The proteins of Plasmodium, the malaria parasite, are strikingly rich in asparagine. Plasmodium depends primarily on host haemoglobin degradation for amino acids and has a rudimentary pathway for amino acid biosynthesis, but retains a gene encoding asparagine synthetase (AS).

Researchers show that deletion of AS in Plasmodium berghei (Pb) delays the asexual- and liver-stage development with substantial reduction in the formation of ookinetes, oocysts and sporozoites in mosquitoes.

In the absence of asparagine synthesis, extracellular asparagine supports suboptimal survival of Pb AS knockout (KO) parasites. Depletion of blood asparagine levels by treating Pb ASKO-infected mice with asparaginase completely prevents the development of liver stages, exflagellation of male gametocytes and the subsequent formation of sexual stages. 

In vivo supplementation of asparagine in mice restores the exflagellation of Pb ASKO parasites. Thus, the parasite life cycle has an absolute requirement for asparagine, which we propose could be targeted to prevent malaria transmission and liver infections.

http://www.nature.com/ncomms/2015/151104/ncomms9775/full/ncomms9775.html