ACIDOS MICOLICOS PDF

Los ácidos micólicos, en específico, poseen funciones biológicas importantes, entre las que se encuentra el papel que desempeñan en la persistencia de la. como los ácidos micólicos, ácido micoserósido, fenoltiocerol, lipoarabinomanano y arabinogalactano contribuyen a la longevidad, a la respuesta inflamatoria. Aunque el análisis de los lípidos de la pared celular (ácidos micólicos) mediante cromatografía líquida de alta presión es una opción Buena y bien conocida, los.

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Targeting tuberculosis and malaria through inhibition of enoyl reductase: Effect of Mycobacterial phospholipids on interaction of Mycobacterium tuberculosis with macrophages.

Microbial pathogenesis of Mycobacterium tuberculosis: Nat Rev Microbiol ; 4: Structural micolocos and mechanism of enoyl reductase inhibition by triclosan. Evaluation of Mycobacterium smegmatis as a possible surrogate screen for selecting molecules active against micoolicos resistant Mycobacterium tuberculosis.

De estudios sobre virulencia hacia herramientas para su control. Enzymatic characterization of the target for isoniazid in Mycobacterium tuberculosis. Clarity through the scope of genetics. The envelope of mycobateria.

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The global tuberculosis situation: The history of the Ziehl-Neelsen stain. Ciudad de la Habana, Cuba. Heterocyclic acid hydrazides and derivatives. Pathogenic and potentially pathogenic microorganisms as contaminants of fresh water from different sources.

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Inhibition of the Staphylococcus aureus NADPH-dependent enoyl-acyl carrier protein reductase by triclosan and hexachlorophene. Triclosan targets lipid synthesis. Single nucleotide polymorphisms in genes associated with isoniazid resistance in Mycobacterium tuberculosis.

Services on Demand Journal. Cepa bacteriana y condiciones de crecimiento. Infection and Immunity ; Does antibody to mycobacterial antigens, including lipoarabinomannan, limit dissemination in childhood tuberculosis?

Surface glycopeptidolipids of M. Tuberculosis, Mycobacterium smegmatis, lipids. The enoyl-reductases are essential enzymes in the fatty acids elongation pathway towards the mycolic acids, the main mycobacteria cell wall constituents, biosynthesis and so they are potential targets to the rational new antimycobacteria drug design.

Chemotherapy of experimental tuberculosis – V. Receptor-independent four-dimensional quantitative structure-activity relationship analysis of a set of isoniazid derivatives. Lipid biosynthesis as a target for antibacterial agents. The synthesis of acid hydrazides, their derivatives and related compounds. These results indicate the relevance acixos continuing immunoprotection studies with mycobacterial lipid antigens.

Ácido micólico – Wikipedia, a enciclopedia libre

Infect Dis Clin N Am ; La pared celular de M. A triclosan-resistant bacterial enzyme.

All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License.

An application to a set of peptidometic rennin inhibitors. Mechanism of action of diazaborines. Obtainment and partial characterization of a lipidic fragment of the outer membrane of Mycobacterium smegmatis. Annu Rev Biochem ; Preparation and antibacterial activities of new 1,2,3-diazaborine derivatives and analogues.

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Rational design of new antituberculosis agents: The mabA gene from the inhA operon of Mycobacterium tuberculosis encodes a 3-ketoacyl reductase micilicos fails to confer isoniazid resistance. This paper highlights recent approaches regarding the design of new anti-TB agents, particularly, the enoyl-ACP reductase inhibitors.

Pyrrolidine carboxamides as a novel class of inhibitors of enoyl acyl carrier protein reductase from Mycobacterium tuberculosis. Rational approach in the new antituberculosis agent design: A study of the structure-activity relationship for diazaborine inhibition of Escherichia coli enoyl-acp reductase. High affinity InhA inhibitors with micolicso against drug-resistant strains of Mycobacterium tuberculosis.

Ácido micólico

Em geral, as tiofeno-diazoborinas foram os inibidores mais potentes, seguidos pelas benzo-diazoborinas e furano-diazoborinas, enquanto que as pirrol-diazoborinas foram totalmente inativas. The envelope of mycobacteria.

Probing mechanisms of resistance to the tuberculosis drug isoniazid: Conformational changes caused by inhibition of InhA, the enoyl reductase from Mycobacterium tuberculosis.