PCR–DGGE fingerprints of microbial succession during a manufacture of traditional water buffalo mozzarella cheese

• Published in: Journal of applied microbiology 2004-02, Vol.96 (2), p.263-270
• Main Authors: Ercolini, D., Mauriello, G., Blaiotta, G., Moschetti, G., Coppola, S.
• Format: Article
• Language: English
• Subjects: Animals; Biodiversity; Biological and medical sciences; Cheese - microbiology; Colony Count, Microbial - methods; Culture Media; DNA Fingerprinting - methods; DNA, Bacterial - analysis; Electrophoresis - methods; Food Handling - methods; Food industries; Food Microbiology; Fundamental and applied biological sciences. Psychology; Lactic Acid - metabolism; microbial diversity; Microbiology; Milk - microbiology; Milk and cheese industries. Ice creams; natural whey culture; PCR–DGGE analysis; Polymerase Chain Reaction - methods; product identity; quality control; starter effectiveness; Streptococcus - isolation & purification; tracing system; water buffalo mozzarella cheese
• ISSN: 1364-5072; 1365-2672
• DOI: 10.1046/j.1365-2672.2003.02146.x

Aims:  To monitor the process and the starter effectiveness recording a series of fingerprints of the microbial diversity occurring at different steps of mozzarella cheese manufacture and to investigate the involvement of the natural starter to the achievement of the final product. Methods and Results:  Samples of raw milk, natural whey culture (NWC) used as starter, curd after ripening and final product were collected during a mozzarella cheese manufacture. Total microbial DNA was directly extracted from the dairy samples as well as bulk colonies collected from the plates of appropriate culture media generally used for viable counts of mesophilic and thermophilic lactic acid bacteria (LAB) and used in polymerase chain reaction–denaturing gradient gel electrophoresis (PCR–DGGE) experiments. The analysis of the DGGE profiles showed a strong influence of the microflora of the NWC on the whole process because after the starter addition, the profile of all the dairy samples was identical to the one shown by the NWC. Simple indexes were calculated for the DGGE profiles to have an objective estimation of biodiversity and of technological importance of specific groups of organisms. LAB grown on Man Rogosa Sharp (MRS) and Rogosa agar at 30°C showed high viable counts and the highest diversity in species indicating their importance in the cheese making, which had not been considered so far. Moreover, the NWC profiles were shown to be the most similar to the curd profile suggesting to be effective in manufacture. Conclusions:  The PCR–DGGE analysis showed that in premium quality manufacture the NWC used as starter had a strong influence on the microflora responsible for process development. Significance and Impact of the Study:  The molecular approach appeared to be valid as a tool to control process development, starter effectiveness and product identity as well as to rank cheese quality.