Esters are the major flavor compounds produced by Acetobacter sp. during vi
negar production. The two genes encoding the esterases in the bacteria were
disrupted, and the effects of the disruptions studied. When cultured in th
e presence of ethanol,, the est1 gene-disrupted mutant (DE1K) did not produ
ce any ethyl acetate or isoamyl acetate. However, the disruption of est2 di
d not affect the ester production. Ethyl acetate production by N-23 (pME122
P) and DE1K (pME122P), which contain est1, was 1.7-fold higher than that by
the wild type, N-23. On analyzing the relationship between ethyl acetate p
roduction and the extracellular ethanol and acetic acid concentrations, we
found that the highest amount of ethyl acetate was produced when the molar
ratio of ethanol and acetic acid was 1 : 1. These results indicate that the
ester production by Acetobacter sp. is mostly catalyzed by the intracellul
ar esterase, esterase-l, with ethanol and acetic acid used as the substrate
s.