Electrochemical deoxyribonucleic acid biosensor based on carboxyl functionalized graphene oxide and poly-l-lysine modified electrode for the detection of tlh gene sequence related to vibrio parahaemolyticus

[Display omitted] ► Ploy-l-lysine modified glassy carbon electrode was prepared by electropolymerization. ► A carboxyl functionalized graphene oxide was synthesized and decorated on PLLy/GCE. ► Electrochemical DNA biosensor based on GO-COOH/PLLy/GCE was fabricated. ► The tlh gene related to vibrio p...

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Veröffentlicht in:Analytica chimica acta 2012-11, Vol.752, p.39-44
Hauptverfasser: Sun, Wei, Zhang, Yuanyuan, Ju, Xiaomei, Li, Guangjiu, Gao, Hongwei, Sun, Zhenfan
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creator Sun, Wei
Zhang, Yuanyuan
Ju, Xiaomei
Li, Guangjiu
Gao, Hongwei
Sun, Zhenfan
description [Display omitted] ► Ploy-l-lysine modified glassy carbon electrode was prepared by electropolymerization. ► A carboxyl functionalized graphene oxide was synthesized and decorated on PLLy/GCE. ► Electrochemical DNA biosensor based on GO-COOH/PLLy/GCE was fabricated. ► The tlh gene related to vibrio parahaemolyticus was detected successfully. A carboxyl functionalized graphene oxide (GO-COOH) and electropolymerized ploy-l-lysine (PLLy) modified glassy carbon electrode (GCE) was fabricated and used for the construction of an electrochemical deoxyribonucleic acid (DNA) biosensor. The NH2 modified probe ssDNA sequences were immobilized on the surface of GO-COOH/PLLy/GCE by covalent linking with the formation of amide bonds, which was stable and furthur hybridized with the target ssDNA sequence. Differential pulse voltammetry (DPV) was used to monitor the hybridization events with methylene blue as electrochemical indicator, which gave a sensitive reduction peak at −0.287V (vs. SCE). Under the optimal conditions the reduction peak current was proportional to the concentration of tlh gene sequence in the range from 1.0×10−12 to 1.0×10−6molL−1 with a detection limit as 1.69×10−13molL−1 (3σ). The polymerase chain reaction products of tlh gene from oyster samples were detected with satisfactory results, indicating the potential application of this electrochemical DNA sensor.
doi_str_mv 10.1016/j.aca.2012.09.009
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A carboxyl functionalized graphene oxide (GO-COOH) and electropolymerized ploy-l-lysine (PLLy) modified glassy carbon electrode (GCE) was fabricated and used for the construction of an electrochemical deoxyribonucleic acid (DNA) biosensor. The NH2 modified probe ssDNA sequences were immobilized on the surface of GO-COOH/PLLy/GCE by covalent linking with the formation of amide bonds, which was stable and furthur hybridized with the target ssDNA sequence. Differential pulse voltammetry (DPV) was used to monitor the hybridization events with methylene blue as electrochemical indicator, which gave a sensitive reduction peak at −0.287V (vs. SCE). Under the optimal conditions the reduction peak current was proportional to the concentration of tlh gene sequence in the range from 1.0×10−12 to 1.0×10−6molL−1 with a detection limit as 1.69×10−13molL−1 (3σ). The polymerase chain reaction products of tlh gene from oyster samples were detected with satisfactory results, indicating the potential application of this electrochemical DNA sensor.</description><identifier>ISSN: 0003-2670</identifier><identifier>EISSN: 1873-4324</identifier><identifier>DOI: 10.1016/j.aca.2012.09.009</identifier><identifier>PMID: 23101650</identifier><identifier>CODEN: ACACAM</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Amino Acid Sequence ; Analytical chemistry ; Biological and medical sciences ; Biosensing Techniques ; Biosensors ; Biotechnology ; Carboxyl functionalized graphene oxide ; Chemistry ; Deoxyribonucleic acid ; DNA - chemistry ; DNA, Single-Stranded - chemistry ; DNA, Single-Stranded - genetics ; Electrochemical deoxyribonucleic acid biosensor ; Electrochemical methods ; Electrochemical Techniques ; Electrodes ; Exact sciences and technology ; Fundamental and applied biological sciences. Psychology ; General, instrumentation ; Genes ; Glassy carbon electrode ; Graphene ; Graphite - chemistry ; Methods. Procedures. Technologies ; Monitors ; Oxides ; Oxides - chemistry ; Ploy-l-lysine ; Polylysine - chemistry ; Polymerase Chain Reaction ; Reduction ; Various methods and equipments ; Vibrio parahaemolyticus ; Vibrio parahaemolyticus - genetics</subject><ispartof>Analytica chimica acta, 2012-11, Vol.752, p.39-44</ispartof><rights>2012 Elsevier B.V.</rights><rights>2014 INIST-CNRS</rights><rights>Copyright © 2012 Elsevier B.V. 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A carboxyl functionalized graphene oxide (GO-COOH) and electropolymerized ploy-l-lysine (PLLy) modified glassy carbon electrode (GCE) was fabricated and used for the construction of an electrochemical deoxyribonucleic acid (DNA) biosensor. The NH2 modified probe ssDNA sequences were immobilized on the surface of GO-COOH/PLLy/GCE by covalent linking with the formation of amide bonds, which was stable and furthur hybridized with the target ssDNA sequence. Differential pulse voltammetry (DPV) was used to monitor the hybridization events with methylene blue as electrochemical indicator, which gave a sensitive reduction peak at −0.287V (vs. SCE). Under the optimal conditions the reduction peak current was proportional to the concentration of tlh gene sequence in the range from 1.0×10−12 to 1.0×10−6molL−1 with a detection limit as 1.69×10−13molL−1 (3σ). 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A carboxyl functionalized graphene oxide (GO-COOH) and electropolymerized ploy-l-lysine (PLLy) modified glassy carbon electrode (GCE) was fabricated and used for the construction of an electrochemical deoxyribonucleic acid (DNA) biosensor. The NH2 modified probe ssDNA sequences were immobilized on the surface of GO-COOH/PLLy/GCE by covalent linking with the formation of amide bonds, which was stable and furthur hybridized with the target ssDNA sequence. Differential pulse voltammetry (DPV) was used to monitor the hybridization events with methylene blue as electrochemical indicator, which gave a sensitive reduction peak at −0.287V (vs. SCE). Under the optimal conditions the reduction peak current was proportional to the concentration of tlh gene sequence in the range from 1.0×10−12 to 1.0×10−6molL−1 with a detection limit as 1.69×10−13molL−1 (3σ). The polymerase chain reaction products of tlh gene from oyster samples were detected with satisfactory results, indicating the potential application of this electrochemical DNA sensor.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>23101650</pmid><doi>10.1016/j.aca.2012.09.009</doi><tpages>6</tpages></addata></record>
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subjects Amino Acid Sequence
Analytical chemistry
Biological and medical sciences
Biosensing Techniques
Biosensors
Biotechnology
Carboxyl functionalized graphene oxide
Chemistry
Deoxyribonucleic acid
DNA - chemistry
DNA, Single-Stranded - chemistry
DNA, Single-Stranded - genetics
Electrochemical deoxyribonucleic acid biosensor
Electrochemical methods
Electrochemical Techniques
Electrodes
Exact sciences and technology
Fundamental and applied biological sciences. Psychology
General, instrumentation
Genes
Glassy carbon electrode
Graphene
Graphite - chemistry
Methods. Procedures. Technologies
Monitors
Oxides
Oxides - chemistry
Ploy-l-lysine
Polylysine - chemistry
Polymerase Chain Reaction
Reduction
Various methods and equipments
Vibrio parahaemolyticus
Vibrio parahaemolyticus - genetics
title Electrochemical deoxyribonucleic acid biosensor based on carboxyl functionalized graphene oxide and poly-l-lysine modified electrode for the detection of tlh gene sequence related to vibrio parahaemolyticus
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