Delftia sp. PY-12对乙酰氨基酚的生物降解特性:性能、降解动力学和途径

IF 3.7 3区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Yanxue Pei , Muchen Yin , Yanan Cui , Fan Yang , Xueying Bian , Jun Li , Yaodong Wu
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引用次数: 0

摘要

对乙酰氨基酚(APAP)因其解热特性而被广泛使用,在废水中普遍存在,对水生生态系统有潜在威胁。微生物降解已被证明是去除APAP的有效方法。然而,能够高效降解APAP的菌株很少,对APAP生物降解动力学的研究也不足。本研究从活性污泥中分离到一株新型apap降解菌,经形态学鉴定和16S rRNA基因测序鉴定为Delftia sp. PY-12。采用Box-Behnken响应面设计优化实验条件,发现PY-12在pH为7.11、30℃、转速为163 rpm的条件下,在24 h内降解100 mg/L APAP的效果优于其他菌株。底物抑制模型对比分析表明Aiba和Tiesser最适合PY-12的底物抑制特性。模型表明,即使在浓度为446.919 mg/L和554.215 mg/L时,PY-12仍能降解APAP。通过电位酶活性测定,确定了PY-12对APAP的降解途径。APAP先经氨基水解酶转化为4-氨基酚(4-AP),再经脱氨酶转化为对苯二酚(HQ),对苯二酚再经对苯二酚1,2-双加氧酶转化为4-羟基半醛,最终进入TCA循环。本研究揭示了PY-12在APAP降解中的潜在应用价值,它可能是环境修复中APAP污染微生物修复的有力候选菌株。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Biodegradation characteristics of acetaminophen by Delftia sp. PY-12: Performance, degradative kinetics, and pathway
Acetaminophen (APAP) is widely used for its antipyretic properties and is commonly found in wastewater, potentially threatening aquatic ecosystems. Microbial degradation has been proven effective in removing APAP. However, strains capable of efficiently degrading APAP are rare, and the research on the biodegradation kinetics of APAP is insufficient. In this study, a novel APAP-degrading strain, identified as Delftia sp. PY-12 by morphological characterization and 16S rRNA gene sequencing, was isolated from activated sludge. Experimental conditions were optimized using the Box-Behnken response surface design, revealing that PY-12 degraded 100 mg/L APAP under pH 7.11, 30℃, and 163 rpm within 24 h, outperforming most other strains. Comparative analysis of substrate inhibition models shows that the Aiba and Tiesser were most suitable for the substrate inhibition characteristics of PY-12. The models indicate that PY-12 can still degrade APAP even at concentrations of 446.919 mg/L and 554.215 mg/L. Through potential enzyme activity measurements, the degradation pathway of APAP by PY-12 was determined. APAP is first converted by amidohydrolase into 4-aminophenol (4-AP) and then converted by deaminase into hydroquinone (HQ), which is further converted by hydroquinone 1,2-dioxygenase to form 4-hydroxymuconic semialdehyde, ultimately entering the TCA cycle. This study revealed the potential application value of PY-12 in APAP degradation, which could be a strong candidate strain for microbial bioremediation of APAP pollution in environmental remediation.
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来源期刊
Biochemical Engineering Journal
Biochemical Engineering Journal 工程技术-工程:化工
CiteScore
7.10
自引率
5.10%
发文量
380
审稿时长
34 days
期刊介绍: The Biochemical Engineering Journal aims to promote progress in the crucial chemical engineering aspects of the development of biological processes associated with everything from raw materials preparation to product recovery relevant to industries as diverse as medical/healthcare, industrial biotechnology, and environmental biotechnology. The Journal welcomes full length original research papers, short communications, and review papers* in the following research fields: Biocatalysis (enzyme or microbial) and biotransformations, including immobilized biocatalyst preparation and kinetics Biosensors and Biodevices including biofabrication and novel fuel cell development Bioseparations including scale-up and protein refolding/renaturation Environmental Bioengineering including bioconversion, bioremediation, and microbial fuel cells Bioreactor Systems including characterization, optimization and scale-up Bioresources and Biorefinery Engineering including biomass conversion, biofuels, bioenergy, and optimization Industrial Biotechnology including specialty chemicals, platform chemicals and neutraceuticals Biomaterials and Tissue Engineering including bioartificial organs, cell encapsulation, and controlled release Cell Culture Engineering (plant, animal or insect cells) including viral vectors, monoclonal antibodies, recombinant proteins, vaccines, and secondary metabolites Cell Therapies and Stem Cells including pluripotent, mesenchymal and hematopoietic stem cells; immunotherapies; tissue-specific differentiation; and cryopreservation Metabolic Engineering, Systems and Synthetic Biology including OMICS, bioinformatics, in silico biology, and metabolic flux analysis Protein Engineering including enzyme engineering and directed evolution.
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