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Carbohydrate metabolism in the developing endosperm of rice grains

Tipo de material: TextoTextoSeries ; Plant & Cell Physiology, 30(6), p.833-839, 1989Trabajos contenidos:
  • Nakamura, Y
  • Yuki, K
  • Park, S.-Y
  • Ohya, T
Tema(s): Recursos en línea: Resumen: The metabolism of carbohydrates in developing rice endosperm was characterized by a comparison of levels of activities of 33 major enzymes between the endosperm and green leaves of rice. Activities of ADPglucose pyrophosphorylase, starch synthase and branching enzyme (Q-enzyme), compared on the basis of soluble protein content, were markedly higher in endosperm than in green leaves. The high levelsof Q-enzyme may be responsible for the efficientproduction of starch in the rice endosperm. The GIP is converted to starch by the concerted reactions of ADPglucose pyrophosphorylase, starch synthase and Q-enzyme.measurement of levelsof metabolic intermediates and the localization of key enzymes in isolated amyloplasts from rice endosperm support the view that sucrose is metabolized in the cytoplasm via the pathway: sucrose-+UDPglucose-+hexose-P-+FBP -+triose-P. Triose-P then enters the amyloplast, where it is converted to G1P via FBP and, finally,
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The metabolism of carbohydrates in developing rice endosperm was characterized by a comparison of levels of activities of 33 major enzymes between the endosperm and green leaves of rice. Activities of ADPglucose pyrophosphorylase, starch synthase and branching enzyme (Q-enzyme), compared on the basis of soluble protein content, were markedly higher in endosperm than in green leaves. The high levelsof Q-enzyme may be responsible for the efficientproduction of starch in the rice endosperm. The GIP is converted to starch by the concerted reactions of ADPglucose pyrophosphorylase, starch synthase and Q-enzyme.measurement of levelsof metabolic intermediates and the localization of key enzymes in isolated amyloplasts from rice endosperm support the view that sucrose is metabolized in the cytoplasm via the pathway: sucrose-+UDPglucose-+hexose-P-+FBP -+triose-P. Triose-P then enters the amyloplast, where it is converted to G1P via FBP and, finally,

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