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A continuous fluorescence assay to measure nicotianamine synthase activity.
Pasin, Thiago M; Meneely, Kathleen M; Ruiz, Deegan M; Lamb, Audrey L.
Afiliación
  • Pasin TM; Department of Chemistry, University of Texas at San Antonio, San Antonio, TX, United States.
  • Meneely KM; Department of Chemistry, University of Texas at San Antonio, San Antonio, TX, United States.
  • Ruiz DM; Department of Chemistry, University of Texas at San Antonio, San Antonio, TX, United States.
  • Lamb AL; Department of Chemistry, University of Texas at San Antonio, San Antonio, TX, United States. Electronic address: audrey.lamb@utsa.edu.
Methods Enzymol ; 702: 51-74, 2024.
Article en En | MEDLINE | ID: mdl-39155120
ABSTRACT
S-adenosylmethionine (SAM) is most widely known as the biological methylating agent of methyltransferases and for generation of radicals by the iron-sulfur dependent Radical SAM enzymes. SAM also serves as a substrate in biosynthetic reactions that harvest the aminobutyrate moiety of the methionine, producing methylthioadenosine as a co-product. These reactions are found in the production of polyamines such as spermine, siderophores derived from nicotianamine, and opine metallophores staphylopine and pseudopaline, among others. This procedure defines a highly sensitive, continuous fluorescence assay for the determination of steady state kinetic parameters for enzymes that generate the co-product methylthioadenosine.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: S-Adenosilmetionina / Pruebas de Enzimas Idioma: En Revista: Methods Enzymol Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: S-Adenosilmetionina / Pruebas de Enzimas Idioma: En Revista: Methods Enzymol Año: 2024 Tipo del documento: Article