Immunomagnetic separation and rapid detection of bacteria using bioluminescence and microfluidics

被引:76
作者
Qiu, Jingmin [2 ]
Zhou, Yun [1 ]
Chen, Hui [1 ]
Lin, Jin-Ming [1 ,2 ]
机构
[1] Tsinghua Univ, Dept Chem, Key Lab Bioorgan Phosphorus Chem & Chem Biol, Beijing 100084, Peoples R China
[2] Chinese Acad Sci, Ecoenvironm Sci Res Ctr, State Key Lab Environm Chem & Ecotoxicol, Beijing 100085, Peoples R China
基金
中国国家自然科学基金;
关键词
Immunomagnetic bead; Bacteria; Salmonella; Staphylococcus aureus; Bioluminescence; Microfluidics; CATIONIC LIPOSOMES; INTRACELLULAR ATP; ASSAY;
D O I
10.1016/j.talanta.2009.05.003
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
This paper describes an immunomagnetic separation of target bacterial cells from others by using magnetic bead. The surface of bead was coated with antibodies which can capture specific organism. The binding efficiency of immunomagnetic bead (IMB) capturing target bacterial cells was higher than 98% when the concentrations of target and interferent bacterial cells were at the same level. The concentration of bacteria was determined indirectly by detecting adenosine 5'-triphosphate (ATP) employing bioluminescence (BL) reaction of firefly luciferin-ATR Benzalkonium chloride (BAC) was used as an ATP extractant from living bacterial cells. We found that BAC could enhance the light emission when the concentration of BAC was less than 5.3 x 10(-2)% (w/v) and the BL intensity reached its maximum at the concentration of BAC was 2.7 x 10(-2)%, which was 10-fold stronger than that without BAC. Based on the principle of the IMB, a microfluidic chip combined with immunofluorescence assay for separating and detecting bacteria simultaneously was also developed. The IMBs were magnetically fixed in the bead-beds of chip channels with a 3-mm diameter of NdFeB permanent magnet. The target bacterial cells can be captured magnetically and observed by a fluorescent microscope. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:787 / 795
页数:9
相关论文
共 25 条
[1]   Quantification of bacterial cells based on autofluorescence on a microfluidic platform [J].
Bao, Ning ;
Jagadeesan, Balarnurugan ;
Bhunia, Arun K. ;
Yao, Yuan ;
Lu, Chang .
JOURNAL OF CHROMATOGRAPHY A, 2008, 1181 (1-2) :153-158
[2]   An alternative mechanism of bioluminescence color determination in firefly luciferase [J].
Branchini, BR ;
Southworth, TL ;
Murtiashaw, MH ;
Magyar, RA ;
Gonzalez, SA ;
Ruggiero, MC ;
Stroh, JG .
BIOCHEMISTRY, 2004, 43 (23) :7255-7262
[3]   Yellow-green and red firefly bioluminescence from 5,5-dimethyloxyluciferin [J].
Branchini, BR ;
Murtiashaw, MH ;
Magyar, RA ;
Portier, NC ;
Ruggiero, MC ;
Stroh, JG .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (10) :2112-2113
[4]   Rapid prototyping of microfluidic systems in poly(dimethylsiloxane) [J].
Duffy, DC ;
McDonald, JC ;
Schueller, OJA ;
Whitesides, GM .
ANALYTICAL CHEMISTRY, 1998, 70 (23) :4974-4984
[5]   An approach to the rapid control of oil spill bioremediation by bioluminescent method of intracellular ATP determination [J].
Efremenko, EN ;
Azizov, RE ;
Raeva, AA ;
Abbasov, VM ;
Varfolomeyev, SD .
INTERNATIONAL BIODETERIORATION & BIODEGRADATION, 2005, 56 (02) :94-100
[6]   Particulate platform for bioluminescent immunosensing [J].
Fromell, Karin ;
Hulting, Greta ;
Ilichev, Alexander ;
Larsson, Anders ;
Caldwell, Karin D. .
ANALYTICAL CHEMISTRY, 2007, 79 (22) :8601-8607
[7]   Immunomagnetic T cell capture from blood for PCR analysis using microfluidic systems [J].
Furdui, VI ;
Harrison, DJ .
LAB ON A CHIP, 2004, 4 (06) :614-618
[8]   Reusable immunomagnetic beads in an enzyme immunoassay [J].
Han, F. C. ;
Luo, J. ;
Guo, H. F. ;
Zhang, W. H. ;
He, D. C. ;
Yan, X. J. .
WORLD JOURNAL OF MICROBIOLOGY & BIOTECHNOLOGY, 2007, 23 (08) :1041-1045
[9]   Enhanced microbial biomass assay using mutant luciferase resistant to benzalkonium chloride [J].
Hattori, N ;
Sakakibara, T ;
Kajiyama, N ;
Igarashi, T ;
Maeda, M ;
Murakami, S .
ANALYTICAL BIOCHEMISTRY, 2003, 319 (02) :287-295
[10]   Firefly bioluminescent assay of ATP in the presence of ATP extractant by using liposomes [J].
Kamidate, T ;
Yanashita, K ;
Tani, H ;
Ishida, A ;
Notani, M .
ANALYTICAL CHEMISTRY, 2006, 78 (01) :337-342