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Chinese Journal of Biotechnology ; (12): 478-481, 2005.
Artículo en Chino | WPRIM | ID: wpr-305247

RESUMEN

Human manganese superoxide dismutase (hMn-SOD) cDNA was amplified by RT-PCR from total RNA of human liver cell (L02), and cloned into yeast expression vector pPIC9K containing AOX1 promoter and the alpha-factor signal peptide sequence. The resultant pPIC9K-MnSOD was transformed to P. pastoris GS115, screened for Mut+ carrying multiple copies of hMn-SOD. The positive transformants were fermented in flasks and induced by 0.5% methanol. After 4 days of methanol induction, the expressed hMn-SOD was up to 32% of the total proteins in the supernatant by SDS-PAGE with specific activity of 247.7 u/mg.


Asunto(s)
Humanos , Clonación Molecular , ADN Complementario , Genética , Pichia , Genética , Metabolismo , Proteínas Recombinantes , Genética , Superóxido Dismutasa , Genética
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