214 resultados para AChE
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本研究利用淡水鲫鱼肝脏为主要原材料提取乙酰胆碱酯酶(acetylcholinesterase,AChE),并设计正交试验确定了鲫鱼肝脏中乙酰胆碱酯酶的最佳提取条件:通过酶抑制法衡量敌敌畏、辛硫磷、三唑磷、乐果等四种不同种类有机磷农药对粗酶液的抑制作用;将鱼肝和鱼脑中乙酰胆碱酯酶活性及蛋白含量的进行对比研究。研究结果表明:提取液pH值、提取液种类以及原料与提取液的质量体积比对酶液的活性影响显著;被测四种有机磷农药中,敌敌畏对AChE活性抑制作用最强。鱼脑的AChE比酶活是肝脏的AChE比酶活的3~7倍。
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以鲫鱼肌肉为原料提取乙酰胆碱酯酶(Acetylcholinesterase,AChE),然后采用改进的Ellman方法按照正交试验设计分别测定不同环境条件(pH值,温度,时间)下粗酶液活性,得到测定AChE活性的最佳条件组合。再将粗酶液依次通过DEAE-Sephadex A-50和Sephadex G-200柱层析纯化。结果表明,3个因素对AChE活性影响的顺序为温度>pH值>时间;最佳酶活性测定条件组合为环境温度35℃,体系pH值8.0,反应时间30 min;经Sephadex A-50柱层析后的纯化倍
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提取不同生长期的鲫鱼脑中乙酰胆碱酯酶(acetylcholinesterase,AChE)并做比较,以Ellman法测定其酶活。并用正交试验方法确定了最佳测定条件。采用体外实验法研究了在最佳条件下鲫鱼脑AChE对三种有机磷农药的敏感性。研究结果表明,以体长12cm左右的鲫鱼体内AChE活性最高,正交试验得出AChE最佳测定条件组合为:酶的剂量为40μl、底物最终浓度为120mmol/L、pH值7.5、温度35℃;时间15min。鲫鱼脑AChE对农药的敏感性为敌敌畏>辛硫磷>乐果。
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Among the variety of applications for biosensors one of the exciting frontiers is to utilize those devices as post-synaptic sensing elements in chemical coupling between neurons and solid-state systems. The first necessary step to attain this challenge is to realize highly efficient detector for neurotransmitter acetylcholine (ACh). Herein, we demonstrate that the combination of floating gate configuration of ion-sensitive field effect transistor (ISFET) together with diluted covalent anchoring of enzyme acetylcholinesterase (AChE) onto device sensing area reveals a remarkable improvement of a four orders of magnitude in dose response to ACh. This high range sensitivity in addition to the benefits of peculiar microelectronic design show, that the presented hybrid provides a competent platform for assembly of artificial chemical synapse junction. Furthermore, our system exhibits clear response to eserine, a competitive inhibitor of AChE, and therefore it can be implemented as an effective sensor of pharmacological reagents, organophosphates, and nerve gases as well. © 2007 Materials Research Society.
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The potential use of biochemical and physiological responses as biomarkers of organophosphate exposure and/or effect were assessed in the shore crab (Carcinus maenas). Male crabs were assigned to one of four dimethoate treatments (0, 0.5, 1.0 or 2.0 mg 1(-1)). Cardiac activity was measured non-invasively before and during dimethoate exposure using automated interpulse duration assessment. Heart rates decreased significantly in a concentration-dependent manner (p
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A series of novel naphthyridine derivatives 3 and 4 was prepared from substituted pyridine 2 and ketones using ZnCl2 as catalyst under microwave irradiation conditions. All the compounds were evaluated for AChE inhibitory activity and promising compounds 3d, 3e, 4b, and 4g was identified. Representative compounds 3d and 3e were found to show insignificant THLE-2 liver cell viability/toxicity. The binding mode between X-ray crystal structure of human AChE and compounds was studied using molecular docking method and fitness scores were found to be in good correlation with the activity data.
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We have identified two mutations in the ace1 gene of Aphis gossypii that are associated with insensitivity of acetylcholinesterase (AChE) to carbamate and organophosphate insecticides. The first of these, S431F (equivalent to F331 in Torpedo californica), is associated with insensitivity to the carbamate insecticide pirimicarb in a range of A. gossypii clones. The S431F mutation is also found in the peach-potato aphid, Myzus persicae (Sulzer), and a rapid RFLP diagnostic allows the identification of individuals of both aphid species with a resistant genotype. This diagnostic further revealed the presence of S431 in several other pirimicarb-susceptible aphid species. The serine at this position in the wild-type enzyme has only been reported for aphids and provides a molecular explanation of why pirimicarb has a specific aphicidal action. A less specific insensitivity to a wide range of carbamates and organophosphates is associated with a second mutation, A302S (A201 in T. californica).
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Chronic back pain is one of the eight most important symptoms of mankind in several lifetime prevalence studies. In the chronification process, an utmost important role is devoted to psychosocial influences, whereas structural abnormalities normally do not have a primal function in this process. The author also includes the discussion of the possibilities for the generalist to influence early the chronification process with the aim to keep the patient in his/her working environment.
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Chromosome 7q22 has been the focus of many cytogenetic and molecular studies aimed at delineating regions commonly deleted in myeloid leukemias and myelodysplastic syndromes. We have compared a gene-dense, GC-rich sub-region of 7q22 with the orthologous region on mouse chromosome 5. A physical map of 640 kb of genomic DNA from mouse chromosome 5 was derived from a series of overlapping bacterial artificial chromosomes. A 296 kb segment from the physical map, spanning Ache to Tfr2, was compared with 267 kb of human sequence. We identified a conserved linkage of 12 genes including an open reading frame flanked by Ache and Asr2, a novel cation-chloride cotransporter interacting protein Cip1, Ephb4, Zan and Perq1. While some of these genes have been previously described, in each case we present new data derived from our comparative sequence analysis. Adjacent unfinished sequence data from the mouse contains an orthologous block of 10 additional genes including three novel cDNA sequences that we subsequently mapped to human 7q22. Methods for displaying comparative genomic information, including unfinished sequence data, are becoming increasingly important. We supplement our printed comparative analysis with a new, Web-based program called Laj (local alignments with java). Laj provides interactive access to archived pairwise sequence alignments via the WWW. It displays synchronized views of a dot-plot, a percent identity plot, a nucleotide-level local alignment and a variety of relevant annotations. Our mouse–human comparison can be viewed at http://web.uvic.ca/~bioweb/laj.html. Laj is available at http://bio.cse.psu.edu/, along with online documentation and additional examples of annotated genomic regions.
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1. ptie. Monuments de la vallée du Polvar-Roud.--2. ptie. Monuments de Persépolis.--3. ptie. La sculpture persépolitaine.--4. ptie. Les monuments voutés de l'époque achéménide.--5. ptie. Monuments parthes et sassanides.
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Mode of access: Internet.
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Performed with the greatest applause, at the theatre, Philadelphia.