A rapid method for detecting Lactobacillus brevis, L. casei, and L. plantarum from beer was developed using the polymerase chain reaction (PCR). Regions of the 16S rRNA sequences unique to each organism were used to generate species-specific PCR products, which were visualized by gel electrophoresis. Small numbers of these bacteria were isolated from water and beer by membrane filtration and membrane dissolution, before the PCR reaction. This method for detecting spoilage lactic acid bacteria was rapid and sensitive and allowed identification at the species level. However, beer contained a PCR inhibitor that decreased sensitivity.
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DiMichele et al. (1993) studied this question.
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