O objetivo deste estudo foi avaliar o efeito inibitório de Lactobacillus rhamnosus sobre as contagens de Staphylococcus aureus e Listeria monocytogenes, aspergidos isoladamente ou em combinação sobre a superfície de queijo Minas Frescal, durante armazenamento por 21 dias a 7ºC. O delineamento consistiu em esquema fatorial 2x2x2, sendo 8 tratamentos com 4 repetições. As características físico-químicas (pH, atividade de água, umidade, teor de gordura, proteína e perfil de textura) foram determinadas nos queijos dos tratamentos sem adição de L. rhamnosus ou contendo este probiótico (T1 e T2, respectivamente). Verificaramse as contagens de L. rhamnosus, S. aureus e L. monocytogenes nos queijos de todos os tratamentos nos dias 1, 7, 14 e 21 de armazenamento. Foram também analisados os percentuais de sobrevivência dos microrganismos submetidos a condições de simulação do trato gastrointestinal (TGI) utilizando ensaios in vitro. Não houve efeito significativo (P>0,05) entre os parâmetros físico-químicos dos queijos dos tratamentos T1 e T2. As contagens de L. rhamnosus aumentaram (P<0,05) em todos os tratamentos a partir do dia 7 de armazenamento, estabilizando ao redor de 108 UFC/g, sendo que a presença concomitante de L. monocytogenes e/ou S. aureus nos queijos não influenciou a contagem de L. rhamnosus. L. rhamnosus diminuiu em cerca de 1 ciclo log as contagens de L. monocytogenes, e não exerceu efeito inibitório sobre S. aureus após 21 dias. S. aureus não sobreviveu ao teste de simulação ao TGI. No entanto, L. rhamnosus e L. monocytogenes apresentaram percentuais de sobrevivência entre 74,6% a 86,4%, e entre 75,8% a 94,1%, respectivamente. Os resultados demonstraram que a adição de L. rhamnosus não alterou as características físico-químicas dos queijos Minas frescal, porém exerceu efeito inibitório sobre L. monocytogenes, mas nenhum efeito sobre S. aureus. A utilização de L. rhamnosus como probiótico apresenta um potencial para inibição de L. monocytogenes na fabricação de queijos Minas frescal. São necessários estudos sobre os mecanismos envolvidos na competição entre as bactérias por substratos no alimento, bem como sua sobrevivência nas condições do TGI em ensaios in vivo. / The aim of this study was to evaluate the effects of Lactobacillus rhamnosus on growth of Staphylococcus aureus and Listeria monocytogenes in Minas frescal cheese during 21 days of storage at 7ºC. The experimental design was totally randomized, in a 2x2x2 factorial arrangement with 8 treatments and 4 replicates per treatment. Physical chemical parameters such as pH, moisture, water activity, fat, protein and texture profile analysis were carried out in cheeses where no microorganism were inoculated (T1) and in the cheeses inoculated with the probiotic bacteria, L. rhamnosus (T2). The counts of L. rhamnosus, S. aureus and L. monocytogenes were examined on days 1, 7, 14, 21 of storage. Survival percentage of the bacteria after exposure to simulated gastrointestinal conditions was studied in vitro. Statistical analysis indicated that there were no significant differences (P>0,05) among the means of the physical chemical parameters analyzed in treatments 1 and 2. From day 7 on, the counts of L. rhamnosus increased (P<0,05) in all treatments, stabilizing and reaching up to 108 CFU/g. It was noticed that the concurring presence of L. monocytogenes and/or S. aureus in the cheese samples did not show influence in the counts of the probiotic bacteria. The L. rhamnosus caused about 1 log cycle reduction in the counts of L. monocytogenes, but showed no inhibitory effect on S. aureus at the end of the period of storage. S. aureus did not survive the exposure to simulated gastrointestinal conditions. However, L. rhamnosus and L. monocytogenes showed survival percentages varying from 74,6% to 86,4%, and from 75,8% to 94,1%, respectively. The results showed that the addition of L. rhamnosus had no influence on the physical chemical characteristics of the Minas frescal cheese and no inhibitory effect on S. aureus, nevertheless demonstrated inhibitory effect on L. monocytogenes. The addition of probiotic strains of L. rhamnosus in Minas frescal cheese represents potential for L. monocytogenes inhibition. It is essential to carry out studies on the mechanisms involved in the competition for substrate by bacteria, as well as their survival to simulated gastrointestinal conditions in in vivo experiments.

O objetivo deste estudo foi avaliar o efeito inibitório de Lactobacillus rhamnosus sobre as contagens de Staphylococcus aureus e Listeria monocytogenes, aspergidos isoladamente ou em combinação sobre a superfície de queijo Minas Frescal, durante armazenamento por 21 dias a 7ºC. O delineamento consistiu em esquema fatorial 2x2x2, sendo 8 tratamentos com 4 repetições. As características físico-químicas (pH, atividade de água, umidade, teor de gordura, proteína e perfil de textura) foram determinadas nos queijos dos tratamentos sem adição de L. rhamnosus ou contendo este probiótico (T1 e T2, respectivamente). Verificaramse as contagens de L. rhamnosus, S. aureus e L. monocytogenes nos queijos de todos os tratamentos nos dias 1, 7, 14 e 21 de armazenamento. Foram também analisados os percentuais de sobrevivência dos microrganismos submetidos a condições de simulação do trato gastrointestinal (TGI) utilizando ensaios in vitro. Não houve efeito significativo (P>0,05) entre os parâmetros físico-químicos dos queijos dos tratamentos T1 e T2. As contagens de L. rhamnosus aumentaram (P<0,05) em todos os tratamentos a partir do dia 7 de armazenamento, estabilizando ao redor de 108 UFC/g, sendo que a presença concomitante de L. monocytogenes e/ou S. aureus nos queijos não influenciou a contagem de L. rhamnosus. L. rhamnosus diminuiu em cerca de 1 ciclo log as contagens de L. monocytogenes, e não exerceu efeito inibitório sobre S. aureus após 21 dias. S. aureus não sobreviveu ao teste de simulação ao TGI. No entanto, L. rhamnosus e L. monocytogenes apresentaram percentuais de sobrevivência entre 74,6% a 86,4%, e entre 75,8% a 94,1%, respectivamente. Os resultados demonstraram que a adição de L. rhamnosus não alterou as características físico-químicas dos queijos Minas frescal, porém exerceu efeito inibitório sobre L. monocytogenes, mas nenhum efeito sobre S. aureus. A utilização de L. rhamnosus como probiótico apresenta um potencial para inibição de L. monocytogenes na fabricação de queijos Minas frescal. São necessários estudos sobre os mecanismos envolvidos na competição entre as bactérias por substratos no alimento, bem como sua sobrevivência nas condições do TGI em ensaios in vivo. / The aim of this study was to evaluate the effects of Lactobacillus rhamnosus on growth of Staphylococcus aureus and Listeria monocytogenes in Minas frescal cheese during 21 days of storage at 7ºC. The experimental design was totally randomized, in a 2x2x2 factorial arrangement with 8 treatments and 4 replicates per treatment. Physical chemical parameters such as pH, moisture, water activity, fat, protein and texture profile analysis were carried out in cheeses where no microorganism were inoculated (T1) and in the cheeses inoculated with the probiotic bacteria, L. rhamnosus (T2). The counts of L. rhamnosus, S. aureus and L. monocytogenes were examined on days 1, 7, 14, 21 of storage. Survival percentage of the bacteria after exposure to simulated gastrointestinal conditions was studied in vitro. Statistical analysis indicated that there were no significant differences (P>0,05) among the means of the physical chemical parameters analyzed in treatments 1 and 2. From day 7 on, the counts of L. rhamnosus increased (P<0,05) in all treatments, stabilizing and reaching up to 108 CFU/g. It was noticed that the concurring presence of L. monocytogenes and/or S. aureus in the cheese samples did not show influence in the counts of the probiotic bacteria. The L. rhamnosus caused about 1 log cycle reduction in the counts of L. monocytogenes, but showed no inhibitory effect on S. aureus at the end of the period of storage. S. aureus did not survive the exposure to simulated gastrointestinal conditions. However, L. rhamnosus and L. monocytogenes showed survival percentages varying from 74,6% to 86,4%, and from 75,8% to 94,1%, respectively. The results showed that the addition of L. rhamnosus had no influence on the physical chemical characteristics of the Minas frescal cheese and no inhibitory effect on S. aureus, nevertheless demonstrated inhibitory effect on L. monocytogenes. The addition of probiotic strains of L. rhamnosus in Minas frescal cheese represents potential for L. monocytogenes inhibition. It is essential to carry out studies on the mechanisms involved in the competition for substrate by bacteria, as well as their survival to simulated gastrointestinal conditions in in vivo experiments.

Ce travail de thèse a permis d’étudier l’influence de l’ajout d’ingrédients fonctionnels laitiers sur l’encapsulation de L. rhamnosus GG (LGG). Deux ingrédients laitiers (ß-lactoglobuline et membrane des globules gras du lait - MFGM) ont été identifiés comme étant capables d’adhérer fortement à LGG par l’intermédiaire de ses pili. Le rôle clé de ces adhésions dans la localisation spatiale des bactéries dans la matrice laitière a été mis en évidence, ainsi que le rôle des constituants de la matrice dans sa structuration. Cela a permis de sélectionner, in vitro, une matrice d’encapsulation capable de protéger de manière efficace les bactéries des conditions gastriques et de libérer les bactéries vivantes au niveau de l’intestin. En parallèle, la MFGM dans l’encapsulation des bactéries s’est révélée prometteuse. Ce travail a également démontré l’importance primordiale du choix de la matrice d’encapsulation. En effet, une compétition entre l’adhésion de LGG aux cellules intestinales et l’adhésion de LGG à certains composants de la matrice laitière a été démontrée. Les deux phénomènes impliquent probablement les mêmes mécanismes : adhésion aux pili glycosylés de LGG. Pour terminer, un procédé de séchage par atomisation a été développé pour encapsuler LGG. Il permet une bonne survie des bactéries après séchage et la production de microparticules présentant des propriétés fonctionnelles innovantes liées à la température du milieu de réhydratation / The aim of this work was to understand how functional dairy components influence L. rhamnosus GG (LGG) encapsulation. First, two dairy components (-lactoglobulin and milk fat globule membrane - MFGM) able to strongly adhere to LGG through their pili are identified. The key role of these adhesions on bacteria spatial location in the matrix is highlighted, as well as the role of matrix dairy components in their structuration. This allowed to select, in vitro, a matrix able to protect bacteria in gastric conditions and to release them viable in the intestine. Simultaneously, the use of MFGM in bacteria encapsulation has proven to be promising. This work demonstrated the importance of the matrix choice in the encapsulation procedure. Results demonstrated that adhesion between LGG and dairy matrix may compete with adhesion of LGG to epithelial intestinal cell. The two phenomena likely involve the same mechanisms: adhesion to glycosylated pili of LGG. To finish, a spray drying encapsulation process is developed to encapsulate bacteria. It leads to a high bacteria survival after drying and the production of microparticles with innovative properties depending on rehydration temperature

<p>Pivski trop čini približno 85% od ukupnih sporednih proizvoda proizvodnje piva, i dostupan je po veoma niskim cenama tokom čitave godine. Pivski trop ima veliku perspektivu za primenu u biotehnologiji i proizvodnji visoko vrednih proizvoda. Jedna od veoma ekolo&scaron;ki i ekonomski isplativih alternativa je upotreba pivskog tropa u proizvodnji mlečne kiseline, jer se poslednjih par decenija uočava intenzivan rast potražnje za mlečnom kiselinom. Mlečna kiselina je najvažnija hidroksikarbonska kiselina &scaron;iroko rasprostranjena u prirodi, sa velikom primenom u prehrambenoj, farmaceutskoj, tekstilnoj i hemijskoj industriji i industriji prerade kože.<br />Cilj istraživanja ove doktorske disertacije je ispitivanje primene pivskog tropa u proizvodnji mlečne kiseline. Prvo je izvr&scaron;ena optimizacija enzimske hidrolize pivskog tropa u cilju dobijanja &scaron;to je moguće veće koncentacije redukujućih &scaron;ećera neophodne za mlečno-kiselu fermentaciju. Hidrolizat pivskog tropa je dobijen enzimskom hidrolizom dodatkom komercijalnih enzima za razgradnju skroba i celuloze. Parametri čiji je uticaj na efikasnost enzimske hidrolize ispitanu su: pH vrednost, temperatura hidrolize i količina dodatih enzima. Nakon &scaron;to su određeni najbolji uslovi razgranje pivskog tropa, dobijeni postupak hidrolize je primenjen u proizvodnji hidrolizata pivskog tropa koji je kori&scaron;ćen u mlečno-kiselim fermentacijama.<br />Nakon toga je ispitana mlečno-kisela fermentacija sa dva proizvodna mikoorganizma. Kao proizvodni mikroorganizmi u mlečno-kiselim fermentacijama primenjena su dva soja bakterija mlečne kiseline: Lactobacillus fermentum PL-1 i Lactobacillus rhamnosus ATCC 7469. Ispitan je uticaj dodatka različitih koncentracija ekstrakta kvasca (0,5-5,0%) uz korekciju pH vrednosti tokom fermentacije sa dodatkom kalcijum-karbonata. U zavisnosti od udela L-(+)- i D-(-)-mlečne kiseline koje nastaju tokom fermentacije izabran je proizvodni mikroorganizam koji proizvodi vi&scaron;e L-(+)-mlečne kiseline.<br />U daljim ispitivanjima je ispitan uticaj korekcije pH pomoću natrijum-hidroksida kao i dodatak različitih koncentracija ekstrakta kvasca (0,5-5,0%) i redukujućih &scaron;ećera (2,7; 5,4 i 8,1%) u hidrolizatu pivskog tropa na mlečno-kiselu fermentaciju pomoću odabranog soja bakterija mlečne kiseline. Na osnovu dobijenih rezultata izabrana je najbolja koncentracija redukujućih &scaron;ećera i ekstrakta kvasca koji će se koristiti u daljim istraživanjima.<br />Takođe je ispitana i mogućnost zamene skupog ekstrakta kvasca i glukoze sa obnovljivim sirovinama, kao &scaron;to su pivski kvasac, džibra i bistra džibra.<br />Ispitan je uticaj dodatka različitih koncentracija pivskog kvasca (0,5-5,0%), džibre (5-20%) i bistre džibre (5-50%) pre fermentacije kao i dodatak bistre džibre u dolivnoj fermentaciji, na mlečno-kiselu fermentaciju hidrolizata pivskog tropa.<br />Ispitan je i dolivni postupak fermentacije hidrolizata pivskog tropa dodatkom glukoze, glukoze i ekstrakta kvasca i sladovine. Takođe je ispitana mogućnost izvođenja vi&scaron;e uzastopnih fermentacija sa imobilisanim ćelijama odabranog soja bakterija mlečne kiseline u kalcijum-alginatu.<br />Na osnovu eksperimentalnih rezultata zaključujeno je da je dodatak kalcijum-karbonata imao pozitivan uticaj na proizvodnju mlečne kiseline sa L. fermentum i L. rhamnosus. Sa dodatkom kalcijum-karbonata povećali su se utro&scaron;ak redukujućih &scaron;ećera, koncentracija i prinos mlečne kiseline i vijabilnost ćelija L. fermentum i L. rhamnosus. Ekstrakt kvasca i kalcijum-karbonat su imali značajan uticaj na proizvodnju mlečne kiseline sa L. fermentum i L. rhamnosus. U fermentacijama sa L. fermentum najveći prinos ukupne mlečne kiseline (44%) je postignut sa dodatkom 5,0% ekstrakta kvasca i 2,0% kalcijum-karbonata. U fermentacijama sa L. rhamnosus najveći prinos ukupne mlečne kiseline (98%) i L-(+)-mlečne kiseline (96%) je ostvaren u fermentaciji sa dodatkom 2,0% ekstrakta kvasca i 2,0% kalcijum-karbonata. Na osnovu rezultata odlučeno je da se u daljim ispitivanjima mlečno-kisele fermentacije hidrolizata pivskog tropa kao proizvodni mikoorganizam koristi L. rhamnosus.<br />Primenom natrijum-hidroksida za korekciju pH je skratila fermentaciju za 48 sati a ostvareno je i značajno povećanje zapreminske produktivnosti L-(+)-mlečne kiseline (za 200%, povećanje sa 0,21 na 0,63 g/l&middot;h-1). Korekcija pH u svim daljim istraživanjima je vr&scaron;ena sa dodatkom natrijum-hidroksida.<br />U mlečno-kiselim fermentacijama sa različitim početnim koncentracijama redukujućih &scaron;ećera (2,7; 5,4 i 8,1%) i sa dodatkom različitih koncentracija ekstrakta kvasca (0,5-5,0%), najveći prinos L-(+)-mlečne kiseline i zapreminska produktivnost od 91,29% i 1,69 g/l&middot;h-1, kao i vijabilnost ćelija L. rhamnosus od 9,7&middot;109 CFU/ml ostvareni su u fermentaciji sa početniom koncentracijom redukujućih &scaron;ećera od 5,4% i dodatkom 5,0% ekstrakta kvasca.<br />Na osnovu ostvarenih rezultata u istraživanjima sa dodatkom džibre i dodacima tokom fermentacije kao i u fermentacijama sa imobilisanim ćelijama je kori&scaron;ćen hidrolizat pivskog tropa sa početnom koncentracijom redukujućih &scaron;ećera od 5,4%.<br />U mlečno kiseloj fermentaciji sa dodatkom pivskog kvasca najveći prinos L-(+)-mlečne kiseline (89,01%) i zapreminska produktivnost (0,89 g/l&middot;h-1) L-(+)-mlečne kiseline su ostvareni u fermentaciji sa dodatkom 5,0% pivskog kvasca i korekcijom početne koncentracije redukujućih &scaron;ećera na 5,0%. Na osnovu rezultata utvrđeno je da se može izvr&scaron;iti delimična ili potpuna zamena ekstrakta kvasca pivskim kvascem uz značajno smanjenje cene podloge za mlečno-kiselu fermentaciju, bez značajnog smanjenja efikasnosti mlečno-kisele fermentacije.<br />U mlečno-kiseloj fermentaciji sa dodatkom džibre i bistre džibre najveć koncetracija, prinos i zapreminska produktivnost L-(+)-mlečne kiseline od 31,03 g/l, 86,15% i 0,93 g/l&middot;h-1, ostvareni su u fermentaciji sa dodatkom 50% bistre džibre. Najvi&scaron;a koncentracija, prinos i zapreminska produktivnost L-(+)-mlečne kiseline ostvareni u dolivnoj fermentaciji sa dodatkom glukoze i bistre džibre tokom mlečno-kisele fermentacije su iznosili su 48,02 g/l, 87,82% i 0,96 g/l&middot;h-1.<br />U fermentacijama sa dodatkom nutritijenata tokom mlečno-kisele fermentacije najveća vrednost koncetracije, prinosa i zapreminske produktivnosti L-(+)-mlečne kiseline od 116,08 g/l, 93,32% i 2,04 g/L&middot;h-1, su ostvarene u fermentaciji sa dodatkom glukoze i ekstrakta kvasca tokom fermentacije. Na osnovu rezultata utvrđeno je da se dolivni postupak fermentacije može koristiti u cilju povećanja efikasnosti mlečno-kisele fermentacije.<br />Izvr&scaron;ena je imobilizacija ćelija L. rhamnosus u kalcijum-alginatu uz izuzetno visoku vijabilnost (1010 CFU/ml). Imobilisane ćelije L. rhamnosus su uspe&scaron;no kori&scaron;ćene u tri mlečno-kisele fermentacije. Prinos L-(+)-mlečne kiseline i zapreminska produktivnost su u sve tri fermentacije bili izuzetno visoki, pri čemu su najveći prinos L-(+)-mlečne kiseline i zapreminska produktivnost od 95,2% i 1,76 g/l&middot;h-1, ostvareni u drugoj fermentaciji. Upotrebom imobilisanih ćelija L. rhamnosus je osim povećanja prinosa i zapreminske produktivnosti L-(+)-mlečne kiseline skraćena fermentacija za 12 sati u poređenju sa &scaron;aržnim fermentacijama.</p> / <p>Brewers spent grain represents (BSG) about 85% of the total by-products from brewing process and is available at low price during the whole year. Due to its chemical composition BSG has great potential use in biotechnology and production of high-value products. One of very eco-friendly and economical alternative uses of BSG is in production of lactic acid (LA), since in the last few decades the demand for the LA has significantly risen, mostly because of development of biodegradable lactic polymers, which are eco-friendly and nontoxic.<br />Lactic acid is the most important hydrocarboxylic acid with an asymmetrical carbon atom, widely distributed in nature, and it has shown great potential in fields of food, pharmaceutical, textile, leather and chemical industries.<br />The aim of this doctoral thesis was to investigate the application of BSG in lactic acid production. First, the optimization of enzymatic hydrolysis of BSG was conducted, with the goal to achieve high reducing sugar concentrations, as much as possible, that are necessary on LA fermentation. BSG hydrolysis was conducted by usage of commercial enzymes for degradation of starch and cellulose. Effect of pH value, temperature and enzyme dosage on BSG hydrolysis efficiency was investigated. After the best conditions for BSG hydrolysis were determined, the optimized procedure for BSG hydrolysis was used for the production of BSG hydrolysate that will be used in LA fermentations.<br />After optimization of BSG hydrolysis, LA fermentation by two LA producing microorganisms was investigated. The strains investigated were two LA bacteria strains: Lactobacillus fermentum PL-1 and Lactobacillus rhamnosus ATCC 7469. The effect of yeast extract (0.5; 1.0; 2.0; 3.0; 4.0, and 5.0%) addition in BSG hydrolysate, with the correction of pH value during LA fermentation by the addition of calcium-carbonate, on LA fermentation was investigated. Based on the results achieved for L-(+)- and D-(-)-LA ratio the LAB strains that produced more L-(+)-LA was chosen for further research.<br />In further research the effect of pH correction (with addition of NaOH), yeast extract (0.5, 1.0, 2.0, 3.0, 4.0, and 5.0%) addition and reducing sugar concentration (2.7; 5.4 and 8.1%) in BSG hydrolysate on LA fermentation was investigated. Based on the results achieved the best yeast extract and reducing sugars concentrations was determined and used in further analysis or research. Also the possible replacement of expensive yeast extract and glucose with cheap alternatives, like brewer`s spent grain and stillage was investigated. The effect of brewer`s spent grain (0.5; 1.0; 2.0; 3.0; 4.0, and 5.0%), whole stillage (5, 10, 15 i 20%) and thin stillage (5, 10, 15, 20, 30, 40, 50%) addition before fermentation as well as thin stillage addition in fed-batch fermentation in BSG hydrolysate on LA fermentation were investigated.<br />Also fed-batch fermentation procedure (addition of glucose, glucose and yeast extract and wort during fermentation) was investigated. The possible application of cells immobilized in Ca-alginate for LA fermentation of BSG hydrolysate was also investigated.<br />Based on the results it was concluded that BSG can be successfully utilized as a raw material in production of LA, after optimization of hydrolysis and addition of nitrogen source.<br />According to the results of chemical composition before and after optimized hydrolysis 78.6% of total cellulose was hydrolyzed.<br />Addition of calcium-carbonate had positive effect on LA production by L. fermentum i L. rhamnosus. With the addition of calcium-carbonate reducing sugar utilization, LA yield and concentration and cell viability (both L. fermentum i L. rhamnosus) increased. Addition of calcium-carbonate and yeast extract had a positive effect on LA fermentation by L. fermentum and L. rhamnosus. In LA fermentation by L. fermentum the highest LA yield (44%) was achieved with addition of 5.0% of yeast extract and 2.0% of calcium-carbonate. In L. rhamnosus fermentations the highest total LA yield (98%) and L-(+)-LA yield (96%) was reached when 2.0% of yeast extract and 2.0% of calcium-carbonate were added.<br />Based on the results achieved it was concluded that BSG hydrolysate, with the addition of yeast extract, is a good fermentation media for LA fermentation with L. rhamnosus, and it was decided that L. rhamnosus will be used in further research of LA fermentation on BSG hydrolysate.<br />Addition of NaOH instead of calcium-carbonate for the pH correction shortened the fermentation time by 48 h and increased the L-(+)-LA volumetric productivity (by 200%, from 0.21 to 0.63 g/L&middot;h-1). Based on this results pH correction in further experiments was done by addition of NaOH.<br />In LA fermentation with different reducing sugar (2.7, 5.4 and 8.1%) and yeast extract concentrations (0.5-5.0%), the highest L-(+)-LA yield and volumetric productivity of 91.29%, and 1.69 g/L&middot;h-1, respectively, as well as L. rhamnosus cell viability (9.67 log CFU/mL), were achieved with the reducing sugar content of 5.4% and yeast extract content of 5.0%.<br />Based on this results in further experiment with the addition of stillage, in fed-batch fermentation and fermentation with immobilized cell BSG hydrolysate with 5.4% of reducing sugars and 5.0% yeast extract was used.<br />In fermentation with the addition of brewer&rsquo;s spent yeast the highest L-(+)-LA yield (89.01%) and volumetric productivity (0.89 g/L&middot;h-1) were achieved in the fermentation of BSG hydrolysate with 5.0% of reducing sugar and 5.0% of brewer&rsquo;s yeast. Based on the results achieved it was concluded that yeast extract can be partial or complete replaced by brewer&rsquo;s spent yeast with significant decrease of media cost, without the decrease in LA fermentation efficiency.<br />In fermentation with the addition of thin stillage the highest L-(+)-LA concentration, yield, and volumetric productivity of 31.03 g/L, 86.15%, and 0.93 g/L&middot;h-1, respectively, was obtained in fermentation with the addition of 50% of thin stillage. The highest L-(+)-LA concentration, yield, and volumetric productivity achieved in fed-batch fermentation with the addition of glucose and thin stillage during fermentation, were 48,02 g/L, 87,82% i 0,96 g/L&middot;h-1.<br />In fed-batch fermentation the highest L-(+)-LA concentration, yield, and volumetric productivity of 116.08 g/L, 93.32%, and, 2.04 g/L h-1, respectively, were achieved in fermentation with glucose and yeast extract addition during fermentation. The results showerd that fed-batch fermentation could be used to increase L-(+)-LA fermentation efficiency<br />Immobilization of L. rhamnosus cells with high viability (1010 CFU/mL) in Ca-alginate was conducted. Immobilized cells we successfully utilized in three repeated batch fermentation. L-(+)-LA yield and volumetric productivity were very high in all three batch fermentation, with the highest results achieved (95.20% and 1.76 g/L&middot;h-1, respectively) in second fermentation. Application of immobilized L. rhamnosus cells increased L-(+)-LA yield and volumetric productivity and shortened the fermentation time for 12 h in comparison with batch fermentation.</p>

Preterm birth remains a major challenge in obstetrics. It complicates up to 13% of all pregnancies and accounts for approximately 80% of neonatal mortality and morbidity. Bacterial Vaginosis (BV) is associated with a 1.4-fold increased risk of preterm birth. Due to ineffectiveness of antibiotics in preventing preterm labour, probiotics have been proposed to serve as an alternative for treatment of BV and prevention of preterm birth. The objectives of this thesis were to determine 1) the effect of Lactobacillus rhamnosus GR-1 (L. rhamnosus GR-1) supernatant on cytokine profile and prostaglandin (PG)-regulating enzyme expression in lipopolysaccharide (LPS)-stimulated human chorion and placental trophoblast cells from human placentae, 2) the potential signaling pathways through which lactobacilli act and 3) the potential role of immune and placental trophoblast cells in initiating a response to LPS and L. rhamnosus GR-1 treatments. Primary cultures of human placental trophoblast cells were pre-treated with lactobacilli supernatant and then with LPS. In addition, immune cells were removed from cell suspensions using a magnetic purification technique to determine their role in modulating cytokine levels. The expression of pro- and anti-inflammatory cytokines and prostaglandin-regulating enzymes was then determined. We found sex-specific differences in the ability of LPS to increase the output of TNF-α, IL-10, and PTGS2. We also showed that L. rhamnosus GR-1 is able to act through the JAK/STAT and MAPK pathways to increase IL-10 and G-CSF, and independently down-regulates PTGS2 and TNF-α and up-regulates PGDH. The increase in G-CSF and PGDH were only observed in women carrying a female fetus. L. rhamnosus GR-1 may serve as an alternative to antibiotics in preventing some infection/inflammation-mediated cases of preterm birth.

Preterm birth remains a major challenge in obstetrics. It complicates up to 13% of all pregnancies and accounts for approximately 80% of neonatal mortality and morbidity. Bacterial Vaginosis (BV) is associated with a 1.4-fold increased risk of preterm birth. Due to ineffectiveness of antibiotics in preventing preterm labour, probiotics have been proposed to serve as an alternative for treatment of BV and prevention of preterm birth. The objectives of this thesis were to determine 1) the effect of Lactobacillus rhamnosus GR-1 (L. rhamnosus GR-1) supernatant on cytokine profile and prostaglandin (PG)-regulating enzyme expression in lipopolysaccharide (LPS)-stimulated human chorion and placental trophoblast cells from human placentae, 2) the potential signaling pathways through which lactobacilli act and 3) the potential role of immune and placental trophoblast cells in initiating a response to LPS and L. rhamnosus GR-1 treatments. Primary cultures of human placental trophoblast cells were pre-treated with lactobacilli supernatant and then with LPS. In addition, immune cells were removed from cell suspensions using a magnetic purification technique to determine their role in modulating cytokine levels. The expression of pro- and anti-inflammatory cytokines and prostaglandin-regulating enzymes was then determined. We found sex-specific differences in the ability of LPS to increase the output of TNF-α, IL-10, and PTGS2. We also showed that L. rhamnosus GR-1 is able to act through the JAK/STAT and MAPK pathways to increase IL-10 and G-CSF, and independently down-regulates PTGS2 and TNF-α and up-regulates PGDH. The increase in G-CSF and PGDH were only observed in women carrying a female fetus. L. rhamnosus GR-1 may serve as an alternative to antibiotics in preventing some infection/inflammation-mediated cases of preterm birth.

Les probiotiques font partie du microbiote commensal. Ils ont le potentiel de stimuler la réponse immunitaire intestinale et systémique. Le virus de la grippe est à l’origine de morbidité importante. De plus, il favorise les infections bactériennes secondaires telles que Neisseria meningitidis. Nous nous sommes intéressés à l’étude des mécanismes de protections conférées par la souche Lactobacillus paracasei CNCM I-1518 sur une infection par le virus de la grippe dans un modèle de souris. Nos résultats ont montré que le gavage des souris avec la souche L. paracasei pendant 7 jours avant l’infection grippale a permis une activation des cytokines pro-inflammatoires et un recrutement massif des cellules immunitaires dans les poumons. Cette activation du système immunitaire est responsable après infection grippale d’une meilleure clairance du virus de la grippe et d’une réponse inflammatoire moins importante comparée aux souris témoins. L’administration orale à des souris du peptidoglycane de la souche L. paracasei a permis de retrouver partiellement le phénotype protecteur observé avec la bactérie entière. Les effets protecteurs induits par L. paracasei CNCM I-1518 lui sont spécifiques car l’utilisation de 2 souches L. rhamnosus CNCM I-3690 et L. paracasei CNCM I-3689 n’ont pas conférées aux souris une protection contre la grippe. L’étude de l’impact de la souche L. paracasei CNCM I-1518 sur une infection secondaire par N. meningitidis après infection grippale a montré que le gavage des souris par la souche L. paracasei permet un meilleur état clinique associé à une modulation de la réponse immunitaire et une clairance de l’infection bactérienne secondaire plus efficace / Probiotics are part of the commensal microbiota. They play a potential role in stimulating the intestinal and systemic immune response. Several clinical studies addressed beneficial effect of probiotics against respiratory infections in particular on influenza infections. These infections are responsible for significant morbidity. The burden of flu is also worsened by secondary bacterial infections such as Neisseria meningitidis. In this work, we investigated the mechanisms of protection against influenza infection conferred by Lactobacillus paracasei CNCM I-1518 strain in mice. Our results showed that, L. paracasei consumption allow an early activation of pro-inflammatory cytokines and a massive recruitment of immune cells in the lungs prior to influenza infection. This activation of immune system was associated with a faster clearance of influenza virus after infection. We able to show that feeding mice with purified peptidoglycan from L. paracasei reproduced partially the above mentioned effects observed with L. paracasei bacteria feeding.The protective effects induced by L. paracasei CNCM I-1518 against the flu infection are strain specific as L. rhamnosus CNCM I-3690 and L. paracasei CNCM I-3689, tested under the same conditions did not confer to mice protection against influenza infection. Subsequently, we investigated the impact of L. paracasei CNCM I-1518 on secondary bacterial infection with N. meningitidis following influenza infection. Our results showed that consumption of L. paracasei CNCM I-1518 strain was associated with a better clinical status and a modulation of the immune response with a better clearance of secondary bacterial infection