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Colorimetric biosensing of nopaline synthase terminator using Fe3O4@Au and hemin-functionalized reduced graphene oxide.
Cao, Xiaodong; Xia, Zihao; Yan, Wuwen; He, Shudong; Xu, Xuan; Wei, Zhaojun; Ye, Yongkang; Zheng, Haisong.
Afiliação
  • Cao X; School of Food Science and Biological Engineering, Hefei University of Technology, Hefei, 230009, China.
  • Xia Z; School of Food Science and Biological Engineering, Hefei University of Technology, Hefei, 230009, China.
  • Yan W; School of Food Science and Biological Engineering, Hefei University of Technology, Hefei, 230009, China.
  • He S; School of Food Science and Biological Engineering, Hefei University of Technology, Hefei, 230009, China.
  • Xu X; College of Chemistry and Molecular Engineering, Nanjing Tech University, Nanjing, 211816, China.
  • Wei Z; School of Food Science and Biological Engineering, Hefei University of Technology, Hefei, 230009, China.
  • Ye Y; School of Food Science and Biological Engineering, Hefei University of Technology, Hefei, 230009, China. Electronic address: yongkang.ye@hfut.edu.cn.
  • Zheng H; Technology Center of Hefei Customs, Hefei, 230032, China.
Anal Biochem ; 602: 113798, 2020 08 01.
Article em En | MEDLINE | ID: mdl-32505706
ABSTRACT
In this paper, we present a simple and label-free colorimetric biosensor for detection of the nopaline synthase (NOS) terminator in genetically modified (GM) plants. The "signal on" colorimetric biosensor was developed using a nanocomposite consisted of gold nanoparticles doped magnetic Fe3O4 nanoparticles (Fe3O4@Au NP), capture probe DNA (cDNA), and hemin-functionalized reduced graphene oxide nanosheets (H-GN). The nanocomposite was successfully prepared by means of Au-S bonds and the strong π interactions between cDNA and H-GN. The sensing approach is based on the excellent peroxidase-mimicking activity of H-GN and its different electrostatic interactions with single-stranded DNA (ssDNA) and double-stranded DNA (dsDNA). In presence of the target NOS, the cDNA in the nanocomposite will hybridize with its complementary sequence, and form dsDNA structure. Due to the weak π interactions between dsDNA and H-GN, a portion of H-GN will be released from the surface of Fe3O4@Au NPs and transferred into solution. After magnetic separation was performed, the supernatant was incubated with 3,3',5,5'-tetramethylbenzidine (TMB) in the presence of H2O2. The released H-GN can catalyze the oxidation reaction of TMB and turn the colorless solution blue. This "signal-on" colorimetric biosensor shows a broad linear range of 0.5-100 nM for the target NOS, with a 0.19 nM detection limit. The application of the biosensor for determination of NOS segments in samples of GM and non-GM tomatoes shows that it can discriminate between GM and non-GM plants. The reliability of the method for samples of NOS-spiked GM tomato suggests satisfactory recoveries in the range of 93.6%-94.2%.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Técnicas Biossensoriais / Colorimetria / Aminoácido Oxirredutases Limite: Humans Idioma: En Revista: Anal Biochem Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Técnicas Biossensoriais / Colorimetria / Aminoácido Oxirredutases Limite: Humans Idioma: En Revista: Anal Biochem Ano de publicação: 2020 Tipo de documento: Article