PRIMARY STRUCTURE AND EXPRESSION OF THE DIHYDROPTEROATE SYNTHETASE GENE OF PLASMODIUM-FALCIPARUM

被引:256
作者
TRIGLIA, T
COWMAN, AF
机构
[1] Walter Eliza Hall Inst. of Med. Res., Melbourne
基金
英国惠康基金;
关键词
MALARIA; SULFADOXINE; DRUG RESISTANCE; FOLATE;
D O I
10.1073/pnas.91.15.7149
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The enzyme dihydropteroate synthetase (DHPS) from Plasmodium falciparum is involved in the mechanism of action of the sulfone/sulfonamide group of drugs. We describe the cloning and sequencing of the gene encoding the P. falciparum DHPS enzyme and show that it is a bifunctional enzyme that includes dihydro-6-hydroxymethylpterin pyrophosphokinase (PPPK) at the N terminus of DHPS. The gene encodes a putative protein of 83 kDa that contains two domains that are homologous with the DHPS and PPPK enzymes of other organisms. The PPPK-DHPS gene is encoded on chromosome 8 and has two introns. An antibody raised to the PPPK region of the protein was found to recognize a 68-kDa protein that is expressed throughout the asexual life cycle of the parasite. We have determined the sequence of the DHPS portion of the gene from sulfadoxine-sensitive and -resistant P. falciparum clones and identified sequence differences that may have a role in sulfone/sulfonamide resistance.
引用
收藏
页码:7149 / 7153
页数:5
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