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1.
Nanoscale ; 7(43): 18337-42, 2015 Nov 21.
Artigo em Inglês | MEDLINE | ID: mdl-26488340

RESUMO

We investigate the optoelectronic properties of the semiconducting (6,5) species of single-walled carbon nanotubes by measuring ultrafast transient transmission changes with 20 fs time resolution. We demonstrate that photons with energy below the lowest exciton resonance efficiently lead to linear excitation of electronic states. This finding challenges the established picture of a vanishing optical absorption below the fundamental excitonic resonance. Our result points towards below-gap electronic states as an intrinsic property of semiconducting nanotubes.

2.
Biotechnol Bioeng ; 76(2): 126-31, 2001 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-11505382

RESUMO

Plant-derived glucosides have attracted much attention due to their widespread applications. This class of products is difficult to isolate or to synthesize in pure form because of the resulting low yields. Thus, simple approaches for the generation of such glucosides would be highly beneficial. We purified and characterized a novel glucosyltransferase from plant cell suspension cultures of Rauvolfia serpentina, which showed rather low substrate specificity. We obtained its cDNA and expressed the active recombinant protein in bacteria (Escherichia coli) with excellent plant-specific glucosylation efficiencies. Compared with the plant system, the bacteria delivered the new enzyme, which was in the form of a soluble or matrix-bound enzyme, approximately 1800 times more efficiently for the synthesis of a wide range of glucosides. More importantly, the engineered E. coli strain allowed for in vivo glucosylation and release of the product into the culture medium, as shown by the formation of arbutin, which is a potent inhibitor of human melanin biosynthesis with commercial value.


Assuntos
Arbutina/metabolismo , Escherichia coli/metabolismo , Glucosídeos/biossíntese , Rauwolfia/citologia , Arbutina/isolamento & purificação , Células Cultivadas , Clonagem Molecular , Escherichia coli/genética , Engenharia Genética , Vetores Genéticos , Glucosiltransferases/metabolismo , Fenol , Fenóis/metabolismo , Plasmídeos , Proteínas Recombinantes/genética , Proteínas Recombinantes/isolamento & purificação , Proteínas Recombinantes/metabolismo , Sensibilidade e Especificidade , Especificidade por Substrato , Suspensões , Transformação Genética
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