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Auswahl der wissenschaftlichen Literatur zum Thema „Bifidobacterium infantis“
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Zeitschriftenartikel zum Thema "Bifidobacterium infantis"
Sakurai, Takuma, Toshitaka Odamaki und Jin-zhong Xiao. „Production of Indole-3-Lactic Acid by Bifidobacterium Strains Isolated fromHuman Infants“. Microorganisms 7, Nr. 9 (11.09.2019): 340. http://dx.doi.org/10.3390/microorganisms7090340.
Der volle Inhalt der QuelleChen, Yuan Yao, Xin Zhao, Wolfgang Moeder, Hein M. Tun, Elinor Simons, Piushkumar J. Mandhane, Theo J. Moraes et al. „Impact of Maternal Intrapartum Antibiotics, and Caesarean Section with and without Labour on Bifidobacterium and Other Infant Gut Microbiota“. Microorganisms 9, Nr. 9 (31.08.2021): 1847. http://dx.doi.org/10.3390/microorganisms9091847.
Der volle Inhalt der QuelleYoung, Sarah L., Mary A. Simon, Margaret A. Baird, Gerald W. Tannock, Rodrigo Bibiloni, Kate Spencely, Juliette M. Lane et al. „Bifidobacterial Species Differentially Affect Expression of Cell Surface Markers and Cytokines of Dendritic Cells Harvested from Cord Blood“. Clinical Diagnostic Laboratory Immunology 11, Nr. 4 (Juli 2004): 686–90. http://dx.doi.org/10.1128/cdli.11.4.686-690.2004.
Der volle Inhalt der QuelleSakurai, T., A. Yamada, N. Hashikura, T. Odamaki und J. Z. Xiao. „Degradation of food-derived opioid peptides by bifidobacteria“. Beneficial Microbes 9, Nr. 4 (15.06.2018): 675–82. http://dx.doi.org/10.3920/bm2017.0165.
Der volle Inhalt der QuelleHiraku, Akari, Setsuko Nakata, Mai Murata, Chendong Xu, Natsumi Mutoh, Satoshi Arai, Toshitaka Odamaki et al. „Early Probiotic Supplementation of Healthy Term Infants with Bifidobacterium longum subsp. infantis M-63 Is Safe and Leads to the Development of Bifidobacterium-Predominant Gut Microbiota: A Double-Blind, Placebo-Controlled Trial“. Nutrients 15, Nr. 6 (14.03.2023): 1402. http://dx.doi.org/10.3390/nu15061402.
Der volle Inhalt der QuellePozo-Rubio, T., J. R. Mujico, A. Marcos, E. Puertollano, I. Nadal, Y. Sanz und E. Nova. „Immunostimulatory effect of faecal Bifidobacterium species of breast-fed and formula-fed infants in a peripheral blood mononuclear cell/Caco-2 co-culture system“. British Journal of Nutrition 106, Nr. 8 (31.05.2011): 1216–23. http://dx.doi.org/10.1017/s0007114511001656.
Der volle Inhalt der QuelleHilliard, Margaret A., und David A. Sela. „Transmission and Persistence of Infant Gut-Associated Bifidobacteria“. Microorganisms 12, Nr. 5 (27.04.2024): 879. http://dx.doi.org/10.3390/microorganisms12050879.
Der volle Inhalt der QuelleTaft, Diana H., Zachery T. Lewis, Nhu Nguyen, Steve Ho, Chad Masarweh, Vanessa Dunne-Castagna, Daniel J. Tancredi et al. „Bifidobacterium Species Colonization in Infancy: A Global Cross-Sectional Comparison by Population History of Breastfeeding“. Nutrients 14, Nr. 7 (29.03.2022): 1423. http://dx.doi.org/10.3390/nu14071423.
Der volle Inhalt der QuellePeirotén, A., J. L. Arqués, M. Medina und E. Rodríguez-Mínguez. „Bifidobacterial strains shared by mother and child as source of probiotics“. Beneficial Microbes 9, Nr. 2 (27.02.2018): 231–38. http://dx.doi.org/10.3920/bm2017.0133.
Der volle Inhalt der QuelleHaarman, Monique, und Jan Knol. „Quantitative Real-Time PCR Assays To Identify and Quantify Fecal Bifidobacterium Species in Infants Receiving a Prebiotic Infant Formula“. Applied and Environmental Microbiology 71, Nr. 5 (Mai 2005): 2318–24. http://dx.doi.org/10.1128/aem.71.5.2318-2324.2005.
Der volle Inhalt der QuelleDissertationen zum Thema "Bifidobacterium infantis"
Gann, Reed N. „Host Signaling Response to Adhesion of Bifidobacterium infantis“. DigitalCommons@USU, 2010. https://digitalcommons.usu.edu/etd/586.
Der volle Inhalt der QuelleBahaka, Driss. „Analyse phenotypique et genotypique des souches du genre bifidobacterium appartenant ou apparentees aux especes b. Breve, b. Infantis et b. Longum“. Lille 2, 1993. http://www.theses.fr/1993LIL2P254.
Der volle Inhalt der QuelleHung, Ming-Ni 1962. „Biochemical and genomic analysis of -galactosidases from Bifidobacterium infantis HL96“. Thesis, McGill University, 2001. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=36953.
Der volle Inhalt der QuelleTwo genes, beta-galI and beta-galIII, located on 4.6 and 4.4 kb DNA fragments respectively, were cloned into E. coli, and the nucleotide sequences were determined. The 3,069 by-long beta-galI, encoded a polypeptide with a Mr of 113 kDa. A putative ribosome-binding site and a promoter sequence were recognized at the 5' flanking region of beta-galI. A partial sequence of an ORF transcribing divergently from beta-galI resembled a lactose permease gene. The beta-galIII gene, which is 2,076 bp long, encoded a polypeptide with a Mr of 76 kDa. A rho-independent, transcription terminator-like sequence was found 25 bp downstream of the termination codon.
The amino acid sequences of beta-GalI and beta-GalIII were homologous to those in the LacZ and LacG families, respectively. The acid-base, nucleophilic, and substrate recognition sites conserved in the LacZ family were found in beta-GalI, and a possible acid-base site proposed for the LacG family was located in beta-GalIII, containing a glutamate at residue 160. beta-GalI and beta-GalIII were over-expressed 35 and 96 times respectively in E. coli by using a pET expression system.
Both beta-GalI and beta-GalIII were specific for beta-D -anomeric linked galactosides, but beta-GalI showed more hydrolytic and synthetic activities toward lactose than beta-GalIII. The galacto-oligosaccharides (GaOS) production mediated by beta-GalI at 37°C in 20% (w/v) lactose was 130 mg/ml, which is six times higher than that of beta-GalIII. The yield of GaOS further increased to 190 mg/ml in 30% (w/v) lactose. A major tri-saccharide produced by beta-GalI was characterized as O-beta- D-galactopyranosyl-(1-3)-O-beta-D-galactopyranosyl-(1-4)- D-glucopyranose.
beta-GalI was purified by ammonium sulphate precipitation, and anion-exchange (Mono-Q) and gel filtration (Superose 12) chromatographic steps. The enzyme appeared to be a tetramer, with a Mr of 470 kDa as estimated by native PAGE and gel-filtration chromatography. The optimum temperature and pH for ONPG and lactose as substrates were 60°C, pH 7.5, and 50°C, pH 7.5, respectively. The enzyme was stable over the pH range of 5~8.5, and was particularly active at 50°C for more than 80 min. The enzyme was significantly activated by reducing agents, especially glutathione, as well as by Na+ and K+ cations. Maximal activity required both Na+ and K+ at a concentration of 10 mM. The enzyme was strongly inhibited by p-chloromercuribenzoic acid, and by most bivalent metal ions. Hydrolytic activity using 20 mM lactose as substrate was significantly inhibited by 10 mM galactose. The Km and Vmax values for ONPG and lactose were 2.6 mM, 262 U/mg, and 73.8 mM, 1.28 U/mg, respectively.
The objectives of this research were to characterize beta-galactosidases of B. infantis HL96 at the molecular and biochemical levels, and to over-express the enzymes in Escherichia coli. Two beta-galactosidase isoenzymes with unique properties were genetically characterized for the first time. beta-GalI properties included a neutral pH optimum, relatively higher temperature stability and a high transgalactosylic activity that makes it very competitive for GaOS synthesis. The results were also important for the advancement of knowledge on the catalytic mechanism and the evolutionary aspect of this enzyme.
Tu, Liwen. „Cloning and sequence analysis of multiple genes from Bifidobacterium infantis /“. free to MU campus, to others for purchase, 2004. http://wwwlib.umi.com/cr/mo/fullcit?p3137758.
Der volle Inhalt der QuelleDaigle, André. „Production d'un fromage à pâte ferme contenant des cellules vivantes de Bifidobacterium infantis“. Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1997. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp05/mq25545.pdf.
Der volle Inhalt der QuelleSousa, Ana Lucia Orlandini Pilleggi de. „Viabilidade de Bifidobacterium animalis subsp. lactis HN019 em fórmulas infantis probióticas durante o armazenamento a 4 ºC“. Universidade de São Paulo, 2011. http://www.teses.usp.br/teses/disponiveis/9/9133/tde-22082013-122441/.
Der volle Inhalt der QuelleThis study proposed to study infant formulas as vehicles for Bifidobacterium animalis ssp.lactis HNOI9. Three dairy and three non-dairy matrices were employed for the preparation of fermented or unfermented products using Bifidobacterium animalis ssp. lactis HN019 resulting in twelve different probiotic infant formulas. Acidification profile of the probiotic was determined at 42°C until pH 4.7. Physicochemical determination (total solids, protein, fat, ash, carbohydrates and calories, density and pH) was conducted, and counts viable bacteria (in dairy and non dairy infant formulas fermented and unfermented) during cold storage was focused on. The chemical characterization of the dairy and non-dairy matrix showed different results, the exception FSL2, all were in accordance to the Codex Alimentarius. The acidification profile of B. animalis ssp. lactis HN019 differed according to the matrix. During storage of products at 4°C counts of viable bacteria were stable as well as post-acidification, and were in accordance with the recommendations of the Brazilian legislation. Process (fermentation or addition) and matrix type (dairy and non-dairy) influenced post-acidification and viability of B. animalis ssp. lactis BN019 . Infant formulas could be considered good vehicles for Bifidobacterium animalis ssp. lactis HN019.
Yam, Godward Georgia Nga-Mun, of Western Sydney Hawkesbury University, Faculty of Science and Technology und of Science Food and Horticulture School. „Studies on enhancing the viability and survival of probiotic bacteria in dairy foods through strain selection and microencapsulation“. THESIS_FST_SFH_YamGodward_G.xml, 2000. http://handle.uws.edu.au:8081/1959.7/411.
Der volle Inhalt der QuelleMaster of Science (Hons)
Andrade, Samir de Deus Elian. „Efeitos da administração intragástrica de Bifidobacterium longum subsp. infantis CHCC2228 em um modelo murino agudo de colite ulcerativa induzida por sulfato sódico de dextrana (DSS)“. Universidade Federal de Minas Gerais, 2013. http://hdl.handle.net/1843/BUOS-9KKHBA.
Der volle Inhalt der QuelleDoenças inflamatórias intestinais (IBDs) são condições inflamatórias crônicas, marcadas por remissões e recidivas, de origem idiopática, mas que possuem mediação imunológica. A colite ulcerativa (UC), uma das principais formas de IBDs, tem como tratamento padrão o uso de anti-inflamatórios e corticosteróides. O uso de antibióticos também tem sido relatado, mas aqui devem ser considerados os efeitos colaterais associados. Nos últimos anos, a utilização de probióticos no tratamento de IBDs vem ganhando atenção na comunidade médica. Este trabalho objetivou avaliar os efeitos de Bifidobacterium longum subsp. infantis CHCC2228 no tratamento de UC em um modelo murino. Para a indução da colite em camundongos BALB/c fêmeas, a água foi suplementada com 3,5% de DSS (sulfato sódico de dextrana) a 3,5% por 7 dias. Durante este período os animais foram avaliados quanto à variação de peso, consistência fecal e presença de sangue nas fezes. No sétimo dia os animais foram eutanasiados para coleta dos órgãos para realização de análises histológica do fígado, do intestino delgado e do cólon. Foram, ainda, realizados: dosagem de imunoglobulina secretada (sIgA) no intestino delgado; avaliação da permeabilidade intestinal; avaliação indireta dos infiltrados de neutrófilos pela enzima mieloperoxidase (MPO), eosinófilos pela peroxidase eosinofílica (EPO) e macrófagos pela N-acetil-glicosaminidase (NAG); dosagem das citocinas KC e eotaxina-1; avaliação da permeabilidade e do estresse oxidativo no intestino. O tratamento com o probiótico melhorou o quadro clínico provocado pelo DSS nos animais. As análises histológicas e morfométricas mostraram que houve uma tendência à redução de áreas de lesão e edema nos animais, mas não houve aumento na produção de mucina. A dosagem de sIgA mostrou-se maior no grupo com colite e reduzido no grupo com colite e tratado com o probiótico. Houve, ainda, uma redução no quadro inflamatório do cólon, com redução das atividades enzimáticas de EPO e MPO, mas sem alteração na atividade de NAG. A permeabilidade intestinal, que está tipicamente aumentada durante o acometimento das IBD, mostrou-se reduzida após o tratamento com a bifidobactéria. Não foram observadas diferenças nas taxas de geração de espécies reativas de oxigênio (ROS). Baseado nestes dados pode-se concluir que a bactéria B. Longum subsp. infantis CHCC2228 possui potencial probiótico no modelo estudado e é um bom candidato para o tratamento para o tratamento da colite ulcerativa.
Yam, Godward Georgia Nga-Mun. „Studies on enhancing the viability and survival of probiotic bacteria in dairy foods through strain selection and microencapsulation“. Thesis, View thesis View thesis, 2000. http://handle.uws.edu.au:8081/1959.7/411.
Der volle Inhalt der QuelleWatterlot, Laurie. „Analyse des effets de souches probiotiques anti-inflammatoires“. Phd thesis, AgroParisTech, 2010. http://pastel.archives-ouvertes.fr/pastel-00570505.
Der volle Inhalt der QuelleBücher zum Thema "Bifidobacterium infantis"
Cheng, Ronshan. Growth, physiological characteristics and plasmid profiles of Bifidobacterium species. 1989.
Den vollen Inhalt der Quelle findenBuchteile zum Thema "Bifidobacterium infantis"
Trujillo-de Santiago, G., und C. Rojas-de Gante. „Influence of Moisture Content and Temperature on the Stability of a Dehydrated Probiotic Dairy Product Containing Bifidobacterium infantis or Lactobacillus acidophilus“. In Food Engineering Series, 461–68. New York, NY: Springer New York, 2015. http://dx.doi.org/10.1007/978-1-4939-2578-0_40.
Der volle Inhalt der QuelleLau, Amy Sie-Yik, Jin-Zhong Xiao und Min-Tze Liong. „Bifidobacterium for Infants: Essence and Efficacy“. In Microbiology Monographs, 39–72. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-23213-3_3.
Der volle Inhalt der QuelleFarzini, Yusha, Mat Nor Rohana und Abdul Khalil Khalilah. „Survivability characteristics of bifidobacterium spp. Isolates from newborn meconium and breast-fed/ formulated infant feces in acidic-simulated intestinal conditions“. In Bioresources Technology in Sustainable Agriculture, 193–205. Waretown, NJ: Apple Academic Press, 2017.: Apple Academic Press, 2018. http://dx.doi.org/10.1201/9781315365961-14.
Der volle Inhalt der Quelle„Bifidobacterium Infantis“. In Hale’s Medications & Mothers’ Milk™ 2019. New York, NY: Springer Publishing Company, 2018. http://dx.doi.org/10.1891/9780826150356.0104.
Der volle Inhalt der QuelleQuigley, E. M. M. „Bifidobacterium longum spp. infantis“. In The Microbiota in Gastrointestinal Pathophysiology, 143–44. Elsevier, 2017. http://dx.doi.org/10.1016/b978-0-12-804024-9.00017-3.
Der volle Inhalt der QuelleGhatani, Kriti, Shankar Prasad Sha, Subarna Thapa, Priya Chakraborty und Sagnik Sarkar. „Bifidobacterial Genome Editing for Potential Probiotic Development“. In Genome Editing in Bacteria (Part 1), 62–87. BENTHAM SCIENCE PUBLISHERS, 2024. http://dx.doi.org/10.2174/9789815165678124010007.
Der volle Inhalt der QuelleSancar Bozkurt, Hüseyin, und Havva Bozkurt. „Single Strain Probiotic Bifidobacteria Approach in Health and Non-Health Fields“. In Prebiotics and Probiotics - From Food to Health [Working Title]. IntechOpen, 2021. http://dx.doi.org/10.5772/intechopen.99712.
Der volle Inhalt der QuelleLewis, Zachery T., und David A. Mills. „Differential Establishment of Bifidobacteria in the Breastfed Infant Gut“. In Intestinal Microbiome: Functional Aspects in Health and Disease, 149–59. S. Karger AG, 2017. http://dx.doi.org/10.1159/000455399.
Der volle Inhalt der QuelleHack, Shirley, und Ari Bergwerk. „Lactose Intolerance“. In Pediatric Nutrition In Chronic Diseases And Developmental Disorders, 340–45. Oxford University PressNew York, NY, 2005. http://dx.doi.org/10.1093/oso/9780195165647.003.0050.
Der volle Inhalt der QuelleGupta, Charu, Consuelo Pacheco und Dhan Prakash. „Lactoserum“. In Nutraceutical and Functional Foods in Disease Prevention, 432–56. IGI Global, 2019. http://dx.doi.org/10.4018/978-1-5225-3267-5.ch015.
Der volle Inhalt der QuelleKonferenzberichte zum Thema "Bifidobacterium infantis"
Smilowitz, Jennifer T., Melissa A. Breck, Jackelyn Moya, Annette Fineberg und Mark Underwood. „Safety and Tolerability in Consuming Bifidobacterium Longum Subspecies Infantis in Exclusively Breastfed Term Infants“. In Selection of Abstracts From NCE 2016. American Academy of Pediatrics, 2018. http://dx.doi.org/10.1542/peds.141.1_meetingabstract.559.
Der volle Inhalt der QuelleFrese, Steven Alex, Andra Hutton, Lindsey Contreras, Claire Shaw, Jackelyn Moya, Melissa A. Breck, Annette Fineberg, Mark Underwood und Jennifer T. Smilowitz. „The Imprint (infant Microbiota and Probiotic Intake) Study: Microbiome Remodeling in Breast-fed Term Infants Following Supplementation and Subsequent Colonization of a Keystone Bifidobacterium Species“. In Selection of Abstracts From NCE 2016. American Academy of Pediatrics, 2018. http://dx.doi.org/10.1542/peds.141.1_meetingabstract.565.
Der volle Inhalt der QuelleLouro, Beatriz Marques Barbosa, JÉSSICA MARTINS PIMENTA MIRANDA, NATHÁLIA TENÓRIO DE HOLANDA CABRAL COSTA und YASMMYN DOS SANTOS REBOUÇAS. „ASPECTOS DA VIDA GESTACIONAL E NEONATAL E A DEFESA IMUNOLÓGICA DO RECÉM-NASCIDO“. In II Congresso Brasileiro de Imunologia On-line. Revista Multidisciplinar em Saúde, 2022. http://dx.doi.org/10.51161/ii-conbrai/6208.
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