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Sunflower HaGPAT9-1 is the predominant GPAT during seed development.
Payá-Milans, Miriam; Aznar-Moreno, Jose Antonio; Balbuena, Tiago S; Haslam, Richard P; Gidda, Satinder K; Pérez-Hormaeche, Javier; Mullen, Robert T; Thelen, Jay J; Napier, Johnathan A; Salas, Joaquín J; Garcés, Rafael; Martínez-Force, Enrique; Venegas-Calerón, Mónica.
Afiliação
  • Payá-Milans M; Department of Biochemistry and Molecular Biology of Plant Products, Instituto de la Grasa (CSIC), Campus Universitario Pablo de Olavide, 41013 Seville, Spain; Department of Entomology & Plant Pathology, University of Tennessee, Knoxville, TN 37996, United States.
  • Aznar-Moreno JA; Department of Biochemistry and Molecular Biology of Plant Products, Instituto de la Grasa (CSIC), Campus Universitario Pablo de Olavide, 41013 Seville, Spain; Department of Biochemistry & Molecular Biophysics, Kansas State University, Manhattan, KS 66506, United States.
  • Balbuena TS; Department of Biochemistry and Interdisciplinary Plant Group, University of Missouri, Columbia, MO 65211, United States; Department of Technology, São Paulo State University, Jaboticabal, São Paulo, Brazil.
  • Haslam RP; Department of Biological Chemistry and Crop Protection, Rothamsted Research, Harpenden, Hertfordshire AL5 2JQ, United Kingdom.
  • Gidda SK; Department of Molecular and Cellular Biology, University of Guelph, Guelph, Ontario, N1G 2W1, Canada.
  • Pérez-Hormaeche J; Department of Biochemistry and Molecular Biology of Plant Products, Instituto de la Grasa (CSIC), Campus Universitario Pablo de Olavide, 41013 Seville, Spain.
  • Mullen RT; Department of Molecular and Cellular Biology, University of Guelph, Guelph, Ontario, N1G 2W1, Canada.
  • Thelen JJ; Department of Biochemistry and Interdisciplinary Plant Group, University of Missouri, Columbia, MO 65211, United States.
  • Napier JA; Department of Biological Chemistry and Crop Protection, Rothamsted Research, Harpenden, Hertfordshire AL5 2JQ, United Kingdom.
  • Salas JJ; Department of Biochemistry and Molecular Biology of Plant Products, Instituto de la Grasa (CSIC), Campus Universitario Pablo de Olavide, 41013 Seville, Spain.
  • Garcés R; Department of Biochemistry and Molecular Biology of Plant Products, Instituto de la Grasa (CSIC), Campus Universitario Pablo de Olavide, 41013 Seville, Spain.
  • Martínez-Force E; Department of Biochemistry and Molecular Biology of Plant Products, Instituto de la Grasa (CSIC), Campus Universitario Pablo de Olavide, 41013 Seville, Spain.
  • Venegas-Calerón M; Department of Biochemistry and Molecular Biology of Plant Products, Instituto de la Grasa (CSIC), Campus Universitario Pablo de Olavide, 41013 Seville, Spain. Electronic address: mvc@ig.csic.es.
Plant Sci ; 252: 42-52, 2016 Nov.
Article em En | MEDLINE | ID: mdl-27717477
ABSTRACT
In oil crops, triacylglycerol biosynthesis is an important metabolic pathway in which glycerol-3-phosphate acyltransferase (GPAT) performs the first acylation step. Mass spectrometry analysis of developing sunflower (Helianthus annuus) seed membrane fractions identified an abundant GPAT, HaGPAT9 isoform 1, with a N-terminal peptide that possessed two phosphorylated residues with possible regulatory function. HaGPAT9-1 belongs to a broad eukaryotic GPAT family, similar to mammalian GPAT3, and it represents one of the two sunflower GPAT9 isoforms, sharing 90% identity with HaGPAT9-2. Both sunflower genes are expressed during seed development and in vegetative tissues, with HaGPAT9-1 transcripts accumulating at relatively higher levels than those for HaGPAT9-2. Green fluorescent protein tagging of HaGPAT9-1 confirmed its subcellular accumulation in the endoplasmic reticulum. Despite their overall sequence similarities, the two sunflower isoforms displayed significant differences in their enzymatic activities. For instance, HaGPAT9-1 possesses in vivo GPAT activity that rescues the lethal phenotype of the cmy228 yeast strain, while in vitro assays revealed a preference of HaGPAT9-1 for palmitoyl-, oleoyl- and linoleoyl-CoAs of one order of magnitude, with the highest increase in yield for oleoyl- and linoleoyl-CoAs. By contrast, no enzymatic activity could be detected for HaGPAT9-2, even though its over-expression modified the TAG profile of yeast.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas de Plantas / Glicerol-3-Fosfato O-Aciltransferase / Helianthus Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas de Plantas / Glicerol-3-Fosfato O-Aciltransferase / Helianthus Idioma: En Ano de publicação: 2016 Tipo de documento: Article