纳米银在诺氟沙星胁迫下对黄孢原毛平革菌的毒物兴奋效应

丁文东, 崔康平, 郭志, 高斯研. 纳米银在诺氟沙星胁迫下对黄孢原毛平革菌的毒物兴奋效应[J]. 生态毒理学报, 2020, 15(6): 141-150. doi: 10.7524/AJE.1673-5897.20200403001
引用本文: 丁文东, 崔康平, 郭志, 高斯研. 纳米银在诺氟沙星胁迫下对黄孢原毛平革菌的毒物兴奋效应[J]. 生态毒理学报, 2020, 15(6): 141-150. doi: 10.7524/AJE.1673-5897.20200403001
Ding Wendong, Cui Kangping, Guo Zhi, Gao Siyan. Hormesis of Silver Nanoparticles on Phanerochaete chrysosporium under Norfloxacin Stress[J]. Asian Journal of Ecotoxicology, 2020, 15(6): 141-150. doi: 10.7524/AJE.1673-5897.20200403001
Citation: Ding Wendong, Cui Kangping, Guo Zhi, Gao Siyan. Hormesis of Silver Nanoparticles on Phanerochaete chrysosporium under Norfloxacin Stress[J]. Asian Journal of Ecotoxicology, 2020, 15(6): 141-150. doi: 10.7524/AJE.1673-5897.20200403001

纳米银在诺氟沙星胁迫下对黄孢原毛平革菌的毒物兴奋效应

    作者简介: 丁文东(1994-),男,硕士研究生,研究方向为环境微生物学,E-mail:hfutding@163.com
    通讯作者: 郭志, E-mail: guozhi@hfut.edu.cn
  • 基金项目:

    国家自然科学基金资助项目(51809068);国家重点研发计划资助项目(SQ2019YFC040023);安徽省科技重大专项(17030801031);安徽省科技重大专项(201903a07020009);长丰县-合肥工业大学产业创新引导资金资助项目;中央高校基本科研业务费专项资金资助项目(JZ2020HGTB0022,JZ2018HGBZ0311)

  • 中图分类号: X171.5

Hormesis of Silver Nanoparticles on Phanerochaete chrysosporium under Norfloxacin Stress

    Corresponding author: Guo Zhi, guozhi@hfut.edu.cn
  • Fund Project:
  • 摘要: 具有生物毒性的纳米银(AgNPs)在低浓度下能产生毒物兴奋效应,可以刺激细胞的活性增强。研究了在诺氟沙星胁迫下,AgNPs对黄孢原毛平革菌活性的影响,并通过探究AgNPs的迁移转化以及细胞外蛋白质浓度的变化,结合扫描电镜、X射线衍射以及傅里叶红外光谱分析进行机理探索。结果表明,AgNPs在0.001 mg·L-1和0.01 mg·L-1浓度下可以将黄孢原毛平革菌的细胞活性提高1.29倍与1.51倍,而在1.3 mg·L-1 AgNPs的刺激下,细胞活性降低64%,同时,相同浓度的Ag离子仅对细胞产生毒性抑制作用。低浓度AgNPs可以在溶液相与生物相之间进行迁移,触发细胞生物学特性的变化,刺激细胞在面临诺氟沙星胁迫时产生较多的胞外蛋白质来减轻毒性抑制作用。黄孢原毛平革菌的菌丝表面存在的羟基、醛、酮和巯基等官能团可以将Ag离子还原为纳米氯化银和硫化银,在细胞表面聚集。
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  • 卢雪蓉, 冯晓丽, 刘朝莹, 等. 纳米银的迁移转化对环境微生物毒性的影响[J]. 生态毒理学报, 2018, 13(5):49-57

    Lu X R, Feng X L, Liu Z Y, et al. Impact of migration and transformation of AgNPs on its toxicity towards environmental microorganism[J]. Asian Journal of Ecotoxicology, 2018, 13(5):49-57(in Chinese)

    衣俊, 黄俊, 程金平. 纳米银在水环境中的环境行为和毒性效应研究进展[J]. 生态毒理学报, 2015, 10(1):101-109

    Yi J, Huang J, Cheng J P. Review of environmental behavior and toxicity of silver nanoparticles in the aquatic environment[J]. Asian Journal of Ecotoxicology, 2015, 10(1):101-109(in Chinese)

    Xiu Z M, Zhang Q B, Puppala H L, et al. Negligible particle-specific antibacterial activity of silver nanoparticles[J]. Nano Letters, 2012, 12(8):4271-4275
    Arora S, Jain J, Rajwade J M, et al. Cellular responses induced by silver nanoparticles:In vitro studies[J]. Toxicology Letters, 2008, 179(2):93-100
    Shin S H, Ye M K, Kim H S, et al. The effects of nano-silver on the proliferation and cytokine expression by peripheral blood mononuclear cells[J]. International Immunopharmacology, 2007, 7(13):1813-1818
    Braydich-Stolle L, Hussain S, Schlager J J, et al. In vitro cytotoxicity of nanoparticles in mammalian germline stem cells[J]. Toxicological Sciences, 2005, 88(2):412-419
    Li H B, Chen J, Hou H J, et al. Sustained molecular oxygen activation by solid iron doped silicon carbide under microwave irradiation:Mechanism and application to norfloxacin degradation[J]. Water Research, 2017, 126:274-284
    González-Plaza J J, Blau K, Milakovic' M, et al. Antibiotic-manufacturing sites are hot-spots for the release and spread of antibiotic resistance genes and mobile genetic elements in receiving aquatic environments[J]. Environment International, 2019, 130:104735
    Kivits T, Broers H P, Beeltje H, et al. Presence and fate of veterinary antibiotics in age-dated groundwater in areas with intensive livestock farming[J]. Environmental Pollution, 2018, 241:988-998
    Zhang Q Q, Ying G G, Pan C G, et al. Comprehensive evaluation of antibiotics emission and fate in the river basins of China:Source analysis, multimedia modeling, and linkage to bacterial resistance[J]. Environmental Science & Technology, 2015, 49(11):6772-6782
    汪皓琦, 董玉瑛, 汪灵伟, 等. 4种喹诺酮类抗生素对发光菌毒性作用研究[J]. 生态毒理学报, 2017, 12(3):453-459

    Wang H Q, Dong Y Y, Wang L W, et al. The toxicity of four quinolones to Photobacterium phosphoreum[J]. Asian Journal of Ecotoxicology, 2017, 12(3):453-459(in Chinese)

    Guo Z, Chen G Q, Zeng G M, et al. Determination of inequable fate and toxicity of Ag nanoparticles in a Phanerochaete chrysosporium biofilm system through different sulfide sources[J]. Environmental Science:Nano, 2016, 3(5):1027-1035
    Chen A W, Zeng G M, Chen G Q, et al. Plasma membrane behavior, oxidative damage, and defense mechanism in Phanerochaete chrysosporium under cadmium stress[J]. Process Biochemistry, 2014, 49(4):589-598
    Cornelis G, Kirby J K, Beak D, et al. A method for determination of retention of silver and cerium oxide manufactured nanoparticles in soils[J]. Environmental Chemistry, 2010, 7(3):298
    Huang Z Z, Chen G Q, Zeng G M, et al. Polyvinyl alcohol-immobilized Phanerochaete chrysosporium and its application in the bioremediation of composite-polluted wastewater[J]. Journal of Hazardous Materials, 2015, 289:174-183
    谭琼. 废水处理中复合纳米生物材料白腐真菌的生理响应机制研究[D]. 长沙:湖南大学, 2015:9-10 Tan Q. Physiological response mechanism of composite nano-biomaterial Phanerochaete chrysosporium in the wastewater[D]. Changsha:Hunan University, 2015:9

    -10(in Chinese)

    Deraman A M, Talib I A, Omar M R, et al. Microcrystallite dimension and total active surface area of carbon electrode from mixtures of pre-carbonized oil palm empty fruit bunches and green petroleum cokes[J]. Sains Malaysiana, 2010, 39(1):83-86
    Chen G Q, Zou Z J, Zeng G M, et al. Coarsening of extracellularly biosynthesized cadmium crystal particles induced by thioacetamide in solution[J]. Chemosphere, 2011, 83(9):1201-1207
    Lad U, Kale G M, Bryaskova R. Glucose oxidase encapsulated polyvinyl alcohol-silica hybrid films for an electrochemical glucose sensing electrode[J]. Analytical Chemistry, 2013, 85(13):6349-6355
    Zuo Y N, Chen G Q, Zeng G M, et al. Transport, fate, and stimulating impact of silver nanoparticles on the removal of Cd(Ⅱ) by Phanerochaete chrysosporium in aqueous solutions[J]. Journal of Hazardous Materials, 2015, 285:236-244
    Sanghi R, Verma P. A facile green extracellular biosynthesis of CdS nanoparticles by immobilized fungus[J]. Chemical Engineering Journal, 2009, 155(3):886-891
    Verma D K, Hasan S H, Ranjan D, et al. Modified biomass of Phanerochaete chrysosporium immobilized on Luffa sponge for biosorption of hexavalent chromium[J]. International Journal of Environmental Science and Technology, 2014, 11(7):1927-1938
    Calabrese E J. Overcompensation stimulation:A mechanism for hormetic effects[J]. Critical Reviews in Toxicology, 2001, 31(4-5):425-470
    Wang Z, Xia T, Liu S J. Mechanisms of nanosilver-induced toxicological effects:More attention should be paid to its sublethal effects[J]. Nanoscale, 2015, 7(17):7470-7481
    Nel A E, Mädler L, Velegol D, et al. Understanding biophysicochemical interactions at the nano-bio interface[J]. Nature Materials, 2009, 8(7):543-557
    Xie X L, Sun T C, Xue J Z, et al. Targeted antibacterial therapy:Ag nanoparticles cluster with pH-triggered reassembly in targeting antimicrobial applications (Adv. Funct. Mater. 17/2020)[J]. Advanced Functional Materials, 2020, 30(17):2070106
    Bae S, Hwang Y S, Lee Y J, et al. Effects of water chemistry on aggregation and soil adsorption of silver nanoparticles[J]. Environmental Health and Toxicology, 2013, 28:e2013006
    Huang Z Z, Chen G Q, Zeng G M, et al. Toxicity mechanisms and synergies of silver nanoparticles in 2,4-dichlorophenol degradation by Phanerochaete chrysosporium[J]. Journal of Hazardous Materials, 2017, 321:37-46
    Akaighe N, Maccuspie R I, Navarro D A, et al. Humic acid-induced silver nanoparticle formation under environmentally relevant conditions[J]. Environmental Science & Technology, 2011, 45(9):3895-3901
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  • 收稿日期:  2020-04-03

纳米银在诺氟沙星胁迫下对黄孢原毛平革菌的毒物兴奋效应

    通讯作者: 郭志, E-mail: guozhi@hfut.edu.cn
    作者简介: 丁文东(1994-),男,硕士研究生,研究方向为环境微生物学,E-mail:hfutding@163.com
  • 1. 合肥工业大学资源与环境工程学院, 合肥 230009;
  • 2. 合肥工业大学纳米矿物与污染控制安徽普通高校重点实验室, 合肥 230009
基金项目:

国家自然科学基金资助项目(51809068);国家重点研发计划资助项目(SQ2019YFC040023);安徽省科技重大专项(17030801031);安徽省科技重大专项(201903a07020009);长丰县-合肥工业大学产业创新引导资金资助项目;中央高校基本科研业务费专项资金资助项目(JZ2020HGTB0022,JZ2018HGBZ0311)

摘要: 具有生物毒性的纳米银(AgNPs)在低浓度下能产生毒物兴奋效应,可以刺激细胞的活性增强。研究了在诺氟沙星胁迫下,AgNPs对黄孢原毛平革菌活性的影响,并通过探究AgNPs的迁移转化以及细胞外蛋白质浓度的变化,结合扫描电镜、X射线衍射以及傅里叶红外光谱分析进行机理探索。结果表明,AgNPs在0.001 mg·L-1和0.01 mg·L-1浓度下可以将黄孢原毛平革菌的细胞活性提高1.29倍与1.51倍,而在1.3 mg·L-1 AgNPs的刺激下,细胞活性降低64%,同时,相同浓度的Ag离子仅对细胞产生毒性抑制作用。低浓度AgNPs可以在溶液相与生物相之间进行迁移,触发细胞生物学特性的变化,刺激细胞在面临诺氟沙星胁迫时产生较多的胞外蛋白质来减轻毒性抑制作用。黄孢原毛平革菌的菌丝表面存在的羟基、醛、酮和巯基等官能团可以将Ag离子还原为纳米氯化银和硫化银,在细胞表面聚集。

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