Applied and Environmental Microbiology, January 2001, p. 125-132, Vol. 67, No. 1
0099-2240/01/$04.00+0 DOI: 10.1128/AEM.67.1.125-132.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
ID TNO Animal Nutrition, Lelystad,1 and Department of Microbiology, University of Groningen, Haren,2 The Netherlands
Received 15 May 2000/Accepted 11 October 2000
The degradation of lactic acid under anoxic conditions was studied
in several strains of Lactobacillus buchneri and in close relatives such as Lactobacillus parabuchneri,
Lactobacillus kefir, and Lactobacillus
hilgardii. Of these lactobacilli, L. buchneri and
L. parabuchneri were able to degrade lactic acid under
anoxic conditions, without requiring an external electron acceptor.
Each mole of lactic acid was converted into approximately 0.5 mol of acetic acid, 0.5 mol of 1,2-propanediol, and traces of ethanol. Based
on stoichiometry studies and the high levels of NAD-linked 1,2-propanediol-dependent oxidoreductase (530 to 790 nmol
min
1 mg of protein
1), a novel pathway for
anaerobic lactic acid degradation is proposed. The anaerobic
degradation of lactic acid by L. buchneri does not support
cell growth and is pH dependent. Acidic conditions are needed to induce
the lactic-acid-degrading capacity of the cells and to maintain the
lactic-acid-degrading activity. At a pH above 5.8 hardly any lactic
acid degradation was observed. The exact function of anaerobic lactic
acid degradation by L. buchneri is not certain, but some
results indicate that it plays a role in maintaining cell viability.
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