DENOVO BIOSYNTHESIS OF HEME OFFERS A NEW CHEMOTHERAPEUTIC TARGET IN THE HUMAN MALARIAL PARASITE

被引:96
作者
SUROLIA, N [1 ]
PADMANABAN, G [1 ]
机构
[1] INDIAN INST SCI, JAWAHARLAL NEHRU CTR ADV SCI RES, BANGALORE 560012, KARNATAKA, INDIA
关键词
D O I
10.1016/0006-291X(92)91258-R
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The human malarial parasite, Plasmodium falciparum, has been found to synthesize heme de novo, despite the accumulation of large quantities of polymeric heme derived from the hemoglobin of the red cell host. The parasite δ-aminolevulinate dehydrase level is significantly lower than that of the host and its inhibition by succinylacetone leads to inhibition of parasite protein synthesis and viability. © 1992.
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收藏
页码:744 / 750
页数:7
相关论文
共 19 条
[1]   HEME IS A POSITIVE REGULATOR OF CYTOCHROME-P-450 GENE-TRANSCRIPTION [J].
BHAT, GJ ;
PADMANABAN, G .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1988, 264 (02) :584-590
[2]   SUCCINYLACETONE, A POTENT INHIBITOR OF HEME-BIOSYNTHESIS - EFFECT ON CELL-GROWTH, HEME CONTENT AND DELTA-AMINOLEVULINIC-ACID DEHYDRATASE ACTIVITY OF MALIGNANT MURINE ERYTHROLEUKEMIA-CELLS [J].
EBERT, PS ;
HESS, RA ;
FRYKHOLM, BC ;
TSCHUDY, DP .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1979, 88 (04) :1382-1390
[3]   LYSIS OF PLASMODIUM-FALCIPARUM BY FERRIPROTOPORPHYRIN-IX AND A CHLOROQUINE-FERRIPROTOPORPHYRIN-IX COMPLEX [J].
FITCH, CD ;
CHEVLI, R ;
BANYAL, HS ;
PHILLIPS, G ;
PFALLER, MA ;
KROGSTAD, DJ .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1982, 21 (05) :819-822
[4]  
FITCH CD, 1983, CIBA F SYMP, V94, P222
[5]  
FITCH CD, 1987, J BIOL CHEM, V262, P15552
[6]  
GARDNER LC, 1991, J BIOL CHEM, V266, P22010
[7]  
GARDNER MJ, 1989, MOL BIOCHEM PARASIT, V35, P97
[8]  
Granick S, 1978, Adv Enzymol Relat Areas Mol Biol, V46, P33
[9]   RAPID ACTION OF QINGHAOSU AND RELATED DRUGS ON INCORPORATION OF [ISOLEUCINE-H-3 BY PLASMODIUM-FALCIPARUM INVITRO [J].
GU, HM ;
WARHURST, DC ;
PETERS, W .
BIOCHEMICAL PHARMACOLOGY, 1983, 32 (17) :2463-2466
[10]  
KANNANGARA CG, 1988, TRENDS BIOCHEM SCI, V13, P139