Simple Screening Method for Staurosporine in Bacterial
Cultures using Liquid Chromatography-Tandem
Mass Spectrometry |
| Amitha K. Hewavitharana1*, P. Nicholas Shaw1, Yi K. Ng2, John A. Fuerst2 |
1School of Pharmacy, The University of Queensland, Brisbane, Queensland 4072, Australia |
| 2School of Molecular and Microbial Sciences, The University of Queensland, Brisbane, Queensland 4072, Australia |
| *Corresponding author: |
Dr. Amitha K. Hewavitharana, School of Pharmacy,
The University of Queensland, Brisbane,
Queensland 4072, Australia,
Tel : +61-7-3365-8853,
Fax : +61-7-3365-1688,
E-mail : a.hewavitharana@pharmacy.uq.edu.au |
|
| Received November 10, 2009; Accepted December 20, 2009; Published December 21, 2009 |
Citation: Hewavitharana AK, Shaw PN, Ng YK, Fuerst JN (2009) Simple
Screening Method for Staurosporine in Bacterial Cultures using Liquid
Chromatography-Tandem Mass Spectrometry. J Bioanal Biomed 1: 001-
004. doi: 10.4172/1948-593X.1000001 |
Copyright: © 2009 Hewavitharana AK, et al. This is an open-access
article distributed under the terms of the Creative Commons Attribution
License, which permits unrestricted use, distribution, and reproduction
in any medium, provided the original author and source are credited. |
| Abstract |
Staurosporine has been shown to possess an array of important
biological properties such as anti-fungal, anti-bacterial, antihypertensive
and anti-cancer. Methods available to screen any
plant or bacterial extract for this compound are lengthy and laborious.
We present here a simple HPLC-MS-MS method for
the highly selective identification of Staurosporine in various
strains of the marine sponge-derived bacterium Salinispora.
Gradient elution using acetonitrile/water/ammonium acetate was
used to separate Staurosporine from the matrix and positive ionelectrospray
mass spectrometry was used for detection and confirmation.
Presence of Staurosporine in bacterial extracts was
confirmed by matching retention times and parent-daughter ion
mass spectra (using Multiple Reaction Monitoring, MRM mode)
of the standard Staurosporine with those of the bacterial extracts.
Detection of Staurosporine was achieved down to 11 ng/mL
bacterial extract. This method can be easily adapted to screen
any plant extract for Staurosporine. The simplicity and the speed
of this method make it possible for the analyst to screen a large
number of extracts before embarking on lengthy and costly isolation
and purification of Staurosporine in a selected few. |
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