Nantana Nuchtavorn, Fritz Bek, Mirek Macka, Worapot Suntornsuk, Leena Suntornsuk
Index: Electrophoresis 33(9-10) , 1421-6, (2012)
Full Text: HTML
Rapid detection of microorganisms by alternative methods is desirable. Electromigration separation methods have the capability to separate microorganisms according to their charge and size and laser-induced fluorescence (LIF) detection have single-cell detection capability. In this work, a new combined separation and detection scheme was introduced using chip-based capillary electrophoresis (chip-CE) platform with LIF detection. Three microorganisms Escherichia coli, Staphylococcus aureus, and Candida albicans were selected as representatives of Gram-positive bacteria, Gram-negative bacteria, and fungi. While their cells carry an overall negative charge in neutral to alkaline pH, staining them with nile blue (NB) provided highly sensitive LIF detection with excitation and emission wavelengths at 635 nm and 685 nm, respectively, and at the same time, the overall charge was converted to positive. Electrolyte pH and concentration of polyethylene oxide (PEO) significantly affected the resolution of the microorganisms. Their optimal separation in the 14 mm separation channel was achieved in less than 30 s (R(s) > 5.3) in an electrolyte consisting of 3.94 mM Tris, 0.56 mM boric acid, 0.013 mM ethylenediaminetetraacetic acid disodium salt dihydrate (pH 10.5), and 0.025% PEO, with injection/separation voltages of +1000/+1000 V. The separation mechanism is likely employing contributions to the overall cationic charge from both the prevalently anionic membrane proteins and the cationic NB. Importantly, the resulting cationic NB-stained cells exhibited excellent separation selectivity and efficiency of ∼38000 theoretical plates for rapid separations within 30-40 s. The results indicate the potential of chip-CE for microbial analysis, which offers separations of a wide range of species with high efficiency, sensitivity, and throughput.© 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
| Structure | Name/CAS No. | Molecular Formula | Articles |
|---|---|---|---|
![]() |
Nile Blue A (sulfate)
CAS:3625-57-8 |
C20H20N3O3S0.5 | |
![]() |
NILE BLUE A PERCHLORATE
CAS:53340-16-2 |
C20H20ClN3O5 |
|
Heterogeneous immunoassay for soy protein determination usin...
2011-09-09 [Anal. Chim. Acta 701(2) , 194-9, (2011)] |
|
Stepwise fluorescence changes of quantum dots: single-molecu...
2012-01-18 [Chem. Commun. (Camb.) 48(5) , 723-5, (2012)] |
|
Evaluation of three bait materials and their food transfer e...
2012-10-01 [J. Econ. Entomol. 105(5) , 1758-65, (2012)] |
|
Assessment of iontophoretic and passive ungual penetration b...
2012-12-01 [Pharm. Res. 29(12) , 3464-74, (2012)] |
|
Electrochemical properties of interstrand cross-linked DNA d...
2012-12-11 [Langmuir 28(49) , 17211-6, (2012)] |
Home | MSDS/SDS Database Search | Journals | Product Classification | Biologically Active Compounds | Selling Leads | About Us | Disclaimer
Copyright © 2026 ChemSrc All Rights Reserved

