Direct selective detection of genomic DNA from coliform using a fiber optic biosensor

被引:31
作者
Almadidy, A
Watterson, J
Piunno, PAE
Raha, S
Foulds, IV
Horgen, PA
Castle, A
Krull, U
机构
[1] Univ Toronto, Dept Chem, Mississauga, ON L5L 1C6, Canada
[2] FONA Technol Inc, Waterloo, ON N2V 2K1, Canada
[3] Univ Toronto, Dept Biol, Mississauga, ON L5L 1C6, Canada
[4] Brock Univ, Dept Biol, St Catharines, ON L2S 3A1, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
genomic DNA; coliform; biosensor;
D O I
10.1016/S0003-2670(02)00243-X
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Fiber optic biosensors operated in a total internal reflection format were prepared based on covalent immobilization of 25mer lacZ single-stranded nucleic acid probe. Genomic DNA from Escherichia coli was extracted and then sheared by sonication to prepare fragments of approximately 300mer length. Other targets included a 25mer fully complementary lacZ sequence, 100mer polymerase chain reaction (PCR) products containing the lacZ sequence at various locations, and non-complementary DNA including genomic samples from salmon sperm. Non-selective adsorption of non-complementary oligonucleotides (ncDNA) was found to occur at a significantly faster rate than hybridization of complementary oligomers (cDNA) in all cases. The presence of ncDNA oligonucleotides did not inhibit selective interactions between immobilized DNA and cDNA in solution. The presence of high concentrations of non-complementary genomic DNA had little effect on extent or speed of hybridization of complementary oligonucleotides. Detection of genomic fragments containing the lacZ sequence was possible in as little as 20 s by observation of the steady-state fluorescence intensity increase or by time-dependent rate of fluorescence intensity changes. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:37 / 47
页数:11
相关论文
共 27 条
[11]  
KERN W, 1970, RCA REV, V31, P187
[12]   FRACTAL REACTION-KINETICS [J].
KOPELMAN, R .
SCIENCE, 1988, 241 (4873) :1620-1626
[13]   PROTEIN-RESISTANT SURFACES PREPARED BY PEO-CONTAINING BLOCK COPOLYMER SURFACTANTS [J].
LEE, JH ;
KOPECEK, J ;
ANDRADE, JD .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 1989, 23 (03) :351-368
[14]   Rapid detection and identification of biological and chemical agents by immunoassay, gene probe assay and enzyme inhibition using a silicon-based biosensor [J].
Lee, WE ;
Thompson, HG ;
Hall, JG ;
Bader, DE .
BIOSENSORS & BIOELECTRONICS, 2000, 14 (10-11) :795-804
[15]   Molecular beacons for DNA biosensors with micrometer to submicrometer dimensions [J].
Liu, XJ ;
Farmerie, W ;
Schuster, S ;
Tan, WH .
ANALYTICAL BIOCHEMISTRY, 2000, 283 (01) :56-63
[16]   Light-directed synthesis of high-density oligonucleotide arrays using semiconductor photoresists [J].
McGall, G ;
Labadie, J ;
Brock, P ;
Wallraff, G ;
Nguyen, T ;
Hinsberg, W .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (24) :13555-13560
[17]   Considerations for the quantitative transduction of hybridization of immobilized DNA [J].
Piunno, PAE ;
Watterson, J ;
Wust, CC ;
Krull, UJ .
ANALYTICA CHIMICA ACTA, 1999, 400 :73-89
[18]  
PIUNNO PAE, 2000, ACS SYM SER, V762, P257
[19]  
Pon Richard T., 1993, V20, P465
[20]   Steric factors influencing hybridisation of nucleic acids to oligonucleotide arrays [J].
Shchepinov, MS ;
CaseGreen, SC ;
Southern, EM .
NUCLEIC ACIDS RESEARCH, 1997, 25 (06) :1155-1161