Development of a fluorometric sensor for the measurement of phycobilin pigment and application to freshwater phytoplankton
โ Scribed by Ryoichi Asai; Scott McNiven; Kazunori Ikebukuro; Isao Karube; Yasuo Horiguchi; Shuichi Uchiyama; Akira Yoshida; Yuzo Masuda
- Publisher
- John Wiley and Sons
- Year
- 2000
- Weight
- 466 KB
- Volume
- 4
- Category
- Article
- ISSN
- 1086-900X
No coin nor oath required. For personal study only.
โฆ Synopsis
A two-channel fluorometric sensor system for the detection of the waterbloom phytoplankton Microcystis aeruginosa has been developed. Excitation wavelengths of 620 and 440 nm were used, the former for detecting the cyanobacteria themselves, and the latter for subtracting the interference due to eukaryotic algae present in the sample. The fluorescence of the cyanobacteria and eukaryotic algae was measured at 645 and 680 nm, respectively. A linear relationship between phycocyanin fluorescence was established for the species examined in the range of to 10 0 g/ml ุ1 chlorophyll a.
ุ4 10 Furthermore, upon ultrasonic treatment of a colony of cyanobacteria, the relationship between fluorescence intensity and cell concentration was improved. Applied to real samples in Lake Kasumigaura, Japan, after ultrasonication, this fluorometric method could detect waterbloom. This system is capable of the rapid determination of phycocyanin; the time required for one measurement cycle is approximately 25 min including sonication and rinsing for 5 min. The detection limit of this method is suitable for detecting phycocyanin in the early stage of waterbloom formation. Furthermore, a device based on
๐ SIMILAR VOLUMES
A capillary precolumn was coupled directly into a valve switching system for the rapid analysis of discrete solution phase library samples. The samples, provided in dimethyl sulphoxide, are loaded onto the precolumn in an aqueous mobile phase and the trapped analytes are eluted into the mass spectro