristics. This led us to define key residues and inter-residue interaction fingerprints in each subfamily. The comparison of these fingerprints allows, on a rational basis, the design of mutants likely to modulate the activity and/or specificity of the target sod, in good agreement with the available experimental results on known mutants. The key residues and interaction fingerprints are furthermore used to predict if a novel sequence corresponds to a sod enzyme, and if so, what type of sod it is. The predictions of this fingerprint method reach much higher scores and present much more discriminative power than the commonly used method that uses pairwise sequence comparisons.     

Asymmetric Rate Behavior of Si Anodes for Lithium‐Ion Batteries: Ultrafast De‐Lithiation versus Sluggish Lithiation at High Current Densities

The combined effect of lithium‐ion diffusion, potential‐concentration gradient, and stress plays a critical role in the rate capability and cycle life of Si‐based anodes of lithium‐ion batteries. In this work, Si nanofilm anodes are shown to exhibit an asymmetric rate performance: around 72% of the total available capacity can be delivered during de‐lithiation under a high current density of 420 A g^‐1 (100C where C is the charge‐rate) in 22 s; in striking contrast, only 1% capacity can be delivered during lithiation. A mathematical model of single‐ion diffusion is established to elucidate the asymmetric rate performance, which can be mainly attributed to the potential‐concentration profile associated with the active material and the ohmic voltage shift under high currents; the difference in chemical diffusion coefficients during lithiation and de‐lithiation also plays a role. This clarifies that the charge and discharge rates of lithium‐ion‐battery electrodes should be evaluated separately due to the asymmetric effect in the electrochemical system.     

铜、铅、镉、锌、汞和银离子复合污染对水螅的急性毒性效应

以水螅(Hydrasp)为例,通过单因子静态急性毒性试验方法和等毒性溶液法,分别研究Hg2 、Cu2 、Cd2 、Ag 、Zn2 和Pb2 对其单一和复合毒性效应。单一实验结果表明,它们对水螅毒性大小顺序为Hg2 >Cu2 >Cd2 >Ag >Zn2 >Pb2 。复合毒性实验表明,Zn2 与Cu2 、Hg2 、Pb2 、Ag ;Pb2 与Cu2 ;Hg2 与Ag ;Pb2 与Ag 这些组合对水螅联合急性毒性总体上表现出拮抗作用,Cd2 与Cu2 、Hg2 、Pb2 、Ag 组合总体上则是协同作用,Zn2 与Cd2 、Pb2与Hg2 、Cu2 与Hg2 ,Ag 在不同的浓度水平组合下明显表现出不同的毒性效应。     

若尔盖高原湿地不同微地貌区甲烷排放通量特征

若尔盖高原是我国泥炭沼泽湿地的主要分布区、青藏高原的主要甲烷(CH₄)排放中心。为了研究湿地微地貌环境对高原湿地CH₄排放通量的影响, 2014年5-10月, 采用静态箱和快速温室气体分析仪原位测量若尔盖高原湖滨湿地3种泥炭沼泽5种微地貌环境下的CH₄排放通量特征。结果表明: (1)常年性淹水泥炭湿地洼地(P-hollow)和草丘(P-hummock)生长季平均CH₄排放通量为68.48和40.32 mg·m^-2·h^-1, 季节性淹水的泥炭湿地洼地(S-hollow)和草丘(S-hummock)平均CH₄排放通量为2.38和0.63 mg·m^-2·h^-1, 而无淹水平坦地(Lawn)平均CH₄排放通量为3.68 mg·m^-2·h^-1; (2)湿地5种微地貌区CH₄排放通量为(23.10 ± 30.28) mg·m^-2·h^-1 (平均值±标准偏差)), 变异系数为131%。分析显示这5种微地貌区CH₄排放通量的平均值与其水位深度平均值存在显著的线性正相关关系(R² = 0.919, p < 0.01), 表明水位深度是控制湿地微地貌区CH₄排放通量空间变化的主要因子; (3) P-hummock、P-hollow和S-hummock的CH₄排放通量存在显著的季节变化, Lawn和S-hollow无明显的季节性变化, 但5种微地貌区在夏季或秋季均观测到CH₄排放通量峰值, 其影响因子可能与水位深度、土壤温度和凋落物输入密切相关; (4) P-hollow可能时常发生冒泡式CH₄排放, 这可能导致过去低估了若尔盖高原湿地的CH₄排放量。     

Ca~(++)促进大麦根K~+吸收的过程分析

吸收溶液中CaCl_2促进了大麦根K~+净吸收,Ca~(++)本身对H~+分泌无影响,Cl~-减少了H~+净分泌量。 含有~(86)Rb的大麦根在1m mol/L KCl溶液中发生~(86)Rb外流,在H_2O、1m mol/L NaCl或0.5 m mol/L CaCl_2中没有明显外流。VO_4~(3-)、NaN_3和4℃低温均可以减少根段在1m mol/L KCl溶液中的~(86)Rb外流量。Ca~(++)抑制K~+(~(86)Rb~+)的外流,EDTA加剧外流,Ca~(++)可以逆转EDTA的效应。 Ca~(++)抑制K~+(~(86)Rb)外流和促进K~+净吸收的趋势相吻合。K~+吸收的通量分析结果表明,Ca~(++)抑制K~+通过质膜的外流,促进K~+由细胞质向液泡中转运,而不影响K~+通过质膜的内流速率。     

A catalytic dyad modulates conformational change in the CO2-fixing flavoenzyme 2-ketopropyl coenzyme M oxidoreductase/carboxylase

2-Ketopropyl-coenzyme M oxidoreductase/carboxylase (2-KPCC) is a member of the flavin and cysteine disulfide containing oxidoreductase family (DSOR) that catalyzes the unique reaction between atmospheric CO₂ and a ketone/enolate nucleophile to generate acetoacetate. However, the mechanism of this reaction is not well understood. Here, we present evidence that 2-KPCC, in contrast to the well-characterized DSOR enzyme glutathione reductase, undergoes conformational changes during catalysis. Using a suite of biophysical techniques including limited proteolysis, differential scanning fluorimetry, and native mass spectrometry in the presence of substrates and inhibitors, we observed conformational differences between different ligand-bound 2-KPCC species within the catalytic cycle. Analysis of site-specific amino acid variants indicated that 2-KPCC-defining residues, Phe501-His506, within the active site are important for transducing these ligand induced conformational changes. We propose that these conformational changes promote substrate discrimination between H⁺ and CO₂ to favor the metabolically preferred carboxylation product, acetoacetate.