145 resultados para rp
Resumo:
Jussiaea repens L. (JRL) is an edible medicinal plant and is also used as a vegetable by the local people in southwestern China. The crude extract and its four fractions derived from JRL were evaluated for the 1,1-diphenyl-2-picrylhydrazyl radical-scavenging ability, hydroxyl radical-scavenging capacity and the potassium ferricyanide reduction property. The ethyl acetate-soluble fraction (EAF) and EAF6 (a subfraction derived from EAF) were the most valuable fraction and subfraction, respectively. Furthermore, bioactivity-guided chromatographic fractionation revealed that three pure compounds greatly contributed to the antioxidant activities. Qualitative and quantitative analyses of the major antioxidant constituents in the extract were systematically conducted by NMR, mass spectral analyses and RP-HPLC. The result demonstrated that rosmarinic acid (2.00 mg g(-1) JRL dry weight) quercetin 3-O-beta-D-glucopyranoside (9.88 mg g(-1) JRL dry weight), and kaempferol 3-O-beta-D-glucopyranoside (1.85 mg g(-1) JRL dry weight) were the major antioxidative constituents in JRL. These compounds are reported for the first time from this plant.
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In our screening of marine Streptomycetes for bioactive principles, two novel antitumor antibiotics designated as chinikomycins A (2a) and B (2b) were isolated together with manumycin A (1), and their structures were elucidated by a detailed interpretation of their spectra. Chinikomycins A (2a) and B (2b) are chlorine-containing aromatized manumycin derivatives of the type 64-pABA-2 with an unusual para orientation of the side chains. They exhibited antitumor activity against different human cancer cell lines, but were inactive in antiviral, antimicrobial, and phytotoxicity tests.
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In our screening of marine actinomycetes for bioactive principles, three novel antibiotics designated as chandrananimycin A (3c), B (3d) and C (4) were isolated from the culture broth of a marine Actinomadura sp. isolate M045. The structures of the new antibiotics were determined by detailed interpretation of mass, 1 D and 2 D NMR spectra.
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The extracts obtained from 28 species of marine algae were evaluated for their antioxidant activity (AA) versus the positive controls butylated hydroxytoluene (BHT), gallic acid (GA), and ascorbic acid (AscA). Most of the tested samples displayed antioxidant activity to various degrees. Among them, the extract of Symphyocladia latiuscula exhibited the strongest AA, which was comparable to BHT, GA, and AscA in radical scavenging activity, as shown in the DPPH (alpha,alpha-diphenyl-beta-picrylhydrazyl) assay, and higher than those of the positive controls in beta-carotene-linoleate assay system. In addition, the ethyl acetate-soluble fraction isolated from the crude extract of S. latiuscula exhibited the highest antioxidant activity in both assay systems. This fraction was further fractionated into seven subfractions (F1-F7) by vacuum liquid chromatography (VLC). F1 and F4 were found to be the most effective subfractions in scavenging DPPH radical assay and in the beta-carotene-linoleate assay, respectively. The total phenolic content (TPC) and reducing power (RP) for all of the extracts, fractions, and subfractions (F1-F7) were also determined. The TPC of the 28 extracts ranged from 0.10 to 8.00 gallic acid equivalents (mg/g seaweed dry weight) while the RP ranged from 0.07 to 11.60 ascorbic acid equivalents (mg center dot g(-1) seaweed dry weight). Highly positive relationships between AA and TPC as well as between AA and RP were found for the extracts and fractions, while for the subfractions F1-F7 only weak or no such relations were found. The results obtained from this study indicate that further analysis is needed of those marine algal species that contain the most antioxidant activity in order to identify the active principles.
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Peptidoglycan recognition protein (PGRP) is an essential molecule in innate immunity for both invertebrates and vertebrates, owing to its prominent ability in detecting and eliminating the invading bacteria. Several PGRPs have been identified from mollusk, but their functions and the underlined mechanism are still unclear. In the present study, the mRNA expression profiles, location, and possible functions of PGRP-S1 from Zhikong scallop Chlamys farreri (CfPG RP-St) were analyzed. The CfPGRP-S1 protein located in the mantle, gill, kidney and gonad of the scallops. Its mRNA expression in hemocytes was up-regulated extremely after PGN stimulation (P < 0.01), while moderately after the stimulations of LPS (P < 0.01) and beta-glucan (P < 0.05). The recombinant protein of CfPGRP-S1 (designated as rCfPGRP-S1) exhibited high affinity to PGN and moderate affinity to LPS, but it did not bind beta-glucan. Meanwhile, rCfPGRP-S1 also exhibited strong agglutination activity to Gram-positive bacteria Micrococcus luteus and Bacillus subtilis and weak activity to Gram-negative bacteria Escherichia coli. More importantly, rCfPGRP-S1 functioned as a bactericidal amidase to degrade PGN and strongly inhibit the growth of E. coli and Staphyloccocus aureus in the presence of Zn2+. These results indicated that CfPGRP-S1 could not only serve as a pattern recognition receptor recognizing bacterial PGN and LPS, but also function as a scavenger involved in eliminating response against the invaders. (C) 2010 Elsevier Ltd. All rights reserved.
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海洋生物具有产生丰富多样的次生代谢产物的能力,其中红藻门松节藻科海藻卤代次生代谢产物以其结构新颖、生物活性独特引起了天然产物化学家的重视。 本论文对海洋红藻多管藻和松节藻进行了化学成分研究,综合利用各种色谱学方法 (硅胶柱层析、反相硅胶柱层析、凝胶Sephadex LH-20柱层析、半制备高效液相色谱以及重结晶等) 和现代波谱学技术 (IR、UV、EI-MS、FAB-MS、HR-ESI-MS、CD、1H-NMR、13C-NMR、DEPT、1H-1H COSY、HSQC、HMBC等),共分离鉴定了100个化合物,发现25个新化合物。 从多管藻中分离鉴定38个化合物 (24个溴酚化合物),其中7个新化合物 (均为溴酚化合物),包括1个菲并呋喃结构溴酚 (P1), 2个二氢菲结构溴酚 (P2, P3),1个含 5,7-dihydrodibenzo[c,e]oxepine 结构溴酚 (P4)和3个简单溴酚 (P5, P6, P7)。P1 (urceolatin) 属首例报道的具有菲并呋喃结构的天然产物,从该种中分离的化合物P12 和 P13 可能是其生源合成的前体。P2和P3为第二例报道的具有二氢菲结构的溴酚化合物。 从松节藻中分离并鉴定了62 个化合物,其中18 个为溴酚类新化合物,44 个为已知化合物。化合物具有多变的取代基团,包括2 个脲基吡咯烷酮溴酚化合物 (R1, R2), 4 个γ-脲基丁酸溴酚化合物 (R3-R6),5 个酰胺溴酚化合物 (R7, R8, R9, R13, R14),1 个溴酚砜化合物 (R12), 1 个Xanthene 溴酚化合物 (R10)和5 个简单溴酚化合物 (R11, R15, R16, R17, R18)。R1、R2 是首例报道的含有脲基吡咯烷酮片段的天然产物,R10 为首次报道的溴代Xanthene 类天然产物。 对分离到的化合物进行了清除DPPH 和ABTS两种自由基活性的筛选。结果发现溴酚类天然产物具有显著的DPPH自由基清除活性,其中R3 的IC50 仅为3.3 μM, 其活性强度约为阳性对照BHT (IC50 为82.1 μM) 的24倍。另外,溴酚类天然产物对ABTS自由基有较强的清除活性,R2 的TEAC(Trolox efficency activity capacity)值为5.2 mM,约为阳性对照 (ascorbic acid, 1.02 mM) 的 5 倍。初步的构效关系研究发现,稠环分子、多羟基和邻位甲氧基等结构特点能有效增强DPPH 自由基清除活性;特殊取代基如脲基、吡咯烷酮等含有氮原子的基团,能有效增强ABTS 自由基清除活性,多羟基、溴代等结构特点也使其活性有所增强。 本研究结果丰富了海藻卤代化合物的结构类型,为多管藻和松节藻的合理利用提供了一定的科学依据。
Resumo:
海洋设施长期处于恶劣的腐蚀环境中,如不加以防护,一旦发生应力腐蚀开裂(SCC),损失就会极为惨重。海底泥土区环境十分重要,因为管线和平台桩腿等都埋在海底泥中。海底泥中硫酸盐还原菌(SRB)十分活跃,而且为了防止腐蚀,海泥中的设施无一例外地采取了阴极保护,相当于设施处在长期稳定的充氢状态。因此非常有必要研究海泥中的活性SRB和极化电位对海洋结构用钢在海泥中的氢渗透行为和SCC敏感性造成的影响,弄清SCC发生和发展的过程以便采取相应的措施减缓或防止SCC。 本文通过慢应变速率拉伸实验(SSRT)、电化学阻抗谱(EIS)技术、动电位扫描极化曲线测定实验和氢渗透实验等研究了海泥中SRB和极化电位对16Mn钢和管线钢X56(API X56)的SCC敏感性造成的影响。 从渤海海泥中富集得到SRB菌种,并做出了SRB在海泥中的生长曲线;在荧光显微镜下观察SRB为弧状,可以归为脱硫弧菌属,为革兰氏阴性菌;海泥中活性SRB数量与硫电位等主要腐蚀环境因子具有一定的对应关系。 SSRT结果表明,施加阴极极化电位可以使试样断裂脆性特征明显,SCC敏感性增大;海泥中活性SRB浓度越高,断裂脆性特征越明显,SCC敏感性越大。在含SRB海泥中或阴极极化电位条件下,两种钢都容易发生SCC,氢脆(HIC)起主要作用。 随着浸泡天数的增加,试样在灭菌海泥中的Rp一直增大;在含SRB海泥中Rp先增大,又变小,并呈现出显著的Warburg阻抗特征;在灭菌海泥中,两种试样在阳极电位范围内无SCC敏感区,而在阴极电位范围内有明显的SCC敏感区;在含SRB海泥中,在阳极电位范围和阴极电位范围内均有SCC敏感区;SRB代谢产物既有阳极去极化作用,又有阴极去极化作用,能使腐蚀电流密度增加。 活性SRB的存在能够促进试样在海泥中的氢渗透;在实海工程应用中,两种钢在含SRB海泥中的氢渗透电流密度大约是在不含SRB海泥中的3~4倍。阴极极化电位能够促进试样在灭菌海泥中的氢渗透。在含SRB海泥中对试样施加阴极极化电位,氢渗透电流密度大于不加阴极极化电位时的氢渗透电流密度,也大于在不含SRB的海泥中的氢渗透电流密度。
Resumo:
海洋微生物拥有丰富多样的次生代谢途径,其中海洋生物内生真菌次生代谢产物研究日益受到天然产物化学界的重视。本论文以菌丝体生物量、发酵产物重量、抗菌与细胞毒活性、薄层色谱分析结果以及高效液相色谱分析结果等为评价依据对采自青岛沿海的13株海藻内生真菌在四种液体培养基上的静置发酵产物进行了综合评价,并从中选择了黑曲霉Aspergillus niger EN-13(分离自褐藻囊藻Colpomenia sinuosa)和杂色曲霉A. versicolor EN-7(分离自褐藻鼠尾藻Sargassum thunbergii)两株真菌进行了30升规模发酵(分别采用GPYM培养基和PDB培养)和化学成分的研究,对分离得到的大部分化合物进行了初步的生物活性筛选。 发酵提取物采用常规的硅胶柱层析、反相硅胶柱层析,凝胶Sephadex LH-20柱层析、制备薄层层析、半制备高效液相色谱以及重结晶等分离手段,得到单体化合物。利用各种现代波谱技术(IR、UV、EI-MS、FAB-MS、HR-ESI-MS、1H-NMR、13C-NMR、DEPT、1H-1H COSY、HSQC、HMBC等)并结合化学方法从两种菌株发酵提取物中鉴定了55个化合物的结构。其中从菌株A. niger EN-13分离鉴定了31个化合物,发现9个新化合物,包括2个鞘酯类化合物(AN-1~2)、3个萘并-γ-吡喃酮类化合物(AN-3~5)、3个苯乙基取代的α-吡喃酮类化合物(AN-17, AN-19~20)和1个甾体Diels-Alder加成产物(AN-21),另有1个新的天然环二肽(AN-27)被分离鉴定;从菌株A. versicolor EN-7分离鉴定了24个化合物,发现2个新化合物,为蒽醌AV-12与AV-17,另外,从前一菌株(A. niger EN-13)中鉴定的2个新鞘酯类化合物(AN-1~2)在A. versicolor EN-7中也被再次分离到。 对大部分单体化合物进行了抗菌活性、DPPH自由基清除活性和细胞毒活性测试。结果显示新化合物AN-1、AN-5和AN-20具有弱或中等强度的抑制白色念珠菌生长的活性,AN-4、AN-5、AN-21显示了弱或中等强度的抑制黑曲霉生长的活性,AV-12、AV-17显示了弱的抑制大肠杆菌生长的活性。在DPPH自由基清除活性筛选中,AN-5显示了中等强度的活性,其EC50为109.3 mM,与阳性对照BHT相近(EC50为81.8 mM)。其它部分已知化合物在抗菌和DPPH自由基清除活性的筛选中也显示了弱或中等强度的活性。在针对人肝癌细胞株SMMC-7721和人肺腺癌细胞株A549的体外细胞毒活性筛选中,所测样品均未显示显著活性。
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A 21-d laboratory experiment was conducted to study, the phosphorus (P) utilization of two different diets by redlip mullet Liza haematocheila T. & S. Sand-filtered water in salinity 30 and temperature 25 degrees C was used. Twenty-nine fish individuals were divided into three groups: 11 to group 1 (G1) fed on diet 1, 11 to group 2 (G2) fed on diet 2, and 7 to contrast group. Diet 1 was a commercial feed, more valuable in nutrition than diet 2 that similar to natural detritus. The results show the intake phosphorus (IP) of G1 was significantly higher than that of G2, and both increased linearly with body size at a certain amount of diet. The retention phosphorus (RP) in fish of G1 was lower than G2. The relationship between retention phosphorus and body size was positive and stronger in G2. Significant difference in faecal phosphorus (FP) was found between G1 and G2. Body size significantly impacted the excretion phosphorus (EP) in G1 but G2. The loss of intake phosphor-us in G1 was 10.83-20.27 mg per g fish weight gain, higher than that in G2 for 6.63-9.56. Of the phosphor-us, about 10% was allocated into growth, 50% in faeces, and the rest lost in excretion. The main part of phosphorus was lost in faeces but excretion. The phosphorus budget of the fish could be described as 100IP = 7.40RP + 47.39FP + 36.63EP (Diet 1) or 100IP = 11.93RP + 56.64FP + 21.76EP (Diet 2).
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采用薄层色谱法(TLC)和反相高效液相色谱法(RP-HPLC)对藏药材圆萼刺参中的芦丁,熊果酸和齐墩果酸进行定性和定量的分析.定性分析:TLC法检定芦丁和熊果酸和齐墩果酸成分,薄层色谱条件是以V(乙酸乙酯)∶V(丁酮)∶V(甲酸)∶V(水)=10∶6∶1∶2为展开剂,喷以10 g/L.NaNO_2的1%甲醇溶液在105℃检定芦丁,以V(CHCl3)∶V(乙酸乙酯)=1∶1为展开剂,喷以V(H2SO4)∶V(甲醇)=1∶2溶液在105℃检定熊果酸和齐墩果酸.定量分析:RP-HPLC法测定圆萼刺参中芦丁,流动相:V(甲醇)∶V(0.4%H_3PO_4溶液)=38∶62;检测波长340 nm;RP-HPLC法测定熊果酸和齐墩果酸,流动相:V(甲醇)∶V(0.2%H_3PO_4)溶液=85∶15;检测波长215 nm;圆萼刺参中的齐墩果酸,在本种植物中首次发现.
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采用反相高效液相色谱一二极管阵列的检测方法,分析了不同产地11批麻花秦艽药材,建立麻花秦艽药材的指纹图谱,进行野生药材与栽培药材的对比研究。结果表明:最佳条件可较全面的反映麻花秦艽药材的主要成分,栽培药材与野生药材相似度较好。
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目的:建立反相高效液相色谱法同时测定四川及青海地区部分獐牙菜中獐牙菜苦苷、龙胆苦苷、芒果苷、当药醇苷、异荭草苷、1,8-二羟基-3-甲氧基(口山)酮的含量.方法:采用RP-HPLC,使用Kromasil C_(18)(4.6 mm×250mm,5 μm)柱;流动相甲醇-水(含0.02%磷酸);梯度洗脱程序为0~50 min,甲醇的体积分数(下同)由20%上升至80%;50~55 min由80%增至100%,55~60 min为100%,流速1 mL•min~(-1),检测波长254 nm;柱温35 ℃.结果:6种成分均达到基线分离,线性良好.结论:该方法快速、准确、重复性好,为该类药材的入药提供了理论依据.
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利用硅胶柱层析、Sephadex LH-20及反相硅胶RP-18分离及纯化技术,从辐状肋柱花全草乙醇提取物的正丁醇萃取部分得到7个水溶性成分,经^1H NMR、^13C NMR等波谱技术鉴定为异荭草苷、芒果苷、Swertipunicoside、当药醇苷、异牡荆苷、当药黄素、和7-O-[α-L-吡喃鼠李糖-(1-2)-β-D-吡喃木糖]-1,8-二羟基-3-甲氧基[口山]酮。除异荭草苷外,其余化合物均首次从该植物中得到。
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选用西宁地区人工栽培的高山植物唐古特大黄(Rheum tanguticum)、山莨菪(Anisodus tanguticus)和麻花艽(Gentiana straminea),比较了3种高山植物之间光合作用的光响应和CO2响应特性,叶片光合色素以及UV—B吸收物质的差异;并以低海拔植物菘蓝(Isatis indigotica)为对比,分析了高山植物与低海拔植物的差异。结果表明:与低海拔植物菘蓝相比,3种高山植物光合作用的表观量子效率(AQY)都偏低;唐古特大黄叶片的AQY、羧化效率(CE)和光呼吸速率(Rp)都很低,净光合速率(Pn)的光响应曲线在全日照光辐射范围内并没有达到完全饱和,这与单位面积叶片具有较高的光合色素以及UV—B吸收物质有关;麻花艽植物与唐古特大黄一样,具有较高的UV-B吸收物质和光合色素含量,但其Rp较高,加之Pn受气孔限制较为明显,故其光合作用的饱和光强很低,Pn相对于其它3种植物也较低;山莨菪与低海拔植物菘蓝的光合特性很相似,都具有较高的AQY和CE。这些结果表明,3种高山植物的光合特性有较大差异,但并没有一致的相对于低海拔植物的共性。4种植物Pn的胞间CO2浓度(G)响应曲线在CO2饱和点以后都表现为无机磷(Pi)再生限制,其吃的变化与CO2饱和点以后的最大Pn的变化基本一致。
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研究了花锚中去甲氧基花锚甙和花锚甙的含量随着不同生长期的变化趋势,为药材的合理栽培和采收提供科学依据.RP-HPLC法,使用VP-ODS C18柱,流动相为乙腈∶磷酸∶水(1‰),梯度洗脱程序:0~5.00 min乙腈的体积分数(以下同)为15%、5.01~14.00 min由15%增至25%、14.01~30.00 min由25%增至40%,流速为1 mL/min,柱温25℃,检测波长:254 nm.花锚甙和去甲氧基花锚甙、在花锚全草中的含量在不同生长期有明显变化.