Fe^2＋-H2O2体系降解壳聚糖

Fe2 -H2O2体系能够有效地降解壳聚糖,反应介质的pH值、反应时间、反应温度、Fe2 浓度及H2O2浓度等实验因素对壳聚糖的降解效果都有程度不同的影响,其中以反应介质的pH值和H2O2浓度对降解反应的影响为最大.在pH值为3～5时Fe2 -H2O2体系降解壳聚糖的活性最高.适当增大H2O2的用量可以增大壳聚糖的降解程度,但当其用量增大至一定程度后,壳聚糖降解产物分子量的下降趋势明显变缓.合理的Fe2 -H2O2体系降解壳聚糖的实验条件为:介质pH值3～5;温度,室温;时间60～90 min;壳聚糖:H2O2:Fe2 =240:12～24:1～2(摩尔比).     

Convenient Synthesis of 2′-Deoxy-2-fluoroadenosine from 2-Fluoroadenine

Abstract

A convenient synthesis of 2′-deoxy-2-fluoroadenosine from commercially available 2-fluoroadenine is described. The coupling reaction of silylated 2-fluoroadenine with phenyl 3,5-bis[O-(t-butyldimethylsilyl)]-2-deoxy-1-thio-D-erythro-pentofuranoside gave the corresponding 2-fluoro-2′-deoxyadenosine derivative (α/β =1:1) in good yield. The α- and β-anomers were separated by chromatography, and then desilylated to give compounds 1a and 1b.     

TXA2/PGI2与心血管疾病

血栓素(Thromboxane,TXA2)和前列环素(Prostacyclin,PGI2)均为花生四烯酸的代谢物,是前列腺素(Prostaglandins,PGs)中生物活性最强的一对。在正常情况下,二者在体内保持一定的平衡,相互拮抗、相互协调,共同维持血液循环畅通,与心血管疾病关系密切。本文即就其生物特性及与心血管病的关系等进行综述,对人们全面认识TXA2/PGI2具有一定的参考价值。     

再论2πω2的最优性

证明了用角2πω~2/(1 ω~2)、2π(3 ω~2)和2π/(2 ω~2)在圆周上作插分得到任意n个分点并将圆周分为11个角时,其最小角与最大角之比也至少是ω~2．根据叶序的基本功能,用模糊数学的综合评判理论证明了角2πω~2优于角2πω~2/(1 ω~2)、2π/(3 ω~2)和2π/(2 ω~2),从而从理论上说明了2πω~2作为互生植物的叶序分数所对应的极限角是合理的．     

固氮酶催化还原C_2H_2和N_2的探讨

自从Dilworth等发现固氮酶对C_2H_2的还原活性以来,用乙炔还原法研究生物固氮作用的文献大大超过~(15)N示踪的方法,这可能是前一方法更灵敏简便.近年来化学模拟生物固氮研究也把催化乙炔还原为乙烯的反应作为固氮酶活性中心模拟物络合活化底物的一种判据,依其还原活性的大小推测模型物与固氮酶活性中心的相似程度,用以指导模型物的合成.然而,固氮酶对乙炔的还原活性是否完全     

H_2O_2诱导Neuro-2a细胞死亡机理的研究

细胞内线粒体呼吸链过程中的电子漏和神经细胞代谢的酶类如单胺氧化酶(MAO)等可产生活性氧物质(ROS)如H_2O_2等。ROS对细胞有毒性作用,导致细胞死亡,在许多疾病特别是神经退行性疾病中具有重要作用。我们用H_2o_2诱导N-2a神经母细胞瘤细胞,利用光镜、荧光显微镜、透射电镜观察了诱导的N-2a细胞的死亡,结果表明其死亡形式不同于典型的细胞凋亡,而类似于Ⅱ型神经细胞编程性死亡,死亡细胞染色质呈团块状凝集,细胞核膜仍保持完整。DNA不降解形成ladder,且不需要caspase-3,1的活性,但是H_2O_2诱导的Neuro-2a细胞死亡可以被Bcl-X_L,抑制。我们的结果可以说明,ROS介导的细胞毒性作用是导致Ⅱ型神经细胞编程性死亡的一个原因。     

脱落酸和己糖激酶抑制剂对高表达C4-PEPC转基因稻苗耐旱性的影响

为了研究高表达转玉米C₄-磷酸烯醇式丙酮酸羧化酶（phosphoenolpyruvate carboxylase,PEPC）基因水稻（PC）的耐旱性机制,本研究以PC和未转基因野生型原种kitaake为材料,分别在光照和黑暗预处理24 h,其中光照处理中光强为600 μmol·m^-2·s^-1,预处理后稻苗再在15％聚乙二醇-6000模拟干旱胁迫下,同时使用药理学的方法,通过加入脱落酸和己糖激酶的专一性抑制剂100 μmol·L^-1去甲二氢愈创木酸和10 mmol·L^-1葡萄糖胺,观察两种水稻4~5叶期稻苗耐旱表现。结果发现,与WT水稻相比,在PEG-6000处理后,经过光预处理的PC水稻叶片相对含水量下降较少,始终比WT的高,而且丙二醛含量则较少,脯氨酸诱导增加,表现耐旱;而经过暗预处理后PC植株显著降低这个优势,表明光预处理有利于PC耐旱性的表现;黑暗预处理均显著下调了2供试材料植株叶片中可溶性糖的含量,而对可溶性蛋白的含量影响不显著;而光预处理后PC水稻叶片内可溶性糖含量比WT增加,而在黑暗预处理则PC的显著低于WT的,其中葡萄糖胺对光预处理下PC的可溶性糖含量的下调作用最显著;暗预处理逆转或消除了NO,H₂O₂和钙离子含量变化趋势,这些变化与暗预处理减少了两材料叶片蔗糖和葡萄糖含量变化同步;光暗预处理对两材料的PEPC酶活性的差异影响不大,表明外源玉米C₄-PEPC在水稻中是组成型表达。可见PC叶片可部分通过糖组分,参与内源糖介导ABA和HXK信号途径,缓解干旱处理对叶片的伤害,稳定光合能力。     

甲基紫精对水稻幼苗根细胞膜微囊Ca^2＋-ATP酶活性的影响

10μmol／L甲基紫精(MV)预处理水稻幼苗可明显提高其抗冷力,但这种功效可被钙的螯合剂EGTA(10 mmol／L)和钙调素(CaM)的抑制剂氯丙嗪(CPZ,0．5mmol／L)所抑制。MV预处理提高了幼苗质膜、液泡膜Ca^2 -ATP酶活性,同时也有提高质膜Fe(CN)6^3-还原速率和这些活性的冷适应性,但这些效果均可被EGTA和CPZ所抑制。离体条件下,膜微囊的Ca^2 -ATP酶活性对H2O2、O2^-、-0H敏感。结果显示,MV预处理提高幼苗的抗冷力可能是通过钙信使介导起作用的,钙信使或CaM可能刺激了质膜、液泡膜Ca^2 -ATP酶活性;而该预处理有增加质膜、液泡膜Ca^2 -ATP酶的冷稳定性则可能与该处理有提高细胞抗氧化能力、稳定冷胁迫下细胞膜系统结构有关。     

The phosphorylation of Sorghum leaf phosphoenolpyruvate carboxylase is a Ca++-calmodulin dependent process

Regulation of the in vitro phosphorylation process of the photosynthetic form (G form) of Sorghum leaf Phosphoenolpyruvate carboxylase (PEPC: EC 4.1.1.31) was studied. Results established that: 1) PEPC was efficiently phosphorylated on seryl residues in crude leaf extract 2) Pyruvate, orthophosphate dikinase (EC 2.7.9.1.) which has been supposed to interfere with the process, was found not to be significantly phosphorylated in our experimental conditions 3) KF, as well as both Ca++ and Mg++ ions increased the radioactive signal detected 4) addition of EDTA or EGTA nullified it and Ca++ alone was found to reverse the inhibitory effect exerted by both chelators 5) addition of anti-Calmodulin antibodies to the medium also abolished the PEPC phosphorylation. Present data demonstrated that the post-translational modification of the C4-plant photosynthetic PEPC is a Ca++/Calmodulin dependent process.     

Ca2+和钙调素对H2O2诱导的玉米幼苗耐热性的调控

外源H2O2预处理提高了玉米幼苗内源H2O2的含量和钙调素(CaM)活性,缓解了高温处理过程中CaM活性的下降,增加了玉米幼苗在高温胁迫下的存活率.H2O2诱导的玉米幼苗耐热性的形成可被外源Ca2 处理所加强,被Ca2 螯合剂EGTA、质膜Ca2 通道阻塞剂La3 、胞内Ca2 通道阻断剂RR(钌红),以及CaM抑制剂CPZ(氯丙嗪)和TFP(三氟拉嗪)所抑制,表明Ca2 和CaM参与了H2O2诱导的玉米幼苗耐热性形成的调控.     

Hydrogen peroxide induces loss of dopamine transporter activity: a calcium-dependent oxidative mechanism

H2O2 dose dependently inhibited dopamine uptake in PC12 cells and in striatal synaptosomes. Treatment with H2O2 resulted in a reversible reduction in Vmax, with no effect on its Km value. This suppressive effect of H2O2 could be relieved by reducing agents (dithiothreitol and cysteine). Furthermore, an oxidizer (dithiodipyridine) also markedly suppressed the dopamine transporter (DAT). Oxidative stress therefore might contribute to the action of H2O2. H2O2 appeared to modify DAT at both extracellular and intracellular sites because cumene-H2O2 (a radical generator mostly restricted to plasma membranes) at high concentrations also slightly suppressed DAT activity and the intracellular overexpression of catalase ameliorated the inhibitory effect of H2O2. Internalization was unlikely to be involved because concanavalin A, which blocked endocytosis, did not prevent the H2O2-evoked inhibition of DAT activity. Interestingly, H2O2 treatment evoked a Ca2+ influx in PC12 cells. Moreover, removal of external calcium by EGTA or reduction in the intracellular calcium level using BAPTA-AM reversed the inhibitory effect of H2O2. Conversely, depletion of intracellular calcium stores using thapsigargin did not affect the reduction in DAT activity by H2O2. Collectively, our results indicate that the DAT, one of the most important proteins controlling the dopaminergic system, is also a redox sensor. In addition, H2O2 might suppress the DAT by a Ca2+-dependent oxidative pathway.     

不同钙-醇溶解体系丝素蛋白的制备及表征研究

采用 ４种中性盐溶液 Ｃａ（ＮＯ３）２４Ｈ２Ｏ 甲醇、Ｃａ（ＮＯ３）２４Ｈ２Ｏ 乙醇、ＣａＣｌ２ 甲醇 水和 ＣａＣｌ２ 乙醇 水（摩尔比分别为 １∶２、１∶２、１∶２∶８、１∶２∶８）处理蚕丝纤维,透析后经冷冻干燥制成固体,利用ＳＤＳ ＰＡＧＥ、电镜扫描和红外光谱对制得的固体进行表征。ＳＤＳ ＰＡＧＥ结果表明：Ｃａ（ＮＯ３）２４Ｈ２Ｏ 醇体系降解丝素蛋白较 ＣａＣｌ２ 醇 水体系降解程度高;电镜扫描的结果表明 Ｃａ（ＮＯ３）２４Ｈ２Ｏ 甲醇和 ＣａＣｌ２ 乙醇 水溶解体系处理的丝素蛋白溶解比较完全,Ｃａ（ＮＯ３）２４Ｈ２Ｏ 甲醇处理的丝素蛋白冻干后为颗粒状,而 ＣａＣｌ２ 乙醇 水处理的丝素蛋白冻干后为片状。红外光谱的结果表明：４种溶液处理后的丝素蛋白构象均介于 β折叠和无规则卷曲之间,从而为丝素蛋白在药物缓释载体领域的应用提供了一定的理论依据。     

H(2)O(2) mediates Ca(2+)- and MLC(20) phosphorylation-independent contraction in intact and permeabilized vascular muscle

One purpose of the current study was to establish whether vasoconstriction occurs in all vessel types in response to H(2)O(2). Isometric force was measured in pulmonary venous and arterial rings, and isobaric contractions were measured in mesenteric arteries and veins in response to H(2)O(2). A second purpose was to determine whether H(2)O(2)-induced contraction is calcium independent. The addition of H(2)O(2) to calcium-depleted (using the Ca(2+) ionophore ionomycin in zero calcium EGTA buffer) muscle caused contraction. Furthermore, permeabilized muscle contracted in response to H(2)O(2) even in zero Ca(2+). The final purpose was to determine whether the 20-kDa regulatory myosin light chain (MLC(20)) phosphorylation plays a role in H(2)O(2)-induced contraction. Pulmonary arterial strips were freeze-clamped at various time points during H(2)O(2)-induced contractions, and the relative amounts of phosphorylated MLC(20) were measured. H(2)O(2) caused dose-dependent contractions that were independent of MLC(20) phosphorylation. ML-9, a myosin light chain kinase inhibitor, had no effect on the H(2)O(2) contractile response. In conclusion, H(2)O(2) induces Ca(2+)- and MLC(20) phosphorylation-independent contraction in pulmonary and systemic arterial and venous smooth muscle.     

Expression of the Na(+)/Ca(2+) exchanger ameliorates ionomycin-induced cell death

PC12 cells were stably transfected with cDNA encoding the Na(+)/Ca(2+) exchanger (NCX1.4). A robust Na(+)-dependent Ca(2+) uptake confirmed the functional expression of the protein. When NCX1. 4 expressing cells (NO) and vector transfected control cells (VC) were exposed to 0.5-20 microM ionomycin for 6 h, a dose-dependent increase in LDH release was observed. LDH release was significantly reduced in NO when compared with VC. When either VC and NO were treated with 3 microM ionomycin and 1.1 mM EGTA, the increase in LDH release was nearly abolished. However, when VC and NO were treated with ionomycin and then EGTA was added 2 min later, LDH release remained elevated. These data suggest ionomycin-induced cell death was Ca(2+) dependent and expressing NCX1.4 may have ameliorated cell death by reducing elevated [Ca(2+)](I).