نتایج جستجو برای: katg mutants

تعداد نتایج: 76510  

Journal: :Chemical communications 2013
Xiangbo Zhao Hans-Petter Hersleth Janan Zhu K Kristoffer Andersson Richard S Magliozzo

Peroxidatic activation of the anti-tuberculosis pro-drug isoniazid by Mycobacterium tuberculosis catalase-peroxidase (KatG) is regulated by gating residues of a heme access channel. The steric restriction at the bottleneck of this channel is alleviated by replacement of residue Asp137 with Ser, according to crystallographic and kinetic studies.

Journal: :Journal of clinical microbiology 2016
B Molina-Moya G Kazdaglis A Lacoma C Prat A Gómez R Villar-Hernández E García-García L Haba J Maldonado S Samper J Ruiz-Manzano J Domínguez

The aim of this study was to evaluate the GenoFlow DR-MTB array test (DiagCor Bioscience, Hong Kong) on 70 cultured isolates and 50 sputum specimens. The GenoFlow array test showed good sensitivity and specificity compared to the phenotypic Bactec 460TB. This array accurately detected mutations inrpoB,katG, andinhAassociated with resistance to rifampin and isoniazid.

Journal: :Journal of clinical microbiology 1994
M Goyal D Young Y Zhang P A Jenkins R J Shaw

PCR amplification of a species-specific 2-kb KpnI fragment of variable size located 10 kb upstream of the katG gene was used to subdivide 130 clinical isolates of Mycobacterium tuberculosis. Seven subtypes were identified, and their frequencies were distributed normally with respect to the size of the amplified product.

2014
M. Galarza D. Tarazona V. Borda J. C. Agapito H. Guio

We report the genome sequence of Mycobacterium tuberculosis INS-MDR from Peru, a multidrug-resistant tuberculosis (MDR-TB) and Latin American-Mediterranean (LAM) lineage strain. Our analysis showed mutations related to drug resistance in the rpoB (D516V), katG (S315T), kasA (G269S), and pncA (Q10R) genes. Our evidence suggests that INS-MDR may be a clonal expansion related to the African strain...

E Mohiti R Pourahmad Jaktaji

Quinolones are a large and widely consumed class of synthetic drugs. Expanded-spectrum quinolones, like ciprofloxacin are highly effective against Gram-negative bacteria, especially Escherichia coli. In E. coli the major target for quinolones is DNA gyrase. This enzyme is composed of two subunits, GyrA and GyrB encoding by gyrA and gyrB, respectively. Mutations in either of these genes cause qu...

Jalal Mardaneh, Mohsen Rashidi, Samira Zolfaghari, Sattar Ostadhadi, Vahid Nikoui,

Appearance of bacteria resistant to antibacterial agents puts physicians in trouble and threatens the health of the world. The rapid development of bacterial resistance in Escherichia coli to ciprofloxacin makes difficult the treatment of infectious diseases. So, detection of the locations of possible mutations in gyrase A gene ( gyrA ) in these mutants is very important to determine the mech...

Journal: :Journal of bacteriology 1997
B González-Flecha B Demple

The exponential phase of aerobic growth is associated with risk of endogenous oxidative stress in which cells need to cope with an approximately 10-fold increase in the rate of H2O2 generation. We addressed this issue by studying the regulation of the intracellular concentration of H2O2 in aerobically growing Escherichia coli. Intracellular H2O2 was kept at an almost constant steady-state value...

Journal: :Antimicrobial agents and chemotherapy 2006
Manzour Hernando Hazbón Michael Brimacombe Miriam Bobadilla del Valle Magali Cavatore Marta Inírida Guerrero Mandira Varma-Basil Helen Billman-Jacobe Caroline Lavender Janet Fyfe Lourdes García-García Clara Inés León Mridula Bose Fernando Chaves Megan Murray Kathleen D Eisenach José Sifuentes-Osornio M Donald Cave Alfredo Ponce de León David Alland

The molecular basis for isoniazid resistance in Mycobacterium tuberculosis is complex. Putative isoniazid resistance mutations have been identified in katG, ahpC, inhA, kasA, and ndh. However, small sample sizes and related potential biases in sample selection have precluded the development of statistically valid and significant population genetic analyses of clinical isoniazid resistance. We p...

2017
Mussie Brhane Ameha Kebede Yohannes Petros

BACKGROUND Molecular methods that target drug resistance mutations are suitable approaches for rapid drug susceptibility testing to detect multidrug-resistant tuberculosis (MDR-TB). The aim of the study was to determine MDR-TB cases and to analyze the frequency of gene mutations associated with rifampicin (RIF) and/or isoniazid (INH) resistance of Mycobacterium tuberculosis among smear-positive...

2016
Jody Phelan Francesc Coll Ruth McNerney David B. Ascher Douglas E. V. Pires Nick Furnham Nele Coeck Grant A. Hill-Cawthorne Mridul B. Nair Kim Mallard Andrew Ramsay Susana Campino Martin L. Hibberd Arnab Pain Leen Rigouts Taane G. Clark

BACKGROUND Combating the spread of drug resistant tuberculosis is a global health priority. Whole genome association studies are being applied to identify genetic determinants of resistance to anti-tuberculosis drugs. Protein structure and interaction modelling are used to understand the functional effects of putative mutations and provide insight into the molecular mechanisms leading to resist...

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