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1.
Metab Eng ; 17: 23-9, 2013 May.
Artículo en Inglés | MEDLINE | ID: mdl-23466419

RESUMEN

3-Hydroxyalkanoic acids (3HA) are precious precursors for synthesis of value added chemicals. According to their carbon chain lengths, 3HA can be divided into two groups: short-chain-length (SCL) 3HA consisting of 3-5 carbon atoms and medium-chain-length (MCL) 3HA containing 6-14 carbon atoms. To produce MCL 3HA, a metabolic engineered pathway expressing tesB gene, a thioesterase encoding gene that has been reported to catalyze acyl-CoA to free fatty acids, was constructed in Pseudomonas entomophila L48. When tesB of Escherichia coli encoding thioesterase II was introduced into polyhydroxyalkanoate (PHA) synthase and ß-oxidation pathway deleted mutant of P. entomophila LAC31 derived from wild type P. entomophila L48, 6.65g/l 3-hydroxytetradecanoic acid (3HTD) and 4.6g/l 3-hydroxydodecanoic acid (3HDD) were obtained, respectively, when tetradecanoic acid or dodecanoic acid as related carbon sources was added in shake flask cultures. Moreover, 1.8g/l of 3-hydroxydecanoic (3HD) acid was also produced by P. entomophila LAC31 harboring PTE1 gene cloned from Saccharomyces cerevisiae using corresponding fatty acid decanoic acid. Interestingly, shake flask studies indicated that PTE1 harboring strain showed advantages over tesB expressing one for 3HDD and 3HD production, while tesB favored 3HTD production by P. entomophila LAC31. For the first time our study revealed that fine chemicals 3HTD, 3HDD or 3HD could be efficiently produced by metabolic engineered ß-oxidation in Pseudomonas spp grown on related fatty acids.


Asunto(s)
Eliminación de Gen , Mejoramiento Genético/métodos , Hidroxiácidos/metabolismo , Operón/genética , Oxidorreductasas/metabolismo , Pseudomonas/enzimología , Pseudomonas/genética , Hidroxiácidos/química , Hidroxiácidos/aislamiento & purificación , Ingeniería Metabólica/métodos , Peso Molecular , Oxidación-Reducción , Oxidorreductasas/genética , Pseudomonas/clasificación , Especificidad de la Especie
2.
Biomacromolecules ; 12(10): 3559-66, 2011 Oct 10.
Artículo en Inglés | MEDLINE | ID: mdl-21838281

RESUMEN

A medium-chain-length (MCL) polyhydroxyalkanoates (PHAs) producer Pseudomonas entomophila L48 was investigated for microbial production of 3-hydroxydodecanote homopolymer. Pseudomonas entomophila L48 was found to produce MCL PHA consisting of 3-hydroxyhexanoate (3HHx), 3-hydroxyoctanoate (3HO), 3-hydroxydecanoate (3HD), and 3-hydroxydodecanoate (3HDD) from related carbon sources fatty acids. In this study, some of the genes encoding key enzymes in ß-oxidation cycle of P. entomophila such as 3-hydroxyacyl-CoA dehydrogenase, 3-ketoacyl-CoA thiolase, and acetyl-CoA acetyltransferase were deleted to study the relationship between ß-oxidation and PHA synthesis in P. entomophila. Among the mutants constructed, P. entomophila LAC26 accumulated over 90 wt % PHA consisting of 99 mol % 3HDD. A fed-batch fermentation process carried out in a 6 L automatic fermentor produced 7.3 g L(-1) PHA consisting of over 97 mol % 3HDD fraction. Properties of MCL PHA were significantly improved along with increasing 3HDD contents. P(2.1 mol % 3HD-co-97.9 mol % 3HDD) produced by P. entomophila LAC25 had the widest temperature range between T(g) and T(m), which were -49.3 and 82.4 °C, respectively, in all MCL PHA reported so far. The new type of PHA also represented high crystallinity caused by side-chain crystallization compared with short side chain PHA. For the first time, P(3HDD) homopolymers were obtained.


Asunto(s)
Proteínas Bacterianas/metabolismo , Microbiología Industrial/métodos , Organismos Modificados Genéticamente/genética , Polihidroxialcanoatos , Pseudomonas/enzimología , 3-Hidroxiacil-CoA Deshidrogenasas/deficiencia , 3-Hidroxiacil-CoA Deshidrogenasas/genética , Acetil-CoA C-Acetiltransferasa/deficiencia , Acetil-CoA C-Acetiltransferasa/genética , Acetil-CoA C-Aciltransferasa/deficiencia , Acetil-CoA C-Aciltransferasa/genética , Proteínas Bacterianas/genética , Reactores Biológicos , Cromatografía de Gases , Cristalización , Ácidos Grasos/metabolismo , Fermentación , Eliminación de Gen , Espectroscopía de Resonancia Magnética , Organismos Modificados Genéticamente/crecimiento & desarrollo , Oxidación-Reducción , Polihidroxialcanoatos/biosíntesis , Polihidroxialcanoatos/genética , Polihidroxialcanoatos/aislamiento & purificación , Pseudomonas/genética
3.
Biomacromolecules ; 12(9): 3166-73, 2011 Sep 12.
Artículo en Inglés | MEDLINE | ID: mdl-21863836

RESUMEN

Polyhydroxyalkanoates (PHA) synthesis genes phbC and orfZ cloned from Ralstonia eutropha H16 were transformed into beta-oxidation weakened Pseudomonas putida KTOY08ΔGC, a mutant of P. putida KT2442. The recombinant P. putida strain termed KTHH06 was able to produce a short-chain-length PHA block copolymer consisting of poly(3-hydroxybutyrate) (P3HB) as one block and poly(4-hydroxybutyrate) (P4HB) as another block. One-dimensional and two-dimensional nuclear magnetic resonance (NMR) clearly indicated the polymer was a diblock copolymer consisting of 20 mol % P3HB as one block and 80 mol % P4HB as another one. Differential scanning calorimetric (DSC) showed that P3HB block melting temperatures (T(m)) in the block copolymer P3HB-b-P4HB was shift to low temperature compared with homopolymer P3HB and a blend of P3HB and P4HB. The block copolymer with a number average molecular weight of 50000 Da and a polydispersity of 3.1 demonstrated a better yield and tensile strength compared with that of its related random copolymer and blend of homopolymers of P3HB and P4HB.


Asunto(s)
Aciltransferasas/metabolismo , Materiales Biocompatibles/química , Cupriavidus necator/genética , Genética Microbiana/métodos , Polihidroxialcanoatos/biosíntesis , Pseudomonas putida/genética , Ingeniería de Tejidos/métodos , 4-Butirolactona/metabolismo , Aciltransferasas/química , Aciltransferasas/genética , Proteínas Bacterianas/química , Proteínas Bacterianas/genética , Proteínas Bacterianas/metabolismo , Materiales Biocompatibles/farmacología , Biodegradación Ambiental , Rastreo Diferencial de Calorimetría , Clonación Molecular , Cupriavidus necator/enzimología , Hidroxibutiratos/metabolismo , Peso Molecular , Resonancia Magnética Nuclear Biomolecular , Plásmidos , Poliésteres/metabolismo , Polihidroxialcanoatos/análisis , Pseudomonas putida/enzimología , Proteínas Recombinantes/química , Proteínas Recombinantes/genética , Proteínas Recombinantes/metabolismo , Temperatura , Resistencia a la Tracción , Transformación Bacteriana
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