948 resultados para G-f 20
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The nano ZnFe2O4 compound was prepared by eco-friendly hydrothermal method. The characterization of the sample for its structure, morphology and composition were done by powder X-ray diffraction (PXRD), scanning electron microscopy (SEM), dynamic light scattering, Fourier transform infrared spectroscopy, zeta surface profiler and UV-Visible spectroscopy studies. The PXRD measurement reveals that the compound shows spinel cubic phase belong Fd (3) over barm (227) space group. Morphology of the compound from SEM and surface profile shows nearly spherical agglomerated particles with well defined grains and grain boundaries. The material shows the semiconducting behavior with E-g of 2.3 eV at room temperature (RT). The variation in the magnetic ordering was observed for wide range of temperature. The compound behaves like a soft magnetic material with ferrimagnetic at various temperatures except at RT. Both magnetic and EPR studies supports the superparamagnetic behavior of the the sample. The DC conductivity, dielectric and AC conductivity behavior of the 1000 degrees C pellets sintered for 2 h shows good frequency dependent transport properties. The present study facilitate in selecting the suitable materials for the nanoelectronics and spintronic applications. (C) 2013 Elsevier B.V. All rights reserved.
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Effects of Basudine and Gammalin 20 on the fingerlings of Aphyosemin gairdneri were investigated using static bioassays and continuous aeration over a period of 48 hours. The 48 hours LC sub(50) of the exposed fish to Basudine and Gammalin 20 were determined to be 194.99 mu g dm super(3) and 95.50 mu g dm super(3) respectively. Gammalin 20 was more toxic than Basudine. The behavioural responses observed include agitation, erratic swimming, loss of equilibrium, period of quiescence and death. It is concluded that repeated applications of these herbicides should be avoided before stocking ponds with fish
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This dissertation describes studies of G protein-coupled receptors (GPCRs) and ligand-gated ion channels (LGICs) using unnatural amino acid mutagenesis to gain high precision insights into the function of these important membrane proteins.
Chapter 2 considers the functional role of highly conserved proline residues within the transmembrane helices of the D2 dopamine GPCR. Through mutagenesis employing unnatural α-hydroxy acids, proline analogs, and N-methyl amino acids, we find that lack of backbone hydrogen bond donor ability is important to proline function. At one proline site we additionally find that a substituent on the proline backbone N is important to receptor function.
In Chapter 3, side chain conformation is probed by mutagenesis of GPCRs and the muscle-type nAChR. Specific side chain rearrangements of highly conserved residues have been proposed to accompany activation of these receptors. These rearrangements were probed using conformationally-biased β-substituted analogs of Trp and Phe and unnatural stereoisomers of Thr and Ile. We also modeled the conformational bias of the unnatural Trp and Phe analogs employed.
Chapters 4 and 5 examine details of ligand binding to nAChRs. Chapter 4 describes a study investigating the importance of hydrogen bonds between ligands and the complementary face of muscle-type and α4β4 nAChRs. A hydrogen bond involving the agonist appears to be important for ligand binding in the muscle-type receptor but not the α4β4 receptor.
Chapter 5 describes a study characterizing the binding of varenicline, an actively prescribed smoking cessation therapeutic, to the α7 nAChR. Additionally, binding interactions to the complementary face of the α7 binding site were examined for a small panel of agonists. We identified side chains important for binding large agonists such as varenicline, but dispensable for binding the small agonist ACh.
Chapter 6 describes efforts to image nAChRs site-specifically modified with a fluorophore by unnatural amino acid mutagenesis. While progress was hampered by high levels of fluorescent background, improvements to sample preparation and alternative strategies for fluorophore incorporation are described.
Chapter 7 describes efforts toward a fluorescence assay for G protein association with a GPCR, with the ultimate goal of probing key protein-protein interactions along the G protein/receptor interface. A wide range of fluorescent protein fusions were generated, expressed in Xenopus oocytes, and evaluated for their ability to associate with each other.
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The FIDAWOG workshop held at the Tom Mboya Labour College in Kisumu was the fourth stock assessment workshop held under the LVFRP programme. There were two main objectives: training in paper and report writing and presentation, and presentation of research results collected to date.
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The morphology, increase and systematica of Sphaerotilus natans is studied and culture methods examined.
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postprint
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Over 20 years, successive openings and closures of the Sumilon Island marine reserve to fishers have provided unique opportunities to examine the effects of marine reserves on populations and communities of fishes and upon local fisheries. The history of the reserve also highlights the problems and frustrations of educating and convincing people of the need for rational management of renewable marine resources. Yet, it is a symbol of hope in that it has provided a unique example of the potential benefits of marine reserves in fisheries management, particularly in the developing world.
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G蛋白参与了哺乳动物内多种细胞信号途径,但其在植物花粉萌发和花粉管发育过程中的细胞学定位、生化特性及功能研究比较滞后,有关这方面的研究报道较少。在显花植物授粉受精过程中,具顶端极性生长特性的花粉管是雄性生殖单位的载体,也是研究细胞生长分子调控机理的理想体系。与被子植物相比,裸子植物具有生长周期长,花粉管生长缓慢、易分叉等特点,具有不同于被子植物花粉发育的独特发育模式。对于裸子植物花粉萌发和花粉管生长的调控机理,目前尚不十分清楚。本文以松类植物中比较有代表性的裸子植物青杆(Piceawillsonii)和白皮松(Pinus bungeana)花粉为试材,应用免疫分析和间接免疫荧光显微镜技术,结合药理学实验和FTIR手段,研究了异三聚体G蛋白和小G蛋白在花粉管细胞中的定位、生化特性及其在花粉管发育中的调控作用。结果如下: 应用Western Blotting技术和来自于抗哺乳动物中不同序列G蛋白O【亚基抗体,我们在白皮松花粉管中检测到一条分子量为40 kDa左右的蛋白。去污剂处理显示,该蛋白与质膜偶联。间接免疫荧光显微镜实验发现,在花粉管发育的整个时期,代表Ga蛋白的荧光均一的分布在整个质膜区域,尤其在尖端皮层区域荧光最亮,显示此处该蛋白浓度最高。无论是在正常发育的花粉管抑或是发生弯曲或扭曲生长的花粉管,均呈现同样的分布模式。随着花粉管发育,Ga蛋白表达量发生变化。在花粉管发育中期,Ga蛋白表达量比较高;随着花粉管离体培养时间的延长,Ga蛋白表达量下降。另外,在花粉刚刚萌发时,Ga蛋白表达量也比较低。 对白皮松花粉萌发进行的药理学实验显示,G蛋白调节剂 CTX和PTX对白皮松花粉管的影响呈现双阶段效应。当添加的药剂浓度小于400 ng mL-I时,无论CTX还是PTX均抑制了花粉萌发和花粉管生长,且花粉管容易破裂;而当二者浓度分别升至500 ng mL-I时,同对照相比,花粉管生长明显受到促进。这一结果不支持Ma等人在百合花粉中的研究结果。进一步应用FTIR技术分析发现,当用浓度为400 ng mL-I CTX或PTX处理花粉管时,花粉管细胞壁酚类物质增加,而纤维素、半纤维素、木聚糖等物质下降,这可能是导致此浓度处理下花粉管易破裂的原因。这些结果显示了G蛋白a亚基参与了白皮松花粉管生长,CTX和PTX可能通过下游对其敏感的功能蛋白而非Ga本身,影响着花粉管生长并调控着花粉管壁的建成。 利用来源于烟草的抗NtRacl抗体和拟南芥的抗ROPs抗体,应用WeternBlotting技术,我们在青杆花粉管中检测到分子量为23kDa的多肽。间接免疫荧光显微镜实验显示,在花粉萌发18和24小时后,Rac蛋白主要定位于花粉管尖端质膜区域,时而会延伸到顶端两侧区域,但从尖端到基部存在浓度梯度,这种分布模式多在花粉管发育的后期观察到。Rac蛋白在青杆花粉管不同发育时期的分布模式变化可能和花粉管的生长状态有关,在花粉管发育早期和中期,正是花粉管旺盛生长期,Rac蛋白的尖端定位保证了花粉管的极性生长。对Rac蛋白在花粉管的分布进行的连续切片扫描发现,Rac蛋白不但分布在质膜上,并与质膜偶联,而且在胞质中亦有分布。通过对一系列正常发育(即极性生长的花粉管)和畸形发育的花粉管进行观察发现,Rac蛋白主要分布在旺盛生长的花粉管尖端质膜或离顶端20 Vm处,在分叉的生长缓慢的分枝端分布较少。而在那些发生分叉生长的花粉管中,处于次要位置的基本停止生长的分枝端几乎没有Rac蛋白存在。在顶端发生膨大的花粉管中,Rac蛋白均匀分布在花粉管整个质膜上,丧失浓度梯度,失去极性生长。这些结果显示了Rac蛋白参与了青杆花粉管生长。 应用抗NtRacl抗体进行的间接免疫荧光显微镜定位实验,我们在正在生长的花粉管的管核中观察到明亮的荧光,显示了有Rac蛋白的存在。当精细胞在花粉粒中未移动到花粉管中时,几乎没有观察到荧光信号。随着花粉管发育,两个精细胞的位置发生变化,当其中一个较大的精细胞移动到花粉管中时,观察到明亮的荧光信号,这些结果显示了Rac蛋白可能参与了管核或精细胞在花粉管内的移动。