54
Views
4
CrossRef citations to date
0
Altmetric
Original Articles

LIQUID CHROMATOGRAPHY DETERMINATION AND LC-ESI-MS ANALYSIS OF MICROCYSTIN-LR FROM PCC STRAINS OF MICROCYSTIS AERUGINOSA

&
Pages 865-875 | Received 01 Oct 2001, Published online: 11 Dec 2006
 

Abstract

Cyanobacteria (blue-green algae) have been shown to produce unique biologically active peptides such as microcystins, mainly from different species of Microcystis aeruginosa. Presence of these toxic peptides (hepatotoxin) in fresh water supplies are of increasing concern and has emphasized the need for a suitable analytical method. Amounts of microcystin-LR were estimated in the laboratory cultures of PCC strains viz. PCC-7806, 7820, and PCC-7941, using high performance liquid chromatography. The identity of microcystin-LR was confirmed by LC-ESI-MS. The lower detection limit of quantification is 1.0 μg/L.

ACKNOWLEDGMENTS

We thank Dr. R.V. Swamy, Chief Controller, Defense Research and Development Organization, New Delhi, for his encouragement and helpful advice. We are also thankful to Prof. Wayne. W. Carmichael of Wright State University Dayton, Ohio, USA, for providing the standard reference and Dr. P.V.L. Rao of DRDE Gwalior, for providing the cultured samples. M.N. is indebted to DRDO New Delhi for financial support.

Log in via your institution

Log in to Taylor & Francis Online

PDF download + Online access

  • 48 hours access to article PDF & online version
  • Article PDF can be downloaded
  • Article PDF can be printed
USD 61.00 Add to cart

Issue Purchase

  • 30 days online access to complete issue
  • Article PDFs can be downloaded
  • Article PDFs can be printed
USD 583.00 Add to cart

* Local tax will be added as applicable

Related Research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.