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1.
Biotechnol Bioeng ; 116(10): 2640-2651, 2019 10.
Artículo en Inglés | MEDLINE | ID: mdl-31184369

RESUMEN

Microbial production of 1,5-diaminopentane (DAP) from renewable feedstock is a promising and sustainable approach for the production of polyamides. In this study, we constructed a ß-glucosidase (BGL)-secreting Corynebacterium glutamicum and successfully used this strain to produce DAP from cellobiose and glucose. First, C. glutamicum was metabolically engineered to produce l-lysine (a direct precursor of DAP), followed by the coexpression of l-lysine decarboxylase and BGL derived from Escherichia coli and Thermobifida fusca YX (Tfu0937), respectively. This new engineered C. glutamicum strain produced 27 g/L of DAP from cellobiose in CGXII minimal medium using fed-batch cultivation. The yield of DAP was 0.43 g/g glucose (1 g of cellobiose corresponds to 1.1 g of glucose), which is the highest yield reported to date. These results demonstrate the feasibility of DAP production from cellobiose or cellooligosaccharides using an engineered C. glutamicum strain.


Asunto(s)
Proteínas Bacterianas , Celobiosa/metabolismo , Corynebacterium glutamicum , Diaminas/metabolismo , Ingeniería Metabólica , beta-Glucosidasa , Proteínas Bacterianas/genética , Proteínas Bacterianas/metabolismo , Corynebacterium glutamicum/genética , Corynebacterium glutamicum/metabolismo , beta-Glucosidasa/genética , beta-Glucosidasa/metabolismo
2.
Bioresour Technol ; 245(Pt B): 1684-1691, 2017 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-28599919

RESUMEN

Xylooligosaccharide-assimilating Corynebacterium glutamicum strains were constructed using metabolic engineering and cell surface display techniques. First, C. glutamicum was metabolically engineered to create lysine-producing strains. Beta-xylosidase BSU17580 derived from Bacillus subtilis was then expressed on the C. glutamicum cell surface using PorH anchor protein, and enzymes involved in the xylose assimilation pathway were also expressed. Metabolic engineering had no effect on the activity of beta-xylosidase. The engineered strains efficiently consumed xylooligosaccharides and produced 12.4mM of lysine from 11.9g/L of xylooligosaccharides as the carbon source. Finally, co-expression of lysine decarboxylase enabled production of 11.6mM of 1,5-diaminopentane (cadaverine) from 13g/L of consumed xylooligosaccharides.


Asunto(s)
Corynebacterium glutamicum , Ingeniería Metabólica , Xilosidasas , Cadaverina , Glucuronatos , Oligosacáridos
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