Zobrazeno 1 - 10
of 54
pro vyhledávání: '"Murty V. V. S. Madiraju"'
Autor:
Anna Nitecka-Blaźlak, Magdalena Kowalewicz-Kulbat, Marek Fol, Murty V. V. S. Madiraju, Joël Pestel, Magdalena Druszczyńska, Wiesława Rudnicka, Piotr Szpakowski
Publikováno v:
Archives of Biological Sciences, Vol 68, Iss 2, Pp 263-271 (2016)
Dendritic cells (DCs) play a key-role in the immune response against intracellular bacterial pathogens, including mycobacteria. Monocyte-derived dendritic cells (MoDCs) are considered to behave as inflammatory cell populations. Different immunomagnet
Autor:
Jarosław Dziadek, Akash T. Satsangi, Malini Rajagopalan, Robert J. Donnelly, Purushotham Gorla, Renata Plocinska, Murty V. V. S. Madiraju, Emmanuel Vijay Paul Pandeeti, Krishna Sarva
Publikováno v:
Frontiers in Microbiology
Frontiers in Microbiology, Vol 9 (2018)
Frontiers in Microbiology, Vol 9 (2018)
The biological processes regulated by the essential response regulator MtrA and the growth conditions promoting its activation in Mycobacterium tuberculosis, a slow grower and pathogen, are largely unknown. Here, using a gain-of-function mutant, MtrA
Autor:
Ewelina Blaszczyk, Luis Martinez, Malini Rajagopalan, Purushotham Gorla, Krishna Sarva, Emmanuel Vijay Paul Pandeeti, Jarosław Dziadek, Renata Plocinska, Murty V. V. S. Madiraju
Publikováno v:
Journal of Bacteriology. 196:4120-4129
The septal association of Mycobacterium tuberculosis MtrB, the kinase partner of the MtrAB two-component signal transduction system, is necessary for the optimal expression of the MtrA regulon targets, including ripA , fbpB , and ftsI , which are inv
Autor:
Malini Rajagopalan, Krishna Sarva, Murty V. V. S. Madiraju, Renata Plocinska, Przemysław Płociński, Luis Martinez
Publikováno v:
ResearcherID
We recently showed that two small membrane proteins of Mycobacterium tuberculosis, CwsA and CrgA, interact with each other, and that loss of CwsA in M. smegmatis is associated with defects in the cell division and cell wall synthesis processes. Here
Autor:
Malini Rajagopalan, Na Yi, Buka Samten, Krishna Sarva, Murty V. V. S. Madiraju, Stewart Fannin
Publikováno v:
Tuberculosis (Edinburgh, Scotland).
Mycobacterium tuberculosis secretes a number of proteins into the extracellular milieu during growth. Several of these proteins have been associated with modulation of the host immune response. Antigen 84, or Wag31, is one such protein that is conser
Publikováno v:
Tuberculosis. 91:S150-S155
Acidic phospholipids such as cardiolipin (CL) have been shown to modulate Mycobacterium tuberculosis (Mtb) DnaA interactions with ATP. In the present study, using nonyl acridine orange fluorescent dye we localized CL-enriched regions to midcell septa
Autor:
Krishna Sarva, Murty V. V. S. Madiraju, Malini Rajagopalan, Maha Al Zayer, Renata Dziedzic, Dorota L. Stankowska
Publikováno v:
Plasmid. 65:210-218
The genetic and biochemical aspects of the essential Mycobacteriumtuberculosis MtrAB two-component regulatory signal transduction (2CRS) system have not been extensively investigated. We show by bacterial two-hybrid assay that the response regulator
Publikováno v:
Tuberculosis. 89:S65-S69
The ParA and ParB family proteins are required for accurate partitioning of replicated chromosomes. The Mycobacterium tuberculosis genome contains parB, parA and two parA homologs, Rv1708 and Rv3213c. It is unknown if parA and its homologs are functi
Autor:
Malini Rajagopalan, Hava Lofton, Rasmus Jensen, Ashwini Chauhan, Murty V. V. S. Madiraju, Manjot Kiran, Renata Dziedzic, Erin Maloney
Publikováno v:
Tuberculosis. 89:S60-S64
Summary Optimal levels of ftsZ gene product are shown to be required for initiation of the cell division process in Mycobacterium tuberculosis. Here, we report that the ftsZ gene expression is sharply down-regulated during starvation and hypoxia, con
Autor:
Malini Rajagopalan, Syed Muniruzzaman, Renata Dziedzic, Murty V. V. S. Madiraju, Rebecca Greendyke, Naveen K Nair
Publikováno v:
Molecular Microbiology. 71:291-304
The genetic aspects of oriC replication initiation in Mycobacterium tuberculosis are largely unknown. A two-step genetic screen was utilized for isolating M. tuberculosis dnaA cold-sensitive (cos) mutants. First, a resident plasmid expressing functio