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PMID: 3093227 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Purification and structural analysis of pyocyanin and 1-hydroxyphenazine.

European journal of biochemistry ·Vol. 159 ·No. 2 ·1986-09-01 ·Pages 309-13

Watson D, MacDermot J, Wilson R, Cole PJ, Taylor GW

Abstract

Pyocyanin and related members of the phenazine family are produced by Pseudomonas aeruginosa and have been associated with events of pathophysiological importance. Pyocyanin and its base hydrolysis product 1-hydroxyphenazine were purified to homogeneity by reverse-phase high-pressure liquid chromatography. Their mass spectrometric behaviour was examined with a view to evaluating the use of high-resolution chromatography/mass spectrometry in studying phenazine-mediated effects in man. The molecular mass of naturally derived pyocyanin was determined as 210 Da by thermospray liquid chromatography/mass spectrometry and confirmed by desorption electron-impact mass spectrometry. Mass spectrometric data could not be obtained by fast-atom bombardment or desorption chemical ionisation, techniques commonly used to determine molecular mass of polar or thermally labile species. The thermal lability of underivatised pyocyanin precluded analysis by gas chromatography/mass spectrometry. In contrast to pyocyanin, mass spectrometric data were readily obtained for 1-hydroxyphenazine, using direct probe analysis as well as with gas and liquid chromatography inlet systems.

MeSH Terms
Chromatography, Gas Chromatography, High Pressure Liquid Gas Chromatography-Mass Spectrometry Phenazines/analysis,isolation & purification Pseudomonas aeruginosa/analysis Pyocyanine/analysis,isolation & purification
Chemicals
Phenazines 1-hydroxyphenazine Pyocyanine
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Watson D
MacDermot J
Wilson R
Cole P J
Taylor G W
Article Info
Journal
European journal of biochemistry
Abbr.
Eur J Biochem
ISSN
0014-2956
Published
1986-09-01
Pages
309-13
Language
English
Region
England
NLM ID
0107600
Subset
IM
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