Expression and characterization of a codon-optimized butyrylcholinesterase for analysis of organophosphate insecticide residues

التفاصيل البيبلوغرافية
العنوان: Expression and characterization of a codon-optimized butyrylcholinesterase for analysis of organophosphate insecticide residues
المؤلفون: Yuan-hong Xie, Xiang-ning Chen, Wen-tao Xu, Li Xu, Yong Lu, Jing-jing Tian, Bin Du
المصدر: Journal of Integrative Agriculture, Vol 15, Iss 3, Pp 684-693 (2016)
بيانات النشر: Elsevier BV, 2016.
سنة النشر: 2016
مصطلحات موضوعية: 0301 basic medicine, Agriculture (General), Plant Science, Biochemistry, Michaelis–Menten kinetics, S1-972, Pichia pastoris, Toxicology, 03 medical and health sciences, chemistry.chemical_compound, Food Animals, Affinity chromatography, expression, Dichlorvos, Butyrylcholinesterase, chemistry.chemical_classification, Chromatography, Ecology, biology, Organophosphate, organophosphate insecticide residues, biology.organism_classification, codon-optimized, 030104 developmental biology, Enzyme, chemistry, butyrylcholinesterase, Animal Science and Zoology, Specific activity, Agronomy and Crop Science, Food Science
الوصف: Organophosphate insecticide residues on vegetable, fruit, tea and even grains are primary cause of food poisoning. Organophosphate compounds can cause irreversible inhibition of the activity of acetylcholinesterase and butyrylcholinesterase (BChE, EC 3.1.1.8), which are both candidates for rapid detection of organophosphate pesticides. To develop an easy-to-handle method for detecting organophosphate pesticides using BChE, BChE from human was optimized according to the codon usage bias of Pichia pastoris and successfully expressed in P. pastoris GS115. The codon-optimized cDNA shared 37.3% of the codon identity with the native one. However, the amino acid sequence was identical to that of the native human butyrylcholinesterase gene ( hBChE ) as published. The ratio of guanine and cytosine in four kinds of bases ((G+C) ratio) was simultaneously increased from 40 to 47%. The recombinant hBChE expression reached a total protein concentration of 292 mg mL –1 with an activity of 14.7 U mL –1 , which was purified 3.2×10 3 -fold via nickel affinity chromatography with a yield of 68% and a specific activity of 8.1 U mg –1 . Recombinant hBChE was optimally active at pH 7.4 and 50°C and exhibited high activity at a wide pH range (>60% activity at pH 4.0 to 8.0). Moreover, it had a good adaptability to high temperature (>60% activity at both 50 and 60°C up to 60 min) and good stability at 70°C. The enzyme can be activated by Li + , Co + , Zn 2+ and ethylene diamine tetraacetic acid (EDTA), but inhibited by Mg 2+ , Mn 2+ , Fe 2+ , Ag + and Ca 2+ . Na + had little effect on its activity. The values of hBChE of the Michaelis constant (K m ) and maximum reaction velocity (V m ) were 89.4 mmol L –1 and 1721 mmol min –1 mg –1 , respectively. The bimolecular rate constants (K i ) of the hBChE to four pesticides were similar with that of electric eel AChE (EeAChE) and higher than that of horse BChE (HoBChE). All values of the half maximal inhibitory concentration of a substance (IC 50 ) for hBChE were lower than those for HoBChE, but most IC 50 for hBChE were lower than those for EeAChE except dichlorvos. The applicability of the hBChE was further verified by successful detection of organophosphate insecticide residues in six kinds of vegetable samples. Thus, hBChE heterologously over-expressed by P . pastoris would provide a sufficient material for development of a rapid detection method of organophosphate on spot and produce the organophosphate detection kit.
تدمد: 2095-3119
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aca10721f82e8d2ef7ebe7828c14ea9c
https://doi.org/10.1016/s2095-3119(15)61139-x
حقوق: OPEN
رقم الأكسشن: edsair.doi.dedup.....aca10721f82e8d2ef7ebe7828c14ea9c
قاعدة البيانات: OpenAIRE