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Bacterial community dynamics during industrial malting, with an emphasis on lactic acid bacteria
A Justé1, S Malfliet2, M Waud1
1Laboratory for Process Microbial Ecology and Bioinspirational Management (PME&BIM), Department of Microbial and Molecular Systems (M(2)S), KU Leuven, Campus De Nayer, B-2860 Sint-Katelijne-Waver, Belgium; Scientia Terrae Research Institute, B-2860 Sint-Katelijne-Waver, Belgium; Leuven Food Science and Nutrition Research Centre (LFoRCe), KU Leuven, Belgium; Leuven Institute for Beer Research (LIBR), KU Leuven, Belgium.
Abstract:
Characterization of the microflora during malting is an essential step towards process management and optimization. Up till now, however, microbial characterization in the malting process has mostly been done using culture-dependent methods, probably leading to biased estimates of microbial diversity. The aim of this study was to characterize the bacterial communities using two culture-independent methods, including Terminal Restriction Fragment Length Polymorphism (T-RFLP) and 454 pyrosequencing, targeting the 16S rRNA gene. Studied samples originated from two harvest years and two malting houses malting the same batch of barley. Besides targeting the entire bacterial community (T-RFLP), emphasis was put on lactic acid bacteria (LAB) (T-RFLP and 454 pyrosequencing). The overall bacterial community richness was limited, but the community structure changed during the process. Zooming in on the LAB community using 454 pyrosequencing revealed a total of 47 species-level operational taxonomic units (OTUs). LAB diversity appeared relatively limited since 88% of the sequences were covered by the same five OTUs (representing members of Weissella, Lactobacillus and Leuconostoc) present in all samples investigated. Fluctuations in the relative abundances of the dominant LAB were observed with the process conditions. In addition, both the year of harvest and malting house influenced the LAB community structure.
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