Ultrasensitive behavior in the synthesis of storage polysaccharides in cyanobacteria

The glycogen synthetic pathway operates ultrasensitively as a function of the ADPglucose pyrophosphorylase (ADPGlcPPase) allosteric effectors, 3-phosphoglycerate and Pi, in permeabilized cells of the cyanobacterium Anabaena PCC 7120. In vitro data previously showed that the ultrasensitive behavior o...

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Bibliographic Details
Authors: Gomez Casati, Diego Fabian, Cortassa, Sonia del Carmen, Aon, Miguel A., Iglesias, Alberto Alvaro
Format: article
Status:Published version
Publication Date:2003
Country:Argentina
Institution:Consejo Nacional de Investigaciones Científicas y Técnicas
Repository:CONICET Digital (CONICET)
Language:English
OAI Identifier:oai:ri.conicet.gov.ar:11336/93436
Online Access:http://hdl.handle.net/11336/93436
Access Level:Open access
Keyword:Permeabilized cyanobacteria
ADPGLUCOSE PYROPHOSPHORYLASE
ANABAENA
MOLECULAR CROWDING
PERMEABILIZED CYANOBACTERIA
https://purl.org/becyt/ford/1.6
https://purl.org/becyt/ford/1
Description
Summary:The glycogen synthetic pathway operates ultrasensitively as a function of the ADPglucose pyrophosphorylase (ADPGlcPPase) allosteric effectors, 3-phosphoglycerate and Pi, in permeabilized cells of the cyanobacterium Anabaena PCC 7120. In vitro data previously showed that the ultrasensitive behavior of ADPGlcPPase depends upon cross-talk between the two allosteric effectors, the enzyme's response being additionally modulated by molecular crowding [D.F. Gómez Casatiet al. (2000) Biochem J 350:139–147]. In the present work we show, experimentally and with a mathematical model, that α-1,4-glucan synthesis is also ultrasensitive in cells due to the propagation of the switch-like behavior of ADPGlcPPase to the synthetic pathway. Amplifications of up to 20-fold in storage-polysaccharide synthesis can be achieved with a modest 6.7-fold increase in 3-phosphoglycerate in the presence of 5 mM Pi in contrast to the 30-fold necessary in its absence. This is the first time that this phenomenon has been reported to occur in the glycogen synthetic pathway of a photosynthetic prokaryote. The implications of the results for plant cell physiology during light–dark transitions are discussed.