Zhang Heng, Yang Chao, Li Chaokun, Li Lin, Zhao Qiao, Qiao Chuanling
State Key Laboratory of Integrated Management of Pest Insects & Rodents, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China.
J Agric Food Chem. 2008 Sep 10;56(17):7897-902. doi: 10.1021/jf801684g. Epub 2008 Aug 12.
Organophosphorus pesticides (OPs) cause serious environmental problems, and bioremediation using bacterial enzymes may provide an efficient and economical method for their detoxification. Green fluorescent protein (GFP) is a stable and easily detectable marker in monitoring genetically engineered microorganisms (GEMs) in the environment. In our research, the methyl parathion hydrolase gene (mpd) and enhanced green fluorescent protein gene (egfp) were successfully coexpressed using pETDuet vector in E. coli BL21 (DE3). The coexpression of methyl parathion hydrolase (MPH) and enhanced green fluorescent protein (EGFP) were confirmed by determining MPH activity and fluorescence intensity. The recombinant protein MPH showed high enzymatic degradative activity of several widely used OP residues on vegetables determined by GC analysis. Subsequently, a dual-species consortium comprising engineered E. coli and a natural p-nitrophenol (PNP) degrader Ochrobactrum sp. strain LL-1 for complete mineralization of dimethyl OPs was studied. It could completely mineralize methyl parathion (MP) via MP through PNP and hydroquinone and eventually through the TCA cycle as determined by HPLC analysis. The accumulation of PNP in suspended culture was prevented. The consortium could be further utilized for complete mineralization of PNP-substituted OPs in a laboratory-scale bioreactor and easily monitored by fluorescence of EGFP for its activity and fate.
有机磷农药(OPs)造成了严重的环境问题,利用细菌酶进行生物修复可能为其解毒提供一种高效且经济的方法。绿色荧光蛋白(GFP)是监测环境中基因工程微生物(GEMs)时一种稳定且易于检测的标记物。在我们的研究中,甲基对硫磷水解酶基因(mpd)和增强型绿色荧光蛋白基因(egfp)利用pETDuet载体在大肠杆菌BL21(DE3)中成功实现了共表达。通过测定MPH活性和荧光强度,证实了甲基对硫磷水解酶(MPH)和增强型绿色荧光蛋白(EGFP)的共表达。通过气相色谱分析测定,重组蛋白MPH对蔬菜上几种广泛使用的OP残留显示出高酶促降解活性。随后,研究了一种由工程化大肠杆菌和天然对硝基苯酚(PNP)降解菌 Ochrobactrum sp.菌株LL-1组成的双物种联合体,用于二甲基OPs的完全矿化。通过高效液相色谱分析测定,它可以通过PNP和对苯二酚将甲基对硫磷(MP)完全矿化,最终通过三羧酸循环实现。悬浮培养中PNP的积累得到了防止。该联合体可进一步用于实验室规模生物反应器中PNP取代的OPs的完全矿化,并可通过EGFP的荧光轻松监测其活性和去向。