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Appl Environ Microbiol, June 1998, p. 2291-2294, Vol. 64, No. 6
School of Biology and
Biochemistry1 and
the QUESTOR
Centre,2 The Queen's University of Belfast,
Belfast, Northern Ireland
Received 22 December 1997/Accepted 10 April 1998
A strain of Burkholderia cepacia isolated by enrichment
culture utilized L-2-amino-3-phosphonopropionic acid
(phosphonoalanine) at concentrations up to 20 mM as a carbon, nitrogen,
and phosphorus source in a phosphate-insensitive manner. Cells
contained phosphoenolpyruvate phosphomutase activity, presumed to be
responsible for cleavage of the C---P bond of phosphonopyruvate, the
transamination product of L-phosphonoalanine; this was
inducible in the presence of phosphonoalanine.
0099-2240/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Phosphoenolpyruvate Phosphomutase Activity in
an L-Phosphonoalanine-Mineralizing Strain of
Burkholderia cepacia
*
Corresponding author. Present address: Biotechnology
Research Unit, School of Applied Biological and Chemical Sciences,
University of Ulster, Cromore Road, Coleraine, Co. Londonderry,
Northern Ireland BT52 1SA. Phone: 44 (0) 1265 323063. Fax: 44 (0) 1265 324906. E-mail: ng.ternan{at}ulst.ac.uk.
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