广西师范大学学报(自然科学版) ›› 2012, Vol. 30 ›› Issue (2): 99-105.

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5-溴-4-氯-3-吲哚基磷酸盐共振散射光谱法检测碱性磷酸酯酶

梁爱惠, 刘高伞, 蒋治良   

  1. 广西师范大学环境与资源学院,珍稀濒危动植物生态与环境保护省部共建教育部重点实验室,广西桂林541004
  • 收稿日期:2012-04-16 出版日期:2012-06-20 发布日期:2018-12-03
  • 通讯作者: 梁爱惠(1965—),女,广西岑溪人,广西师范大学研究员,硕士生导师。E-mail:ahliang2008@163.com
  • 基金资助:
    国家自然科学基金资助项目(21165005,21075023);广西研究生科研创新项目资助(2011106020830M62)

Resonance Scattering Spectral Assay for Alkaline Phosphatase Using BCIP as Substrate

LIANG Ai-hui, LIU Gao-san, JIANG Zhi-liang   

  1. Key Laboratory of Ecology of Rare and Endangered Species and Environmental Protection,Ministry of Education, School of Environment and Resource,Guangxi Normal University,Guilin Guangxi 541004,China
  • Received:2012-04-16 Online:2012-06-20 Published:2018-12-03

摘要: 在pH8.0的Tris-HCl缓冲溶液及32 mg/L PEG20000的存在下,碱性磷酸酯酶(ALP)催化底物5-溴-4-氯-3-吲哚基磷酸盐(BCIP)水解生成不溶性的蓝色BCIP二聚体微粒,该微粒在710 nm波长处产生一个共振散射峰。在选定条件下,随着ALP活性增大,710 nm波长处的共振散射峰强度线性增大,碱性磷酸酯酶浓度在0.078~1.25 U/L与共振散射强度增大值ΔI呈良好线性关系,其回归方程为:ΔI=512.6C+17.8,检出限为9.6×10-3 U/L。该法用于合成样品中碱性磷酸酯酶的测定,结果满意。

关键词: 5-溴-4-氯-3-吲哚基磷酸盐, 碱性磷酸酯酶, 共振散射光谱法

Abstract: In pH 8.0 Tris-HCl buffer solutions and in the presence of 32 mg/L PEG20000,using EDTANa2 as terminated agent to stop the enzymatic reaction,alkaline phosphatase (ALP) catalyzed the hydrolysis of 5-bromo-4-Chloro-3-indolylphosphat (BCIP) substrate to form blue BCIP dimer particles,which exhibited a strongresonance scattering (RS) peak at 710 nm.In the selected conditions,with theALP activity increased,the RS intensity (ΔI) linearly increased.ALP activitylinear range was 0.078~1.25 U/L,with a regression equation of ΔI=512.6C+17.8,and a detection limit of 9.6×10-3 U/L.

Key words: 5-bromo-4-chloro-3-indolyl phosphate, alkaline phosphatase, resonance scattering spectroscopy

中图分类号: 

  • O657.3
[1] COLEMAN J E.Structure and mechanism of alkaline phosphatase[J].Annual Review of Biophysics and Biomolecular Structure,1992,21:441-483.
[2] 吉尔鲍特.酶法分析[M].缪辉南译.北京:科学出版社,1977:58-205.
[3] KIM H J,KWAK J.Electrochemical determination of total alkaline phosphatasein human blood with a micropatterned ITO film[J].Journal of Electroanalytical Chemistry,2005,577:243-248.
[4] TIJSSEN P.Practice and theory of enzyme immunoassay[M].Amsterdam:Elsevier,1985:211-219.
[5] OHKUMA H,ABE K,ITO M,et al.Development of a highly sensitive enzyme-linked immunosorbent assay for bis-phenol A in Serum[J].Analyst,2002,127:93-97.
[6] ZHU Xiao-jing,JIANG Chong-qiu.8-Quinolyl phosphate as a substrate for thefluorimetric determination of alkaline phosphatase[J].Clinica Chimica Acta,2007,377(1/2):150-153.
[7] 张娜,边玮玮,李耀辉.荧光光度法测定血清中碱性磷酸酶[J].分析化学,2009,37(5):721-724.
[8] ZHU Xiao-jing,LIU Qi-kui,JIANG Chong-qiu.2-carboxy-1-naphthyl phosphate as a substrate for the fluorimetric determination of alkaline phosphatase[J].Analytica Chimica Acta,2006,570(7):29-33.
[9] FENOLL J,JOURQUIN G,KAUFFMANN J M.Fluorimetric determination ofalkalinephosphatase in solid and fluid dairy products[J].Talanta,2002,56:1021-1026.
[10] CHRISTOPOULOS T K,DIAMANDIS E P.Enzymically amplified time-resolved fluorescence immunoassay with te-rbium chelates[J].Anal Chem,1992,64(4):342-346.
[11] SERRA B,MORALES M D,REVIEJO A J,et al.Rapid and highly sensitive electrochemical determination of alkaline phosphatase using a composite tyrosinase biosensor[J].Analytical Biochemistry,2005,336:289-294.
[12] 孙伟,焦奎,刘光源.磷酸苯酯-碱性磷酸酯酶伏安酶联免疫分析新体系的研究[J].分析试验室,2002,21(1):13-15.
[13] 焦奎,孙伟,王海玉.以对硝基磷酸苯酯为底物电化学分析法检测碱性磷酸酯酶[J].分析化学,2001,10(29):1174-1177.
[14] RóBERT E G,ANDREA B,GéZA N,et al.Amperometric microcells for alkaline phosphatase assay[J].Analyst,2002,127:235-240.
[15] 陈国千,陈蕾,王亚平,等.BCIP/NBT比色法测定碱性磷酸酶活力[J].上海医学检验杂志,1999,14(2):69-71.
[16] EBERSOLE R C,WARD M D.Amplified mass immunosorbent assay with aquartz crystal microbalance[J].Journal of the American Chemical,1988,110:8623-8628.
[17] JIANG Zhi-liang,HUANG Yu-juan,LIANG Ai-hui,et al.Resonancescattering detection of trace microalbumin using immunonanogold probe as the catalyst of Fehling reagent-glucose reaction[J].Biosense and Bioelectron,2009,24:1674-1678.
[18] TAO Hui-lin,WEI Li-li,LIANG Ai-hui,et al.Highly sensitiveresonance scattering detection of DNA hybridization using aptamer modified gold nanopaticle as catalyst[J].Plasmonics,2010,5(2):189-198.
[19] LIANG Ai-hui,ZHANG Yi,FAN Yan-yan,et al.Catalysis of aptamer-modified AuPd nanoalloy probe and its application to resonance scattering detection of trace UO2+2[J].Nanoscale,2011,3(8):3178-3184.
[20] 江波,张骏,胡庆红,等.孔雀石绿的催化共振散射法测定痕量过氧化氢[J].广西师范大学学报:自然科学版,2009,27(1):67-70.
[21] 蒋治良,蒋彩娜,梁爱惠,等.催化共振散射光谱法测定木瓜蛋白酶活力[J].广西师范大学学报:自然科学版,2008,26(1):76-79.
[22] WEI Xiao-ling,MA Ji,LIANG Ai-hui,et al.A new enzyme-catalytic resonancescattering assay for glucose in serum using cationic surfactant[J].Analytical Science,2009,25(7):887-890.
[23] JIANG Zhi-liang,LIANG Yue-yuan,HUANG Guo-xia,et al.Catalytic resonancescattering spectral determination of ultratrace horseradish peroxidase using rhodamine S[J].Luminescence,2009,24(3):144-149.
[24] 张诒亮,杨红梅,董淑萍,等.碱性磷酸酶参考值的探讨[J].医学检验与临床,2006,5:45-49.
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