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Functional analysis of phosphoethanolamine N-methyltransferase in plants and parasites: Essential S-adenosylmethionine-dependent methyltransferase in choline and phospholipid metabolism.
Bare, Alex; Thomas, Jaime; Etoroma, Daniel; Lee, Soon Goo.
Afiliação
  • Bare A; Department of Chemistry and Biochemistry, University of North Carolina Wilmington, Wilmington, NC, United States.
  • Thomas J; Department of Chemistry, University of Manitoba, Winnipeg, MB, Canada.
  • Etoroma D; Department of Chemistry and Biochemistry, University of North Carolina Wilmington, Wilmington, NC, United States.
  • Lee SG; Department of Chemistry and Biochemistry, University of North Carolina Wilmington, Wilmington, NC, United States. Electronic address: lees@uncw.edu.
Methods Enzymol ; 680: 101-137, 2023.
Article em En | MEDLINE | ID: mdl-36710008
ABSTRACT
Phospholipids play an essential role as a barrier between cell content and the extracellular environment and regulate various cell signaling processes. Phosphatidylcholine (PtdCho) is one of the most abundant phospholipids in plant, animal, and some prokaryote cell membranes. In plants and some parasites, the biosynthesis of PtdCho begins with the amino acid serine, followed mainly through a phosphoethanolamine N-methyltransferase (PMT)-mediated biosynthetic pathway to phosphocholine (pCho). Because the PMT-mediated pathway, referred to as the phosphobase methylation pathway, produces a series of important primary and specialized metabolites for plant development and stress response, understanding the PMT enzyme is a key aspect of engineering plants with improved stress tolerance and fortified nutrients. Importantly, given the very limited phylogenetic distribution of PMTs, functional analysis and the identification of inhibitors targeting PMTs have potential and positive impacts in humans and in veterinary and agricultural fields. Here, we describe detailed basic knowledge and practical research methods to enable the systematic study of the biochemical and biophysical functions of PMT. The research methods described in this chapter are also applicable to the studies of other ubiquitous S-adenosyl-l-methionine (SAM)-dependent methyltransferases in all kingdoms.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Parasitos / Metiltransferases Limite: Animals / Humans Idioma: En Revista: Methods Enzymol Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Parasitos / Metiltransferases Limite: Animals / Humans Idioma: En Revista: Methods Enzymol Ano de publicação: 2023 Tipo de documento: Article