Creating a Halotolerant Degrader for Efficient Mineralization of p-Nitrophenol-Substituted Organophosphorus Pesticides in High-Saline Wastewater

IF 3.5 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Biotechnology and Bioengineering Pub Date : 2025-01-16 DOI:10.1002/bit.28923
Yujie Liu, Weini Xiong, Yuting Jiang, Yan Meng, Wanwan Zhao, Chao Yang, Ruihua Liu
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Abstract

The bioaugmentation performance is severely reduced in the treatment of high-saline pesticide wastewater because the growth and degradation activity of pesticide degraders are significantly inhibited by high salt concentrations. In this study, a heterologous biodegradation pathway comprising the seven genes mpd/pnpABCDEF responsible for the bioconversion of p-nitrophenol (PNP)-substituted organophosphorus pesticides (OPs) into β-oxoadipate and the genes encoding Vitreoscilla hemoglobin (VHb) and green fluorescent protein (GFP) were integrated into the genome of a salt-tolerant chassis Halomonas cupida J9, to generate a genetically engineered halotolerant degrader J9U-MP. RT-PCR assays demonstrated that the nine exogenous genes are successfully transcribed to mRNA in J9U-MP. Gas chromatography analysis of methyl parathion (MP) and its intermediates demonstrated that the expressed MP hydrolase and PNP-degrading enzymes PnpABCD show obvious degradation activity toward the specific substrates in J9U-MP. Stable isotope analysis showed that J9U-MP is able to efficiently convert 13C6-PNP into 13CO2, demonstrating the complete mineralization of MP in high-salt media. J9U-MP is genetically stable during passage culture, and genomic integration of exogenous genes does not negatively influence the growth of J9U-MP. Under oxygen-limited conditions, VHb-expressing J9U-MP does not show obvious growth inhibition and a significant reduction in the MP degradation rate. A real-time monitoring system with enhanced GFP is used to track the motion and activity of J9U-MP during bioremediation. Moreover, 50 mg/L MP and its intermediates (i.e., PNP and HQ) were completely degraded by J9U-MP within 12 h in wastewater supplemented with 60 g/L NaCl. After 3 days of incubation, 25 mg/L 13C6-PNP was converted into 13CO2 by J9U-MP in wastewater supplemented with 60 g/L NaCl. Our results highlight the power of synthetic biology for creating new halotolerant pollutant-mineralizing strains. The strong competitive advantages of J9U-MP in high-salinity and low-oxygen environments make this degrader suitable for in situ bioaugmentation of OP wastewater.

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高盐废水中对硝基酚取代有机磷农药高效矿化的耐盐降解剂研究
在高盐农药废水处理中,由于高盐浓度显著抑制了农药降解体的生长和降解活性,导致生物增强性能严重降低。本研究将对硝基苯酚(PNP)取代的有机磷农药(OPs)转化为β-氧己二酸酯的7个基因mpd/pnpABCDEF以及玻璃状蛋白(VHb)和绿色荧光蛋白(GFP)的编码基因整合到耐盐底盘盐单胞菌(Halomonas cupida) J9的基因组中,生成耐盐降解物J9U-MP。RT-PCR结果表明,9个外源基因在J9U-MP中成功转录为mRNA。对甲基对硫磷及其中间体的气相色谱分析表明,所表达的甲基对硫磷水解酶和甲基对硫磷降解酶PnpABCD对J9U-MP中的特定底物具有明显的降解活性。稳定同位素分析表明,J9U-MP能够有效地将13C6-PNP转化为13CO2,表明MP在高盐介质中完全矿化。J9U-MP在传代培养过程中遗传稳定,外源基因的基因组整合对J9U-MP的生长没有负面影响。在限氧条件下,表达vhb的J9U-MP不表现出明显的生长抑制,MP降解率明显降低。利用增强GFP实时监测系统跟踪J9U-MP在生物修复过程中的运动和活性。在添加60 g/L NaCl的废水中,50mg /L的MP及其中间体(即PNP和HQ)在12 h内被J9U-MP完全降解。培养3天后,在添加60 g/L NaCl的废水中,25 mg/L的13C6-PNP通过J9U-MP转化为13CO2。我们的研究结果突出了合成生物学在创造新的耐盐污染物矿化菌株方面的力量。J9U-MP在高盐度和低氧环境中的强大竞争优势使其适合于OP废水的原位生物强化。
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来源期刊
Biotechnology and Bioengineering
Biotechnology and Bioengineering 工程技术-生物工程与应用微生物
CiteScore
7.90
自引率
5.30%
发文量
280
审稿时长
2.1 months
期刊介绍: Biotechnology & Bioengineering publishes Perspectives, Articles, Reviews, Mini-Reviews, and Communications to the Editor that embrace all aspects of biotechnology. These include: -Enzyme systems and their applications, including enzyme reactors, purification, and applied aspects of protein engineering -Animal-cell biotechnology, including media development -Applied aspects of cellular physiology, metabolism, and energetics -Biocatalysis and applied enzymology, including enzyme reactors, protein engineering, and nanobiotechnology -Biothermodynamics -Biofuels, including biomass and renewable resource engineering -Biomaterials, including delivery systems and materials for tissue engineering -Bioprocess engineering, including kinetics and modeling of biological systems, transport phenomena in bioreactors, bioreactor design, monitoring, and control -Biosensors and instrumentation -Computational and systems biology, including bioinformatics and genomic/proteomic studies -Environmental biotechnology, including biofilms, algal systems, and bioremediation -Metabolic and cellular engineering -Plant-cell biotechnology -Spectroscopic and other analytical techniques for biotechnological applications -Synthetic biology -Tissue engineering, stem-cell bioengineering, regenerative medicine, gene therapy and delivery systems The editors will consider papers for publication based on novelty, their immediate or future impact on biotechnological processes, and their contribution to the advancement of biochemical engineering science. Submission of papers dealing with routine aspects of bioprocessing, description of established equipment, and routine applications of established methodologies (e.g., control strategies, modeling, experimental methods) is discouraged. Theoretical papers will be judged based on the novelty of the approach and their potential impact, or on their novel capability to predict and elucidate experimental observations.
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