Changes in the gene expression profile of Acetobacter aceti during growth on ethanol

J Biosci Bioeng. 2012 Mar;113(3):343-8. doi: 10.1016/j.jbiosc.2011.11.005. Epub 2011 Dec 5.

Abstract

Acetobacter aceti NBRC 14818 shows a diauxic growth profile and temporarily accumulates acetate when grown in medium containing ethanol. However, the mechanisms underlying the metabolic switching between the incomplete oxidation of ethanol and overoxidation of acetate, and the control of stress resistance systems in A. aceti cells grown on ethanol are not fully understood. In this study, time-dependent transcriptome changes in cells during growth on ethanol were analyzed by DNA microarray. In A. aceti, ethanol is oxidized to acetate via acetaldehyde by sequential reactions of alcohol dehydrogenase (ADH) and aldehyde dehydrogenase (ALDH). We found that the genes encoding pyrroloquinoline quinone-dependent ADH, membrane-bound ALDH, and two NAD(+)-ADHs were expressed constitutively in cells throughout the culture period. In contrast, the expression levels of genes encoding tricarboxylic acid (TCA) cycle enzymes were low during acetate accumulation until ethanol was consumed, but were significantly upregulated after the accumulated acetate was started to be consumed. This result suggests that changes in the carbon metabolic flow through the TCA cycle are important for the metabolic switching from acetate accumulation to the overoxidation of acetate. In addition, the genes for glyoxylate pathway enzymes were significantly upregulated soon after the cells began oxidizing ethanol, indicating that this pathway is important for the utilization of ethanol as a carbon source.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetobacter / enzymology*
  • Acetobacter / genetics*
  • Acetobacter / metabolism
  • Alcohol Dehydrogenase / genetics*
  • Alcohol Dehydrogenase / metabolism
  • Ethanol / metabolism*
  • Gene Expression Profiling
  • Gene Expression Regulation, Bacterial*
  • Oligonucleotide Array Sequence Analysis

Substances

  • Ethanol
  • Alcohol Dehydrogenase