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1.
Appl Microbiol Biotechnol ; 90(1): 107-16, 2011 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-21221570

RESUMEN

Vanillin can be produced on a commercial scale by depolymerising renewable lignin. One product of microbial metabolism of vanillin by common soil microbes, such as Acinetobacter baylyi, is a tricarboxylic acid with a butadiene backbone known as 3-carboxy muconate (3CM). Three enzymes, 4-hydroxy benzaldehyde dehydrogenase, vanillate monooxygenase and protocatechuate 3,4-dioxygenase, catalyse the biotransformation of vanillin to 3CM. These three enzymes were metabolically engineered into an Escherichia coli host, giving a biocatalyst that converted vanillin into 3CM. The biocatalyst was found to give 100% yield of 3CM from 1 mM of vanillin after 39 h. The rate-limiting reaction was identified as the conversion of vanillate to 3,4-dihydroxybenzoate catalysed by vanillate monooxygenase. Low expression of the reductase subunit of this enzyme was identified as contributing to the reduced rate of this reaction. Proof of principle of a novel application for 3CM was demonstrated when it was converted into a trimethyl ester derivative and copolymerised with styrene.


Asunto(s)
Benzaldehídos/metabolismo , Biopolímeros/metabolismo , Escherichia coli/metabolismo , Ácido Sórbico/análogos & derivados , Benzaldehídos/química , Biopolímeros/química , Biotransformación , Escherichia coli/genética , Ingeniería Genética , Ácido Sórbico/química , Ácido Sórbico/metabolismo
2.
Bioorg Med Chem Lett ; 20(15): 4555-7, 2010 Aug 01.
Artículo en Inglés | MEDLINE | ID: mdl-20591665

RESUMEN

A series of novel polyacetylene substituted 2-hydroxy acids and derivatives were prepared and characterized. Alkylation of butane-2,3-diacetal (BDA) protected glycolic acid with iodoalkyl substituted polyacetylene compounds gave the corresponding diacetal protected polyacetylene substituted 2-hydroxy acids. Diacetal deprotection through acid mediated hydrolysis, transesterification or aminolysis afforded the 2-hydroxy-polyacetylenic acid, ester or amide derivatives. Twenty one of these novel compounds were tested against 10 microbes of clinical importance and several of them showed good antimicrobial activity, in particular against Pseudomonas aeruginosa.


Asunto(s)
Amidas/química , Antifúngicos/química , Hidroxiácidos/química , Poliinos/química , Antifúngicos/síntesis química , Antifúngicos/farmacología , Ésteres , Pruebas de Sensibilidad Microbiana , Poliinos/síntesis química , Poliinos/farmacología , Pseudomonas aeruginosa/efectos de los fármacos , Relación Estructura-Actividad
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