결핵균 검출을 위한 모세관 중합효소연쇄반응의 적정조건

Other Titles
Optimization of Capillary-Polymerase Chain Reaction for Detection of M.tuberculosis
Authors
김재룡전동석박헌찬전효진
Department
Dept. of Laboratory Medicine (진단검사의학)
Issue Date
1993
Citation
Keimyung Medical Journal, Vol.12(4) : 520-530, 1993
Abstract
For detection of M. tuberculosis using hot-air capillary-thermocycler, FTC-2000[Daehan Medical System Co, Korea], We amplified 188 base pair IS986 fragment from chromosomal DNA of M. tuberculosis H37Rv strain by two-step nested method, and the concentrations of each component of polymerase chain reaction(PCR) mixture and the temperatures and times of each PCR stage were indivisually optimized. When compared to conventional heating-block method, only one tenth of reaction volume and time were required, i. e. 10ul and 10-30 minute, respectively. Final concentrations of each component at optimal condition were 0.5uM each primer, 0.2mM each dNTP, 50mM Tris-HCI(pH 8.3), 500ug/ml bovine serum albumin(BSA), 4mM MgCl₂and 0.5-1U Taq polymerase per reaction. Optimal temperatures and times of each stage were 94℃ and 1 sec of predenaturation, 45-55℃ and 1 sec of annealing, 72℃ and 10-20 sec of post-elongation, and optimal cycles of each nested-PCR were 30-50. Among various condition of capillary-PCR, BSA, annealing temperature and MgCl₂effect most critically on PCR result. At an annealing temperature of 45℃ with 3.5mM MgCl₂or 55℃ with 3mM MgCl₂, two-step nested-PCR gave greatest yield and highest sensitivity. At these optimal condition of capillary-PCR, 0.5fg of M. tuberculosis H37Rv DNA(same amout of DNA extracted from a single tubercle bacillus) was amplified effectively.
Keywords
CapillaryM.tuberculosisOptimal conditionPolymerase chain reaction
URI
http://kumel.medlib.dsmc.or.kr/handle/2015.oak/14851
Appears in Collections:
1. Journal Papers (연구논문) > 1. School of Medicine (의과대학) > Dept. of Laboratory Medicine (진단검사의학)
2. Keimyung Medical Journal (계명의대 학술지) > 1993
Keimyung Author(s)
전효진; 전동석; 김재룡
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