期刊
MOLECULAR AND BIOCHEMICAL PARASITOLOGY
卷 115, 期 2, 页码 217-226出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/S0166-6851(01)00293-6
关键词
Leishmania donovani; spermidine synthase; gene knockouts; polyamines
资金
- NIAID NIH HHS [AI10096, AI41622] Funding Source: Medline
The polyamine biosynthetic pathway of protozoan parasites has been validated as a target in antiparasitic chemotherapy. To investigate this pathway at the biochemical and genetic level in a model parasite, the gene encoding spermidine synthase: (SPDSYN), a key polyamine biosynthetic enzyme, has been cloned and sequenced from Leishmania donovani. The L. donovani SPDSYN gene encodes a polypeptide of 300 amino acids that exhibits 56% amino acid identity with the human counterpart. SPDSYN is present as a single copy gene in the leishmanial genome and encodes a 1.6 kb transcript. Employing SPDSYN Banking sequences to construct drug resistance cassettes, a Delta spdsyn knockout strain of L. donovani was created by double targeted gene replacement. This Delta spdsyn line could not convert putrescine to spermidine and was auxotrophic for polyamines. The polyamine auxotrophy could be circumvented by exogenous spermidine but not by putrescine (1,4-diaminobutane), cadaverine (1,5-diaminopentane). 1,3-diaminopropane, or spermine. Incubation of the null mutant in polyamine-deficient medium resulted in a rapid depletion in the intracellular spermidine level with a concomitant elevation of the putrescine pool. In addition, the level of trypanothione, a spermidine-containing thiol. was reduced. whereas the glutathione pool increased 3-4-fold, These data establish that SPDSYN is an essential enzyme in L. donovani promastigotes. The molecular and cellular reagents created in this investigation provide a foundation For subsequent structure-function and inhibitor design studies on this keg polyamine biosynthetic enzyme. (C) 2001 Elsevier Science B.V. All rights reserved.
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