Functional analysis of the acetic acid resistance (aar) gene cluster in Acetobacter aceti strain 1023

Main Article Content

Elwood A. Mullins
T. Joseph Kappock *
(*) Corresponding Author:
T. Joseph Kappock |


Vinegar production requires acetic acid bacteria that produce, tolerate, and conserve high levels of acetic acid. When ethanol is depleted, aerobic acetate overoxidation to carbon dioxide ensues. The resulting diauxic growth pattern has two logarithmic growth phases, the first associated with ethanol oxidation and the second associated with acetate overoxidation. The vinegar factory isolate Acetobacter aceti strain 1023 has a long intermediate stationary phase that persists at elevated acetic acid levels. Strain 1023 conserves acetic acid despite possessing a complete set of citric acid cycle (CAC) enzymes, including succinyl-CoA:acetate CoA-transferase (SCACT), the product of the acetic acid resistance (aar) gene aarC. In this study, cell growth and acid production were correlated with the functional expression of aar genes using reverse transcription-polymerase chain reaction, Western blotting, and enzyme activity assays. Citrate synthase (AarA) and SCACT (AarC) were abundant in A. aceti strain 1023 during both log phases, suggesting the transition to acetate overoxidation was not a simple consequence of CAC enzyme induction. A mutagenized derivative of strain 1023 lacking functional AarC readily oxidized ethanol but was unable to overoxidize acetate, indicating that the CAC is required for acetate overoxidation but not ethanol oxidation. The primary role of the aar genes in the metabolically streamlined industrial strain A. aceti 1023 appears to be to harvest energy via acetate overoxidation in otherwise depleted medium

Downloads month by month


Download data is not yet available.

Article Details

Author Biographies

Elwood A. Mullins, Department of Biochemistry, Purdue University, West Lafayette, Indiana; Department of Chemistry, Washington University in St. Louis, St. Louis, Missouri

Graduate Student

T. Joseph Kappock, Department of Biochemistry, Purdue University, West Lafayette, Indiana

Assistant Professor