Cultivation and preservation of vinegar bacteria

Abstract Ten strains of acetic acid bacteria were investigated for their characteristics of growth and metabolism. The strains were identified as those presently in use for industrial vinegar production in southern Germany. At the time of isolation from industrial acetators the total concentrations, i.e. acetic acid (w/v) plus ethanol (v/v), of the fermenting vinegars were 6.1–14.9%. The applicability of a previously described method for starter preparation was examined for the various isolates as well as for the type strains of species of the genera Gluconobacter and Acetobacter . Isolates from cider or wine vinegar fermentations grew readily in RAE-medium to total counts of >1×10 9 cells ml −1 . For the cultivation of strains isolated from spirit vinegar fermentations AE-medium proved most suitable. Cultures of these strains exhibited lag phases of 2–5 days and grew up to total counts of 9 cells ml −1 . All type strains could be grown on RAE-agar. The use of 20% malt extract as cryo-protectant was effective for the preservation of all strains. Upon revitalization the cultures were suitable as inoculum for starting fermentations in pilot acetators. 16S rRNA-targeted oligonucleotide probes were constructed which were species specific for Gluconobacter oxydans or Acetobacter aceti or group specific for Acetobacter europaeus / Acetobacter xylinum . The probes hybridized with the DNA of the respective type strains. Four isolates were allotted to A. europaeus / A. xylinum applying the group specific probe. The DNA of six of the Acetobacter sp. hybridized with none of the probes.

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