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1.
Electron. j. biotechnol ; 19(3): 1-9, May 2016. ilus
Artículo en Inglés | LILACS | ID: lil-787003

RESUMEN

Background: Human is an essential cellular enzyme that is found in all human cells. As this enzyme is upregulated in cancer cells exceedingly, it is used as a target for cancer chemotherapeutic drug development. As such, producing the in-house enzyme for the purpose to speed up the search for more cost-effective and target specific hTopoI inhibitors is warranted. This study aims to compare the optimised conditions for the expression of hTopoI in KM71H (MutS) and X33 (Mut+) strains of Pichia pastoris. P. pastoris transfected with an hTopoI recombinant vector was used for the optimization of a higher level of hTopoI expression. Results: In the process, fed-batch cultivation parameters that influence the expression of hTopoI, such as culture temperature, methanol induction and feeding strategy, were optimised in the transfected KM71H and X33 P. pastoris strains in a shake flask system. The cell density and total protein concentration (protein level) of transfected P. pastoris were compared to determine the optimum culture conditions for each transfected P. pastoris strain. A higher hTopoI level was observed in the transfected KM71H culture supernatant (2.26 ng/mL) when the culture was incubated in the optimum conditions. Conclusions: This study demonstrated that MutS strain (KM71H) expressed and secreted a higher level of hTopoI heterologous protein in the presence of methanol compared to the Mut+ strain; X33 (0.75 ng/mL). However, other aspects of optimization, such as pH, should also be considered in the future, to obtain the optimum expression level of hTopoI in P. pastoris.


Asunto(s)
Pichia , Proteínas Recombinantes , ADN-Topoisomerasas de Tipo I , Técnicas de Cultivo , Concentración de Iones de Hidrógeno
2.
Journal of Southern Medical University ; (12): 2655-2657, 2010.
Artículo en Chino | WPRIM | ID: wpr-267715

RESUMEN

<p><b>OBJECTIVE</b>To determine the distribution of HCV genotypes among volunteer blood donors in Guangzhou.</p><p><b>METHODS</b>Six-nine HCV RNA-positive samples were collected from volunteer blood donors in Guangzhou. NS5B fragments of HCV were amplified followed by DNA sequencing and phylogenetic analysis.</p><p><b>RESULTS</b>HCV genotypes were determined for 67 samples. Among them, the subtypes 1b, 2a, 3a, 3b, 6a and 6n were detected at the frequencies of 37.31%, 4.48%, 7.46%, 4.48%, 44.78% and 1.49%, respectively.</p><p><b>CONCLUSION</b>HCV 1b and 6a are the most predominant two subtypes among volunteer blood donors in Guangzhou.</p>


Asunto(s)
Humanos , Donantes de Sangre , China , Genotipo , Hepacivirus , Clasificación , Genética , Filogenia , ARN Viral , Genética , Análisis de Secuencia de ADN
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