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A mass spectrometric method for quantifying C3 and C6 phosphorylation of starch.
Carpenter, Margaret; Joyce, Nigel; Butler, Ruth; Genet, Russell; Timmerman-Vaughan, Gail.
Afiliación
  • Carpenter M; The New Zealand Institute for Plant & Food Research Ltd., Christchurch 8140, New Zealand. Margaret.Carpenter@plantandfood.co.nz
Anal Biochem ; 431(2): 115-9, 2012 Dec 15.
Article en En | MEDLINE | ID: mdl-22982506
The glucosyl residues comprising starch can be phosphorylated at either the C3 or the C6 position of the molecule because of the activities of two distinct dikinase enzymes. After hydrolysis of the starch, the C6 phosphorylation is easy to measure using a routine enzyme assay for glucose 6-phosphate, but the C3 phosphorylation is more difficult to assay. A mass spectrometric (MS) method has been developed that, in a single run, can distinguish and quantify the glucose 3-phosphate and glucose 6-phosphate produced by hydrolysis of starch and can also measure the glucose content to give an accurate estimate of the starting material. The MS method involves quantification by LC/MS with external standards, using normal-phase hydrophilic interaction liquid chromatography and selective reaction monitoring. The MS method has been used to determine degrees of starch phosphorylation in a diverse group of potato lines, revealing threefold differences in phosphorylation between high- and low-phosphate lines. The method was also used to show that cold storage of potato tubers for up to 24weeks had little substantive effect on the levels of starch phosphorylation. MS provided an effective and efficient means of determining both the C6 and the C3 phosphorylation of starch.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Espectrometría de Masas / Almidón / Solanum tuberosum Idioma: En Revista: Anal Biochem Año: 2012 Tipo del documento: Article País de afiliación: Nueva Zelanda

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Espectrometría de Masas / Almidón / Solanum tuberosum Idioma: En Revista: Anal Biochem Año: 2012 Tipo del documento: Article País de afiliación: Nueva Zelanda