Antimicrobial activity of clove and cinnamon essential oils against Listeria monocytogenes in pasteurized milk

The antimicrobial activity of essential oils (EOs) of cinnamon bark, cinnamon leaf, and clove against Listeria monocytogenes Scott A were studied in semiskimmed milk incubated at 7 degrees C for 14 days and at 35 degrees C for 24 h. The MIC was 500 ppm for cinnamon bark EO and 3,000 ppm for the cinnamon leaf and clove EOs. These effective concentrations increased to 1,000 ppm for cinnamon bark EO, 3,500 ppm for clove EO, and 4,000 ppm for cinnamon leaf EO when the semiskimmed milk was incubated at 35 degrees C for 24 h. Partial inhibitory concentrations and partial bactericidal concentrations were obtained for all the assayed EOs. The MBC was 3,000 ppm for the cinnamon bark EO, 10,500 ppm for clove EO, and 11,000 ppm for cinnamon leaf EO. The incubation temperature did not affect the MBC of the EOs but slightly increased the MIC at 35 degrees C. The increased activity at the lower temperature could be attributed to the increased membrane fluidity and to the membrane-perturbing action of EOs. The influence of the fat content of milk on the antimicrobial activity of EOs was tested in whole and skimmed milk. In milk samples with higher fat content, the antimicrobial activity of the EOs was reduced. These results indicate the possibility of using these three EOs in milk beverages as natural antimicrobials, especially because milk beverages flavored with cinnamon and clove are consumed worldwide and have been increasing in popularity in recent years.     

Properties of Cassava Starch‐Based Edible Coating Containing Essential Oils

Edible coatings were produced using cassava starch (2% and 3% w/v) containing cinnamon bark (0.05% to 0.30% v/v) or fennel (0.05% to 0.30% v/v) essential oils. Edible cassava starch coating at 2% and 3% (w/v) containing or not containing 0.30% (v/v) of each essential oils conferred increased in water vapor resistance and decreased in the respiration rates of coated apple slices when compared with uncoated fruit. Cassava starch coatings (2% w/v) added 0.10% or 0.30% (v/v) fennel or cinnamon bark essential oils showed antioxidant capacity, and the addition of 0.30% (v/v) of each essential oil demonstrated antimicrobial properties. The coating containing cinnamon bark essential oil showed a significant antioxidant capacity, comparing to fennel essential oil. Antimicrobial tests showed that the addition of 0.30% (v/v) cinnamon bark essential oil to the edible coating inhibited the growth of Staphylococcus aureus and Salmonella choleraesuis, and 0.30% fennel essential oil inhibited just S. aureus. Treatment with 2% (w/v) of cassava starch containing 0.30% (v/v) of the cinnamon bark essential oil showed barrier properties, an antioxidant capacity and microbial inhibition.     

Comparative evaluation of antioxidant and anti food-borne bacterial activities of essential oils from some spices commonly consumed in Iran

The antioxidant potency, anti food borne bacterial activity, and total phenolic contents of essential oils (EOs) from avishane shirazi (Zataria multiflora), clove (Syzgium aromaticum), cinnamon (Cinnamomum zeylanicum), cumin (Cuminum cyminum), black cumin (Bunium persicum), spearmint (Mentha spicata), horsemint (Mentha longifolia), coriander (Coriandrum sativum), sage (Salvia officinalis), and ginger (Zingiber officinale) were evaluated. In 2,2-diphenyl-1-picrylhydrazyl (DPPH) assay, free radical scavenging activities of clove and avishane shirazi EOs were 90.69% and 88.63%, respectively. In reducing power assay, the EO of clove showed the highest reducing capacity. The highest concentrations of total phenolics (66.01 mg and 44.81 mg GAE/gram sample) were also detected for the EOs of clove and avishane shirazi, respectively. The results of disc diffusion assay showed that the EOs of avishane shirazi, cinnamon, and clove strongly inhibited growth of the tested bacteria. The EO of cinnamon had the lowest minimal inhibitory concentration (MIC) (0.312 mg/mL).     

Mycotoxicogenic fungal inhibition by innovative cheese cover with aromatic plants

BACKGROUND: The use of aromatic plants and their extracts with antimicrobial properties may be compromised in the case of cheese, as some type of fungal starter is needed during its production. Penicillium verrucosum is considered a common cheese spoiler. The aim of this study was to evaluate the innovative use of certain aromatic plants as natural cheese covers in order to prevent mycotoxicogenic fungal growth (P. verrucosum). A collection of 12 essential oils (EOs) was obtained from various aromatic plants by solvent‐free microwave extraction technology, and volatile characterisation of the EOs was carried out by gas chromatography/mass spectrometry. RESULTS: The most effective EOs against P. verrucosum were obtained from Anethum graveolens, Hyssopus officinalis and Chamaemelum nobile, yielding 50% inhibition of fungal growth at concentration values lower than 0.02 µL mL^?1. All EOs showed high volatile heterogeneity, with α‐phellandrene, pinocamphone, isopinocamphone, α‐pinene, camphene, 1,8‐cineole, carvacrol and trans‐anethole being found to be statistically significant in the antifungal model. CONCLUSION: The use of these aromatic plants as natural covers on cheese can satisfactorily inhibit the growth of some mycotoxicogenic fungal spoilers. Among the volatile compounds present, α‐ and β‐phellandrene were confirmed as the most relevant in the inhibition. © 2012 Society of Chemical Industry     

Application of plant essential oils in prevention of fungal growth on Para rubber wood

Antifungal activities of essential oils (cinnamon, clove, eucalyptus, peppermint and lemongrass oils) against moulds (Penicillium sp., Aspergillus niger and Aspergillus versicolor) isolated from rubber wood surfaces were examined. Clove oil possessed consistent antifungal activity with the minimal inhibitory concentration (MIC) of 5 μl ml^?1 against all these fungi, while cinnamon oil had MICs from 2.5 to 10 μl ml^?1. However, only dip treatment with cinnamon oil inhibited the growth of A. niger on rubber wood for at least 25 weeks.     

Prolonging Storage Time of Baby Ginger by Using a Sand‐Based Storage Medium and Essential Oil Treatment

Wilt and rot occur readily during storage of baby ginger because of its tender skin and high moisture content (MC). A storage medium, which consisted of sand, 20% water, and 3.75% super absorbent polymers delayed weight loss and loss of firmness at 12 °C and 90% relative humidity. Microorganisms were isolated and purified from decayed rhizomes; among these, 3 fungi were identified as pathogens. The results of 18S rDNA sequence analysis showed that these fungi belonged to Penicillium, Fusarium, and Mortierella genera. The use of essential oil for controlling these pathogens was then investigated in vitro. Essential oils extracted from Cinnamomum zeylanicum (cinnamon) and Thymus vulgaris (thyme) completely inhibited the growth of all of the above pathogens at a concentration of 2000 ppm. Cinnamon oil showed higher antifungal activity in the drug sensitivity test with minimal fungicidal concentration (<500 ppm against all pathogens). In the in vivo test, cinnamon fumigation at a concentration of 500 ppm reduced infection rates of Penicillium, Fusarium, and Mortierella by 50.3%, 54.3%, and 60.7%, respectively. We recommended cinnamon oil fumigation combined with medium storage at 12 °C as an integrated approach to baby ginger storage.     

Effect of liquid whey protein concentrate–based edible coating enriched with cinnamon carbon dioxide extract on the quality and shelf life of Eastern European curd cheese

Fresh unripened curd cheese has long been a well-known Eastern European artisanal dairy product; however, due to possible cross-contamination from manual production steps, high moisture content (50–60%), and metabolic activity of present lactic acid bacteria, the shelf life of curd cheese is short (10–20 d). Therefore, the aim of this study was to improve the shelf life of Eastern European acid-curd cheese by applying an antimicrobial protein-based (5%, wt/wt) edible coating. The bioactive edible coating was produced from liquid whey protein concentrate (a cheese production byproduct) and fortified with 0.3% (wt/wt, solution basis) Chinese cinnamon bark (Cinnamomum cassia) CO₂ extract. The effect of coating on the cheese was evaluated within package-free (group 1) and additionally vacuum packaged (group 2) conditions to represent types of cheeses sold by small and big scale manufacturers. The cheese samples were examined over 31 d of storage for changes of microbiological (total bacterial count, lactic acid bacteria, yeasts and molds, coliforms, enterobacteria, Staphylococcus spp.), physicochemical (pH, lactic acid, protein, fat, moisture, color change, rheological, and sensory properties). The controlled experiment revealed that in group 1, applied coating affected appearance and color by preserving moisture and decreasing growth of yeasts and molds during prolonged package-free cheese storage. In group 2, coating did not affect moisture, color, or texture, but had a strong antimicrobial effect, decreasing the counts of yeasts and molds by 0.79 to 1.55 log cfu/g during 31 d of storage. In both groups, coating had no effect on pH, lactic acid, protein, and fat contents. Evaluated sensory properties (appearance, odor, taste, texture, and overall acceptability) of all samples were similar, indicating no effect of the coating on the flavor of curd cheese. The edible coating based on liquid whey protein concentrate with the incorporation of cinnamon extract was demonstrated to efficiently extend the shelf life of perishable fresh curd cheese, enhance its functional value, and contribute to a more sustainable production process.     

Microbiological quality of Port Salut Argentino cheese stored at two temperature treatments

Microbiological quality of Port Salut Argentino cheese was studied during 10 days (after ripening) at two storage temperature treatments: (a) 4°C and (b) a temperature combination of both 4 and 20°C (4/20°C), which implied 12 h at 4°C and 12 h at 20°C. Total coliforms were not higher than 10³ cfu/g among samples. E. coli was detected at both treatments. Thirty three percent of the cheese contained Staphylococcus aureus. Listeria spp. and Salmonella spp. were not detected in any treatment. Bacillus spp. incidence was 50% of the cheese, being B. cereus, B. cereus variety mycoides and B. pumilus. Bacillus cereus and Staphylococcus aureus grew at 4/20°C. Mesophilic aerobic bacteria were between 10⁴ and 10⁷ cfu/g. At 4/20°C counts decreased. At 4°C the behaviour was variable. Moulds were lower than 10⁴ cfu/g and yeasts were between 10⁴ and 10⁵ cfu/g. pH, moisture content and tritatable acidity ranges of samples were 5.5-6, 51-52.3% and 1.215-1.935 g/100 g of lactic acid, respectively. Manufacturing of this cheese includes a short heat treatment and starter culture addition; consequently, our results indicate that this processing may be insufficient for achieving hygienic cheese production. The storage at refrigeration temperature will not always guarantee the cheese safety and quality.     

Applicability of heat-stable deoxyribonuclease assay for assessment of staphylococcal growth and the likely presence of enterotoxin in cheese

The relationships between growth of Staphylococcus aureus and production of deoxyribonuclease and enterotoxin A in cheese were evaluated. Conditions of cheese manufacture, such as the nature of milk used (heated or raw), type of lactic starter, and degree of starter activity, influenced deoxyribonuclease production. There was a close correlation between the S. aureus population and deoxyribonuclease content (correlation .88 in Cheddar and Colby cheeses for normal or inhibited starter, and .85 in Brick cheese for normal starter). Conditions which affected deoxyribonuclease production also had a similar influence on production of enterotoxin A. Detection of the former is especially useful in cheeses which may have had a partial starter failure not detected by the usual criteria of starter activity such as the titratable acidity of whey or the final pH of cheese. While the viable S. aureus population declined during aging, both deoxyribonuclease and enterotoxin A persisted for an extended time (3 yr at 4.4 C) in cheese of normal or inhibited starter.     

A combined morphologic and molecular approach for characterizing fungal microflora from a traditional Italian cheese (Fossa cheese)

Phenotypic and genotypic methods were used to identify filamentous fungi that characterize traditional Italian Fossa cheese and its ripening environment. After ageing for 60 days at a dairy, it was ripened for an additional three months in a pit. In the fully ripened cheese, moulds ranged from 3 to 3.4 log cfu g^?1 and Penicillium was the prevalent species. Pit environmental fungi ranged from 530 to 750 cfu m^?3 (air) and from 130 to 340 cfu cm^?2 (surfaces). The dominant pit strains were Alternaria spp., Aspergillus spp., Cladosporium spp. and Penicillium spp. Phylogenetic analyses of 18S rRNA gene and ITS1-5.8S-ITS2 regions highlighted Penicillium camemberti, Aspergillus nidulans and Aspergillus versicolor as traceable species occurring in both the cheese and pit environment, suggesting their involvement in the development of typical Fossa cheese characteristics. This approach may be used for the identification of microflora on other cheese varieties to better understand the fungal contribution in cheese ripening.     

Preliminary observations on proteolysis in Manchego cheese made with a defined-strain starter culture and adjunct starter (Lactobacillus plantarum) or a commercial starter

Different authors have demonstrated the potential of adding lactobacilli as adjunct cultures to pasteurized milk used in cheese manufacture. The aim of this work was to observe the effect of the use of a defined-strain starter culture and the addition of an adjunct culture (Lactobacillus plantarum) to cheesemilk in order to determine their effect on the ripening of Manchego cheese. Manchego cheeses were manufactured using one of the following starter culture systems: a defined starter consisting of Lactococcus lactis ssp. lactis and Leuconostoc mesenteroides ssp. dextranicum; a defined starter, as described above, and Lb. plantarum, which were isolated from a good quality Manchego cheese made from raw milk, or a commercial starter comprised of two strains of Lc. lactis. The cheeses were sampled at 15, 45, 90 and 150 d of ripening. Principal component analysis of peak heights of reversed-phase HPLC chromatograms of 70% (v/v) ethanol-insoluble and -soluble fractions distributed the samples according to the starter used in their manufacture. Quantitative differences in several peptides were evident between the three cheeses. Cheeses made with the defined-strain starters received higher scores for the flavour quality and intensity and for overall impression than the cheeses made with the commercial starter.     

Effect of spices on the growth of red halophilic cocci isolated from salt cured fish and solar salt

Microbial spoilage limits the shelf life of salt cured fish, mainly due to red halophilic bacteria. To contain the growth of red halophiles, 20 spices have been tested in skim milk salt agar medium up to the 2% (v/v and w/v) level against 18 isolates obtained from salt cured fish infested with red discolouration and from solar salt. The isolates, 12 Salinococcus roseus, five Halococcus turkmenicus, and one Halococcus morrhuae were tested for their sensitivity at a cell concentration of 10⁶ per ml. Cloves and clove oil were very effective at 2 and 0.1% (v/v), respectively. Onion, coriander, garlic, asafetida, mustard and spilanthes showed excellent growth control. Red chillies, turmeric, ginger, cumin seed and fenugreek were very good in inhibiting the growth. Three of the spices tested, viz. cassia, cinnamon and poppy seeds acted as growth promoters of red halophiles. The treatment of 20% natural solar salt brines with clove oil at 0.02 and 0.5% (v/v) concentrations, resulted in the complete elimination of Halomonas spp. and red halophilic bacteria after 30 s and 1 min exposure, respectively. However, slime producing halophilic bacteria survived at very low cell density (0.46 log cycles) even after 10 min of exposure.     

Classification of Swiss cheese starter and adjunct cultures using Fourier transform infrared microspectroscopy

The acceptability of Swiss cheese largely depends on the flavor profile, and strain variations of cheese cultures will affect the final quality. Conventional biochemical methods to identify the cultures at the strain level are time-consuming and expensive, and require skilled labor. Our objective was to develop rapid classification methods of starter cultures at the strain level by using a combination of hydrophobic grid membrane filters and Fourier transform infrared (FTIR) spectroscopy. Forty-four pulsed-field gel electrophoresis-verified strains of starter and nonstarter cultures including Streptococcus thermophilus, Propionibacterium freudenreichii, and Lactobacillus spp. were analyzed. The strains were grown on their respective agar media, transferred to broth media, and incubated. Then, cultures were centrifuged and the pellets were resuspended in saline solution (10 μL). Aliquots (2 μL) of the suspended bacterial solution were placed onto a grid of the hydrophobic grid membrane filters, having 6 grids per each strain analyzed. The dried filters were read by FTIR microspectroscopy fitted with an attenuated total reflectance probe. Collected spectra were statistically analyzed by a soft independent modeling of class analogy (SIMCA) for pattern recognition. Classification models were developed for Streptococcus thermophilus, Propionibacterium freudenreichii, and Lactobacillus spp. strains. The models showed major discrimination in the spectral region from 1,200 to 900 cm⁻¹ associated with signals from phosphate-containing compounds and various polysaccharides in the cell wall. The developed method allowed for rapid classification of several Swiss cheese starter and nonstarter cultures at the strain level. This information provides a detailed overview of microbiological status, which would enable corrective measures to be taken early in the cheese making process, limiting production of inferior quality cheese and minimizing defects. This method could be an effective tool to identify and monitor activity of cheese and other dairy starter cultures.     

MODELLING of TIME-TEMPERATURE EFFECTS ON BACTERIA POPULATIONS DURING COOLING of CHEDDAR CHEESE BLOCKS1

Differences in cooling rate of Cheddar cheese from pressing (35C) to aging temperature (3.5–12C) has been reported to be responsible for flavor variation within a production lot. During aging, starter and nonstarter bacteria contribute extensively to flavor quality. Temperature effects on these bacteria were quantified using cheese from a local processor. At day 1, starter counts were 8 × 10⁷ cfu/g but as aging continued, starter counts decreased and non-starters became dominant. At 35C, starter counts reached 3 × 10⁶ cfu/g by day 3 and were below 10⁶ cfu/g by day 5. At 25, 20, 15 and 12C, starter bacteria were below 10⁶ cfu/g by day 10, 20, 24 and 40, respectively. Nonstarter counts, initially at 10⁴ cfu/g, reached = 10⁸ cfu/g at increasingly shorter times with higher temperatures. Kinetic analysis of growth in cheese and in a liquid medium suggested the possibility of diffusion growth limitations in cheese. Computer simulations for the growth of nonstarters suggests the individual cooling of small blocks (18 kg) would reduce the contribution of nonstarter counts to Cheddar cheese aging.     

Use of surface-smear bacteria for inhibition ofListeria monocytogeneson the rind of smear cheese

Surface-smear micro-organisms isolated from Taleggio cheese were screened for their ability to inhibitListeria monocytogenes. Most of the isolates showing antilisterial activity (19% of the total) consisted of coryneform bacteria, mainly belonging to theMicrobacterium lacticumspecies. The inhibitory activity was observed also after growth at 5°C and pH 6·0. After cross-inhibition tests among inhibitory strains and between these and other pigmented, non-inhibitory strains, two bacterial mixtures were assayed as surface-smear starter of Taleggio cheese. At different ripening stages (1, 20 and 40 days), the cheese surface was contaminated with 2·5×10²cfu cm⁻²L. monocytogenes(Ohio strain) and the growth evaluated over 15 days of incubation at 5°C. Contrary to the laboratory experiments,Listeriacould not be completely inhibited on the cheese surface. With 5·5–6·0 pH range of the cheese rind, (lower than usual values), the growth of surface-smear bacteria was delayed, or even stopped. Nevertheless, a listeriostatic effect was achieved on the surface of cheese samples contaminated at the end of ripening. This seemed to confirm the essential role played by surface-smear bacteria, within the rind microflora, in controlling the development of contaminant micro-organisms, and by competitive bacteria in reducing the overall risks associated with soft cheese. The mechanisms involved in the selection and the growth of competing bacteria on the cheese surface are also discussed.     

Dynamics of starter,adjunct non-starter lactic acid bacteria and propionic acid bacteria in low-fat and full-fat Dutch-type cheese

The microbial dynamics of Dutch-type cheeses differing in starter (commercial DL starter or single strain of Lactococcus lactis ssp. cremoris), adjunct (Lactobacillus or Propionibacterium) and fat contents (10% or 28% fat) were investigated by culture-dependent and culture-independent analysis. The cheese microbiota was dominated by the adjunct Lactobacillus after 4 weeks of ripening and the fat content did not influence the microbial diversity. The Leuconostoc sp., presumably from the DL starter, was detected in cheeses made with added Lactobacillus plantarum and Lactobacillus rhamnosus and was not detected in cheese made with added Lactobacillus paracasei after 4 and 7 weeks. No Lactobacillus spp. were detected in cheese with added Propionibacterium, while Leuconostoc was the only species detected. In cheeses made with Lc. lactis ssp. cremoris as starter, the Lactobacillus microbiota was similar to the cheese milk microbiota after 24 h while after 4 weeks different species of Lactobacillus and Leuconostoc were detected.     

Gas production by Paucilactobacillus wasatchensis WDCO4 is increased in Cheddar cheese containing sodium gluconate

Paucilactobacillus wasatchensis can use gluconate (GLCN) as well as galactose as an energy source and because sodium GLCN can be added during salting of Cheddar cheese to reduce calcium lactate crystal formation, our primary objective was to determine if the presence of GLCN in cheese is another risk factor for unwanted gas production leading to slits in cheese. A secondary objective was to calculate the amount of CO₂ produced during storage and to relate this to the amount of gas-forming substrate that was utilized. Ribose was added to promote growth of Pa. wasatchensis WDC04 (P.waWDC04) to high numbers during storage. Cheddar cheese was made with lactococcal starter culture with addition of P.waWDC04 on 3 separate occasions. After milling, the curd was divided into six 10-kg portions. To the curd was added (A) salt, or salt plus (B) 0.5% galactose + 0.5% ribose (similar to previous studies), (C) 1% sodium GLCN, (D) 1% sodium GLCN + 0.5% ribose, (E) 2% sodium GLCN, (F) 2% sodium GLCN + 0.5% ribose. A vat of cheese without added P.waWDC04 was made using the same milk and a block of cheese used as an additional control. Cheeses were cut into 900-g pieces, vacuum packaged and stored at 12°C for 16 wk. Each month the bags were examined for gas production and cheese sampled and tested for lactose, galactose and GLCN content, and microbial numbers. In the control cheese, P.waWDC04 remained undetected (i.e., <10⁴ cfu/g), whereas in cheeses A, C, and E it increased to 10⁷ cfu/g, and when ribose was included with salting (cheeses B, D, and F) increased to 10⁸ cfu/g. The amount of gas (measured as headspace height or calculated as mmoles of CO₂) during 16 wk storage was increased by adding P.waWDC04 into the milk, and by adding galactose or GLCN to the curd. Galactose levels in cheese B were depleted by 12 wk while no other cheeses had residual galactose. Except for cheese D, the other cheeses with GLCN added (C, E and F) showed little decline in GLCN levels until wk 12, even though gas was being produced starting at wk 4. Based on calculations of CO₂ in headspace plus CO₂ dissolved in cheese, galactose and GLCN added to cheese curd only accounted for about half of total gas production. It is proposed that CO₂ was also produced by decarboxylation of amino acids. Although P.waWDC04 does not have all the genes for complete conversion and decarboxylation of the amino acids in cheese, this can be achieved in conjunction with starter culture lactococcal. Adding GLCN to curd can now be considered another confirmed risk factor for unwanted gas production during storage of Cheddar cheese that can lead to slits and cracks in cheese. Putative risk factors now include having a community of bacteria in cheese leading to decarboxylation of amino acids and release of CO₂ as well autolysis of the starter culture that would provide a supply of ribose that can promote growth of Pa. wasatchensis.     

Determination of microbial contamination sources for use in quality management of cheese industry: “Dil” cheese as an example

The microbiological quality, safety and shelf-life of cheeses depend on manufacture and handling in an environment that meets basic standards for hygiene and the management of hygiene in the process. In this research contamination sources of “Dil” cheese during production in a local dairy plant in Bursa, Turkey were determined. Eighteen different control points (raw milk, pasteurized milk, heated curd, molded cheese before kneading, kneaded cheese, brine solution for kneading, thermophilic culture, rennet, calcium chloride solution, brine solution for cheese, cheese vat, workers hands, production room air, production room floor, production room wall, packaging material and packaged cheese) have been examined for the enumeration of total aerobic mesophilic bacteria, Staphylococci, Enterobacteriaceae, Salmonella spp., Escherichia coli, lactic acid bacteria, Pseudomonas spp. and yeast-moulds. It was determined that viability of lactic acid bacteria in thermophilic culture was not in high numbers and some contaminations to “Dil” cheese were detected from the starter culture. Brine solutions and rennet were contaminated with Staphylococci. Yeast and moulds in production room air were the major sources of contamination. Pasteurization and kneading in hot brine solution can eliminate some of the microorganisms but that was not sufficient in the production of Dil cheese. Finish cheese should meet specific hygienic standards, with respect to regulations post-contaminations to the cheese must be inhibited and a HACCP plan should be established during production.     

Impact of ropy and capsular exopolysaccharide-producing strains of Lactococcus lactis subsp. cremoris on reduced-fat Cheddar cheese production and whey composition

Cheddar cheese mixed starter cultures containing exopolysaccharide (EPS)-producing strains of Lactococcus lactis subsp. cremoris (Lac. cremoris) were characterized and used for the production of reduced-fat Cheddar cheese (15% fat). The effects of ropy and capsular strains and their combination on cheese production and physical characteristics as well as composition of the resultant whey samples were investigated and compared with the impact of adding 0.2% (w/v) of lecithin, as a thickening agent, to cheese milk. Control cheese was made using EPS-non-producing Lac. cremoris. Cheeses made with capsular or ropy strains or their combination retained 3.6–4.8% more moisture and resulted in 0.29–1.19 kg/100 kg higher yield than control cheese. Lecithin also increased the moisture retention and cheese yield by 1.4% and 0.37%, respectively, over the control cheese. Lecithin addition also substantially increased viscosity, total solid content and concentrating time by ultra-filtration (UF) of the whey produced. Compared with lecithin addition, the application of EPS-producing strains increased the viscosity of the resultant whey slightly, while decreasing whey total solids, and prolonging the time required to concentrate whey samples by UF. The amount of EPS expelled in whey ranged from 31 to 53 mg L⁻¹. Retention of EPS-producing strains in cheese curd was remarkably higher than that of non-producing strains. These results indicate the capacity of EPS-producing Lac. cremoris for enhanced moisture retention in reduced-fat Cheddar cheese; these strains would be a promising alternative to commercial stabilizers.     

Characterisation of the microflora during ripening of a Norwegian semi-hard cheese with adjunct culture of propionic acid bacteria

The microflora of a semi-hard, washed curd, Norwegian cheese with an added adjunct culture of propionic acid bacteria (PAB) was investigated throughout ripening by phenotypic and physiological tests, API test and 16S rRNA sequencing. Cheeses were made at two commercial Norwegian dairies using different milk treatments (pasteurisation versus microfiltration plus pasteurisation) and the same type of starter cultures. Microflora in the cheese varied according to different plant site, milk treatment, and ripening time. PAB dominated the microflora throughout the ripening process. Leuconostoc spp., most probably from the starter, dominated among the isolates from the cheese using microfiltered and pasteurised milk; however, after 40 weeks of ripening non-starter lactic acid bacteria specie Lactobacillus casei/paracasei and Leuconostoc spp. dominated at the dairy using pasteurised milk. Cheese made at the two plants on two subsequent days showed almost identical microflora throughout ripening.