INVESTIGADORES
ASENCION DIEZ Matias Damian
artículos
Título:
Characterization of Recombinant UDP- and ADP-Glucose Pyrophosphorylases and Glycogen Synthase To Elucidate Glucose-1-Phosphate Partitioning into Oligo- and Polysaccharides in Streptomyces coelicolor
Autor/es:
ASENCION DIEZ, MATIAS DAMIAN; PEIRÚ, SALVADOR; DEMONTE, ANA MARÍA; GRAMAJO, HUGO; IGLESIAS, ALBERTO A.
Revista:
JOURNAL OF BACTERIOLOGY
Editorial:
AMER SOC MICROBIOLOGY
Referencias:
Lugar: Washington; Año: 2012 vol. 194 p. 1485 - 1493
ISSN:
0021-9193
Resumen:
Streptomyces coelicolor exhibits a major
secondary metabolism, deriving important amounts of glucose to synthesize
pigmented antibiotics. Understanding the pathways occurring in the bacterium
with respect to synthesis of oligo- and polysaccharides is of relevance to
determine a plausible scenario for the partitioning of glucose-1-phosphate into
different metabolic fates. We report the molecular cloning of the genes coding
for UDP- and ADP-glucose pyrophosphorylases as well as for glycogen synthase
from genomic DNA of S.
coelicolor A3(2). Each gene was
heterologously expressed in Escherichia
coli cells to produce and purify to electrophoretic
homogeneity the respective enzymes. UDP-glucose pyrophosphorylase (UDP-Glc
PPase) was characterized as a dimer exhibiting a relatively high Vmax in catalyzing UDP-glucose synthesis (270
units/mg) and with respect to dTDP-glucose (94 units/mg). ADP-glucose
pyrophosphorylase (ADP-Glc PPase) was found to be tetrameric in structure and
specific in utilizing ATP as a substrate, reaching similar activities in the
directions of ADP-glucose synthesis or pyrophosphorolysis (Vmax of 0.15 and 0.27 units/mg, respectively).
Glycogen synthase was arranged as a dimer and exhibited specificity in the use
of ADP-glucose to elongate_-1,4-glucan chains in the
polysaccharide. ADP-Glc PPase was the only of the three enzymes exhibiting
sensitivity to allosteric regulation by different metabolites.
Mannose-6-phosphate, phosphoenolpyruvate, fructose-6-phosphate, and glucose- 6-phosphate
behaved as major activators, whereas NADPH was a main inhibitor of ADP-Glc
PPase. The results support a metabolic picture where glycogen synthesis occurs
via ADP-glucose in S.
coelicolor, with the pathway being strictly regulated in
connection with other routes involved with oligo- and polysaccharides, as well
as with antibiotic synthesis in the bacterium.