Academic literature on the topic 'Biofilm cultures'

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Journal articles on the topic "Biofilm cultures"

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SHEFFIELD, C. L., T. L. CRIPPEN, K. ANDREWS, R. J. BONGAERTS, and D. J. NISBET. "Planktonic and Biofilm Communities from 7-Day-Old Chicken Cecal Microflora Cultures: Characterization and Resistance to Salmonella Colonization†." Journal of Food Protection 72, no. 9 (September 1, 2009): 1812–20. http://dx.doi.org/10.4315/0362-028x-72.9.1812.

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Information implicating bacterial biofilms as contributory factors in the development of environmental bacterial resistance has been increasing. There is a lack of information regarding the role of biofilms within the microbial ecology of the gastrointestinal tract of food animals. This work used a continuous-flow chemostat model derived from the ceca of 7-day-old chicks to characterize these communities and their ability to neutralize invasion by Salmonella enterica serovar Typhimurium. We characterized and compared the biofilm and planktonic communities within these microcosms using automate
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Schooling, S. R., U. K. Charaf, D. G. Allison, and P. Gilbert. "A role for rhamnolipid in biofilm dispersion." Biofilms 1, no. 2 (April 2004): 91–99. http://dx.doi.org/10.1017/s147905050400119x.

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Biofilms are often considered as localized zones of high cell density. Quorum sensing provides a means for control of population processes and has been implicated in the regulation of biofilm activities. We present a role for quorum sensing in programmed detachment and dispersal processes. Biofilms of Pseudomonas aeruginosa PAO1 and its isogenic homoserine lactone (HSL) mutant P. aeruginosa PAO-JP2 were grown in batch culture on glass substrata; differences were found in the rate and extent of formation of biofilm. Climax communities were observed for PAO1 at 24 h. These were later accompanied
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Frederick, Jesse R., James G. Elkins, Nikki Bollinger, Daniel J. Hassett, and Timothy R. McDermott. "Factors Affecting Catalase Expression in Pseudomonas aeruginosa Biofilms and Planktonic Cells." Applied and Environmental Microbiology 67, no. 3 (March 1, 2001): 1375–79. http://dx.doi.org/10.1128/aem.67.3.1375-1379.2001.

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ABSTRACT Previous work with Pseudomonas aeruginosa showed that catalase activity in biofilms was significantly reduced relative to that in planktonic cells. To better understand biofilm physiology, we examined possible explanations for the differential expression of catalase in cells cultured in these two different conditions. For maximal catalase activity, biofilm cells required significantly more iron (25 μM as FeCl3) in the medium, whereas planktonic cultures required no addition of iron. However, iron-stimulated catalase activity in biofilms was still only about one-third that in planktoni
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MINEI, CLÁUDIA C., BRUNA C. GOMES, REGIANNE P. RATTI, CARLOS E. M. D'ANGELIS, and ELAINE C. P. DE MARTINIS. "Influence of Peroxyacetic Acid and Nisin and Coculture with Enterococcus faecium on Listeria monocytogenes Biofilm Formation." Journal of Food Protection 71, no. 3 (March 1, 2008): 634–38. http://dx.doi.org/10.4315/0362-028x-71.3.634.

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Biofilm formation is a matter of concern in food industries because biofilms facilitate the survival of pathogenic bacteria such as Listeria monocytogenes, which may contaminate food-processing equipment and products. In this study, nisin and two Enterococcus faecium strains were evaluated for their effect on biofilm formation by L. monocytogenes cultured in brain heart infusion broth and on stainless steel coupons. Elimination of preformed L. monocytogenes biofilms by peroxyacetic acid also was tested. Adhesion control experiments were performed with pure cultures of L. monocytogenes after sw
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Vidal, Jorge E., Joshua R. Shak, and Adrian Canizalez-Roman. "The CpAL Quorum Sensing System Regulates Production of Hemolysins CPA and PFO To Build Clostridium perfringens Biofilms." Infection and Immunity 83, no. 6 (March 30, 2015): 2430–42. http://dx.doi.org/10.1128/iai.00240-15.

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Clostridium perfringensstrains produce severe diseases, including myonecrosis and enteritis necroticans, in humans and animals. Diseases are mediated by the production of potent toxins that often damage the site of infection, e.g., skin epithelium during myonecrosis. In planktonic cultures, the regulation of important toxins, such as CPA, CPB, and PFO, is controlled by theC. perfringensAgr-like (CpAL) quorum sensing (QS) system. Strains also encode a functional LuxS/AI-2 system. AlthoughC. perfringensstrains form biofilm-like structures, the regulation of biofilm formation is poorly understood
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Wolyniak, E. A., B. R. Hargreaves, and K. L. Jellison. "Retention and Release of Cryptosporidium parvum Oocysts by Experimental Biofilms Composed of a Natural Stream Microbial Community." Applied and Environmental Microbiology 75, no. 13 (May 15, 2009): 4624–26. http://dx.doi.org/10.1128/aem.02916-08.

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ABSTRACT Cryptosporidium parvum oocysts accumulate on biofilm surfaces. The percentage of oocysts attached to biofilms remained nearly constant while oocysts were supplied to the system but decreased to a new steady-state level once oocysts were removed from the feed. More oocysts attached to summer biofilm cultures than winter biofilm cultures.
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Rahmani-Badi, Azadeh, Shayesteh Sepehr, Parisa Mohammadi, Mohammad Reza Soudi, Hamta Babaie-Naiej, and Hossein Fallahi. "A combination of cis-2-decenoic acid and antibiotics eradicates pre-established catheter-associated biofilms." Journal of Medical Microbiology 63, no. 11 (November 1, 2014): 1509–16. http://dx.doi.org/10.1099/jmm.0.075374-0.

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The catheterized urinary tract provides ideal conditions for the development of biofilm populations. Catheter-associated urinary tract infections (CAUTIs) are recalcitrant to existing antimicrobial treatments; therefore, established biofilms are not eradicated completely after treatment and surviving biofilm cells will carry on the infection. Cis-2-decenoic acid (CDA), an unsaturated fatty acid, is capable of inhibiting biofilm formation by Pseudomonas aeruginosa and of inducing the dispersion of established biofilms by multiple types of micro-organisms. Here, the ability of CDA to induce disp
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Bryers, James D., and Huang Ching-Tsan. "Recombinant plasmid retention and expression in bacterial biofilm cultures." Water Science and Technology 31, no. 1 (January 1, 1995): 105–15. http://dx.doi.org/10.2166/wst.1995.0025.

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Any exposure of plasmid recombinant microorganisms to an open system environment, either inadvertently or intentionally, mandates research into those fundamental organism:plasmid processes that influence plasmid retention, transfer and expression. In open environmental systems a majority of the microbial activity occurs associated with an interface, within thin biological layers consisting of the cells and their insoluble extracellular polymer, layers known as biofilms. Thus any study regarding the fate of recombinant DNA sequences in an open system must consider processes that affect plasmid
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Chinnici, Jennifer, Lisa Yerke, Charlene Tsou, Sujay Busarajan, Ryan Mancuso, Nishanth D. Sadhak, Jaewon Kim, and Abhiram Maddi. "Candida albicans cell wall integrity transcription factors regulate polymicrobial biofilm formation with Streptococcus gordonii." PeerJ 7 (October 11, 2019): e7870. http://dx.doi.org/10.7717/peerj.7870.

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Polymicrobial biofilms play important roles in oral and systemic infections. The oral plaque bacterium Streptococcus gordonii is known to attach to the hyphal cell wall of the fungus Candida albicans to form corn-cob like structures in biofilms. However, the role of C. albicans in formation of polymicrobial biofilms is not completely understood. The objective of this study was to determine the role of C. albicans transcription factors in regulation of polymicrobial biofilms and antibiotic tolerance of S. gordonii. The proteins secreted by C. albicans and S. gordonii in mixed planktonic culture
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Kay, Matthew K., Thomas C. Erwin, Robert J. C. McLean, and Gary M. Aron. "Bacteriophage Ecology inEscherichia coliandPseudomonas aeruginosaMixed-Biofilm Communities." Applied and Environmental Microbiology 77, no. 3 (December 3, 2010): 821–29. http://dx.doi.org/10.1128/aem.01797-10.

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ABSTRACTPhage therapy is being reexamined as a strategy for bacterial control in medical and other environments. As microorganisms often live in mixed populations, we examined the effect ofEscherichia colibacteriophage λW60 andPseudomonas aeruginosabacteriophage PB-1 infection on the viability of monoculture and mixed-species biofilm and planktonic cultures. In mixed-species biofilm communities,E. coliandP. aeruginosamaintained stable cell populations in the presence of one or both phages. In contrast,E. coliplanktonic populations were severely depleted in coculture in the presence of λW60. Bo
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Dissertations / Theses on the topic "Biofilm cultures"

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Behnke, Sabrina. "Disinfection susceptibilities of detached biofilm clusters compared to planktonic cells and biofilms in single species and dual species cultures." Diss., Montana State University, 2011. http://etd.lib.montana.edu/etd/2011/behnke/BehnkeS0811.pdf.

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Detachment of cells and clusters from biofilms is an important process in the dissemination of microorganisms in industrial, environmental, and clinical settings but the disinfection susceptibilities of these cell clusters have not been sufficiently characterized. With the help of fluorescent microscopy and image analysis, naturally detaching cells and clusters from single species and dual species biofilms of Burkholderia cepacia and Pseudomonas aeruginosa grown in biofilm tubing reactors were analyzed for cluster size distributions and compared to the cluster sizes in chemostat cultures. The
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au, L. Hughes@murdoch edu, and Leonie Hughes. "Multistage and multiple biomass approaches to efficient biological nitrogen removal using biofilm cultures." Murdoch University, 2008. http://wwwlib.murdoch.edu.au/adt/browse/view/adt-MU20080523.134154.

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Nitrogen removal from wastewater is important for the revention of significant health and environmental impacts such as eutrophication. Nitrogen removal is achieved by the combined action of nitrification and denitrification. Nitrification is performed by autotrophic, slow growing microorganisms that require oxygen and are inhibited in the presence of denitrifiers when oxygen and COD are available due to competition for oxygen. Denitrification however, performed by relatively fast growing heterotrophic bacteria, is inhibited by oxygen and requires COD. This implies that nitrification and denit
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Hughes, Leonie. "Multistage and multiple biomass approaches to efficient biological nitrogen removal using biofilm cultures." Hughes, Leonie (2008) Multistage and multiple biomass approaches to efficient biological nitrogen removal using biofilm cultures. PhD thesis, Murdoch University, 2008. http://researchrepository.murdoch.edu.au/674/.

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Nitrogen removal from wastewater is important for the revention of significant health and environmental impacts such as eutrophication. Nitrogen removal is achieved by the combined action of nitrification and denitrification. Nitrification is performed by autotrophic, slow growing microorganisms that require oxygen and are inhibited in the presence of denitrifiers when oxygen and COD are available due to competition for oxygen. Denitrification however, performed by relatively fast growing heterotrophic bacteria, is inhibited by oxygen and requires COD. This implies that nitrification and denit
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Gillmann, Antoine. "Étude de la survie de contaminants bactériens modèles d’origine industrielle, isolés d’environnements oligotrophes, et élaboration de milieux synthétiques permettant leur croissance." Thesis, Strasbourg, 2015. http://www.theses.fr/2015STRAJ004/document.

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La mise au point de milieux de culture permettant de mettre en évidence rapidement et de manière reproductible des micro-organismes exigeants représenterait une évolution significative dans le contrôle des produits et procédés industriels. Deux milieux de culture synthétiques ont été élaborés pour répondre à ce besoin. Le développement des milieux de culture a été réalisé en combinant l’analyse de composés nutritionnels à l’étude de certains métabolismes bactériens. Les formulations des milieux de culture obtenues permettent ainsi la croissance de micro-organismes aux exigences nutritionnelles
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Pierra, Mélanie. "Couplage de la fermentation sombre et de l’électrolyse microbienne pour la production d’hydrogène : formation et maintenance du biofilm électro-actif." Thesis, Montpellier 2, 2013. http://www.theses.fr/2013MON20150/document.

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L'hydrogène, qui constitue une solution alternative et durable à l’usage d’énergies fossiles, est produit essentiellement par reformage de combustibles fossiles (95%). Des filières de production plus soucieuses de l'environnement sont envisagées. Deux familles de technologies sont explorées: 1) par décomposition thermochimique ou électrochimique de l'eau et 2) à partir de différentes sources de biomasse. Parmi celles-ci, les cellules d'électrolyse microbienne ou «Microbial electrolysis cell (MEC)» permettent de produire de l'hydrogène par électrolyse de la matière organique. Une MEC consiste e
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Phoeurng, Sackona. "Mise en évidence de Listeria spp. Dans le contexte alimentaire au Cambodge et étude du comportement de L. Monocytogenes en biofilm sous l'influence de Pseudomonas fluorescens et de désinfectants." Dijon, 2002. http://www.theses.fr/2002DIJOS054.

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Dastidar, Aniruddha. "ARSENITE OXIDATION BY PURE CULTURES OF THIOMONAS ARSENIVORANS STRAIN B6 IN BIOREACTOR SYSTEMS." UKnowledge, 2010. http://uknowledge.uky.edu/gradschool_diss/70.

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The removal of arsenic toxicity from water is accomplished by a preliminary preoxidative step transforming the most toxic form, arsenite (As (III)), to the least toxic form, arsenate (As (V)). The potential of As (III) oxidation to As (V) was initially investigated in batch reactors using the chemoautotrophic Thiomonas arsenivorans strain b6 under varying initial As (III) and cell concentrations and at optimal pH and temperature conditions (pH 6.0 and temperature 30°C). The strain b6 completely oxidized As (III) to As (V) during exponential growth phase for lower levels of As (III) concentrati
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Borrel, Valérie. "Influence du microenvironnement sur la virulence et la formation de biofilm de Cutibacterium acnes." Thesis, Normandie, 2019. http://www.theses.fr/2019NORMR035/document.

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L’acné vulgaris est considérée comme l’une des maladies de la peau les plus communes. Sa pathologie n’est pas encore totalement élucidée mais Cutibacterium acnes (précédemment Propionibacterium acnes), est considérée comme l’un des facteurs principaux de son développement. Cette bactérie est caractérisée par une importante variabilité génomique et les souches de ribotype 4 et 5 (RT4 et RT5) ont été associées à l’acné tandis que celles de RT6 sont considérées comme commensales. Les différences physiologiques de ces types de C. acnes en fonction de leur environnement (différents milieux de cultu
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Goudot, Sébastien. "Étude des facteurs d'influence de l'écologie de Naegleria fowleri dans les biofilms." Thesis, Université de Lorraine, 2012. http://www.theses.fr/2012LORR0304/document.

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Dans l'objectif d'anticiper et de réduire la prolifération de l'amibe pathogène Naegleria fowleri dans les circuits de refroidissement de certaines centrales électriques, notre travail vise à mieux comprendre l'écologie de cette amibe dans des environnements complexes tels que les biofilms d'eau douce récemment reconnus comme niche écologique préférentielle des amibes libres. Des essais de laboratoire ont été réalisés pour déterminer l'impact des facteurs environnementaux naturels et anthropiques: température, nature du matériau support de la formation du biofilm, charge nutritionnelle et mono
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Pandin, Caroline. "Exploration des mécanismes impliqués dans la bioprotection d'Agaricus bisporus par les biofilms de Bacillus subtilis QST713." Thesis, Université Paris-Saclay (ComUE), 2018. http://www.theses.fr/2018SACLA025/document.

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Les pertes alimentaires mondiales se chiffrent à environ un tiers des aliments destinés à la consommation humaine, soit environ 1,3 milliards de tonnes par an (FAO). Une large fraction de ces pertes est due aux altérations microbiologiques des denrées alimentaires. L’utilisation de produits phytosanitaires reste aujourd’hui la solution la plus largement utilisée en agriculture pour limiter ces pertes. Cependant, avec le plan EcoPhyto 2, le gouvernement français a pour objectif de réduire de 50% l’usage des pesticides chimiques d’ici 2025, en particulier en promouvant l’émergence du biocontrôle
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Books on the topic "Biofilm cultures"

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Ehrlich, Garth D., Patrick J. DeMeo, J. William Costerton, and Heinz Winkler, eds. Culture Negative Orthopedic Biofilm Infections. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-29554-6.

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Crichton, Michael. Rising Sun / The Andromeda Strain / Binary. London: Cresset, 1994.

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Culture Negative Orthopedic Biofilm Infections Springer Series on Biofilms. Springer, 2012.

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Costerton, J. William, Heinz Winkler, Garth D. Ehrlich, and Patrick J. DeMeo. Culture Negative Orthopedic Biofilm Infections. Springer, 2015.

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Clair, Larry St. Biodeterioration of Stone Surfaces: Lichens And Biofilms As Weathering Agents Of Rocks And Cultural Heritage. Springer, 2011.

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L, St Clair Larry, and Seaward M. R. D, eds. Biodeterioration of stone surfaces: Lichens and biofilms as weathering agents of rocks and cultural heritage. Dordrecht: Kluwer Academic Publishers, 2004.

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Mabey, David, Hasan E. Baydoun, and Jamil D. Bayram. Prosthetic Joint Infections. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199976805.003.0048.

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Prosthetic joint infection (PJI), a complication of joint replacement surgery, presents with fever, joint pain, erythema, effusion, and joint loosening. Many advances have decreased the risk of infection, such as the use of perioperative antimicrobial prophylaxis and intraoperative laminar airflow. Joint fluid analysis should be pursued by the orthopedic surgeons; primary and acute care providers should consult the definitive care team and refer these patients for admission. Organisms causing prosthetic joint infections often grow in biofilms, which make them difficult to treat. Surgical treat
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Ely, Roger Lee. Startup and performance of a gas-permeable-membrane-supported (GPMS) biofilm system using a mixed culture of methylotrophs to degrade methylene chloride, chloroform, and carbon tetrachloride. 1986.

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Book chapters on the topic "Biofilm cultures"

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Cappitelli, Francesca, and Federica Villa. "Novel Antibiofilm Non-Biocidal Strategies." In Microorganisms in the Deterioration and Preservation of Cultural Heritage, 117–36. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-69411-1_5.

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AbstractSubaerial biofilm (SAB) formation on cultural heritage objects is often considered an undesirable process in which microorganisms and their by-products, e.g., enzymes and pigments, cause damage or alteration to a surface. Since biofilms are widespread phenomena, there has been a high demand for preventive and control strategies that resist their formation or reduce their negative effects once formed. Up to date, the main strategy to control biofilms has been the use of biocides. Because of their intrinsic properties, biocidal products can pose risks to humans, animals, and the environment. In this chapter, the authors call “green” only those alternative strategies to biocides able to prevent/control biofilms but that do not kill microorganisms, i.e., irrespective of the use of natural compounds. Here, we describe some of the methods that are most commonly used to test the effectiveness of antibiofilm compounds with multiple-species biofilm model systems. A unified terminology and well described protocols and guidelines are still required to compare and test the effectiveness of traditional or novel compounds against biofilms retrieved on heritage surfaces.
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Gu, Ji-Dong, and Yoko Katayama. "Microbiota and Biochemical Processes Involved in Biodeterioration of Cultural Heritage and Protection." In Microorganisms in the Deterioration and Preservation of Cultural Heritage, 37–58. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-69411-1_2.

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AbstractThe world cultural heritage sites face new challenges for an effective protection and management because of destruction and damage initiated by both natural and anthropogenic causes. Fresh rock and sandstone surfaces of buildings are quickly colonized and covered by a layer of microorganisms, including phototrophs, lithotrophs, and heterotrophs to form a biofilm that alters the local conditions of the stone surfaces, especially under the favorable tropical climate conditions for autotrophic microorganisms and plants. Biofilms had been studied with indigenous or pure cultures of isolated microorganisms, but the selective ones that contribute to deterioration of the cultural heritage cannot be confirmed easily. Currently, high-throughput sequencing and metegenomics analyses are capable of obtaining microbial community and composition in great depth, but they also suffer from similar weakness unable to identify the culprits in the community. With these as background, this article presents a different approach by focusing on the biochemical processes and the responsible microorganisms involved to reveal the destruction processes for management and protection. Among these different functional groups of microorganisms, lichens are known as pioneering rock-decomposing microorganisms, and both sulfur-oxidizing bacteria and fungi participate in the decomposition of sandstone via sulfur cycling and initiation of salt attack of the stone afterward, resulting in defoliation and cracking of stone. Other microorganisms including ammonia-oxidizing bacteria and archaea, especially the latter, have been recently detected on sandstone monuments providing evidence on the new organisms involved in the deterioration of cultural heritage and buildings. In addition, fungi can colonize the surfaces of the matured biofilms and play a new role in the removal of them, which has a potential biotechnological application in conservation of cultural heritage. The new proposed approach by focusing the microorganisms with identified biochemical function is more productive than a description of the community composition and assembly when assessing cultural heritage biodeterioration, and this provides basic and useful information for effective protection strategies and management.
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Congestri, Roberta, and Patrizia Albertano. "Benthic Diatoms in Biofilm Culture." In The Diatom World, 227–43. Dordrecht: Springer Netherlands, 2011. http://dx.doi.org/10.1007/978-94-007-1327-7_10.

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Ehrlich, G. D., P. J. DeMeo, and J. W. Costerton. "The Problem of Culture-Negative Infections." In Springer Series on Biofilms, 1–15. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-29554-6_1.

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Ehrlich, G. D., Patrick DeMeo, Michael Palmer, T. J. Sauber, Dan Altman, Greg Altman, Nick Sotereanos, et al. "Culture-Negative Infections in Orthopedic Surgery." In Springer Series on Biofilms, 17–27. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-29554-6_2.

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Spenceley, H., C. S. Dow, and J. T. Holah. "Development of Mixed Culture Biofilms on Stainless Steel." In Biofilms — Science and Technology, 395–402. Dordrecht: Springer Netherlands, 1992. http://dx.doi.org/10.1007/978-94-011-1824-8_33.

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Parvizi, Javad. "Diagnosing Periprosthetic Joint Infection: Cultures, Molecular Markers, and the Ibis Technology." In Springer Series on Biofilms, 77–86. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-29554-6_6.

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Pinna, Daniela. "Microbial Growth and its Effects on Inorganic Heritage Materials." In Microorganisms in the Deterioration and Preservation of Cultural Heritage, 3–35. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-69411-1_1.

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AbstractCultural heritage objects composed of inorganic materials, such as metals and stones, support microbial life. Many factors affect the growth of microorganisms: moisture, pH, light, temperature, nutrients. Their colonization relates closely to the nature of the substrata as well as to the characteristic of the surrounding environment. This chapter contains an overview of the complex relationships among microbial growth, materials, and the environment. It emphasizes issues on bioreceptivity of stones and the factors influencing biological colonization, focusing on the biological alteration of inorganic heritage objects and on the agents of biodeterioration. It outlines the effect of biofilms and lichens in terms of degradation of substrata and includes a discussion on an important topic, the bioprotection of stones by biofilms and lichens. In summary, this chapter aims to discuss these issues and review the recent literature on (i) biofilms and lichens colonizing inorganic materials, (ii) the limiting factors of this colonization, (iii) the deteriorative aspects, and (iv) the protective effects of the colonization.
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Cappitelli, Francesca, Federica Villa, and Andrea Polo. "Culture-Independent Methods to Study Subaerial Biofilm Growing on Biodeteriorated Surfaces of Stone Cultural Heritage and Frescoes." In Methods in Molecular Biology, 341–66. New York, NY: Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4939-0467-9_24.

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King, Rebecca M., and Victoria Korolik. "Characterization of Ligand–Receptor Interactions: Chemotaxis, Biofilm, Cell Culture Assays, and Animal Model Methodologies." In Methods in Molecular Biology, 149–61. New York, NY: Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4939-6536-6_13.

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Conference papers on the topic "Biofilm cultures"

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Bhaduri, S., S. K. Mitra, and A. Kumar. "Understanding Biofilm Growth Dynamics Within a Stagnant Culture of Sporosarcina Pasteurii." In ASME 2014 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2014. http://dx.doi.org/10.1115/imece2014-36778.

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Biofilms are bacterial colonies that form at interfaces, where bacteria are encased in extracellular polymeric substances (EPS). Biofilms are ubiquitous in both artificial systems and our environment. Here we focus on understanding biofilm growth within a stagnant pool of confined diluted culture of the bacteria. Sporosarcina pasteurii is taken as the model bacterium for this study. The motivation behind the choice of this organism stems from the fact that S. Pasteurii has the unique ability to precipitate calcite inside the host media which has tremendous applications in reservoir and restora
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Kussovski, V., V. Mantareva, I. Angelov, L. Avramov, E. Popova, and S. Dimitrov. "Al(III), Pd(II), and Zn(II) phthalocyanines for inactivation of dental pathogen Aggregatibacter actinomycetemcomitans as planktonic and biofilm-cultures." In SPIE Photonics Europe, edited by Jürgen Popp, Wolfgang Drexler, Valery V. Tuchin, and Dennis L. Matthews. SPIE, 2012. http://dx.doi.org/10.1117/12.923050.

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Zahra, R., A. A. Khan, and M. Sajid. "Hydrodynamic Evaluation of Microtiter Plate Assay Using Computational Fluid Dynamics for Biofilm Formation." In ASME-JSME-KSME 2019 8th Joint Fluids Engineering Conference. American Society of Mechanical Engineers, 2019. http://dx.doi.org/10.1115/ajkfluids2019-5425.

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Abstract Biofilms are complex surface associated communities where bacterial cells are enclosed by self-produced extra cellular polymeric substances (EPS), mainly consisting of exopolysaccharides, proteins and extracellular DNA. Treatment of biofilm associated persistent infections is an emerging issue for clinicians as bacterial cells adhere with human epithelial cells or indwelling medical devices such as implants and catheters, used in urinary tract and respiratory infections. Several methods are in practice to assess the biofilm formation of bacterial strains. Most of these are phenotypic
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"Simultaneous Saccharification and Ethanol Fermentation by Co-culture in Biofilm Reactors." In 2016 ASABE International Meeting. American Society of Agricultural and Biological Engineers, 2016. http://dx.doi.org/10.13031/aim.20162456278.

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Natalia, Angel Villegas, Arce Miranda Julio Eduardo, Becerra María Cecilia, Baronetti José Luis, Ravetti Soledad, Sotomayor Claudia Elena, Albesa Inés, and Paraje María Gabriela. "How different culture conditions affect cellular stresses in the biofilms." In MICROBES IN APPLIED RESEARCH - Current Advances and Challenges. WORLD SCIENTIFIC, 2012. http://dx.doi.org/10.1142/9789814405041_0128.

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HANSEL, EZEQUIEL, Alice Costa Kiperstok, Rodrigo Gomes Guimaraes, and Emerson Andrade Sales. "CLAY AS A SUBSTRATUM MATERIAL FOR MICROALGAE BIOFILM CULTIVATION." In I South Florida Congress of Development. CONGRESS PROCEEDINGS I South Florida Congress of Development - 2021, 2021. http://dx.doi.org/10.47172/sfcdv2021-0025.

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The production of microalgae faces several obstacles. The bioreactors and processes used today in microalgae cultivation are expensive or lack optimization to scale up. Furthermore, harvesting, concentrating and dewatering, while using a cheap and suitable photobioreactor are the main problems that we need to be overcome to achieve viability in the process. The Clay Ceramic Bioreactor (CCBR) was built using only clay and wood sawdust and was designed to grow an immobilized microalgal biofilm while having almost complete separation from the liquid culture medium, reducing the consumption of wat
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HANSEL, EZEQUIEL, Alice Costa Kiperstok, Rodrigo Gomes Guimaraes, and Emerson Andrade Sales. "CLAY AS A SUBSTRATUM MATERIAL FOR MICROALGAE BIOFILM CULTIVATION." In I South Florida Congress of Development. CONGRESS PROCEEDINGS I South Florida Congress of Development - 2021, 2021. http://dx.doi.org/10.47172/sfcdv2021-0063.

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The production of microalgae faces several obstacles. The bioreactors and processes used today in microalgae cultivation are expensive or lack optimization to scale up. Furthermore, harvesting, concentrating and dewatering, while using a cheap and suitable photobioreactor are the main problems that we need to be overcome to achieve viability in the process. The Clay Ceramic Bioreactor (CCBR) was built using only clay and wood sawdust and was designed to grow an immobilized microalgal biofilm while having almost complete separation from the liquid culture medium, reducing the consumption of wat
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Hassan, Huzairy, Bo Jin, Sheng Dai, and Cornelius Ngau. "Formation of industrial mixed culture biofilm in chlorophenol cultivated medium of microbial fuel cell." In 4TH INTERNATIONAL CONFERENCE ON FUNDAMENTAL AND APPLIED SCIENCES (ICFAS2016). Author(s), 2016. http://dx.doi.org/10.1063/1.4968084.

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Endicott-Yazdani, T. R. "Concordance of BioFire Pneumonia Panel with Traditional Respiratory Bacterial Culture Results." In American Thoracic Society 2021 International Conference, May 14-19, 2021 - San Diego, CA. American Thoracic Society, 2021. http://dx.doi.org/10.1164/ajrccm-conference.2021.203.1_meetingabstracts.a3869.

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Utkin, A. B., P. Chaves, L. Fernandes, I. V. Pinto, and M. J. Revez. "LIF and SFS Techniques for Early Detection of Biofilms Harmful for Cultural Heritage." In 2018 International Conference Laser Optics (ICLO). IEEE, 2018. http://dx.doi.org/10.1109/lo.2018.8435198.

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Reports on the topic "Biofilm cultures"

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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 resu
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Fields, Matthew W. Identification of Molecular and Cellular Responses of Desulfovibrio vulgaris Biofilms under Culture Conditions Relevant to Field Conditions for Bioreduction. Office of Scientific and Technical Information (OSTI), June 2006. http://dx.doi.org/10.2172/896800.

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Wall, Judy D. Identification of Molecular and Cellular Responses of Desulfovibrio vulgaris Biofilms under Culture Conditions Relevant to Field Conditions for Bioreduction of. Office of Scientific and Technical Information (OSTI), June 2006. http://dx.doi.org/10.2172/896801.

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Judy D. Wall. Identification of Molecular and Cellular Responses of Desulfovibrio vulgaris Biofilms under Culture Conditions Relevant to Field Conditions for Bioreduction of Toxic Metals and Radionuclides. Office of Scientific and Technical Information (OSTI), June 2011. http://dx.doi.org/10.2172/1015868.

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