124 resultados para 530


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The structural stability and redox properties of yeast iso-1-cytochrome c and its mutant, F82H, were studied by surface-enhanced resonance Raman scattering (SERRS) spectroscopy. Phenylalanine, which exists at the position-82 in yeast iso-1-cytochrome c, is replaced by histidine in the mutant. The SERRS spectra of the proteins on the bare silver electrodes indicate that the mutant possesses a more stable global structure with regard to the adsorption-induced conformational alteration. The redox potential of the mutant negatively shifts by about 400 mV, relative to that of yeast iso-1-cytochrome c. This is ascribed to axial ligand switching and higher solvent accessibility of the heme iron in the mutant during the redox reactions.

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meso-Tetra (alpha, alpha, alpha, alpha-O-phenylacetyl benzene) porphyrin was used as a complete antigen to elicit monoclonal antibody 1F2 through the immunization and cell fusion techniques. McAb 1F2 obtained was demonstrated very pure by HPLC and MALDI/TOFMS. The retention time of McAb 1F2 was 2. 63 min. The subtype of McAb 1F2 was IgG2a. The relative molecular weight was 156 678. 8. When the McAb 1F2-porphyrin was formed, the maximal absorption of the porphyrin soret region had a redshift from 408 to 416 nm and hyperchromical effect, showing that the antigen-antibody combination was rigid and intense, and the abzyme constancy was high. But compared with HRP, the activity of the abzyme was only 4. 687 5 U/mg and 1. 899 % of that of HRP. Its K-m was 20. 29 mmol/L, k(cat) 396. 82 min(-1), k(cat)/K-m. 1. 955 7 X 10(4) L . mol(-1) . min(-1).

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利用小分子meso-四(α,α,α,α-O-苯乙酰苯)卟啉作为全抗原免疫小鼠,通过细胞融合等技术制备了单克隆抗体(McAb)1F2,利用高效液相色谱(HPLC)、基质辅助激光解吸飞行时间质谱(MALDI/TOFMS)证明纯化得到的单抗是很纯的.McAb1F2的保留时间是2.63 min,亚型为IgG2a,相对分子量为156 678.8.McAb 1F2-卟啉复合物形成时,卟啉Soret带最大吸收峰从408nm红移到416nm,并有增色效应,说明McAb1F2-卟啉是刚性且紧密结合.抗体酶稳定性很高,但比活力只有4.687 5 U/mg,为天然酶HRP的1.899%.抗体酶的Km=20.29 mmol/L,kcat=396.82 min-1,kcat/Km=1.955 7×104L·mol-1·min-1.

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The singlet-triplet splitting energy gap DeltaE(S.T) = E-S - E-T is calculated for the ortho-, meta-, and para-xylylenes and their heteroatomic analogous by means of AM1-CI approach. It is shown that when the radical centers R-.(R-.=H2C.-,H2N.+- or HN.-) are twisted sufficiently Tar out of conjugation with the benzene ring, DeltaE(S.T) tends to zero or is negative, i.e, ortho-, meta-, and para-phenylenes turn into weak ferromagnetic or antiferromagnetic coupling unit, while they are strong ferromagnetic (meta-isomers) or antiferromagnetic (ortho-, para-isomers) coupling units under planar conformation. It is suggested that serious twisted conformation is not recommended candidate for the design of novel high-spin molecules with stable high-spin ground states by ortho- or para-phenylene coupling unit.

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Three title compounds were prepared and the structure of title compound 2 was characterized by IR, H-1 NMR, C-13 NMR, Sn-119 NMR spectroscopy and the crystal structure of compound 2a was determined by X-ray analysis with the final R indices[I >2 sigma (I)] R-1 = 0.0350 and R-2,R-omega = 0.0888. The crystal of compound 2a belongs to triclinic system, space group P1 with a = 1.0598(6) nm, b = 1.307 4(10) nm, c = 1.378 6(10) nm, alpha = 62.666(7)degrees, beta = 72.530(2)degrees, gamma = 80. 680(2)degrees, V = 1.618 0 nm(3), D-x = 1. 444 g (.) cm(-3), Z = 1, F (000) = 728. The bond length of Sn1-O1 is 0. 2076 nm and Sn1 . . . O2 distance is 0.301 3 nm. The coordination about the tin atom can be considered as a distorted tetrahedral. The detail values of H-1 NMR, C-13 NMR, Sn-119 NMR, (2)J(119Sn-1H) and J(119Sn-13C) were obtained. delta (119Sn) = 23.836, (2)J(119Sn-1H) = 88.0 Hz, (1)J(119Sn-13C) = 347.1 Hz, (2)J(119Sn-13C) = 45.6 Hz.

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Sandwich-like heteropoly molybdochromophosphates of supermolecular compound [NH3(CH2)(6)NH3](2)H-3{Cr[Mo6O15(HPO4)(H2PO4)(3)](2)}. 4H(2)O has been hydrothermally synthesized and the single crystal structure has been determined by X-ray diffraction. The crystal data are has follows: triclinic, space group P (1) over bar a=12.156(2), b=12.809(3), c=13.530(3) Angstrom, alpha=102.46(3)degrees, beta=93.67(3)degrees, gamma=93.46(3)degrees, V=2046.9(7) Angstrom(3), Z=1, M-r=2768.69, D-c=2.246 g/cm(-3), F(000)=1337, mu=2.162 mm(-1). The structure has been refined to R=0.0666 and wR=0.1745 by full-matrix least-squares method. The title compound is composed of 1, 6-diaminohexane, water molecules, and {Cr[Mo6O15(HPO4)(H2PO4)(3)](2)}(7-) anion which consists of six oxygen atoms from two [Mo6P4] units with a sandwich-like transition metal atom Cr located at the center of symmetry.

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Artificial neural network(ANN) approach was applied to classification of normal persons and lung cancer patients based on the metal content of hair and serum samples obtained by inductively coupled plasma atomic emission spectrometry (ICP-AES) for the two groups. This method was verified with independent prediction samples and can be used as an aiding means of the diagnosis of lung cancer. The case of predictive classification with one element missing in the prediction samples was studied in details, The significance of elements in hair and serum samples for classification prediction was also investigated.

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根据人发和血清中微量元素的含量,将人工神经网络(ANN)用于正常人与癌症患者的分类预测.用独立预测样本作了检验,表明该方法可作为肺癌诊断的一种辅助手段.讨论了当预测样本中有元素缺损时ANN的分类预测情况,并研究了人发和血清样品中的元素对分类预测的影响

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合成了H3-xCsxPW(x=0~3),H4-xCsxSiW(x=0~4)两系列杂多酸铯盐,以Hammet指示剂法及NH3-TPD研究了它们的酸性质,用BET法测定了其表面积,并在叔丁醇脱水生成异丁烯的反应中考察了杂多酸铯盐的催化性能,其催化活性高于文献报导的其它杂多化合物在相同条件下的活性,并对该反应作了动力学分析,求得了有关参数,发现杂多酸铯盐的催化活性仅与它们的酸性质有关,与表面积无关,属于拟液相反应。

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氢化物发生-光度分析法是在同一反应系统中,使氢化物的发生、传输、吸收显色同时进行并同步完成的一种新分析方法,具有高灵敏、高选择性,且简单实用的特点。适用于Ge、As、Sn、Sb、Se、Bi、Pb、Te等共价氢化物元素的分析。本文对这一方法的原理及其在吸收显色体系、多元素的同时或连续测定、价态形态分析、干扰的消除方法及分析应用等方面的发展进行了评述。

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本文用傅里叶交换红外光谱、X线衍射、XPS和GPC等手段表征了氧化镁与苯乙烯的辐射接枝共聚物。结果表明,在接枝共聚物的红外谱图和X线衍射图上出现有氧化镁和聚苯乙烯的谱带。氧化镁与聚苯乙烯共混物XPS谱图中的C_(1S)、O_(1S)以及Mg_(2S)能级的峰位分别为285.0、530.0和87.6 eV,而氧化镁与苯乙烯接枝聚合物的C_(1S)、O_(1S)和Mg_(2S)峰位分别为284.0、531.7和88.4 eV。说明氧化镁与苯乙烯辐射接枝聚合时,氧化镁被辐射后镁原子引起照射缺陷而成为接枝活性中心,与苯乙烯碰撞时镁原子与电负性大的碳原子相配位产生自由基。然后按自由基机理进行接枝聚合反应。接枝物中的O/C比随接枝率的增加而下降。接枝共聚物的分子量要比均聚物分子量大,但分子量分布较宽。

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The esrB gene of Edwardsiella tarda, which encodes a regulator protein of the type III secretion system, was mutated by the unmarked deletion method and reintroduced by allelic exchange into the chromosome of E. tarda LSE40 by means of the suicide vector pRE 112. The LSE40 esrB mutant was highly attenuated when inoculated intraperitoneally into turbot Scophthamus maximus L., showing a 50% lethal dose of 10(8.1) cfu/fish. The esrB mutants were not recoverable from the internal organs at 14 days post-inoculation. Vaccination with a single dose of 10(5)-10(7) cfu/fish of the esrB mutant elicited significant protection against the wildtype strain of E. tarda LSE40 (relative percentage survival > 50%). The protection correlated well with the antibody titres in the serum of vaccinated fish. (c) 2006 Elsevier Ltd. All rights reserved.

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Translationally controlled tumor protein (TCTP) is one of the abundant and ubiquitously expressed proteins in metazoans In the present study, the first molluscan TCTP (denoted as VpTCTP) was identified from Venerupis philippinarum haemocytes by EST and RACE approaches The full-length cDNA of VpTCTP consisted of 1148 nucleotides with an open-reading frame of 555 bp encoding 184 amino acids The deduced amino acid sequence of VpTCTP shared high similarity with TCTPs from other species, indicating that VpTCTP should be a new member of TCTP family Several highly conserved motifs, including 5'terminal ologopyrimidine (5'TOP) starting sequence and rich AU and AUUT elements in 3'UTR, were also identified in VpTCTP The tissue and temporal expression of VpTCTP after Vi boo anguillarum challenge was recorded by quantitative real-time RT-PCR. VpTCTP transcript could be detected in all examined tissues with the highest expression level in haemocytes and the lowest in hepatopancreas Concerning the time-course expression in haemocytes, the relative expression of VpTCTP mRNA was down-regulated sharply from 6 h to 12 h post-infection. Then, the expression level was obviously up-regulated and reached 3.4-fold to that in the control group at 48 h post challenge As time progressed, the expression of VpTCTP recovered to the original level at 96 h. All these results indicated that VpTCTP was an acute-phase protein involved in the Immune response of V philippinarum (C) 2010 Elsevier Ltd. All rights reserved.

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本文利用黑潮流域主流轴上的两个柱状沉积物岩芯MD05-2908以及PC-1为研究材料,在AMS14C测年的基础上,利用高分辨率的有机地球化学分析记录结合浮游有孔虫氧、碳同位素,恢复并重建了过去25,000 cal a BP以来黑潮流域古海洋环境演化的历史。以及表层海水生产力以及物质输送状况的演化历史。通过利用Uk’37古海水温度以及盐度指标恢复重建了过去25,000 cal a BP以来海洋表层海水温度、盐度;通过机碳、氮含量以及同位素变化、长链正构烷烃以及正构烷醇等指标重建了过去7000a B.P.以来的陆源物质输入历史;通过长链不饱和烯酮含量以及有机碳同位素指标恢复了过去7000a B.P.以来海水表层生产力的历史。此外,通过基于以上各种指标的环境信息与区域以及全球其它气候记录进行对比研究以及不同环境指标的时间系列分析,探讨了该区表层环流系统以及生产力的演化对于全球气候变化的响应,揭示了不同尺度的短周期高频率全球变化事件在黑潮流域的具体作用过程和响应机制。通过这些研究取得了以下的主要认识: 基于有机地球化学指标的古气候环境记录与黑潮流域已有的研究成果有很好的对应关系,从我们高分辨率的有机地球化学记录中可以识别出全新世黑潮强弱变化的几次明显的事件;25000a B.P.以来黑潮流域的环境变化与全球环境变化有着很好的对应性,黑潮强弱演化总体趋势与全球气候背景演化相一致,黑潮对高频气候变化事件的记录与全球记录具有同步性,这种同步性尤其体现在末次冰消期以来的气候快速高频振荡以及全新世以来的气候突变事件上。 全球性的高频气候事件对黑潮主体本身及黑潮流域的相邻区域的大气和海洋环流都具有重要的控制作用,这种控制作用主要通过副高、ITCZ以及季风三种气候要素之间相互关联、彼此影响造成的。具体表现为:太阳辐射量的减少导致热力差异减小,这种相对减小弱化了热带西太平洋的对流活动,造成了西太平洋副热带高压长期偏南、偏东,ITCZ平均北界位置偏南,降雨带长时间集中在南部地区,增强的降雨量提高了风化剥蚀以及沉积物向海洋搬运的能力,陆源物质供应量增加;同时,辐射量以及热力差的减小又与加强的东亚冬季风相联系,增强的冬季风导致了近底层“雾状层”物质的向海传输,物质传输效率增高。这种物源供应以及搬运量的双重增加导致了冲绳海槽流域物质通量的增加。 基于有机地球化学指标的海洋表层生产力的变化与陆源物质供应量以及黑潮流的强弱变化存在着对应关系,通常情况增加的海洋表层生产力对应着高的陆源物质输入以及相对较弱的黑潮。这种变化与东亚夏季风的以及冬季风的强弱都有很好的一致性。陆源物质的输入增加了表层营养物质的含量,导致生产力的勃发;陆源物质的输入增加又对应着减少的太阳辐射量,偏南的ITCZ北界位置以及副热带高压,这些对应于减弱的东亚夏季风(增强的东亚冬季风)。 黑潮流域的高沉积速率事件对应于减弱的黑潮强度和增加的ENSO频度,这些事件与上述的副热带高压、ITCZ位移和强弱的变化相一致。黑潮流域过去25000a B.P.以来南北温度的差异有冰期加大而全新世减小的趋势,但这种冰期与全新世的差异很小,我们认为末次盛冰期的时候黑潮主流轴没有移出冲绳黑潮,只是由于强度的减弱受陆架水体的影响有所加大。 黑潮流域很好的记录到了包括数千年尺度的D/O旋回周期到大气——海洋系统内部振荡所致的PDO、NAO等数十年尺度的高频振荡,说明黑潮流域对过去全球及区域环境变化事件有很好的响应。黑潮流域各古海洋指标所记录周期上的一致性说明这些环境因子控制机理上具有的一致性,即大背景上受太阳活动所引起的辐射量变化控制,局部的高频快速气候波动又受到局域性的气候因素如海气相互作用的放大影响。