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Development of a Biosensor for Methyl Parathion Detection and Genetic Risk Assessment of Exposed Population

机译:用于甲基对硫磷检测和暴露人群遗传风险评估的生物传感器的开发

摘要

Methyl parathion is one of the highly toxic organophosphate pesticides which contaminates udthe environment and exerts toxic effects in the non-targeted living organisms. Its detection and removal from the environment is needed in order to protect both the public and the environment from its hazardous effects. We studied risk assessment to pesticide toxicity (based on case studies), detection of methyl parathion (by using purified green fluorescent protein as a biosensing molecule) and biodegradation of methyl parathion (by indigenous bacterial isolates immobilized in sol gel matrices).udParaoxonase is a protein with enzymatic function which hydrolyzes toxic metabolites of methyl parathion and other organophosphate pesticides. We determined serum paraoxonase and serum arylesterase activities alongwith genotypes of respective groups recruited for the study. Various groups of the study population included healthy non-pesticide exposed male Punjabis, pesticide users, familial hypercholesterolaemia patients, glaucoma patients and appropriate controls. The results of the healthy population provided a baseline data (normal values). Study on pesticide users indicated significant differences of PON1 genotypes and phenotypes between the healthy pesticide users and the pesticide users who developed toxic effects of pesticides during spraying season. Serum paraoxonase and arylesterase activities were significantly low in hypercholesterolemia patients as compared to controls. There was no significant difference of PON1 genotype or phenotypes between glaucoma patients and age and gender matched controls. However age dependant decrease in serum paraoxonase and arylesterase activities explained the role of PON1 in glaucoma. The results of these studies will be helpful in understanding preventive measures to improve the status of public health.udDetection of methyl parathion is relatively costly with available methods and low cost and easy to use biosensor systems are needed for large scale screening of agricultural areas and other environmental segments. Thus we studied methyl parathion detection based on a simple method of fluorescence quenching. The linear decrease in the fluorescence of green fluorescent protein with increasing concentration of methyl parathion showed that fluorescence quenching based method can be utilized for low cost detection of methyl parathion. In addition, a novel fluorescent protein (HriGFP) was characterized for its physico-chemical properties to provide a baseline for future studies.udBacteria play a major role in degrading pesticides in the environment. Bacterial enzymes (esterases) convert the pesticides into metabolites which can be used as nutrients by the bacteria for their growth and proliferation. We isolated bacterial strains from agricultural areas contaminated with methyl parathion and other pesticides and characterized them for their combined xipotential of antimicrobial and heavy metal resistance and utilizing methyl parathion as a source of nutrients. In addition, a short listed consortium of the bacterial strains was immobilized in sol-gel and their survival in sol gel was studied. The results indicate that these environmental bacteria are capable of utilizing methyl parathion as a source of nutrient and sol gel immobilization can be helpful in co-survival of different bacterial strains for their application in bioremediation.udOn the whole, this thesis describes PON1 genotype and phenotype patterns in Pakistani populations, use of GFP as a biosensor molecule for detection of methyl parathion and isolation and characterization of bacterial strains for methyl parathion degrading activities. The study not only gives insight about the risk assessment and ultimately prevention of toxic effects of methyl parathion but also describes a proof of principle based on simple biotechnology approach for its detection. The results of this thesis will be a valuable source of information for public health managers, clinicians, policy makers, agricultural workers and bio-medical researchers for ultimate improvement of health status of general population as well as pesticide users.
机译:甲基对硫磷是一种剧毒的有机磷酸酯农药,它污染环境并对非目标生物产生毒性作用。为了保护公众和环境免受其有害影响,需要对其进行检测并从环境中清除。我们研究了农药毒性的风险评估(基于案例研究),甲基对硫磷的检测(通过使用纯化的绿色荧光蛋白作为生物传感分子)和甲基对硫磷的生物降解(通过固定在溶胶凝胶基质中的原生细菌分离物)。 udParaoxonase是一种具有酶促功能的蛋白质,可水解甲基对硫磷和其他有机磷酸酯农药的有毒代谢产物。我们确定了血清对氧磷酶和血清芳基酯酶的活性以及为研究募集的各组的基因型。研究人群的各个群体包括健康的非农药暴露男性旁遮普邦,农药使用者,家族性高胆固醇血症患者,青光眼患者和适当的对照组。健康人群的结果提供了基线数据(正常值)。对农药使用者的研究表明,健康农药使用者和在喷药季节产生农药毒性的农药使用者之间,PON1基因型和表型存在显着差异。与对照组相比,高胆固醇血症患者的血清对氧磷酶和芳基酯酶活性明显较低。在青光眼患者与年龄和性别匹配的对照之间,PON1基因型或表型没有显着差异。然而,血清对氧磷酶和芳基酯酶活性的年龄依赖性降低解释了PON1在青光眼中的作用。这些研究的结果将有助于理解预防措施以改善公共卫生状况。 ud检测甲基对硫磷的成本相对较高,且可用的方法成本低廉,并且需要易于使用的生物传感器系统来大规模筛查农业地区和农村地区。其他环境领域。因此,我们研究了基于简单的荧光猝灭方法的甲基对硫磷检测。随着甲基对硫磷浓度的增加,绿色荧光蛋白的荧光线性下降,表明基于荧光猝灭的方法可用于低成本检测甲基对硫磷。此外,新型荧光蛋白(HriGFP)的理化性质得以表征,可为将来的研究提供基准。 ud细菌在降解环境中的农药中起着重要作用。细菌酶(酯酶)可将农药转化为代谢产物,细菌可将其用作营养物以促进其生长和繁殖。我们从受甲基对硫磷和其他农药污染的农业地区分离出细菌菌株,并对其抗菌和重金属抗药性的综合潜力进行了表征,并利用甲基对硫磷作为营养物质。另外,将短名单的细菌菌株财团固定在溶胶-凝胶中,并研究了它们在溶胶-凝胶中的存活。结果表明,这些环境细菌能够利用甲基对硫磷作为营养来源,而溶胶凝胶的固定化可以帮助不同细菌菌株在生物修复中的共同生存。总体上,本文描述了PON1的基因型和巴基斯坦人群的表型模式,使用GFP作为生物传感器分子检测甲基对硫磷以及分离和鉴定具有甲基对硫磷降解活性的细菌菌株。该研究不仅提供了有关甲基对硫磷的风险评估和最终预防毒性作用的见解,而且还描​​述了基于简单生物技术方法进行甲基对硫磷检测的原理证明。本论文的结果将为公共卫生经理,临床医生,政策制定者,农业工作者和生物医学研究人员提供有价值的信息来源,以最终改善普通人群和农药使用者的健康状况。

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    Muhammad Idrees .;

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  • 年度 2015
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