Abstract
Objectives: To detect Cochlodinum polykrikoides in long-term monitoring and high-throughput sampling projects using an integrated sandwich hybridization and nuclease protection assay (NPA-SH). Results: The specificity of the probes was verified with individual and mixed cultures as well as field collection, and the quantity of C. polykrikoides determined by NPA-SH analysis showed a good correlation with that determined by cell-counting with a light microscope. In addition a standard curve for C. polykrikoides was established to represent the correlation between optical absorbance in the NPA-SH assay and cell density. Conclusions: This approach provides an efficient alternative to traditional, morphology-based methods for the rapid identification and quantification of harmful algal species and could be used to monitor phytoplankton in field surveys.
| Original language | English |
|---|---|
| Pages (from-to) | 57-63 |
| Number of pages | 7 |
| Journal | Biotechnology Letters |
| Volume | 38 |
| Issue number | 1 |
| DOIs | |
| State | Published - 1 Jan 2016 |
Keywords
- Algal blooms
- Cochlodinium polykrikoides
- Microalgae detection
- Ribosomal RNA
- S1 enzyme
- Sandwich hybridization integrated with nuclease protection assay (NPA-SH)