| Literature DB >> 33768012 |
Arif Nurkanto1,2, Ghulam Jeelani2, Herbert J Santos2, Yulia Rahmawati2, Mihoko Mori3,4, Yumi Nakamura5, Kana Goto5, Yoko Saikawa5, Takeshi Annoura6, Yuzuru Tozawa7, Takaya Sakura8, Daniel Ken Inaoka8, Kazuro Shiomi3, Tomoyoshi Nozaki2.
Abstract
Coenzyme A (CoA) is a well-known cofactor that plays an essential role in many metabolic reactions in all organisms. In Plasmodium falciparum, the most deadly among Plasmodium species that cause malaria, CoA and its biosynthetic pathway have been proven to be indispensable. The first and rate-limiting reaction in the CoA biosynthetic pathway is catalyzed by two putative pantothenate kinases (PfPanK1 and 2) in this parasite. Here we produced, purified, and biochemically characterized recombinant PfPanK1 for the first time. PfPanK1 showed activity using pantetheine besides pantothenate, as the primary substrate, indicating that CoA biosynthesis in the blood stage of P. falciparum can bypass pantothenate. We further developed a robust and reliable screening system to identify inhibitors using recombinant PfPanK1 and identified four PfPanK inhibitors from natural compounds.Entities:
Keywords: PfPanK1; PfPanK2; Plasmodium falciparum; coenzyme A; inhibitors
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Year: 2021 PMID: 33768012 PMCID: PMC7985445 DOI: 10.3389/fcimb.2021.639065
Source DB: PubMed Journal: Front Cell Infect Microbiol ISSN: 2235-2988 Impact factor: 5.293