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Engineered whole-cell biocatalyst-based detoxification and detection of neurotoxic organophosphate compounds
Authors:Chang Sup Kim  Jeong Hyun Seo  Dong Gyun Kang  Hyung Joon Cha
Affiliation:1. Department of Chemical Engineering, Pohang University of Science and Technology, Pohang 790-784, Republic of Korea;2. School of Chemical Engineering, Yeungnam University, Gyeongsan 712-749, Republic of Korea
Abstract:The development of efficient tools is required for the eco-friendly detoxification and effective detection of neurotoxic organophosphates (OPs). Although enzymes have received significant attention as biocatalysts because of their high specific activity, the uneconomic and labor-intensive processes of enzyme production and purification make their broad use in practical applications difficult. Because whole-cell systems offer several advantages compared with free enzymes, including high stability, a reduced purification requirement, and low preparation cost, they have been suggested as promising biocatalysts for the detoxification and detection of OPs. To develop efficient whole-cell biocatalysts with enhanced activity and a broad spectrum of substrate specificity, several factors have been considered, namely the selected strains, the chosen OP-hydrolyzing enzymes, where enzymes are localized in a cell, and which enhancer will assist the expression, function, and folding of the enzyme. In this article, we review the current investigative progress in the development of engineered whole-cell biocatalysts with excellent OP-hydrolyzing activity, a broad spectrum of substrate specificity, and outstanding stability for the detoxification and detection of OPs.
Keywords:AChE, acetylcholinesterase   CB, carbon black   CBD, cellulose-binding domain   CNT, carbon nanotube   CP, coumaphos   CPF, chlorpyrifos   4-CP, 4-chlorophenol   DZN, diazinon   EDSs, edge-plane-like defective sites   EP, ethyl parathion   EPN, ethyl p-nitrophenol thio benzene phosphonate   FITC, fluorescein isothiocyanate   FNT, fenitrothion   GC, glass carbon   GFP, green fluorescent protein   GPI, glycosylphosphatidylinositol   HEPES, 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid   Ina, ice nucleation   INP, ice nucleation protein   Lpp, lipoprotein   MAP, mussel adhesive protein   MC, mesoporous carbon   MP, methyl parathion   MPH, methyl parathion hydrolase   MWCNT, multi-wall carbon nanotube   OmpA, outer membrane protein A   OPAA, organophosphorus acid anhydrase   OPDA, organophosphorus-degrading enzyme   OPH, organophosphorus hydrolase   OPs, organophosphates   PA, parathion   PNP, p-nitrophenol   PO, paraoxon   POLE, polyoxyethylene 10 lauryl ether   PVA, poly (vinyl alcohol)   SPCE, screen-printed carbon electrode   SRP, signal recognition particle   SWCNT, single-wall carbon nanotube   Tat, twin-arginine translocation   TMAO, trimethylamine N-oxide   VHb, Vitreoscilla hemoglobin
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