Relevant bibliographies by topics / Fermentation of lactic acid

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Academic literature on the topic 'Fermentation of lactic acid'

Author: Grafiati
Published: 4 June 2021
Last updated: 2 February 2022

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Journal articles on the topic "Fermentation of lactic acid"

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Hasalliu, Rozeta. "EVALUATION OF LACTIC ACID BACTERIA GROWTH DURING AUTOCHTHONOUS ALBANIAN KALLMET WINE PRODUCTION WITH SPONTANEOUS AND INOCULATED FERMENTATIONS." CBU International Conference Proceedings 5 (September 24, 2017): 1199–203. http://dx.doi.org/10.12955/cbup.v5.1096.

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The grape used in wine making has many wild microorganisms like lactic acid bacteria, yeast, acetic acid bacteria. During the alcoholic fermentation, the evaluation of these microorganisms depends on their activity. There is an interaction between yeast and lactic acid bacteria during this period of wine making. In this study, we have made wine from the autochthonous Albanian grape Kallmet variety using the spontaneous fermentation and inoculated fermentation with the yeast Saccharomyces bayannus. Yeasts carry out the alcohol fermentation, and lactic acid bacteria make malolactic fermentation in wine. With this fermentation, lactic acid bacteria convert malic acid to lactic acid, reducing the acidity of the wine and create a microbiological stability. During the alcoholic fermentation, the evaluation of lactic acid bacteria is not required. The aim of our study is to evaluate the first quantity of lactic acid bacteria to Kallmet grape, their performance during the two fermentations, spontaneous and inoculated fermentations.
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Franco, Wendy, Ilenys M. Pérez-Díaz, Suzanne D. Johanningsmeier, and Roger F. McFeeters. "Characteristics of Spoilage-Associated Secondary Cucumber Fermentation." Applied and Environmental Microbiology 78, no. 4 (December 16, 2011): 1273–84. http://dx.doi.org/10.1128/aem.06605-11.

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ABSTRACTSecondary fermentations during the bulk storage of fermented cucumbers can result in spoilage that causes a total loss of the fermented product, at an estimated cost of $6,000 to $15,000 per affected tank. Previous research has suggested that such fermentations are the result of microbiological utilization of lactic acid and the formation of acetic, butyric, and propionic acids. The objectives of this study were to characterize the chemical and environmental conditions associated with secondary cucumber fermentations and to isolate and characterize potential causative microorganisms. Both commercial spoilage samples and laboratory-reproduced secondary fermentations were evaluated. Potential causative agents were isolated based on morphological characteristics. Two yeasts,Pichia manshuricaandIssatchenkia occidentalis, were identified and detected most commonly concomitantly with lactic acid utilization. In the presence of oxygen, yeast metabolic activities lead to lactic acid degradation, a small decline in the redox potential (Eh, Ag/AgCl, 3 M KCl) of the fermentation brines, and an increase in pH to levels at which bacteria other than the lactic acid bacteria responsible for the primary fermentation can grow and produce acetic, butyric, and propionic acids. Inhibition of these yeasts by allyl isothiocyanate (AITC) resulted in stabilization of the fermented medium, while the absence of the preservative resulted in the disappearance of lactic and acetic acids in a model system. Additionally, three Gram-positive bacteria,Lactobacillus buchneri, aClostridiumsp., andPediococcus ethanolidurans, were identified as potentially relevant to different stages of the secondary fermentation. The unique opportunity to study commercial spoilage samples generated a better understanding of the microbiota and environmental conditions associated with secondary cucumber fermentations.
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Karovičová, J., and Z. Kohajdová. "Lactic acid fermented vegetable juices." Horticultural Science 30, No. 4 (November 28, 2011): 152–58. http://dx.doi.org/10.17221/3878-hortsci.

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Vegetable juices processed by lactic acid fermentation bring about a change in the beverage assortment for their high nutritive value, high content of vitamins and minerals. Starter cultures of the genus Lactobacillus are added into juices to achieve their desirable properties. This review describes the manufacture of lactic acid fermented vegetable juices and beneficial effects of the lactic acid bacteria (mainly antimicrobial and anticancer effects). A separate part of research is devoted to nutrition aspects of lactic acid fermentation and to the occurrence of biogenic amines in lactic acid fermented vegetables and vegetable juices.  
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Hábová, V., K. Melzoch, and M. Rychtera. "Modern method of lactic acid recovery from fermentation broth." Czech Journal of Food Sciences 22, No. 3 (November 16, 2011): 87–94. http://dx.doi.org/10.17221/3411-cjfs.

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Electrodialysis was used for lactic acid recovery from fermentation broth. In the first step, lactate was recovered and concentrated by desalting electrodialysis, and the second step was electroconversion of lactate to lactic acid by water-splitting electrodialysis. The final lactic acid concentration of 151 g/l was obtained. Total energy required in both electrodialysis processes was about 1.5 kWh per 1 kg of lactic acid obtained. The fermentation broth had to be pretreated prior to the electrodialysis experiments. The pretreatment consisted of ultrafiltration, decolourisation, and the removal of multivalent metal ions.  
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Hwang, Hyelyeon, and Jong-Hee Lee. "Characterization of Arginine Catabolism by Lactic Acid Bacteria Isolated from Kimchi." Molecules 23, no. 11 (November 21, 2018): 3049. http://dx.doi.org/10.3390/molecules23113049.

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Kimchi fermentation depends on diverse lactic acid bacteria, which convert raw materials into numerous metabolites that contribute to the taste of food. Amino acids and saccharides are important primary metabolites. Arginine is nearly exhausted during kimchi fermentation, whereas the concentrations of other amino acids are reported not to increase or decrease dramatically. These phenomena could imply that arginine is an important nutritional component among the amino acids during kimchi fermentation. In this study, we investigated the arginine-catabolism pathway of seven lactic acid bacteria isolated from kimchi and evaluated the products of arginine catabolism (citrulline and ornithine) associated with the bacteria. The arginine content dramatically decreased in cultures of Lactobacillus brevis and Weissella confusa from 300 μg/mL of arginine to 0.14 ± 0.19 and 1.3 ± 0.01 μg/mL, respectively, after 6 h of cultivation. Citrulline and ornithine production by L. brevis and W. confusa showed a pattern that was consistent with arginine catabolism. Interestingly, Pediococcus pentosaceus, Lactobacillus plantarum, Leuconostoc mesenteroides, and Leuconostoc lactis did not show increased citrulline levels after arginine was added. The ornithine contents were higher in all bacteria except for L. lactis after adding arginine to the culture. These results were consistent with the absence of the arginine deiminase gene among the lactic acid bacteria. Arginine consumption and ornithine production were monitored and compared with lactic acid bacteria by metagenomics analysis, which showed that the increment of ornithine production correlated positively with lactic acid bacteria growth.
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Schwan, Rosane Freitas. "Cocoa Fermentations Conducted with a Defined Microbial Cocktail Inoculum." Applied and Environmental Microbiology 64, no. 4 (April 1, 1998): 1477–83. http://dx.doi.org/10.1128/aem.64.4.1477-1483.1998.

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ABSTRACT Cocoa fermentations were performed in wooden boxes under the following four experimental regimens: beans naturally fermented with wild microflora; aseptically prepared beans with no inoculum; and beans inoculated with a defined cocktail containing microorganisms at a suitable concentration either at zero time or by using phased additions at appropriate times. The cocktail used consisted of a yeast,Saccharomyces cerevisiae var. chevalieri, two lactic acid bacterial species, Lactobacillus lactis andLactobacillus plantarum, and two acetic acid bacterial species, Acetobacter aceti and Gluconobacter oxydans subsp. suboxydans. The parameters measured were cell counts (for yeasts, filamentous fungi, lactic acid bacteria, acetic acid bacteria, and spore formers, including reisolation and identification of all residual cell types), sugar, ethanol, acetic acid, and lactic acid contents (and contents of other organic acids), pH, and temperature. A cut test for bean quality and a sensorial analysis of chocolate made from the beans were also performed. The natural fermentation mimicked exactly the conditions in 800-kg boxes on farms. The aseptic box remained largely free of microflora throughout the study, and no significant biochemical changes occurred. With the zero-time inoculum the fermentation was almost identical to the natural fermentation. The fermentation with the phased-addition inoculum was similar, but many changes in parameters were slower and less pronounced, which led to a slightly poorer end product. The data show that the nearly 50 common species of microorganisms found in natural fermentations can be replaced by a judicious selection and concentration of members of each physiological group. This is the first report of successful use of a defined, mixed starter culture in such a complex fermentation, and it should lead to chocolate of more reliable and better quality.
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Moens, Frédéric, Timothy Lefeber, and Luc De Vuyst. "Oxidation of Metabolites Highlights the Microbial Interactions and Role ofAcetobacter pasteurianusduring Cocoa Bean Fermentation." Applied and Environmental Microbiology 80, no. 6 (January 10, 2014): 1848–57. http://dx.doi.org/10.1128/aem.03344-13.

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ABSTRACTFour cocoa-specific acetic acid bacterium (AAB) strains, namely,Acetobacter pasteurianus386B,Acetobacter ghanensisLMG 23848T,Acetobacter fabarumLMG 24244T, andAcetobacter senegalensis108B, were analyzed kinetically and metabolically during monoculture laboratory fermentations. A cocoa pulp simulation medium (CPSM) for AAB, containing ethanol, lactic acid, and mannitol, was used. All AAB strains differed in their ethanol and lactic acid oxidation kinetics, whereby onlyA. pasteurianus386B performed a fast oxidation of ethanol and lactic acid into acetic acid and acetoin, respectively. OnlyA. pasteurianus386B andA. ghanensisLMG 23848Toxidized mannitol into fructose. Coculture fermentations withA. pasteurianus386B orA. ghanensisLMG 23848TandLactobacillus fermentum222 in CPSM for lactic acid bacteria (LAB) containing glucose, fructose, and citric acid revealed oxidation of lactic acid produced by the LAB strain into acetic acid and acetoin that was faster in the case ofA. pasteurianus386B. A triculture fermentation withSaccharomyces cerevisiaeH5S5K23,L. fermentum222, andA. pasteurianus386B, using CPSM for LAB, showed oxidation of ethanol and lactic acid produced by the yeast and LAB strain, respectively, into acetic acid and acetoin. Hence, acetic acid and acetoin are the major end metabolites of cocoa bean fermentation. All data highlight thatA. pasteurianus386B displayed beneficial functional roles to be used as a starter culture, namely, a fast oxidation of ethanol and lactic acid, and that these metabolites play a key role as substrates forA. pasteurianusin its indispensable cross-feeding interactions with yeast and LAB during cocoa bean fermentation.
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Kristek, S., D. Bešlo, H. Pavlović, and A. Kristek. "Effect of starter cultures L. mesenteroides and L. lactis ssp. lactis on sauerkraut fermentation and quality." Czech Journal of Food Sciences 22, No. 4 (November 16, 2011): 125–32. http://dx.doi.org/10.17221/3416-cjfs.

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Abstract: Sauerkraut fermentation course was observed in 3 cycles and 4 replicates under controlled conditions (2.5% NaCl, 21°C) using starter cultures (control; Leuconostoc meseneroides – 700 mil. cfu/ml; Lactococcus lactis ssp. lactis – 500 mil. cfu/ml; preceding fermentation juice). Each of the above mentioned cycles lasted for 28 days. Microbiological and chemical characteristics of the sauerkraut during the 28-day fermentation period were investigated. Lactic acid bacteria content, the concentration of lactic acid, and pH of the medium were monitored daily. The completion of each cycle fermentation was followed by the determination of the final product organoleptic properties which were observed for 6 months with the aim to define the expiration date. The best results relative to sauerkraut quality were obtained by using starter culture L. lactis ssp. lactis, followed by fermentation conducted by natural, spontaneous sauerkraut flora (control variant). Organoleptic properties and expiration date of the final product obtained by the use of lactic acid bacterium L. mesenteroides as a starter culture were better compared to the use of sauerkraut juice obtained from the preceding fermentation cycles and possessing the best organoleptic properties.  
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Vaquero, Cristian, Iris Loira, María Antonia Bañuelos, José María Heras, Rafael Cuerda, and Antonio Morata. "Industrial Performance of Several Lachancea thermotolerans Strains for pH Control in White Wines from Warm Areas." Microorganisms 8, no. 6 (June 1, 2020): 830. http://dx.doi.org/10.3390/microorganisms8060830.

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In the current scenario of climatic warming, the over-ripening of grapes increases the sugar content, producing flat and alcoholic wines with low acidity, high pH and low freshness. Additionally, a high pH makes wines more chemically and microbiologically unstable, requiring a higher sulphite content for preservation. Some strains of Lachancea thermotolerans can naturally lower the pH of wine by producing lactic acid from sugars; this pH reduction can reach 0.5 units. The industrial performance of four selected strains has been compared with that of two commercial strains and with that of Saccharomyces cerevisiae. The yeasts were assessed under variable oenological conditions, measuring lactic acid production and fermentative performance at two fermentation temperatures (17 and 27 °C), and in the presence or absence of sulphites (25 and 75 mg/L). Lactic acid production depends on yeast populations, with higher concentrations being reached when the microbial population is close to or above 7-log CFU/mL. A temperature effect on acidification can also be observed, being more intense at higher fermentation temperatures for most strains. Ethanol yield ranged from 7–11% vol., depending on the fermentation conditions (temperature and SO2) at day 12 of fermentation, compared with 12% for the S. cerevisiae control in micro-fermentations. The production of fermentative esters was higher at 27 °C compared with 17 °C, which favoured the production of higher alcohols. Volatile acidity was moderate under all fermentation conditions with values below 0.4 g/L.
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Orozco, F. G., A. Valadez-González, J. A. Domínguez-Maldonado, F. Zuluaga, L. E. Figueroa-Oyosa, and L. M. Alzate-Gaviria. "Lactic Acid Yield Using Different Bacterial Strains, Its Purification, and Polymerization through Ring-Opening Reactions." International Journal of Polymer Science 2014 (2014): 1–7. http://dx.doi.org/10.1155/2014/365310.

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Laboratory-scale anaerobic fermentation was performed to obtain lactic acid from lactose, using five lactic acid bacteria:Lactococcus lactis, Lactobacillus bulgaricus, L. delbrueckii, L. plantarum,andL. delbrueckii lactis. A yield of 0.99 g lactic acid/g lactose was obtained withL. delbrueckii, from which a final concentration of 80.95 g/L aqueous solution was obtained through microfiltration, nanofiltration, and inverse osmosis membranes. The lactic acid was polymerized by means of ring-opening reactions (ROP) to obtain poly-DL-lactic acid (PDLLA), with a viscosity average molecular weight (Mv) of 19,264 g/mol.
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Dissertations / Theses on the topic "Fermentation of lactic acid"

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De, Silva L. L. S. S. K. "Lactic acid fermentation of shrimp waste." Thesis, Loughborough University, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.314517.

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Pradhan, Nirakar. "Hydrogen and lactic acid synthesis through capnophilic lactic fermentation by Thermotoga neapolitana." Thesis, Paris Est, 2016. http://www.theses.fr/2016PESC1145/document.

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Les énergies non-renouvelables ont été d’un apport capital dans l’industrialisation et l’urbanisation dans les derniers centenaires. L’exploitation excessive des réserves d’hydrocarbures et son impact environnemental ont contribué au developpement de plusieurs technologies durables à caractère néo-carbone neutre. A cet effet, les processus biologiques comme la fermentation pourraient être exploités pour convertir biologiquement le hydrates de carbone en énergies comme l’hydrogène (H2) ou des acides organiques commercialement rentables. Ce travail a étudié les techniques d’ingénierie pour améliorer la synthèse simultanée d’H2 et d’acide lactique à travers des conditions de fermentation capnophile lactique (CLF) par une souche de labo de Thermotoga neapolitana.En un premier temps, une comparaison génotypique entre la souche de labo et celle sauvage a révélé une ressemblance de 88,1 (±2,4) %. En plus, les analyses du génotypage par RiboPrint® et par spectroscopie de masse matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF MS) ont montré une différentiation génétique au-delà du niveau sous-espèce ; et par conséquent la souche de labo a été proposée comme sous-espèce, T. neapolitana subsp. lactica. Basé sur la caractérisation phénotypique, la souche de labo produisait 10-90% plus d’acide lactique que celle sauvage sous les mêmes conditions sans pour autant affecté le taux de production d’H2.La souche de labo a donc été étudiée pour aussi bien optimiser les conditions de croissance que pour estimer les paramètres cinétiques de croissance. Un nouveau modèle cinétique basé sur les principes de fermentation à l’obscurité (DF) et les expressions mathématiques Monod ont été développés pour permettre la simulation de la croissance en biomasse, la consommation de substrat, et la formation de produit. Le modèle n’a cependant pas pu faire une estimation des acides acétique et lactique avec précision du fait que le modèle DF n’a pas considéré la carboxylation de l’acide acétique en acide lactique par l’enzyme pyruvate ferrédoxine oxydoréductase (PFOR) sous les conditions CLF.Le model a été associé avec le mécanisme CLF et les paramètres cinétiques ont été recalibrés. Les paramètres cinétiques que sont le taux d’absorption spécifique maximum (k), la constante semi-saturation (ks), le coefficient en rendement biomasse (Y), et le taux de décomposition interne (kd) étaient de 1,30 l/h, 1,42 g/L, 0,12 et 0,02 l/h. Fait intéressant, le nouveau modèle CLF s’est parfaitement adapté avec les résultats expérimentaux et a estimé que près de 40-80% de la production d’acide lactique est attribué au recyclage de l’acide acétique et le CO2.En plus, l’adsorption de l’acide lactique par le carbone actif et les résines polymères anioniques a été appliquée avec succès comme technique de transformation en aval dans la récupération et la purification de l’acide lactique à partir du modèle de fermentation type T. neapolitana. Pour ce faire, ce travail de recherche constitue une étape majeure dans le domaine de la fermentation bactérienne utilisable pour de vastes applications scientifiques prenant en compte le développement d’énergies renouvelables et la production industrielle d’acide lactique
The environmental impact of excessive exploitation of fossil fuel reserves has inspired the innovation of several sustainable neo-carbon-neutral technologies. To that end, the biological processes like fermentation may be leveraged to bioconvert carbohydrate-rich feedstocks to fuels like hydrogen (H2) or commercially valuable organic acids like lactic acid. This research work investigated the engineering techniques for improving simultaneous synthesis of H2 and lactic acid under capnophilic (CO2-dependent) lactic fermentation (CLF) conditions by a lab strain of Thermotoga neapolitana.Primarily, the genotypic comparison between the lab strain and the wild-type revealed DNA homology of 88.1 (± 2.4)%. Genotyping by RiboPrint® and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) analyses showed a genetic differentiation beyond subspecies level, hence the lab strain was proposed as a new subspecies, T. neapolitana subsp. lactica. The lab strain produced 10-90% more lactic acid, based on the phenotypic characterization, than the wild-type strain under similar operating conditions without impairing the H2 yield.The lab strain was then studied to optimize the growth conditions as well as to estimate the growth kinetic parameters. A new mathematical model based on the dark fermentation (DF) principles and Monod-like kinetic expressions was developed to enable the simulation of biomass growth, substrate consumption and product formation. The model failed to estimate acetic and lactic acid accurately, as the DF model did not consider the carboxylation of acetic acid to lactic acid by the pyruvate:ferredoxin oxidoreductase (PFOR) enzyme under CLF conditions. The model was then incorporated with the CLF mechanism and the kinetic parameters were recalibrated.The calibrated kinetic parameters, i.e. maximum specific uptake rate (k), semi-saturation constant (kS), biomass yield coefficient (Y) and endogenous decay rate (kd) were 1.30 1/h, 1.42 g/L, 0.12 and 0.02 1/h, respectively, under CLF conditions. The new CLF-based model fitted very well with the experimental results and estimated that about 40-80% of the lactic acid production is attributed to the recycling of acetic acid and CO2.In addition, the adsorption of lactic acid by activated carbon and anionic polymeric resins was successfully applied as a downstream processing technique for the recovery of lactic acid from a model T. neapolitana fermentation broth. This research work serves as a practical milestone in the field of microbial fermentation with a scope for wider scientific applications, including the development of bio-based renewable energy and industrial lactic acid production
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Kanagachandran, Kanagasooriyam. "The physiology of lactic acid production by Lactococcus lactis IO-1." Thesis, University of Hertfordshire, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.267963.

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Oliveira, Juliana de. "Poly(Lactic acid) production by conventional and microwave polymerization of lactic acid produced in submerged fermentation." reponame:Repositório Institucional da UFPR, 2016. http://hdl.handle.net/1884/46421.

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Orientador : PhD. Luciana Porto de Souza Vandenberghe
Coorientadores : PhD. Carlos Ricardo Soccol e PhD. Sônia Faria Zawadzki
Tese (doutorado) - Universidade Federal do Paraná, Setor de Tecnologia, Programa de Pós-Graduação em Engenharia de Bioprocessos e Biotecnologia. Defesa: Curitiba, 09/06/2016
Inclui referências : f. 115-128
Área de concentração: Agroindústria e biocombustíveis
Resumo: Poli(ácido lático), poliéster, é um polímero biodegravável aplicado em produtos como embalagens, têxteis, médicos e farmacêuticos. Pode ser obtido a partir do monômero ácido lático (AL) por meio da reação de policondensação direta e pela polimerização por abertura de anel do lactídeo. O AL é um ácido orgânico que apresenta diversas aplicações principalmente na indústria alimentícia, assim como na indústria farmacêutica, química e de polímeros. A produção do AL por fermentação oferece vantagens tais como a produção do isômero opticamente puro. As necessidades nutricionais da bactéria aumentam o custo de produção do AL, portanto substratos alternativos tem sido estudados por apresentarem uma alternativa econômica para este processo. O objetivo deste trabalho foi a produção de ácido lático por Lactobacillus pentosus em fermentação submersa utilizando subproduto do processamento da batata e caldo de cana como substratos para a obtenção de poli(ácido lático). Estes sub-produtos porque possuem alta concentração de fonte de carbono e volumes significativos são gerados anualmente, o que justifica sua a re-utilização e valorização. O sub-produto do processamento da batata foi submetido a hidrólise ácida com o objetivo de converter o amido em glucose. A produção de AL foi otimizada utilizando etapas de planejamento experimental estatístico envolvendo a seleção de bactérias do gênero Lactobacillus, definição da composição do meio de cultivo e estudos de cinética em frascos de Erlenmeyer e biorreator do tipo tanque agitado. A produção de AL chegou a 150 g/L utilizando sub-produto do processamento da batata e 225 g/L utilizando caldo de cana em 96 horas de fermentação. O uso da célula inteira de levedura de panificação como fonte de nitrogênio e a condição de fermentação não estéril demostraram ser boas alternativas para um processo industrial de produção de AL. O processo de separação e recuperação do AL do caldo fermentado foi desenvolvido para obtenção da molécula purificada e estudos de polimerização com o monômero obtido. O processo desenvolvido consistiu no aquecimento do caldo fermentado seguido pela etapa de centrifugação. A etapa de clarificação foi realizada utilizando carvão ativado em pó seguida pela precipitação a baixa temperatura e acidificação do lactato de cálcio para conversão em ácido lático. O processo foi efetivo para remoção de contaminantes que estavam presentes no caldo fermentado. A concentração final de AL em solução aquosa foi de 416 g/L com um rendimento de 51%. Os estudos de polimerização foram desenvolvidos utilizando a técnica de policondensação direta do AL, por meio de dois diferentes sistemas de aquecimento, convencional e micro-ondas. Um polímero com massa molar de 6330 g/mol e 61% de rendimento foi obtido a partir de um AL comercial e utilizando o AL obtido por fermentação resultou em um polímero com massa molar de 2370 g/mol. O processo de aquecimento por micro-ondas proporcionou um maior rendimento, 79% e 76% para o AL comercial e obtido por fermentação, respectivamente. Porém, foi obtida menor massa molar que o processo convencional, 2070 para o AL comercial e 1450 para o AL obtido por fermentação. As propriedades físico-químicas do poli(ácido lático) demonstraram aplicação em encapsulamento de compostos bioativos e engenharia de tecido. As perspectivas de sequência de estudos são a aplicação em encapsulamento de moléculas, modificações do polímeros e desenvolvimento de compósitos. PALAVRAS CHAVE: Poli(ácido lático), sub-produto do processamento da batata, caldo de cana, policondensação
Abstract: Poly (lactic acid) (PLA) is a polyester, which has a predominant role as biodegradable plastic, that is applied in packaging, textile, medical and pharmaceutical products. It can be obtained from lactic acid by direct polycondensation and by ring-opening polymerization (ROP) of lactide. Lactic acid (LA) is an organic acid that presents diverse applications mostly in food industry, as well as in pharmaceutical, chemical industries and polymers. The production of LA by fermentation offers the advantage of producing optically high pure LA. Nutritional requirements of bacteria increase the cost of LA production so alternatives substrates have been studied to bring an economical alternative for this process. The aim of this work was the production of LA by Lactobacillus pentosus in submerged fermentation using potato processing waste and sugarcane juice as substrate in order to obtain poly(lactic acid). The fermentation process was developed using potato processing waste and sugarcane juice because of their high carbon source concentration. Important volumes of both sub-products were generated, which is another reason for their re-use and valorization. Potato processing waste was submitted to hydrolysis in order to convert starch to glucose. LA production by fermentation was optimized using, statistical experimental design approach steps of optimization involved the screening of bacteria of the genus Lactobacillus and definition of medium composition kinetics studies in Erlenmeyer flask and stirred tank reactor were also carried out. LA production reached 150 g/l using potato processing waste, it was and 225 g/l with sugar cane juice after 96 hours of fermentation. The use of baker's yeast as a source of nitrogen and nonsterile conditions demonstrated good alternatives for an industrial production process of LA. The separation and recovery process of LA from fermented broth was developed to obtain a purified molecule for further polymerization studies. The developed process consisted in heating the fermented broth, then a centrifugation step was conducted for removal of the cells and suspended solids. A clarification step was included with powered activated carbon with further precipitation at low temperature and acidification of calcium lactate to convert to LA. The process was effective for removal of contaminants that were present in the fermentation medium. Final concentration of LA in aqueous solution reached 416 g/l and a yield of 51%. Polymerization studies were then carried out using direct polycondensation of LA, that were carried out with two different heating systems, conventional and microwave heating. A polymer with 6330 g/mol of molecular weight and 61% of yield was obtained from commercial LA and using fermented LA resulted in 2370 g/mol. Microwave heating process provided a higher yield, 79% and 76% for commercial and fermented LA, respectively. Nevertheless, the molecular weight was lower than conventional process, 2070 for commercial LA and 1450 for fermented LA. Physicochemical properties of PLA demonstrated application in encapsulation of bioactive compounds and tissue engineering. Perspectives of sequence of the studies: application on encapsulation of molecules, modifications of polymer and development of composites. KEYWORDS: Poly(lactic acid); potato processing waste; sugarcane juice; polycondensation
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Planes, Jordi. "Lactic acid production extractive fermentation in acqueous two-phase systems /." Lund : Dept. of Applied Microbiology, Lund University, 1998. http://catalog.hathitrust.org/api/volumes/oclc/40264909.html.

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Yusof, Rokiah Binti Mohd. "Improved safety of infant weaning foods through lactic acid fermentation." Thesis, University of Surrey, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.359907.

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Altıok, Duygu Tokatlı Figen. "Kinetic modelling of lactic acid production from whey/." [s.l.]: [s.n.], 2004. http://library.iyte.edu.tr/tezler/master/gidamuh/T000471.pdf.

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Elvin, Mark. "Production and structure of exopolysaccharides from thermophilic lactic acid bacteria." Thesis, University of Huddersfield, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.368301.

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Prévot, Flavie. "Valorization of vegetables wastes for the poly(lactic acid) bioproduction." Thesis, Strasbourg, 2015. http://www.theses.fr/2015STRAE008/document.

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Cette thèse s’articule autour de la valorisation de la biomasse lignocellulosique pour la production d’un polymère biosourcé, le poly(acide lactique) PLA. Lors d’une première étude, deux prétraitements de la biomasse lignocellulosique ont été réalisés pour libérer les sucres fermentescibles. Puis plusieurs stratégies de fermentations ont été mises en place et un criblage microorganisme / biomasse a été réalisé en vue de sélectionner la meilleure stratégie de fermentation et le meilleur couple biomasse / microorganisme pour la production d’acide lactique. Les bactéries lactiques, Lactobacillus casei et Lactobacillus delbrueckii et le son de blé ont été retenus pour produire l’acide lactique lors d’une fermentation en milieu liquide sur l’hydrolysat produit par une hydrolyse à l’acide dilué du son de blé. Lors d’une seconde étude, la stratégie choisie a été optimisée et a subi un « scale-up » afin d’augmenter la concentration en acide lactique. Les fermentations en milieu liquide ont été effectuées au sein d’un bioréacteur afin de contrôler les paramètres de croissance bactérienne et de production d’acide lactique (pH, pO2, agitation, production d’acide lactique). Puis une purification de l’acide lactique a été menée par chromatographie échangeuse d’ions. Cette technique a été réalisée en deux étapes clés utilisant successivement une colonne cationique forte et une colonne anionique faible. L’acide lactique purifié a été polymérisé par ouverture de cycle (ROP). Durant toutes ces recherches, la chimie verte a été mise au premier plan d’une part par le sujet de l’étude (valorisation de la biomasse végétale) mais aussi d’autre part par le choix des méthodes employées (pas de solvants, peu de produits chimiques, méthodes propres, économiques et renouvelables)
This thesis is articulated around the lignocellulosic biomass valorization to develop a fully sustainable, green and cheap route of PLA production. During a first study, two pretreatments have been realized on the lignocellulosic biomass in order to release the fermentable sugars. Several fermentations strategies have been considered and a screening of the couples microorganisms / biomasses has been performed in order to select the best strategy and the best couple microorganism / biomass for lactic acid production. The lactic acid bacteria, Lactobacillus casei and Lactobacillus delbrueckii and wheat bran have been selected to produce lactic acid via a liquid state fermentation on the acid hydrolysate obtained thanks to a diluted acid pretreatment on the wheat bran. During a second study, the chosen strategy has been optimized and scaled-up in order to increase the lactic acid concentration. Liquid state fermentations have been made in a bioreactor in order to control parameter needed for the optimal growth and consequently the optimal lactic acid production (pH, pO2, agitation, acid lactic production). Then, the lactic acid purification has been performed by ion exchange chromatography. This technic was made in two key steps using a strong cationic column and a weak anionic column successively. Finally, the purified lactic acid was then polymerized by ring opening polymerization (ROP). During all the researches, the green chemistry has been placed in the first plan in one hand by the choice of the topic of the study (biomass valorization) and in a second hand by the choice of each employed method (no solvent; few chemical products; sustainable, cheap and green methods)
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Acan, Basak. "Equilibrium Studies On The Reactive Extraction Of Lactic Acid From Fermentation Broth." Master's thesis, METU, 2003. http://etd.lib.metu.edu.tr/upload/1120781/index.pdf.

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Lactic acid recovery from dilute fermentation broths is a growing requirement due to the increasing demand for pure lactic acid. Reactive extraction is proposed as an alternative to conventional methods of recovery, since the selectivity of separation is remarkably enhanced in reactive extraction. The aim of this study is to perform the equilibrium studies for the recovery of lactic acid from its synthetic aqueous solutions (not from real fermentation broths) by reactive extraction and investigate the effects of various parameters such as initial lactic acid concentration in the aqueous phase (0.25 - 1.3 M), initial pH of the aqueous phase (2 &ndash
6), organic phase extractant concentration (0.1 &ndash
0.5 M), type of the extractant (chloride, hydrogensulphate and hydroxide salts of tri-n-octylmethylammonium) and the type of diluent (oleyl alcohol or octanol). The results of the experiments showed that the degrees of extraction decreased with increasing use of diluent with the extractant and increasing initial lactic acid concentration of the aqueous phase. Highest degrees of extraction were achieved for undiluted extractants. The performance of the diluents were investigated by performing extraction experiments with solutions of TOMAC in oleyl alcohol or octanol at different pH values and it was observed that octanol had a higher solvating power than oleyl alcohol especially at lower aqueous phase pH values. Higher extraction efficiencies were obtained for TOMAC dissolved in octanol rather than oleyl alcohol. Initial aqueous pH of 6 was identified as the optimum pH for the extraction, also due to its being equal the average fermentation pH for the extractions with Lactobacillus species. Among the different salts of tri-n-octylmethylammonium, hydroxide salt exhibited the highest degrees of extraction (83% with undiluted TOMA(OH) and 78% with 0.5 M TOMA(OH) in octanol for the extraction of 0.316 M lactic acid solutions). The present work is the first step in the design of an industrial reactive extraction process that is going to attempt forward and backward extraction of lactic acid simultaneously in a hollow fiber membrane module that is going to be attached to the lactic acid fermentor to achieve continuous product recovery. The equilibrium data obtained from this study can be combined with the kinetic studies as the next step of designing a separation module.
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Books on the topic "Fermentation of lactic acid"

1

Lactic Acid Bacteria Computer Conference (1st 1993). The lactic acid bacteria: Proceedings of the First Lactic Acid Bacteria Computer Conference. Wymondham, Norfolk, England: Horizon Scientific Press, 1996.

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Feng, Xin-Mei. Microbial dynamics during barley tempeh fermentation. Uppsala: Swedish University of Agricultural Sciences, 2006.

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Holzapfel, Wilhelm H., and Brian J. B. Wood, eds. Lactic Acid Bacteria. Chichester, UK: John Wiley & Sons, Ltd, 2014. http://dx.doi.org/10.1002/9781118655252.

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Kanauchi, Makoto, ed. Lactic Acid Bacteria. New York, NY: Springer New York, 2019. http://dx.doi.org/10.1007/978-1-4939-8907-2.

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Faruk Bozoğlu, T., and Bibek Ray, eds. Lactic Acid Bacteria. Berlin, Heidelberg: Springer Berlin Heidelberg, 1996. http://dx.doi.org/10.1007/978-3-642-61462-0.

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Zhang, Heping, and Yimin Cai, eds. Lactic Acid Bacteria. Dordrecht: Springer Netherlands, 2014. http://dx.doi.org/10.1007/978-94-017-8841-0.

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Chen, Wei, ed. Lactic Acid Bacteria. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-7283-4.

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Chen, Wei, ed. Lactic Acid Bacteria. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-7832-4.

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Auras, Rafael, Loong-Tak Lim, Susan E. M. Selke, and Hideto Tsuji, eds. Poly(Lactic Acid). Hoboken, NJ, USA: John Wiley & Sons, Inc., 2010. http://dx.doi.org/10.1002/9780470649848.

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Yokota, Atsushi, and Masato Ikeda, eds. Amino Acid Fermentation. Tokyo: Springer Japan, 2017. http://dx.doi.org/10.1007/978-4-431-56520-8.

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Book chapters on the topic "Fermentation of lactic acid"

1

Martin, Antonio M. "Fermentation Processes for the Production of Lactic Acid." In Lactic Acid Bacteria, 269–301. Berlin, Heidelberg: Springer Berlin Heidelberg, 1996. http://dx.doi.org/10.1007/978-3-642-61462-0_12.

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Martin, Antonio M. "Role of Lactic Acid Fermentation in Bioconversion of Wastes." In Lactic Acid Bacteria, 219–52. Berlin, Heidelberg: Springer Berlin Heidelberg, 1996. http://dx.doi.org/10.1007/978-3-642-61462-0_10.

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Champomier-Vergès, Marie-Christine, and Monique Zagorec. "Lactobacillus sakeiin Meat Fermentation." In Biotechnology of Lactic Acid Bacteria, 209–15. Chichester, UK: John Wiley & Sons, Ltd, 2015. http://dx.doi.org/10.1002/9781118868386.ch13.

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Lonvaud-Funel, Aline. "Lactic Acid Bacteria and Malolactic Fermentation in Wine." In Biotechnology of Lactic Acid Bacteria, 231–47. Chichester, UK: John Wiley & Sons, Ltd, 2015. http://dx.doi.org/10.1002/9781118868386.ch15.

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Di Cagno, Raffaella, Pasquale Filannino, and Marco Gobbetti. "Vegetable and Fruit Fermentation by Lactic Acid Bacteria." In Biotechnology of Lactic Acid Bacteria, 216–30. Chichester, UK: John Wiley & Sons, Ltd, 2015. http://dx.doi.org/10.1002/9781118868386.ch14.

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De Vuyst, Luc, and Stefan Weckx. "The Functional Role of Lactic Acid Bacteria in Cocoa Bean Fermentation." In Biotechnology of Lactic Acid Bacteria, 248–78. Chichester, UK: John Wiley & Sons, Ltd, 2015. http://dx.doi.org/10.1002/9781118868386.ch16.

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Nout, M. J. R., and P. K. Sarkar. "Lactic acid food fermentation in tropical climates." In Lactic Acid Bacteria: Genetics, Metabolism and Applications, 395–401. Dordrecht: Springer Netherlands, 1999. http://dx.doi.org/10.1007/978-94-017-2027-4_26.

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Arunga, R. O. "Lactic Acid Bacteria in Coffee and Cocoa Fermentation." In The Lactic Acid Bacteria Volume 1, 409–29. Boston, MA: Springer US, 1992. http://dx.doi.org/10.1007/978-1-4615-3522-5_16.

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Zheng, Yizhou, Xinhua Ding, Peilin Cen, Chein-Wen Yang, and George T. Tsao. "Lactic Acid Fermentation and Adsorption on PVP." In Seventeenth Symposium on Biotechnology for Fuels and Chemicals, 627–32. Totowa, NJ: Humana Press, 1996. http://dx.doi.org/10.1007/978-1-4612-0223-3_59.

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Vandamme, E. J., M. Raemaekers, N. Vekemans, and W. Soetaert. "Polysaccharides, Oligosaccharides, Special Sugars and Enzymes Via Leuconostoc Mesenteroides Sp. Fermentations." In Lactic Acid Bacteria, 205–18. Berlin, Heidelberg: Springer Berlin Heidelberg, 1996. http://dx.doi.org/10.1007/978-3-642-61462-0_9.

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Conference papers on the topic "Fermentation of lactic acid"

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STOŠKUS, Robertas, Jonas JATKAUSKAS, Vilma VROTNIAKIENĖ, and Vida JUOZAITIENĖ. "THE EFFECT OF HOMO - AND HETERO - FERMENTATIVE LACTIC ACID BACTERIA MIX ON THE ENSILED LUCERNE FERMENTATION CHARACTERISTICS AND AEROBIC STABILITY IN BIG BALES." In RURAL DEVELOPMENT. Aleksandras Stulginskis University, 2018. http://dx.doi.org/10.15544/rd.2017.029.

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The purpose of this study was to determine the effect of homo- and hetero-fermentative lactic acid bacteria mix on the ensiled lucerne fermentation characteristics and aerobic stability in big bales. The lucerne was ensiled without additives (C) and treated with a mix of bacterial inoculant that contains Lactococcus lactis and Lactobacillus buchneri (50:50) (I). Silage was treated with bacterial inoculant, which significantly increased the total organic acids concentration by 69 %, lactic acid by 92% and acetic acid by 76 %. If the results were compared with the C silage, the inoculation significantly decreased the concentrations of butyric acid by 73 %, ethanol by 53 % and ammonia - N concentration by 33%. Inoculated silage had significantly lowered the yeast count by 59 % and moulds count by 34 %. Compared to the inoculated silage and during the aerobic exposure, the untreated silage maximum temperature was significantly higher (13.9 0C vs 4.6 0C) (P < 0.05). Therefore, the bacterial inoculant improved the quality of fermentation and aerobic stability in lucerne silages.
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"Utilization of Waste Bread for Lactic Acid Fermentation." In 2014 ASABE Annual International Meeting. American Society of Agricultural and Biological Engineers, 2014. http://dx.doi.org/10.13031/aim.20141892862.

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Ifrim, George Adrian, Laurentiu Baicu, Sergiu Caraman, and Mariana Titica. "Dynamic modeling of the pH in lactic acid fermentation processes." In 2015 19th International Conference on System Theory, Control and Computing (ICSTCC). IEEE, 2015. http://dx.doi.org/10.1109/icstcc.2015.7321297.

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Zou, Hui, Qunhui Wang, Yingying Liu, and Wengong Zhou. "The Impact on L-Lactic Acid Fermentation with Jinggangmycin Fermentation Residue as Nitrogen Source." In 2010 International Conference on E-Product E-Service and E-Entertainment (ICEEE 2010). IEEE, 2010. http://dx.doi.org/10.1109/iceee.2010.5661403.

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Zheng Jin, Wang Qunhui, Li Zhengyao, and Liu Yingying. "Lactic acid production from distiller's grains by simultaneous saccharification and fermentation." In 2010 International Conference on Mechanic Automation and Control Engineering (MACE). IEEE, 2010. http://dx.doi.org/10.1109/mace.2010.5535977.

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Yebo Li, Abolghasem Shahbazi, Seku Coulibaly, and Michele R. Mims. "LACTIC ACID RECOVERY FROM CHEESE WHEY FERMENTATION BROTH USING NANOFILTRATION MEMBRANES." In 2005 Tampa, FL July 17-20, 2005. St. Joseph, MI: American Society of Agricultural and Biological Engineers, 2005. http://dx.doi.org/10.13031/2013.19661.

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MATHEWS, A. P., and W. FU. "FERMENTATION KINETICS IN THE PRODUCTION OF LACTIC ACID FROM HIGH STRENGTH WASTEWATERS." In Proceedings of the Third Asia-Pacific Conference. WORLD SCIENTIFIC, 2000. http://dx.doi.org/10.1142/9789812791924_0108.

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Abdullah, Abdullah, and Ima Winaningsih. "Effect of some parameter on lactic acid fermentation from pineapple waste by Lactobacillus delbrueckii." In PROCEEDINGS OF 2ND INTERNATIONAL CONFERENCE ON CHEMICAL PROCESS AND PRODUCT ENGINEERING (ICCPPE) 2019. AIP Publishing, 2020. http://dx.doi.org/10.1063/1.5140929.

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Huang, Liping, Jingjing Sheng, Jingwen Chen, and Ning Li. "Direct Fermentation of Fishmeal Wastewater and Starch Wastewater to Lactic Acid by Rhizopus Oryzae." In 2008 2nd International Conference on Bioinformatics and Biomedical Engineering. IEEE, 2008. http://dx.doi.org/10.1109/icbbe.2008.1134.

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C. Liu and S. Chen. "Effects of nutrient supplements on nisin and lactic acid simultaneous fermentation from cull potatoes." In 2004, Ottawa, Canada August 1 - 4, 2004. St. Joseph, MI: American Society of Agricultural and Biological Engineers, 2004. http://dx.doi.org/10.13031/2013.17028.

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Reports on the topic "Fermentation of lactic acid"

1

Dai, Y., and C. J. King. Modeling of fermentation with continuous lactic acid removal by extraction utilizing reversible chemical complexation. Office of Scientific and Technical Information (OSTI), July 1995. http://dx.doi.org/10.2172/90681.

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Hutchinson, M. L., J. E. L. Corry, and R. H. Madden. A review of the impact of food processing on antimicrobial-resistant bacteria in secondary processed meats and meat products. Food Standards Agency, October 2020. http://dx.doi.org/10.46756/sci.fsa.bxn990.

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For meat and meat products, secondary processes are those that relate to the downstream of the primary chilling of carcasses. Secondary processes include maturation chilling, deboning, portioning, mincing and other operations such as thermal processing (cooking) that create fresh meat, meat preparations and ready-to-eat meat products. This review systematically identified and summarised information relating to antimicrobial resistance (AMR) during the manufacture of secondary processed meatand meat products (SPMMP). Systematic searching of eight literature databases was undertaken and the resultantpapers were appraised for relevance to AMR and SPMMP. Consideration was made that the appraisal scores, undertaken by different reviewers, were consistent. Appraisal reduced the 11,000 initially identified documents to 74, which indicated that literature relating to AMR and SPMMP was not plentiful. A wide range of laboratory methods and breakpoint values (i.e. the concentration of antimicrobial used to assess sensitivity, tolerance or resistance) were used for the isolation of AMR bacteria.The identified papers provided evidence that AMR bacteria could be routinely isolated from SPMMP. There was no evidence that either confirmed or refuted that genetic materials capable of increasing AMR in non-AMR bacteria were present unprotected (i.e. outside of a cell or a capsid) in SPMMP. Statistical analyses were not straightforward because different authors used different laboratory methodologies.However, analyses using antibiotic organised into broadly-related groups indicated that Enterobacteriaceaeresistant to third generation cephalosporins might be an area of upcoming concern in SPMMP. The effective treatment of patients infected with Enterobacteriaceaeresistant to cephalosporins are a known clinical issue. No AMR associations with geography were observed and most of the publications identified tended to be from Europe and the far east.AMR Listeria monocytogenes and lactic acid bacteria could be tolerant to cleaning and disinfection in secondary processing environments. The basis of the tolerance could be genetic (e.g. efflux pumps) or environmental (e.g. biofilm growth). Persistent, plant resident, AMR L. monocytogenes were shown by one study to be the source of final product contamination. 4 AMR genes can be present in bacterial cultures used for the manufacture of fermented SPMMP. Furthermore, there was broad evidence that AMR loci could be transferred during meat fermentation, with refrigeration temperatures curtailing transfer rates. Given the potential for AMR transfer, it may be prudent to advise food business operators (FBOs) to use fermentation starter cultures that are AMR-free or not contained within easily mobilisable genetic elements. Thermal processing was seen to be the only secondary processing stage that served as a critical control point for numbers of AMR bacteria. There were significant linkages between some AMR genes in Salmonella. Quaternary ammonium compound (QAC) resistance genes were associated with copper, tetracycline and sulphonamide resistance by virtue of co-location on the same plasmid. No evidence was found that either supported or refuted that there was any association between AMR genes and genes that encoded an altered stress response or enhanced the survival of AMR bacteria exposed to harmful environmental conditions.
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Stepan, Daniel J., Edwin S. Olson, Richard E. Shockey, Bradley G. Stevens, and John R. Gallagher. RECOVERY OF LACTIC ACID FROM AMERICAN CRYSTAL SUGAR COMPANY WASTEWATER. Office of Scientific and Technical Information (OSTI), April 2001. http://dx.doi.org/10.2172/788118.

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Tsai, S. P., and S. H. Moon. An integrated bioconversion process for the production of L-lactic acid from starchy feedstocks. Office of Scientific and Technical Information (OSTI), July 1997. http://dx.doi.org/10.2172/505310.

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Dr. Sharon Shoemaker. Advanced Biocatalytic Processing of Heterogeneous Lignocellulosic Feedstocks to a Platform Chemical Intermediate (Lactic acid Ester). Office of Scientific and Technical Information (OSTI), September 2004. http://dx.doi.org/10.2172/829962.

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Kotsilkova, Rumiana, and Vladimir Georgiev. Influence of Graphene Size and Content on Thermal Conductivity of Novel Poly(lactic) Acid Nanocomposites. "Prof. Marin Drinov" Publishing House of Bulgarian Academy of Sciences, April 2021. http://dx.doi.org/10.7546/crabs.2021.04.06.

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Snyder, S. W. Scaleable production and separation of fermentation-derived acetic acid. Final CRADA report. Office of Scientific and Technical Information (OSTI), February 2010. http://dx.doi.org/10.2172/971986.

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Solberg, Thomas. Aspects of anuran metabolism : effects of chronic hypoxia on maximal oxygen uptake rates and the fate of lactic acid. Portland State University Library, January 2000. http://dx.doi.org/10.15760/etd.3215.

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Olson, Edwin S. Task 2.0 - Air Quality Assessment, Control, and Analytical Methods Subtask 2.11 - Lactic Acid FGD Additives From Sugar Beet Wastewater. Office of Scientific and Technical Information (OSTI), February 1998. http://dx.doi.org/10.2172/1690.

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Olson, E. S. Task 2.0 -- Air quality assessment, control, and analytical methods: Subtask 2.11 -- Lactic acid FGD additives from sugar beet wastewater. Final report. Office of Scientific and Technical Information (OSTI), June 1998. http://dx.doi.org/10.2172/290962.

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