Renewable microcolumns for automated DNA purification and flow-through amplification: from sediment samples through polymerase chain reaction

被引:29
作者
Bruckner-Lea, CJ
Tsukuda, T
Dockendorff, B
Follansbee, JC
Kingsley, MT
Ocampo, C
Stults, JR
Chandler, DP
机构
[1] Pacific NW Natl Lab, Environm Mol Sci Lab, Richland, WA 99352 USA
[2] Pacific NW Natl Lab, Environm Characterizat & Risk Assessment, Richland, WA 99352 USA
基金
美国能源部;
关键词
DNA; nucleic acid; PCR; renewable microcolumn; microbead; sequential injection; sediment;
D O I
10.1016/S0003-2670(01)01438-6
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
There is an increasing need for field-portable systems for the detection and characterization of microorganisms in the environment. Nucleic acids analysis is frequently the method of choice for discriminating between bacteria in complex systems, but standard protocols are difficult to automate and current microfluidic devices are not configured specifically for environmental sample analysis. In this report, we describe the development of an integrated DNA purification and polymerase chain reaction (PCR) amplification system and demonstrate its use for the automated purification and amplification of Geobacter chapellei DNA (genomic DNA or plasmid targets) from sediments. The system includes renewable separation columns for the automated capture and release of microparticle purification matrices, and can be easily reprogrammed for new separation chemistries and sample types. The DNA extraction efficiency for the automated system ranged from 3 to 25%, depending on the length and concentration of the DNA target. The system was more efficient than batch capture methods for the recovery of dilute genomic DNA even though the reagent volumes were smaller than required for the batch procedure. The automated DNA concentration and purification module was coupled to a flow-through, Peltier-controlled DNA amplification chamber, and used to successfully purify and amplify genomic and plasmid DNA from sediment extracts. Cleaning protocols were also developed to allow reuse of the integrated sample preparation system, including the flow-through PCR tube. (C) 2002 Elsevier Science B.V.
引用
收藏
页码:129 / 140
页数:12
相关论文
共 37 条
[1]  
Ausubel FM, 1995, CURRENT PROTOCOLS MO
[2]  
Belgrader P, 1998, CLIN CHEM, V44, P2191
[3]   Integrated systems for DNA sample preparation and detection in environmental samples [J].
Bruckner-Lea, CJ ;
Anheier, NC ;
Holman, D ;
Tsukuda, T ;
Kingsley, MT ;
Brockman, FJ ;
Price, JM ;
Grate, JW ;
Chandler, DP .
BIOCHEMICAL AND BIOMOLECULAR SENSING, 2000, 4200 :74-81
[4]   Strategies for automated sample preparation, nucleic acid purification, and concentration of low target number nucleic acids in environmental and food processing samples [J].
Bruckner-Lea, CJ ;
Holman, DA ;
Schuck, BL ;
Brockman, FJ ;
Chandler, DP .
PATHOGEN DETECTION AND REMEDIATION FOR SAFE EATING, 1999, 3544 :63-71
[5]   Rotating rod renewable microcolumns for automated, solid-phase DNA hybridization studies [J].
Bruckner-Lea, CJ ;
Stottlemyre, MS ;
Holman, DA ;
Grate, JW ;
Brockman, FJ ;
Chandler, DP .
ANALYTICAL CHEMISTRY, 2000, 72 (17) :4135-4141
[6]   Renewable microcolumns for solid-phase nucleic acid separations and analysis from environmental samples [J].
Chandler, DP ;
Brockman, FJ ;
Holman, DA ;
Grate, JW ;
Bruckner-Lea, CJ .
TRAC-TRENDS IN ANALYTICAL CHEMISTRY, 2000, 19 (05) :314-321
[7]   Affinity capture and recovery of DNA at femtomolar concentrations with peptide nucleic acid probes [J].
Chandler, DP ;
Stults, JR ;
Anderson, KK ;
Cebula, S ;
Schuck, BL ;
Brockman, FJ .
ANALYTICAL BIOCHEMISTRY, 2000, 283 (02) :241-249
[8]   Automated nucleic acid isolation and purification from soil extracts using renewable affinity microcolumns in a sequential injection system [J].
Chandler, DP ;
Schuck, BL ;
Brockman, FJ ;
Bruckner-Lea, CJ .
TALANTA, 1999, 49 (05) :969-983
[9]   Comparison of the ABI 7700 system (TaqMan) and competitive PCR for quantification of IS6110 DNA in sputum during treatment of tuberculosis [J].
Desjardin, LE ;
Chen, Y ;
Perkins, MD ;
Teixeira, L ;
Cave, MD ;
Eisenach, KD .
JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (07) :1964-1968
[10]   CHARACTERIZATION OF ATTACHED BACTERIAL-POPULATIONS IN DEEP GRANITIC GROUNDWATER FROM THE STRIPA RESEARCH MINE BY 16S RIBOSOMAL-RNA GENE SEQUENCING AND SCANNING ELECTRON-MICROSCOPY [J].
EKENDAHL, S ;
ARLINGER, J ;
STAHL, F ;
PEDERSEN, K .
MICROBIOLOGY-UK, 1994, 140 :1575-1583