Chem. J. Chinese Universities ›› 2012, Vol. 33 ›› Issue (04): 678.doi: 10.3969/j.issn.0251-0790.2012.04.007

• Analytical Chemistry • Previous Articles     Next Articles

Detection of E.coli O157: H7 Using Mannose-functionalized Hydrogels

ZHOU Li-Xia1,2,4, HE Ding-Geng2,3,4, HE Xiao-Xiao1,2,4, QING Zhi-He1,2,4, WANG Ke-Min1,2,3,4, CAO Jie2,3,4   

  1. 1. College of Biology, ;
    2. State Key Laboratory of Chemo/Biosensing and Chemometrics, ;
    3. College of Chemistry and Chemical Engineering, ;
    4. Key Laboratory for Bio-Nanotechnology and Molecule Engineering of Hunan Province, Hunan University, Changsha 410082, China
  • Received:2011-06-03 Online:2012-04-10 Published:2012-04-10
  • Supported by:

    科技部国际合作专项(批准号: 2010DFB30300)、湖南省自然科学基金创新研究群体基金项目(批准号: 10JJ7002)、国家自然科学基金(批准号: 21175039, 21190044)和湖南省科技计划重点项目(批准号: 2011FJ2001)资助.

Abstract: By combining hydrogel with the nucleic acid dye SYBR Green Ⅰ, we have engineered mannose-functionalized hydrogel for E.coli O157: H7 detection based on multivalent binding of Con A. In this method, the hydrogel was first synthesized using acrylamide, N,N-dimethylacrylamide and N-acryloxysuccinimide, employing ammonium persulfate(APS) as the catalyst and etramethylethylenediamine(TEMED) as the accelerator. Then, the mannose was conjugated to the surface of the prepared hydrogel. After preparing the functional hydrogel, the sample was incubated with the hydrogel for 1 h and then stained with a nucleic acid dye SYBR Green Ⅰ. Finally the labeled E.coli O157: H7 was determined by the fluorescence in vivo imaging. The detection of E.coli O157: H7 was successfully carried out in buffer and bacterial mixture, respectively. This assay allowed the detection of E.coli O157: H7 in PB buffer as low as 3.7×101 Cells/mL within 2 h.

Key words: Hydrogel, SYBR Green Ⅰ, E.coli O157: H7, In vivo fluorescence imaging

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