基于G-四链体-氯化血红素DNA酶比色法测定银离子和汞离子传感器的构筑
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  • 英文篇名:Fabrication of a Sensor for Colorimetric Determination of Silver and Mercury Ions Based on G-quadruplex-Hemin DNAzymes
  • 作者:肖志友 ; 司恒丹 ; 邓兰清 ; 龙丽 ; 居荣梅 ; 张鑫 ; 刘益飞
  • 英文作者:XIAO Zhi-you;SI Heng-dan;DENG Lan-qing;LONG Li;JU Rong-mei;ZHANG Xin;LIU Yi-fei;School of Chemical Engineering,Guizhou Institute of Technology;
  • 关键词:G-四链体-氯化血红素DNA酶 ; 比色法测定 ; 银离子 ; 汞离子 ; 传感器
  • 英文关键词:G-quadruplex-hemin DNAzymes;;colorimetric determination;;silver ion;;mercury ion;;sensor
  • 中文刊名:TEST
  • 英文刊名:Journal of Instrumental Analysis
  • 机构:贵州理工学院化学工程学院;
  • 出版日期:2019-07-17 14:22
  • 出版单位:分析测试学报
  • 年:2019
  • 期:v.38
  • 基金:国家自然科学基金资助项目(21768002);; 贵州省科学技术基金资助项目(黔科合J字[2013]2263号);; 贵州理工学院高层次人才科研启动经费项目(XJGC20181213);贵州理工学院大学生创新训练项目(201814440229)
  • 语种:中文;
  • 页:TEST201907015
  • 页数:5
  • CN:07
  • ISSN:44-1318/TH
  • 分类号:91-95
摘要
利用G-四链体DNA(5′-CTGGGAGGGAGGGAGGGA-3′)与氯化血红素结合形成G-四链体-Hemin DNA酶,其能高效催化H_2O_2氧化反应底物由无色变为绿色,当溶液中有Ag~+或Hg~(2+)存在时会阻碍该DNA酶的形成,导致绿色溶液变浅。基于此,建立了比色法测定Ag~+和Hg~(2+)的传感器。在最佳实验条件下,溶液的吸光度与Ag~+和Hg~(2+)浓度分别在100.0~1 000.0 nmol/L和80.0~800.0 nmol/L范围内具有良好的线性关系,检出限(3δ/Slope)分别为55.9 nmol/L和64.3 nmol/L。该方法具有较好的选择性,采用该方法对实际样品进行测试,结果满意。
        A sensor for colorimetric determination of silver and mercury ions based on G-quadruplex-hemin DNAzymes was fabricated.The G-quadruplex-hemin DNAzymes was formed by the combination of G-quadruplex(5′-CTGGGAGGGAGGGAGGGA-3′) with hemin,which could catalyze H_2O_2 to oxide the substrate efficiently,and make the colorless solution become green.The presence of Ag~+ or Hg~(2+) in the solution would hinder the formation of the DNAzyme,and the solution color became lighter.Under the optimal experimental conditions,there were good linear relationships for the absorbance of the solution with Ag~+ and Hg~(2+) in the concentration ranges of 100.0-1 000.0 nmol/L and 80.0-800.0 nmol/L,with detection limits(3δ/Slope) of 55.9 nmol/L and 64.3 nmol/L,respectively.This method was of good selectivity,and was applied in the detection of real samples with satisfactory results.
引文
[1] Lu Z,Liu Y,Lu S,Li Y,Liu X,Qin Y,Zheng L.RSC Adv.,2018,8(35):19701-19706.
    [2] Kim S,Choi J E,Choi J,Chung K H,Park K,Yi J,Ryu D Y.Toxicol.Vitro,2009,23(6):1076-1084.
    [3] Jia S M,Liu X F,Li P,Kong D M,Shen H X.Biosens.Bioelectron.,2011,27(1):148-152.
    [4] Xiao Z Y,Guo X T,Ling L S.J.Instrum.Anal.(肖志友,郭晓婷,凌连生.分析测试学报),2013,32(9):1117-1121.
    [5] Zhao Y,Yang X,Cui L,Sun Y,Song Q.Dyes Pigments,2018,150:21-26.
    [6] Chen B,Liu J,Yang T,Chen L,Hou J,Feng C,Huang C Z.Talanta,2019,191:357-363.
    [7] Li L,Wen Y,Xu L,Xu Q,Song S,Zuo X,Yan J,Zhang W,Liu G.Biosens.Bioelectron.,2016,75:433-445.
    [8] Leng T,Ma Y,Chen G.J.Photochem.Photobiol.A,2018,353:143-149.
    [9] Amirjani A,Haghshenas D F.Talanta,2019,192:418-423.
    [10] Kong D M.Prog.Chem.(孔德明.化学进展),2011,23(10):2119-2131.
    [11] Li T,Shi L,Wang E,Dong S.Chem-Eur.J.,2009,15(14):3347-3350.
    [12] Kong D M,Cai L L,Shen H X.Analyst,2010,135(6):1253-1258.
    [13] Zhou X H,Kong D M,Shen H X.Anal.Chem.,2010,82(3):789-793.
    [14] Li T,Dong S,Wang E.Anal.Chem.,2009,81(6):2144-2149.
    [15] Lu N,Shao C,Deng Z.Analyst,2009,134(9):1822-1825.
    [16] Kong D M,Wang N,Guo X X,Shen H X.Analyst,2010,135(3):545-549.
    [17] Cheng X,Liu X,Bing T,Cao Z,Shangguan D.Biochemistry,2009,48(33):7817-7823.
    [18] Kong D M,Cai L L,Guo J H,Wu J,Shen H X.Biopolymers,2010,91(5):331-339.
    [19] Zhu L N,Wang H X,Sun R F,Li P,Kong D M,Li X Z.Chin.J.Inorg.Chem.(朱莉娜,王海仙,孙润丰,李平,孔德明,李孝增.无机化学学报),2013,(10):2215-2224.