Application of Quantum Dots for Gene Detection and Fingerprinting System of Environmental Pathogens

碩士 === 中原大學 === 生物科技研究所 === 102 === An improvement of the detection of environmental pathogens in water is very important because it requires a rapid detection of contamination sources and inhibition of contaminant expansion. Traditional methods usually use selective medium to culture and measure mi...

Full description

Bibliographic Details
Main Authors: Chen-Yen Jao, 饒振彥
Other Authors: Chung-Yung Chen
Format: Others
Language:en_US
Published: 2014
Online Access:http://ndltd.ncl.edu.tw/handle/shernk
id ndltd-TW-102CYCU5111006
record_format oai_dc
spelling ndltd-TW-102CYCU51110062019-05-15T21:23:54Z http://ndltd.ncl.edu.tw/handle/shernk Application of Quantum Dots for Gene Detection and Fingerprinting System of Environmental Pathogens 應用量子點基因指紋鑑定環境病原體之研究 Chen-Yen Jao 饒振彥 碩士 中原大學 生物科技研究所 102 An improvement of the detection of environmental pathogens in water is very important because it requires a rapid detection of contamination sources and inhibition of contaminant expansion. Traditional methods usually use selective medium to culture and measure microorganisms. However, it has some disadvantage in its difficulty of quantification and lengthy incubate time (always 2 to 3 days). Also, there are over a thousand species of micro-organisms present in water and not all species can be detected using the traditional method. The quantum dot platform is consisted of a microparticle binding oligonucleotide and designed probes (internal/reporter probe) coated with quantum dot. In our study, this system could be stable and demonstrate highly specificity and sensitivity. As followed specificity and sensitivity assay, the standard curve could reveal that R2 ratio was 0.9. In addition, the limitation assay could detect Pseudomonas spp. at least 10 bacteria and 0.001 ng/μL Escherichia coli target DNA in water sample. Therefore, an application of a novel detecting technology is needed to resolve these problems. In order to increase specificity and sensitivity efficiency, a quantum-dot detection approach developed a high throughput methodology based on previous study in 2012, called as a DNA fingerprinting system. The Fingerprinting system was established different length of fragments by restriction enzyme cutting site, called as Terminal Restriction Fragment Length Polymorphism (T-RFLP), to diversify sizes for evaluating specificity. Interestingly, our research had a time-efficient and an easier detection system that avoid the use of the ineffective traditional-chip methods and PCR amplification. Our technique obtained (1) highly specific, (2) highly sensitive, (3) accurate quantification, and (4) a DNA fingerprinting analysis of environmental pathogens in water samples. Chung-Yung Chen 陳中庸 2014 學位論文 ; thesis 102 en_US
collection NDLTD
language en_US
format Others
sources NDLTD
description 碩士 === 中原大學 === 生物科技研究所 === 102 === An improvement of the detection of environmental pathogens in water is very important because it requires a rapid detection of contamination sources and inhibition of contaminant expansion. Traditional methods usually use selective medium to culture and measure microorganisms. However, it has some disadvantage in its difficulty of quantification and lengthy incubate time (always 2 to 3 days). Also, there are over a thousand species of micro-organisms present in water and not all species can be detected using the traditional method. The quantum dot platform is consisted of a microparticle binding oligonucleotide and designed probes (internal/reporter probe) coated with quantum dot. In our study, this system could be stable and demonstrate highly specificity and sensitivity. As followed specificity and sensitivity assay, the standard curve could reveal that R2 ratio was 0.9. In addition, the limitation assay could detect Pseudomonas spp. at least 10 bacteria and 0.001 ng/μL Escherichia coli target DNA in water sample. Therefore, an application of a novel detecting technology is needed to resolve these problems. In order to increase specificity and sensitivity efficiency, a quantum-dot detection approach developed a high throughput methodology based on previous study in 2012, called as a DNA fingerprinting system. The Fingerprinting system was established different length of fragments by restriction enzyme cutting site, called as Terminal Restriction Fragment Length Polymorphism (T-RFLP), to diversify sizes for evaluating specificity. Interestingly, our research had a time-efficient and an easier detection system that avoid the use of the ineffective traditional-chip methods and PCR amplification. Our technique obtained (1) highly specific, (2) highly sensitive, (3) accurate quantification, and (4) a DNA fingerprinting analysis of environmental pathogens in water samples.
author2 Chung-Yung Chen
author_facet Chung-Yung Chen
Chen-Yen Jao
饒振彥
author Chen-Yen Jao
饒振彥
spellingShingle Chen-Yen Jao
饒振彥
Application of Quantum Dots for Gene Detection and Fingerprinting System of Environmental Pathogens
author_sort Chen-Yen Jao
title Application of Quantum Dots for Gene Detection and Fingerprinting System of Environmental Pathogens
title_short Application of Quantum Dots for Gene Detection and Fingerprinting System of Environmental Pathogens
title_full Application of Quantum Dots for Gene Detection and Fingerprinting System of Environmental Pathogens
title_fullStr Application of Quantum Dots for Gene Detection and Fingerprinting System of Environmental Pathogens
title_full_unstemmed Application of Quantum Dots for Gene Detection and Fingerprinting System of Environmental Pathogens
title_sort application of quantum dots for gene detection and fingerprinting system of environmental pathogens
publishDate 2014
url http://ndltd.ncl.edu.tw/handle/shernk
work_keys_str_mv AT chenyenjao applicationofquantumdotsforgenedetectionandfingerprintingsystemofenvironmentalpathogens
AT ráozhènyàn applicationofquantumdotsforgenedetectionandfingerprintingsystemofenvironmentalpathogens
AT chenyenjao yīngyòngliàngzidiǎnjīyīnzhǐwénjiàndìnghuánjìngbìngyuántǐzhīyánjiū
AT ráozhènyàn yīngyòngliàngzidiǎnjīyīnzhǐwénjiàndìnghuánjìngbìngyuántǐzhīyánjiū
_version_ 1719113940824227840