A fluorescence quenching based gene assay for Escherichia coli O157:H7 using graphene quantum dots and gold nanoparticles

被引:20
作者
Saad, Suria Mohd [1 ,2 ]
Abdullah, Jaafar [1 ,3 ]
Abd Rashid, Suraya [1 ]
Fen, Yap Wing [4 ]
Salam, Faridah [2 ]
Yih, Lau Han [2 ]
机构
[1] Univ Putra Malaysia, Inst Adv Technol, Serdang 43400, Selangor, Malaysia
[2] Persiaran MARDI UPM, MARDI Headquarters, Ctr Biotechnol & Nanotechnol, Serdang 43400, Malaysia
[3] Univ Putra Malaysia, Dept Chem, Fac Sci, Serdang 43400, Selangor, Malaysia
[4] Univ Putra Malaysia, Dept Phys, Fac Sci, Serdang 43400, Selangor, Malaysia
关键词
Fluorophore; Quencher; Food pathogens; fliC gene; Static quenching; Real samples; Selectivity; SILVER; DNA; AUNPS; FRET;
D O I
10.1007/s00604-019-3913-8
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A fluorometric assay is described for highly sensitive quantification of Escherichia coli O157:H7. Reporter oligos were immobilized on graphene quantum dots (GQDs), and quencher oligos were immobilized on gold nanoparticles (AuNPs). Target DNA was co-hybridized with reporter oligos on the GQDs and quencher oligos on AuNPs. This triggers quenching of fluorescence (with excitation/emission peaks at 400 nm/530 nm). On introducing target into the system, fluorescence is quenched by up to 95% by 100 nM concentrations of target oligos having 20 bp. The response to the fliC gene of E. coli O157:H7 increases with the logarithm of the concentration in the range from 0.1 nM to 150 nM. The limit of detection is 1.1 +/- 0.6 nM for n = 3. The selectivity and specificity of the assay was confirmed by evaluating the various oligos sequences and PCR product (fliC gene) amplified from genomic DNA of the food samples spiked with E. coli O157:H7.
引用
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页数:10
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