Academic literature on the topic 'Rv3852'
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Journal articles on the topic "Rv3852"
Brodin, Priscille, Laleh Majlessi, Laurent Marsollier, Marien I. de Jonge, Daria Bottai, Caroline Demangel, Jason Hinds, et al. "Dissection of ESAT-6 System 1 of Mycobacterium tuberculosis and Impact on Immunogenicity and Virulence." Infection and Immunity 74, no. 1 (January 2006): 88–98. http://dx.doi.org/10.1128/iai.74.1.88-98.2006.
Full textLiu, Zhiqiang, Shuang Qie, Lili Li, Bingshui Xiu, Xiqin Yang, Zhenhua Dai, Xuhui Zhang, et al. "Identification of Novel RD1 Antigens and Their Combinations for Diagnosis of Sputum Smear−/Culture+ TB Patients." BioMed Research International 2016 (2016): 1–10. http://dx.doi.org/10.1155/2016/7486425.
Full textGarg, Rajni, Chinmay Anand, Sohini Ganguly, Sandhya Rao, Rinkee Verma, and Valakunja Nagaraja. "Direct Interaction of Polar Scaffolding Protein Wag31 with Nucleoid-Associated Protein Rv3852 Regulates Its Polar Localization." Cells 10, no. 6 (June 20, 2021): 1558. http://dx.doi.org/10.3390/cells10061558.
Full textWerlang, Isabel C. R., Cristopher Z. Schneider, Jordana D. Mendonça, Mario S. Palma, Luiz A. Basso, and Diógenes S. Santos. "Identification of Rv3852 as a nucleoid-associated protein in Mycobacterium tuberculosis." Microbiology 155, no. 8 (August 1, 2009): 2652–63. http://dx.doi.org/10.1099/mic.0.030148-0.
Full textZhao, Nan, Mingna Sun, Kristin Burns-Huang, Xiuju Jiang, Yan Ling, Crystal Darby, Sabine Ehrt, Gang Liu, and Carl Nathan. "Identification of Rv3852 as an Agrimophol-Binding Protein in Mycobacterium tuberculosis." PLOS ONE 10, no. 5 (May 15, 2015): e0126211. http://dx.doi.org/10.1371/journal.pone.0126211.
Full textLiu, Xiao-Qing, Davinder Dosanjh, Hansa Varia, Katie Ewer, Paul Cockle, Geoffrey Pasvol, and Ajit Lalvani. "Evaluation of T-Cell Responses to Novel RD1- and RD2-Encoded Mycobacterium tuberculosis Gene Products for Specific Detection of Human Tuberculosis Infection." Infection and Immunity 72, no. 5 (May 2004): 2574–81. http://dx.doi.org/10.1128/iai.72.5.2574-2581.2004.
Full textCockle, P. J., S. V. Gordon, A. Lalvani, B. M. Buddle, R. G. Hewinson, and H. M. Vordermeier. "Identification of Novel Mycobacterium tuberculosis Antigens with Potential as Diagnostic Reagents or Subunit Vaccine Candidates by Comparative Genomics." Infection and Immunity 70, no. 12 (December 2002): 6996–7003. http://dx.doi.org/10.1128/iai.70.12.6996-7003.2002.
Full textTiwari, Bhavana, Amarendranath Soory, and Tirumalai R. Raghunand. "An immunomodulatory role for theMycobacterium tuberculosisregion of difference 1 locus proteins PE35 (Rv3872) and PPE68 (Rv3873)." FEBS Journal 281, no. 6 (February 12, 2014): 1556–70. http://dx.doi.org/10.1111/febs.12723.
Full textDemangel, Caroline, Priscille Brodin, Paul J. Cockle, Roland Brosch, Laleh Majlessi, Claude Leclerc, and Stewart T. Cole. "Cell Envelope Protein PPE68 Contributes to Mycobacterium tuberculosis RD1 Immunogenicity Independently of a 10-Kilodalton Culture Filtrate Protein and ESAT-6." Infection and Immunity 72, no. 4 (April 2004): 2170–76. http://dx.doi.org/10.1128/iai.72.4.2170-2176.2004.
Full textMeniche, Xavier, Cécile Labarre, Célia de Sousa-d'Auria, Emilie Huc, Françoise Laval, Marielle Tropis, Nicolas Bayan, et al. "Identification of a Stress-Induced Factor of Corynebacterineae That Is Involved in the Regulation of the Outer Membrane Lipid Composition." Journal of Bacteriology 191, no. 23 (October 2, 2009): 7323–32. http://dx.doi.org/10.1128/jb.01042-09.
Full textDissertations / Theses on the topic "Rv3852"
Werlang, Isabel Cristina Ribas. "Rv3852, uma nova proteína Histone-Like de Mycobacterium tuberculosis." reponame:Biblioteca Digital de Teses e Dissertações da UFRGS, 2009. http://hdl.handle.net/10183/17330.
Full textTuberculosis remains the major cause of mortality due to a bacterial pathogen, Mycobacterium tuberculosis. The emergence of multidrug- and extensively drug-resistant strains have raised the bleak prospect of a future epidemic of virtually untreatable TB. More effective antimycobacterial agents, besides new vaccines or vaccination strategies, are thus needed to improve the treatment of resistant strains, to shorten the treatment course, and to provide more effective treatment of latent infection. The molecular mechanisms by which the bacillus establishes infection and persistence have not been completely elucidated. Studies involving nucleoid-associated proteins, which have been related to the control and influence of virulence genes in pathogenic bacteria, can help unveil the virulence process of M. tuberculosis. In this study, we describe the initial characterization of an open reading frame for the M. tuberculosis putative H-NS. This protein is one of the most studied members of the nucleoid-associated proteins family. The gene was cloned, expressed and its product purified to homogeneity. A qualitative protein-DNA binding assay was carried out by gel-retardation and the protein affinity for specific DNA sequences was assessed quantitatively by surface plasmon resonance. A protein-DNA binding mechanism is proposed. In addition, functional complementation studies of an E. coli hns mutant reinforce the likelihood that Rv3852 protein represents a novel nucleoid-associated protein in M. tuberculosis.
SHANAHAN, Erin Rose. "Molecular investigation of mycobacterium tuberculosis and the critical cell wall lipase culp6." Thesis, The University of Sydney, 2014. http://hdl.handle.net/2123/10066.
Full textGoins, Christopher M. "Structural, Enzymatic, and Inhibitory Studies of Two Mycobacterium tuberculosis- Mycomembrane Lipid Esterases." University of Toledo / OhioLINK, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=toledo1524926557102369.
Full textLi, Yu-Ru, and 李育儒. "To Explore β-Amyloid Induced Oxidative DNA Damage and Repair in Rat Primary Cortical Neurons." Thesis, 2016. http://ndltd.ncl.edu.tw/handle/rv3f22.
Full text國立中山大學
生物科學系研究所
104
Alzheimer''s disease (AD) is one of the common form of age-related neurodegenerative diseases and the leading cause of senile dementia. In the beta-amyloid (Aβ) cascade hypothesis, the aggregation of Aβ is a crucial event that produces amounts of oxidative stress contributed to neurotoxicity. In this study, our hypothesis is that Aβ-peptide aggregation enhances oxidative stress which leads to DNA damage and contributes to neurotoxicity. Therefore, increasing DNA repair efficiency and DNA integrity could rescue neuronal cells from Aβ-induced neuronal death. To test our hypothesis, we utilized lentivirus transduction to overexpress Aβ in rat primary cortical neurons. Results of Western blotting and dihydroethidium (DHE) staining have shown that expression of Aβ reached the peak in the first three days as well as the production of reactive oxygen species (ROS), then both Aβ and ROS levels were decreasing in the following day four to day seven. The DNA damage marker, phosphor-histone 2A (γH2AX), demonstrated that neuronal DNA injury was correlated to both levels of Aβ and ROS. Glucagon-like peptide-1 (GLP-1) is a growth factor which has been proved to have neuroprotective properties. After GLP-1 treatment, the production of Aβ and ROS was reduced, but γH2AX was still remaining in 72 hours. GLP-1 has been proved the effects of decreasing Aβ, inflammation and the improvement of recognition, learning and memory in animal model from previous studies. Although we did not see GLP-1 significantly reducing γH2AX, GLP-1 is still a potential drug involving DNA repair. In Alzheimer’s disease, to elevate DNA repair capability is also a important field to investigate in the future.
Huang, Chao-Ku, and 黃兆谷. "Characterization and improvement of lactic acid production of isolated Bacillus coagulans." Thesis, 2018. http://ndltd.ncl.edu.tw/handle/rv38t7.
Full text國立屏東科技大學
生物科技系所
106
Poly lactic acid, polymerized from of lactic acid, is one of the most potential materials due to reducing pollution. Fermentation of agricultural wastes containing starch and cellulose are able to produce lactic acid, but the most lactic acid bacteria have not amylase and cellulose activity, and such as feedstock needs an extra process to be degraded to small molecules before microbial fermentation. Bacillus coagulans has good amylolytic activity; it also can produce L-lactic acid. However, its production level of lactic acid is not significant. Therefore, our goal is improve the production of lactic acid by optimization of culture medium and protoplast fusion technology in this study. X1 strain, a Gram-positive rod, from wasted food. It can hydrolyse starch to glucose and convert to lactic acid, but it cannot grow in medium containing 7% salt. This strain was identified as Bacillus coagulans based on its phylogenetic analysis. In addition, the strain G3 was also isolated. It did not have catalase and cell oxidase activities, but produced 25.141mg/mL of lactic acid. According to these features. Strain G3 may be belong to lactic acid bacteria. In order to improve the production of lactic acid, the bacterial medium was optimized. The medium contain 1.0% soy peptone, 2.5% potato extract and 1.5% yeast extract can increase the bacterial density. In order to improve the ability of L-lactic acid, the protoplasts of X1 strain and G3 strain were fused. Moreover, acid producing and starch hydrolysis abilities were estimated. The results showed that some the fused strain can produce organic acid, others can degrade starch and amylopectin. No fusion strain has both capabilities at the same time. The strain that can produce organic acid, the production level of lactic acid was about 20mg/mL. It was significantly reduced when compared with the wildtype. Because the fusion strain does not improve production of lactic acid, we want to prove the problem of protoplast fusion system and different bacteria has different characteristic to cause the fusion problem. So use the X1 strain fused with Bacillus amyloliquefaciens and Bacillus subtilis. In the result of fusion showed that there was no significantly change of feature in the fusion strains.
Books on the topic "Rv3852"
(Composer), Antonio Vivaldi, and Maurizo Carnelli (Editor), eds. Concerto in G Minor "L'estate" (Summer) from The Four Seasons RV315, Op.8 No.2: Critical Edition Violin and Piano Reduction. Ricordi, 2003.
Find full textVivaldi, Antonio. Music Minus One Violin: Vivaldi L'Estro Armonico: Violin Concerti in A minor, op. 3, no. 6, RV356; Concerto Grosso in A minor, op. 3, no. 8, RV522; Concerto in D major op. 3, no.9, RV230 (Book & CD). Music Minus One, 1996.
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