In this study, Cu ion complex ink was successfully synthesized by a modified electrolysis method in which the Cu ions generated from bulk metal plates by an electric field were coordinated with complex agents. The synthesized ink was ink-jet-printed on a flexible substrate and converted to a dense Cu pattern after sintering at 250 °C. The pattern was characterized by X-ray diffractometry, field emission scanning electron microscope, and four-point probe method to confirm the crystal structure, microstructure, and electrical conductivity, respectively. The effect of the type of complex agent on the characteristics of a Cu conductive pattern was also determined using the analysis results. Finally, we conducted the direct writing of conductive dots and lines using the Cu ion complex ink, and confirmed that fine patterning for application in electronics is possible with the Cu ion complex ink.
Electrospinning and galvanic displacement reaction are combined to fabricate ultra-long hollow chalcogen and chalcogenide nanofibers in a cost-effective and high throughput manner. This procedure exploits electrospinning to fabricate ultra-long sacrificial nanofibers with controlled dimensions and morphology, thereby imparting control over the composition and shape of the nanostructures evolved during galvanic displacement reaction. It is believed to be a general route to form various ultra-long hollow semiconducting nanofibers.
A recombinant Escherichia coli strain was developed to produce guanosine 5'-diphosphate (GDP)-L-fucose, donor of L-fucose, which is an essential substrate for the synthesis of fucosyloligosaccharides. GDP-D: -mannose-4, 6-dehydratase (GMD) and GDP-4-keto-6-deoxymannose 3, 5-epimerase 4-reductase (WcaG), the two crucial enzymes for the de novo GDP-L-fucose biosynthesis, were overexpressed in recombinant E. coli by constructing inducible overexpression vectors. Optimum expression conditions for GMD and WcaG in recombinant E. coli BL21(DE3) were 25 degrees C and 0.1 mM isopropyl-beta-D-thioglucopyranoside. Maximum GDP-L-fucose concentration of 38.9 +/- 0.6 mg l(-1) was obtained in a glucose-limited fed-batch cultivation, and it was enhanced further by co-expression of NADPH-regenerating glucose-6-phosphate dehydrogenase encoded by the zwf gene to achieve 55.2 +/- 0.5 mg l(-1) GDP-L-fucose under the same cultivation condition.
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