ACETATE UTILIZATION IS INHIBITED BY BENZOATE IN ALCALIGENES-EUTROPHUS- EVIDENCE FOR TRANSCRIPTIONAL CONTROL OF THE EXPRESSION OF ACOE CODING FOR ACETYL-COENZYME-A SYNTHETASE
F. Ampe et Nd. Lindley, ACETATE UTILIZATION IS INHIBITED BY BENZOATE IN ALCALIGENES-EUTROPHUS- EVIDENCE FOR TRANSCRIPTIONAL CONTROL OF THE EXPRESSION OF ACOE CODING FOR ACETYL-COENZYME-A SYNTHETASE, Journal of bacteriology, 177(20), 1995, pp. 5826-5833
During batch growth of Alcaligenes eutrophus on benzoate-acetate mixtu
res, benzoate was the preferred substrate, with acetate consumption be
ing delayed until the rate of benzoate consumption had diminished, Thi
s effect was attributed to a transcriptional control of the synthesis
of acetyl coenzyme A (acetyl-CoA) synthetase, an enzyme necessary for
the entry of acetate into the central metabolic pathways, rather than
to a biochemical modulation of the activity of this enzyme, Analysis o
f a 2.4-kb mRNA transcript hybridizing with the A. eutrophus acoE gene
confirmed this repression effect, In a benzoate-limited chemostat cul
ture, derepression was observed, with no increase in the level of expr
ession following an acetate pulse. Benzoate itself was not the signal
triggering the repression of acetyl-CoA synthetase, This role was play
ed by catechol, which transiently accumulated in the medium when high
specific rates of benzoate consumption were reached. The lack of rapid
inactivation of the functional acetyl-CoA synthetase after synthesis
has been stopped enables A. eutrophus to retain the capacity to metabo
lize acetate for prolonged periods while conserving minimal protein ex
penditure.