TY - JOUR
T1 - A DNA sequence-specific electrochemical biosensor based on alginic acid-coated cobalt magnetic beads for the detection of E. coli
AU - Geng, Ping
AU - Zhang, Xinai
AU - Teng, Yingqiao
AU - Fu, Ying
AU - Xu, Lili
AU - Xu, Min
AU - Jin, Litong
AU - Zhang, Wen
PY - 2011/3/15
Y1 - 2011/3/15
N2 - A new type of DNA sequence-specific electrochemical biosensor based on magnetic beads for the detection of Escherichia coli is reported in the present work. Alginic acid-coated cobalt magnetic beads, capped with 5′-(NH2) oligonucleotide and employed not only for magnetic separation but also as the solid adsorbent, were used as DNA probes to hybridize with the target E. coli DNA sequence. This assay was specific for E. coli detection depending on the uid A gene, which encodes for the enzyme β-d-glucuronidase produced by E. coli strains. When daunomycin (DNR) was used as DNA hybridization indicator, the target sequences of E. coli hybridized with the probes resulted in the decrease of DNR reduction peak current, which was proportional to the E. coli concentration. The optimization of the hybridization detection was carried out and the specificity of the probes was also demonstrated. This DNA biosensor can be employed to detect a complementary target sequence for 3.0×10-10mol/L and denatured PCR products for 0.5ng/μL. The linear range of the developed biosensor for the detection of E. coli cells was from 1.0×102 to 2.0×103cells/mL with a detection limit of 50cells/mL. After a brief enrichment process, a concentration of 10cells/mL E. coli in real water samples was detected by the electrochemical biosensor.
AB - A new type of DNA sequence-specific electrochemical biosensor based on magnetic beads for the detection of Escherichia coli is reported in the present work. Alginic acid-coated cobalt magnetic beads, capped with 5′-(NH2) oligonucleotide and employed not only for magnetic separation but also as the solid adsorbent, were used as DNA probes to hybridize with the target E. coli DNA sequence. This assay was specific for E. coli detection depending on the uid A gene, which encodes for the enzyme β-d-glucuronidase produced by E. coli strains. When daunomycin (DNR) was used as DNA hybridization indicator, the target sequences of E. coli hybridized with the probes resulted in the decrease of DNR reduction peak current, which was proportional to the E. coli concentration. The optimization of the hybridization detection was carried out and the specificity of the probes was also demonstrated. This DNA biosensor can be employed to detect a complementary target sequence for 3.0×10-10mol/L and denatured PCR products for 0.5ng/μL. The linear range of the developed biosensor for the detection of E. coli cells was from 1.0×102 to 2.0×103cells/mL with a detection limit of 50cells/mL. After a brief enrichment process, a concentration of 10cells/mL E. coli in real water samples was detected by the electrochemical biosensor.
KW - DNA electrochemical biosensor
KW - E. coli
KW - Hybridization detection
KW - Magnetic beads
UR - https://www.scopus.com/pages/publications/79951727637
U2 - 10.1016/j.bios.2011.01.007
DO - 10.1016/j.bios.2011.01.007
M3 - 文章
C2 - 21277764
AN - SCOPUS:79951727637
SN - 0956-5663
VL - 26
SP - 3325
EP - 3330
JO - Biosensors and Bioelectronics
JF - Biosensors and Bioelectronics
IS - 7
ER -