The temporal stability and diversity of bacterial species composition as well as the antilisterial potential of two different, complex, and undefined microbial consortia from red-smear soft cheeses were investigated. Samples were collected twice, at 6-month intervals, from each of two food producers, and a total of 400 bacterial isolates were identified by Fourier-transform infrared spectroscopy and 16S ribosomal DNA sequence analysis. Coryneform bacteria represented the majority of the isolates, with certain species being predominant. In addition, Marinolactobacillus psychrotolerans, Halomonas venusta, Halomonas variabilis, Halomonas sp. (10 6 to 10 7 CFU per g of smear), and an unknown, gram-positive bacterium (10 7 to 10 8 CFU per g of smear) are described for the first time in such a consortium. The species composition of one consortium was quite stable over 6 months, but the other consortium revealed less diversity of coryneform species as well as less stability. While the first consortium had a stable, extraordinarily high antilisterial potential in situ, the antilisterial activity of the second consortium was lower and decreased with time. The cause for the antilisterial activity of the two consortia remained unknown but is not due to the secretion of soluble, inhibitory substances by the individual components of the consortium. Our data indicate that the stability over time and a potential antilisterial activity are individual characteristics of the ripening consortia which can be monitored and used for safe food production without artificial preservatives.Traditional production of various foodstuffs such as kefir, sourdough, and red-smear cheeses includes the transfer of complex undefined microbial consortia from mature products to freshly prepared matrices. As of now it is not known whether the repeated transfer to fresh substrates, or their indigenous microflora, influences the composition of the respective consortia over time. In the case of red-smear cheeses, the microbial succession during surface ripening starts with the growth of yeasts, which metabolize the lactic acid present and raise the pH on the cheese surface from about 5.0 to about 6.0. When the pH is about 6.0, a salt-tolerant, usually very complex and undefined bacterial consortium begins to develop (8,13,29) and eventually covers the entire surface of the cheese. Despite their complex and undefined composition, analysis of bacterial surface-ripening floras of 19 different smeared cheeses yielded no indication that nonculturable bacteria contribute significantly to these floras (11). Bacterial surface floras consist mainly of a large number of coryneform species (3,4,14,33,37). Identification of coryneform bacteria usually is performed on the basis of physiological, phenotypic, and biochemical characteristics (18,19,24,32,33). These methods, however, do not always provide satisfactory results (5, 27), and they are both too laborious and too time-consuming to be performed on a routine basis. In contrast, molecular methods such as analysi...