998 resultados para 11-diene synthase


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在完成了眼镜王蛇毒液抽提物CM-11的残基质子谱峰归属和二级结构的判定后,利用1H的NOESY谱和DQF-COSY谱选取了距离约束、测定了Φ角和χ1,并做了部分β1H的立体归属。利用度量矩阵距离几何法计算了其三维空间结构,并进行了结构的优化。同一个系列中挑选的12个低能分子结构中,骨架的RMSD为0.14nm,所有重原子的RMSD为0.20nm,所有的距离约束偏差不超过0.05nm,二面角的偏差不超过3°

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2DNMR谱的自动归属是核磁共振发展的一个方向,CAPRI即是蛋白质1H谱的计算机辅助谱峰归属的一种程序。作者将其应用于眼镜王蛇神经毒素CM-111H谱的归属,讨论了CAPRI的功能和特点以及运用在CM-11后得到的分析结果。

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对不同温度热处理过的Nylon-11样品,采用广角X射线衍射(WAXD),根据X射线衍射强度理论,用多重峰图解分峰方法研究了Nylon-11结构的变化,并导出了计算Nylon-11结晶度的公式.所得结果与密度法、DSC法进行了比较.同时也给出了Nylon-11的有关热力学参数

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合成了六铝酸盐SrNiAl11O19并用XRD、UVDRS、TGDTA和TEM等技术对其进行了表征。在750℃于SrNiAl11O19上进行的甲烷与二氧化碳重整反应表明,这类催化剂较Ni/SrAl12O19具有较大活性和低积碳能力,在催化反应过程中可有效地抑制Ni颗粒的增大。

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The aggregate structure of the discotic compound 2,3,6,7,10,11-hexakispentyloxytriphenylene (HPT) was studied both for the crystalline state and the liquid crystalline state by using electron crystallography and a molecular simulation approach. In the crystalline state, HPT was found to adopt an orthorhombic P-2212 space group with cell parameters a = 36.73 Angstrom, b = 27.99 Angstrom and c = 4.91 Angstrom. Molecular packing calculations were conducted to elucidate the molecular conformation and mutual orientational characteristics in the different states. Phase transitions and relationships are discussed from a structural point of view.

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A super-tough polycarbonate (PC) blend was obtained by using epoxidized ethylene propylene diene (eEPDM) rubber as modifier. The notched Izod impact strength of PC/eEPDM (96/4) blend shows a great improvement, with a value about 25 times of that of pure PC. Finely and homogeneously dispersed rubber particles (0.2-0.8 mu m) in the PC matrix indicated good adhesion between the eEPDM rubber phase and the PC matrix. (C) 1997 Elsevier Science Ltd.

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The king cobra(Ophiophagus hannah) neurotoxin CM-11 is long-chain peptide with 72 amino acid residues. Its complete assignment of H-1-NMR resonances was obtained using various 2D-NMR technologies, including DQF-COSY, clean-TOCSY and NOESY.

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The king cobra neuotoxin CM-11 is a small protein with 72 amino acid residues. After its complete assignments of H-1-NMR resonance's were obtained using various 2D-NMR technologies, including of DQF-COSY, clean-TOCSY AND NOESY, the secondary structure was analysed by studying the various NOEs extracted from the NOESY spectra and the distribution of chemical shifts. The secondary structure was finally determined by MCD as follows: a triple-strand antiparallel beta sheet with I20-W36, R37-A43 and V53--S59 as its beta strands, a short alpha helix formed by W30-G35 and four turns formed by P7-K10, C14-G17, K50-V53 and D61-N64.

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In this paper, epoxidation of ethylene propylene diene rubber by in situ generated performic acid is discussed. The samples have been characterized by infra-red and H-1-nuclear magnetic resonance analyses. Quantitative analysis of the reaction products is made possible by using the methyl deformation band at 1377 cm(-1) as internal standard. The conversion of double bonds increases rapidly within the first 1 h, then gradually, over 2 h, has only a slight increase. The maximum conversion ratio of double bonds is about 70%. The relative content of epoxy groups has a top value at about 7 h. The side reactions are also discussed. (C) 1997 Elsevier Science Ltd.

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Tb(111) and Ca(11) ion equilibria in the Presence of glutamic acid and glutamine were studied by potentiometric titration at 37 degrees C and an ionic strength of 0.15mol/L(NaCl). The stability constants for Tb(111) and Ca(11) complexes in the systems were obtained. The species and their distribution in the systems were discussed.

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In this paper, unepoxidized ethylene propylene diene rubber (uEPDM) was first epoxidized with formic acid and H2O2, and then the epoxidized ethylene propylene diene rubber (eEPDM) was melt-mixed with PET resin in a Brabender-like apparatus. Toughening of PET matrix was achieved by this method. The dispersion of rubber particles and phase structure of the blends were also observed by SEM. It has been suggested that the epoxy groups in the eEPDM could react with PET end groups to form a graft copolymer which could act as an interfacial compatibilizer between the PBT matrix and eEPDM rubber dispersed phase. This is beneficial to the improvement of the impact performance of PBT. (C) 1997 Elsevier Science Ltd.

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眼镜王蛇抽提物CM-11为含72个残基的长链神经毒素,对其进行了DQF-COSY,TOCSY和NOESY等一系列2D-NMR谱测定,借助序列专一归属法完成了CM-11NMR氢谱的完整归属。

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眼镜王蛇毒液抽提物CM-11为含72个残基的长链神经毒素,对其进行了DQF-COSY,TOCSY和NOESY等一系列2D-NMR谱测定,通过系统地分析各种NOE信息、化学位移的分布等数据推测了蛋白质有规律二级结构,最后利用MCD主链引导法确定了它的二级结构。其中有三段反平行β折叠股(I20~W26、R37~A43和V53~S59)、一段α螺旋构象(W30~G35)和四个可能的转角(P7~K10,C14~G17,K50~V53,D61~N64),蛇毒神经毒素CM-11其他肽片段处在伸展构象。

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Blends of poly (butylene terephthalate) (PBT) and epoxided ethylene-propylene-diene terpolymer (EEPDM) were prepared. Their mechanical properties and morphology were studied by Izod impact test machine and scanning electronic microscope respectively, It was found that the notched Izod impact strength of blend PBT/EEPDM was as about 23 times as that of pure PET and about 10 times as that of blend PBT/EPDM at room temperature, The dispersed rubber particles were much smaller and the phase boundary was more blurred in blend PBT/EEPDM than in blend PBT/EPDM. The toughness of blend PBT/EEPDM was much more better than that of blend PET and PBT/EPDM, which was in good agreement with the difference between their morphologies.