Escherichia coli strain F-122 was used to determine if there are addit
ional physiological effects, other than decreasing energetic efficienc
y accompanied by the excretion of the acetate, on foreign protein prod
uction. This organism was the host for expressing HIV582-beta-galactos
idase fusion protein under the control of the trp promoter, with ampic
illin resistance. By comparing parallel batch cultures with in the med
ia did not influence beta-galactosidase activity. In these experiments
, it appears that the low protein productivity often observed during a
cetate formation is the result of inefficient cell metabolism, rather
than acetate acting as a specific inhibitor of protein production.