scholarly journals Resazurin reduction assays for screening of anti-tubercular compounds against dormant and actively growing Mycobacterium tuberculosis, Mycobacterium bovis BCG and Mycobacterium smegmatis

2007 ◽  
Vol 60 (2) ◽  
pp. 288-293 ◽  
Author(s):  
Neetu Kumra Taneja ◽  
Jaya Sivaswami Tyagi
2010 ◽  
Vol 38 (12) ◽  
pp. 4067-4078 ◽  
Author(s):  
J. M. DiChiara ◽  
L. M. Contreras-Martinez ◽  
J. Livny ◽  
D. Smith ◽  
K. A. McDonough ◽  
...  

2017 ◽  
Vol 19 (11) ◽  
pp. 515-526 ◽  
Author(s):  
Varadharajan Sundaramurthy ◽  
Hannelie Korf ◽  
Ashima Singla ◽  
Nicole Scherr ◽  
Liem Nguyen ◽  
...  

2011 ◽  
Vol 51 (4) ◽  
pp. 233-242 ◽  
Author(s):  
Bret E. Betz ◽  
Abul K. Azad ◽  
Jessica D. Morris ◽  
Murugesan V.S. Rajaram ◽  
Larry S. Schlesinger

1999 ◽  
Vol 181 (2) ◽  
pp. 454-461 ◽  
Author(s):  
Carol E. A. Peña ◽  
J. Michelle Kahlenberg ◽  
Graham F. Hatfull

ABSTRACT The temperate mycobacteriophage L5 integrates site specifically into the genomes of Mycobacterium smegmatis,Mycobacterium tuberculosis, and Mycobacterium bovis bacillus Calmette-Guérin. This integrative recombination event occurs between the phage L5 attP site and the mycobacterial attB site and requires the phage-encoded integrase and mycobacterial-encoded integration host factor mIHF. Here we show that attP, Int-L5, and mIHF assemble into a recombinationally active complex, the intasome, which is capable of attB capture and formation of products. The arm-type integrase binding sites within attP play specialized roles in the formation of specific protein-DNA architectures; the intasome is constructed by the formation of intramolecular integrase bridges between one pair of sites, P4-P5, and the attP core, while an additional pair of sites, P1-P2, is required for interaction with attB.


Tuberculosis ◽  
2007 ◽  
Vol 87 (2) ◽  
pp. 155-165 ◽  
Author(s):  
Toshiko Yamamoto ◽  
Todd M. Lasco ◽  
Kazuyuki Uchida ◽  
Yoshitaka Goto ◽  
Amminikutty Jeevan ◽  
...  

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