Academic literature on the topic 'Fresh lactic curd cheese'

This study evaluated the microbial quality, safety, and ecology of a retail delicatessen Galotyri-like fresh acid-curd cheese traditionally produced by mixing fresh natural Greek yogurt with ‘Myzithrenio’, a naturally fermented and ripened whey cheese variety. Five retail cheese batches (mean pH 4.1) were analyzed for total and selective microbial counts, and 150 presumptive isolates of lactic acid bacteria (LAB) were characterized biochemically. Additionally, the most and the least diversified batches were subjected to a culture-independent 16S rRNA gene sequencing analysis. LAB prevailed in all cheeses followed by yeasts. Enterobacteria, pseudomonads, and staphylococci were present as <100 viable cells/g of cheese. The yogurt starters Streptococcus thermophilus and Lactobacillus delbrueckii were the most abundant LAB isolates, followed by nonstarter strains of Lactiplantibacillus, Lacticaseibacillus, Enterococcus faecium, E. faecalis, and Leuconostoc mesenteroides, whose isolation frequency was batch-dependent. Lactococcus lactis isolates were sporadic, except for one cheese batch. However, Lactococcus lactis, Enterobacteriaceae, Vibrionaceae, Salinivibrio, and Shewanellaceae were detected at fairly high relative abundances culture-independently, despite the fact that their viable counts in the cheeses were low or undetectable. Metagenomics confirmed the prevalence of S. thermophilus and Lb. delbrueckii. Overall, this delicatessen Galotyri-like cheese product was shown to be a rich pool of indigenous nonstarter LAB strains, which deserve further biotechnological investigation.

Some of the textural changes that occur early in cheese maturation may be related to the redistribution of water within the cheese matrix. To examine this, a model cheese curd system was devised and explored. Initially, cheese curd was prepared using starter and chymosin and the curd pH was controlled by varying the draining and salting pH values. The quantity of serum that could be centrifuged from the resultant curd was less for lower pH curd and decreased in volume with time. The curd pH decreased with time. In the protocol finally adopted, milk was acidified with lactic acid and coagulated with Rennilase 46L. After cheddaring, salting and light pressing, the samples of this curd were finely diced and mixed with glucono-δ-lactone to give curd samples with comparable moisture contents, similar casein proteolysis rates but different pH values. The quantity of serum that could be centrifuged from these samples was greater for pH 5·6 curd than for pH 5·2 curd and decreased faster for the lower pH curd. Neither the curd moisture nor the pH changed significantly during curd storage and the casein proteolysis was low. These results for the model curd system are consistent with known water absorption characteristics of casein curd under ‘equilibrium’ conditions and the effects of pH and mineral salts on this absorption. It was concluded that, during the early stages of cheese ripening, there may be a redistribution of moisture within the cheese, related to the basic properties of the protein matrix and the transient effects of curd salting, rather than as a direct consequence of glycolytic and proteolytic changes.

Abstract Background: Monitoring the acidity of cheese is an important control mechanism in various stages of manufacture, including aging. Acid development in cheesemaking is essential to cheese flavor, texture, and safety. Objective: The aim of the work was to develop and validate calibration models by using NIR spectroscopy, which allows for the monitoring of changes in cheese acidity (pH and titration acidity) during cheese ripening. Methods: Cheeses were analyzed by an FT-NIR spectrometer. Each of the samples was analyzed three times, and for calibration, an average spectrum was used. A partial least-squares regression was used to develop calibration models. The constructed calibration models were validating by full cross-validation. Results: Calibration models were created with a high correlation coefficient for the following cheese pH levels: blue cheese (0.966), Olomouc curd read smear cheese (0.984), and fresh goat cheese (0.980). Results of the calibration of titratable acidity are functional for fresh goat cheese (0.953) and mozzarella (0.999). Conclusions: The results of these new calibration methods showed the possibility of NIR technology for the fast determination of pH and titratable acidity. Highlights: Detection of cheese acidity using FT-NIR spectrometry enables rapid evaluation of the process of lactic acidification in particular cheese technological operations, including the maturing of cheeses.

Red grape Nero d’Avola cultivar grape pomace powder (GPP) was applied during fresh ovine cheese production in order to increase polyphenol content. Before cheeses were produced, the bacteria of a freeze-dried commercial starter culture were isolated and tested in vitro against GPP. Two dominant strains, both resistant to GPP, were identified. Thestarter culture was inoculated in pasteurized ewe’s milk and the curd was divided into two bulks, one added with 1% (w/w) GPP and another one GPP-free. GPP did not influence the starter culture development, since lactic acid bacteria (LAB) counts were 109 CFU/g in both cheeses at 30 d. To exclude the interference of indigenous LAB, the pasteurized milk was analyzed, and several colonies of presumptive LAB were isolated, purified and typed. Four strains were allotted into Enterococcus and Lacticaseibacillus genera. The direct comparison of the polymorphic profiles of cheese bacteria evidenced the dominance of the starter culture over milk LAB. The addition of GPP increased cheese total phenolic compounds by 0.42 g GAE/kg. Sensory evaluation indicated that GPP-enriched cheese was well appreciated by the judges, providing evidence that GPP is a suitable substrate to increase the availability of total phenolic content in fresh ovine cheese.

The idea was to develop powders for fresh/hard cheese or quark production comprising milk proteins in optimal composition and functional properties for manufacturing each of those cheese types. The aim was to avoid whey protein drainage by their prior removal or by their heat-induced structural integration in the curd. The pre-renneted powders already contain additives such as starter cultures and calcium chloride to instantaneously form homogeneous curds upon reconstitution. The impact of the casein/whey protein ratio (86:14 by ultrafiltration and 98:2 by microfiltration) and upfront heat treatment (80 °C/30 min) on the gelling behavior of reconstituted rennet gels and on the survival rate of integrated Lactobacillus paracasei ssp. paracasei F19 was investigated. The assessment criteria for the rennet gelation were curd firming rate, gel strength, and whey drainage. Furthermore, the amount of integrated whey proteins and the resulting cheese yield were evaluated. It could be shown that heating had a positive effect on the viable cell count of the bacteria after spray drying and on the gelation behavior of the reconstituted ultrafiltration concentrates. The curd firming rate and the gel strength could be increased to higher values than the reconstituted microfiltration concentrate at 25% total solids.

Comlek peyniri is a typical artisanal cheese in Central Anatolia. This type of cheese was made by using the indigenous lactic acid bacteria (LAB) flora of cow or ewes' milk. Majority of the samples were taken from fresh cheese because the aim was to isolate homofermentative LAB. Initially 661 microbial isolates were obtained from 17 cheese samples. Only 107 were found to be homofermentative LAB. These isolates were selected and identified by using both phenotypic and molecular methods. Phenotypic identification included curd formation from skim milk, catalase test, Gram staining and light microscopy, growth at different temperatures and salt concentrations, arginine hydrolysis, gas production from glucose, and carbohydrate fermentation. Molecular identification was based on the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) of the 16S rRNA gene-ITS (internally transcribed spacer) region. By combining the phenotypic and molecular identification results, isolates belonging to each of the following genera were determined at species or subspecies level: 54 Lactococcus lactis subsp. lactis, 21 Enterococcus faecium, 3 Ec. faecalis, 2 Ec. durans, 10 Ec. sp., 15 Lactobacillus paracasei subsp. paracasei, and 2 Lb. casei strains. Technological characterisation was also performed by culturing each of the strains in UHT skim milk, and by monitoring pH change and lactic acid production at certain time intervals through the 24 h incubation. Results of the technological characterisation indicated that 33% of the isolates (35 strains) were capable of lowering the pH of UHT milk below 5·3 after 6 h incubation at 30 °C. Thirty four of these strains were Lc. lactis subsp. lactis, and only one was an Ec. faecium strain.

One of the traditional fresh cheeses in Ecuador is the artisanal leafcheese, a kind of stretched-curd cheese. The artisanal product is wrapped in achira leaves (Canna indica), while the industrial leafcheese is packed at vacuum in high density polyethylene bags. In this study the microbiological quality of both products was compared. The hygienic-sanitary microbial indicators and lactic acid bacteria (LAB) were quantified. The LAB isolated were characterized phenotypically. The samples were obtained from artisanal cheese-making and industrial located in Latacunga city province Cotopaxi. The total aerobic mesophilic count was made based on national regulations (NTE INEN 1529 5); total coliforms, Escherichia coli and Staphylococcus aureus was evaluated using petrifilm methods (AOAC 991.14 – AOAC 2003.07) and to LAB was used PRT-712.02-047. The results show high quantities of total coliforms, E. coli and S. aureus in both products, these data exceed the limits of acceptability established in Ecuadorian regulations, this evidence poor hygienic quality of the processes or incorrect controls of milk as raw material. The lactic acid bacteria count showed statistically significant differences, the industrial cheeses had a reduction of 18,15% of Lactobacillus and 14,27% of Lactococcus compared with artisanal cheeses. A total of 32 strains of lactic acid bacteria were isolated, these showed similar phenotypic characteristics, but these had a different response at the level of pH (4,4;9,4) and NaCl (6,5%). The sensory evaluation will be an important complement in this type of study.

The bacterial community of the artisanal Adobera cheese from Los Altos de Jalisco was described through high-throughput sequencing of 16S rRNA gene libraries. Samples were collected in two different seasons (dry and rainy) during four key steps of the manufacturing process (raw milk, fresh curd, matured curd, and cheese). Bacterial diversity was higher in early steps in comparison with the final elaboration stages. Firmicutes and Proteobacteria were the most abundant phyla, strongly represented by the Streptococcaceae, Enterobacteriaceae and Lactobacillaceae families, and core bacteria genera such as Streptococcus spp., Lactococcus spp., and Lactobacillus spp. Undesirable bacteria, including Pseudomonas spp. and Acinetobacter spp., were also detected in raw milk but almost undetectable at the end of the cheese manufacturing process, and seemed to be displaced by lactic-acid bacteria-related genera. Seasonal effects were observed on the community structure but did not define the core microbiota composition. Predictive metabolism was related to membrane transport, and amino-acid, lipid, and carbohydrate metabolism pathways. Our results contribute to deduce the role of bacteria involved in Adobera cheese manufacturing in terms of the metabolism involved, cheese microbial safety, and how undesirable bacterial populations could be regulated by process standardization as a potential tool to improve safety.

Minas cheese is a typical Brazilian fresh cheese, manufactured by addition of rennin and CaCl2 to milk, followed by draining the curd. The intrinsic characteristics of this product make it favorable for growth of pathogens, including Escherichia coli O157:H7. The influence of the addition of a commercial mesophilic type O lactic culture to this product on the growth of this pathogen during storage at 8.5°C was evaluated. Eight different formulations of Minas cheese were manufactured using raw or pasteurized milk and with or without salt and lactic culture. Individual portions of each formulation were transferred to sterile plastic bags and inoculated with E. coli O157:H7 to yield ca. 103 or 106 CFU/g. After blending by hand massaging the bags, samples were stored at 8.5°C for up to 14 days. E. coli O157:H7 was counted after 1, 2, 7, and 14 days of storage using 3M Petrifilm Test Kit-HEC. Counts in samples without added lactic culture showed a 2-log increase in the first 24 h and remained constant during the following 14 days. Counts in samples with added lactic culture showed a 0.5-log increase in the first 24 h, followed by a decrease. These variations were statistically significant (P &lt; 0.05). No significant variations (P &gt; 0.05) were obtained for cheese samples manufactured with pasteurized or raw milk, with or without salt. Results indicate that the addition of type O lactic culture may be an additional safeguard to well-established good manufacturing practices and hazard analysis and critical control point programs in the control of growth of E. coli O157:H7 in Minas cheese.

Making cheese from donkey and mares milk is considered unfeasible, due to difficulties in coagulation and curd forming. Encyclopedia of Dairy Sciences 2nd edition (2011) reported that no cheese is made from equid milk. However in 2015 a pioneering study of Iannella have reported the first protocols for making fresh donkey and mares cheese, subsequently there have been only a few protocols by other researchers. Anyhow, the low cheese yield of these protocols together with a higher cost of production of the raw material currently limit practical application. Also the processing of camel milk into cheese is technically more difficult than milk from other domestic dairy animals which may relate to the poor rennetability of camel milk. Therefore, a research project was planned by Iannella which has developed a technological procedure to produce cheese from camel, donkey and mares milk with a high transformation yield by the use of locust bean gum, k- carrageenan and lactic coagulation in a dedicated process, thus with a mini mal adjustments in the manufacturing technology and equipment. The whey proteins of milk with this method are withheld and this improve the efficiency of making cheese and increase further yield of cheese however preserving body and texture similar of cheese prepared by conventional processes. In the near future this protocol or similar, they could represent a source of innovative cheese and the development definitive of a new commercial scale of cheese from donkey, mares or camel milk or from others minor milks at the same time improving food and animal biodiversity and therefore all the ensuing benefits.

Outgrowth of spoilage yeasts and moulds and post-processing acidification can limit the shelf-life of some fermented dairy products including fresh lactic curd cheeses. The possibility of using high pressure processing (HPP) for controlling these problems was investigated in a commercially manufactured fresh lactic curd cheese (pH 4.3-4.4) and fermented milk models (pH 4.3-6.5). The effects of HPP at 300 and 600 MPa on inactivation of glycolytic enzymes of lactic acid bacteria were also evaluated. Fresh cheeses made from pasteurised bovine milk using a commercial Lactococcus starter preparation were treated with high pressures ranging from 200 to 600 MPa (less than or equal to 22°C, 5 min) under vacuum packaging conditions and subsequently stored at 4°C for 8 weeks. Treatment at greater than or equal to 300 MPa substantially reduced the viable count of Lactococcus and effectively prevented the outgrowth of yeasts and moulds for 6 to 8 weeks without adversely affecting the sensory and textural attributes of the product. However, it had no significant effects (p less than 0.01) on variation of titratable acidity during storage. Fermented milk models were prepared by individually growing Lactococcus lactis subsp. lactis C10, Lactococcus lactis subsp. cremoris BK5, Streptococcus thermophilus TS1, Lactobacillus acidophilus 2400 and Lactobacillus delbrueckii subsp. bulgaricus 2517 in UHT skim milk and diluting the resulting fermented milk with UHT skim milk up to pH 6.5. Pressure treatment of the milk models at pH 5.2 resulted in substantial inhibition of post-processing acidification during storage and markedly reduced the viable count of Lactococcus at both 300 and 600 MPa and other bacteria only at 600 MPa. Treatment of the milk model at 600 MPa decreased the viable counts of Candida zeylanoides and Candida lipolytica (wildtype spoilage yeasts of lactic curd cheese, added as challenge cultures) from 105 CFU mL-1 to below the detection limit (log 0 CFU mL-1) at all pH levels tested (pH 4.3-6.5) and effectively controlled their outgrowth for 8 weeks. Treatment of milk model at 300 MPa had a similar effect only on C. zeylanoides. The viable count of C. lipolytica was reduced by 2.6, 2.4 and 2.3 logs by treatment at 300 MPa at pH levels of 4.3, 5.2 and 6.5, respectively, which subsequently recovered by 2.9, 2.8 and 3.2 logs within 3 weeks. Glycolytic enzymes of various starter bacteria showed different responses to pressure treatment. The lactate dehydrogenase in L. lactis subsp. lactis and Lb. acidophilus was quite resistant to pressures up to 600 MPa, but it was almost completely inactivated in S. thermophilus at pressure levels as low as 300 MPa. The â-galactosidase in Lb. acidophilus was more pressure stable than â-galactosidase in S. thermophilus and Phospho-â-galactosidase in L. lactis subsp. lactis. The findings of this study suggests HPP at 300-600 MPa as an effective method for controlling the outgrowth of some spoilage yeasts and moulds in fresh lactic curd cheeses. The results obtained with selected lactic acid bacteria in fermented milk models can be used to assist in establishing HPP operating parameters for development of new generation cultured dairy products, of reduced acidity and extended shelf-life.

Mestrado em Engenharia Alimentar - Instituto Superior de Agronomia
The aim of this study was the production of fresh goat cheese, with a soft, easy to spread paste, and slightly acidic flavor, using a production line established in dairy Flor de Cardo, S.A.. To be able to use this line, whose settings are programmed into enzymatic coagulation, and expecting to get a final product with characteristics as close to those for cheese obtained by acid coagulation, it was necessary to adjust the manufacturing process, eventually through induced acidification of the curd. This acidification would cause a decrease in pH, an increase in demineralization of the curd, and consequently a final product with desired textural and taste properties. To achieve this acidification, three different methods were tested: addition of a chemical acidifying agent (gluco-δ-lactone); addition of a direct vat set starter culture before coagulation, and incorporation of a pre-multiplied starter culture, at the same stage. Evaluations showed that the most appropriate methodology was the incorporation of a pre-multiplied starter culture, to promote the lowering of pH values below 5.5, during manufacture, and not during the retention period. Therefore we need a faster acidification, either by adjusting the proportion of inoculum, or by modifying the type of lactic starter used.

O presente estudo teve por finalidade avaliar os efeitos da contagem de células somáticas (CCS) no leite cru (nos níveis de 100-200.000, 400-500.000 e >800.000 céls./mL) sobre as características físicas, químicas, microbiológicas, sensoriais e funcionais dos queijos Minas Frescal e tipo Mussarela. Utilizou-se um delineamento experimental em parcelas subdivididas em blocos, considerando-se a contagem de células somáticas como efeito principal, os dias de análise como subparcelas e os processamentos como blocos. Cada tipo de leite foi obtido da ordenha de animais previamente selecionados de acordo com o nível de células somáticas. As etapas de elaboração dos queijos incluíram a pasteurização do leite (65º C, 30 minutos), adição de cloreto de cálcio, fermento (para a Mussarela) e coalho, coagulação e obtenção do coágulo, dessoragem, salga na massa, filagem, moldagem, salga na salmoura (para a Mussarela), e embalagem dos produtos. Os queijos foram mantidos em B.O.D. a 4 ºC e avaliados nos dias 2, 9, 16, 23 e 30 após a fabricação. A seqüência de elaboração dos queijos Minas e tipo Mussarela foi repetida 5 e 3 vezes, respectivamente, para cada tratamento. As análises realizadas nos queijos foram: pH, acidez, percentuais de gordura, matéria seca (MS), cinzas, nitrogênio total (NT), nitrogênio não protéico (NNP), nitrogênio não caseinoso (NNC), índice de proteólise, ácidos graxos livres (AGL), textura, avaliação sensorial, propriedades funcionais (capacidade de derretimento a 107 ºC e percentual de óleo livre - somente no queijo tipo Mussarela), contagem de mesófilos, psicrotróficos e número mais provável a 35 e 45 ºC. No queijo Minas Frescal, não houve interação entre CCS e dias de armazenamentos nas avaliações físico-químicas, microbiológicas, funcionais e índice de lipólise, porém houve efeito significativo (P<0,05) para índices de proteólise e profundidade da proteólise. Já para mesófilos, psicrotróficos, acidez, matéria seca, firmeza e ácidos graxos livres houve efeito significativo (P<0,05) ao avaliar dias de armazenamento. A avaliação sensorial, no primeiro dia de análise, não apresentou diferença significativa nos atributos, porém o queijo de alta CCS (> 800.000 céls./mL) diferiu dos demais no dia 30, em que recebeu menor nota em todas as características. No queijo tipo Mussarela, houve interação entre CCS e dias de armazenamento apenas para a capacidade de derretimento, resultando em aumento do derretimento no decorrer do tempo. Para as características de pH, ácidos graxos livres, índices de proteólise, extensão e profundidade da proteólise, mastigabilidade e elasticidade houve efeito significativo (P<0,05) para dias de armazenamento. Entre os atributos avaliados na sensorial, apenas a aparência apresentou diferença entre tratamentos. O rendimento dos queijos, Minas frescal e tipo Mussarela, não foram influenciados pela quantidade de células somáticas dos leites. Os resultados do trabalho indicaram que o leite destinado à fabricação dos queijos Minas e tipo Mussarela deve apresentar CCS até 400-500.000 céls./mL, de maneira a evitar alterações na qualidade dos produtos ao longo do período de armazenagem.
The aim of the present study was to evaluate the effect of somatic cells counts (SCC) in raw milk (at levels of 100-200,000, 400-500,000 and 800,000 cells./mL) on physical, chemical, microbiological, sensorial and functional characteristics of Minas frescal and Mozzarella type cheeses. A completely randomized block design was used, considering SCC as the main effect, the days of analysis as sub parcels and the processing batches as the blocks. Each type of milk was obtained from cows previously selected according to its individual SCC. The manufacture of cheeses included: pasteurization of milk (65ºC, 30 minutes), addition of calcium chloride, starter culture (for Mozzarella) and rennet, coagulation and separation of the curd, whey drainage, salting (for Minas cheese), stretching of the curd, kneading and salting in brine (for Mozzarella), and packing the products. The cheeses were stored in a B.O.D. oven at 4ºC and evaluated on days 2, 9, 16 23 and 30 after the manufacture. The sequence of elaboration of the Minas frescal and Mozzarella cheeses was repeated 5 and 3 times, respectively, for each treatment. The analyses carried out in the cheeses were: pH, acidity, percentages of fat, dry matter (DM), ashes, total nitrogen (NT), non-protein-nitrogen (NPN), non-casein nitrogen (NCN), proteolysis, free fatty acids (FFA), texture, sensorial evaluation, functional properties (melting capacity the 107 ºC and percentage of free oil - only in the cheese Mozzarella), mesophile and psychrotrophic counts and the most probable number at 30 and 45ºC. For Minas frescal cheese, no interaction was found between SCC and days of storage when considering the data on chemical, physical, microbiological, functional and lipolysis index. However, a significant effect (P<0.05) was observed for proteolysis and depth of proteolysis. For mesophiles, psychrotrophics, acidity, dry matter, firmness and free fatty acids, there was a significant effect (P<0.05) for days of storage. The sensorial evaluation made on the first day of analysis did not present significant differences for all attributes. However, the Minas cheese made with high SCC (800,000 cells/mL) differed on day 30, when it received worse grades for all the attributes. For the Mozzarella cheese, an interaction between SCC and days of storage was observed only for the melting capacity, which resulted in an increment of the melting along the time of storage. The parameters of pH, free fatty acid, proteolysis, extension and depth of proteolysis, springiness and elasticity had significant effect (P<0.05) for days of storage. Amongst the attributes evaluated in the sensorial, only the appearance presented difference between treatments. The yield of Minas frescal and Mozzarella cheese was not influenced by the amount of somatic cells in the original milk. Results indicated that milk used for the manufacture of Minas frescal and Mozzarella cheeses should present SCC up to 400-500,000 cells/mL, in order to avoid quality changes in those products during storage.

Mestrado em Engenharia Alimentar - Instituto Superior de Agronomia
This work aimed to carry out preliminary studies to develop a fresh goat cheese, with contribution of lactic fermentation, having a sour taste and a spreadable and smooth paste. The experimental tests were carried out in the “Flor de Cardo” dairy, following a Response Surface Methodology experimental design, with two milk-clotting factors, the proportions of coagulant and starter culture The experimental trials were followed by physical-chemical analysis, and cheeses were submitted also to a panel of tasters and to the texture profile analysis. The product closest to the aim of this work was obtained by acid coagulation, but this type of coagulation it’s not viable for the kind of production lines installed in this dairy factory, considering mainly the existing equipment for moulding. The rennet coagulation based procedure, which appeared to be the right type of technology, was unsuitable given the lack of whey draining in the clotting vat, leading to an excess of whey in cheese and extensive in mould acidification, during the storage period in study.

Dissertação de Mestrado em Tecnologia e Segurança Alimentar
[…]. O presente trabalho teve como objectivo a selecção de estirpes BAL previamente isoladas do queijo do Pico (DOP), avaliando a actividade antimicrobiana e a sua eficácia contra a Listeria monocytogenes no queijo fresco. As propriedades tecnológicas e segurança das BAL produtoras de bacteriocinas foram igualmente investigadas para avaliar a capacidade para serem utilizadas como culturas de arranque e/ou adjuntas no fabrico do queijo. Os isolados foram caracterizados pelas suas propriedades tecnológicas: produção de diacetilo, actividades enzimáticas, proteólise e lipólise. A sua segurança foi avaliada através do estudo da actividade β-hemolítica, produção de DNase, gelatinase e histamina, e resistência aos antibióticos. Foi testada a produção de bacteriocinas pelas BAL, bem como a cinética de crescimento, pH e produção de ácido láctico no queijo fresco. Nestes queijos inoculados com as BAL produtoras de bacteriocinas, foi ainda realizada uma avaliação sensorial por um painel de provadores não treinados. […].
ABSTRACT: […]. The purpose of this study was to select LAB strains with antimicrobial activity, previously isolated from Pico cheese, and evaluate their efficacy against Listeria monocytogenes in fresh cheese. In addition, the technological and safety relevant properties from bacteriocin-producing LAB were investigated in order to determine their ability for the efficient use as starter/adjunct cultures in cheese making. Isolates were characterised in terms of their main technological properties: diacetyl production, enzymatic activities, proteolysis and lipolysis. Their safety was also evaluated by studying their β-haemolytic activity, production of DNase, gelatinase and histamine, and antibiotic resistance. Bacteriocin production by LAB was tested in fresh cheese, including LAB growth kinetics, cheese pH and titratable acidity. Additionally, the sensorial attributes of fresh cheeses made with these LAB as adjunct cultures were evaluated by a non-trained panel. […].