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J Biol Chem, Vol. 274, Issue 6, 3781-3788, February 5, 1999
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From the A knockout strain of Leishmania
donovani lacking both ornithine decarboxylase (ODC) alleles has
been created by targeted gene replacement. Growth of
Department of Biochemistry and Molecular
Biology, Oregon Health Sciences University, Portland, Oregon 97201-3098 and ¶ Department of Biochemistry, University of Dundee, Dundee DD1
4HN, Scotland, United Kingdom
odc
cells in polyamine-deficient medium resulted in a rapid and profound
depletion of cellular putrescine pools, although levels of spermidine
were relatively unaffected. Concentrations of trypanothione, a
spermidine conjugate, were also reduced, whereas glutathione
concentrations were augmented. The
odc L. donovani
exhibited an auxotrophy for polyamines that could be circumvented by
the addition of the naturally occurring polyamines, putrescine or
spermidine, to the culture medium. Whereas putrescine supplementation
restored intracellular pools of both putrescine and spermidine,
exogenous spermidine was not converted back to putrescine, indicating
that spermidine alone is sufficient to meet the polyamine requirement,
and that L. donovani does not express the enzymatic
machinery for polyamine degradation. The lack of a polyamine catabolic
pathway in intact parasites was confirmed radiometrically. In addition,
the
odc strain could grow in medium supplemented with
either 1,3-diaminopropane or 1,5-diaminopentane (cadaverine), but
polyamine auxotrophy could not be overcome by other aliphatic diamines
or spermine. These data establish genetically that ODC is
an essential gene in L. donovani, define the polyamine
requirements of the parasite, and reveal the absence of a
polyamine-degradative pathway.
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