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The resultant recombinant P. pastoris was inoculated in a 1-L Erlenmeyer flask with 200 mL of standard medium (1.34% [w/v] yeast nitrogen base, 2% [w/v] peptone, 1% [w/v] yeast extract, 0.4 mg/L biotin, and 100 mM potassium phosphate [pH 6.0]) containing 1% (w/v) glycerol (Buffered Glycerol-complex Medium). The inocula were placed in an incubator shaker at 29°C/250 rpm for 36–38 h until a wet cell weight of 30 g/L was achieved. |
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Protocol tips |
The resultant recombinant P. pastoris was inoculated in a 1-L Erlenmeyer flask with 200 mL of standard medium (1.34% [w/v] yeast nitrogen base, 2% [w/v] peptone, 1% [w/v] yeast extract, 0.4 mg/L biotin, and 100 mM potassium phosphate [pH 6.0]) containing 1% (w/v) glycerol (Buffered Glycerol-complex Medium). The inocula were placed in an incubator shaker at 29°C/250 rpm for 36–38 h until a wet cell weight of 30 g/L was achieved. |
Publication protocol
"The Mut+ strain of Pichia pastoris (Komagataella phaffii) GS115 (His4) was used to express Aspergillus niger PhyA phytase under the control of the inducible AOX1 promoter. The alpha-mating factor secretion signal of S. cerevisiae was also incorporated into the plasmid construct (Han et al., 2018). P. pastoris was grown in liquid and solid media during fermentation in accordance with the procedure used by Rahimi et al. (2019) with slight modifications.
The resultant recombinant P. pastoris was inoculated in a 1-L Erlenmeyer flask with 200 mL of standard medium (1.34% [w/v] yeast nitrogen base, 2% [w/v] peptone, 1% [w/v] yeast extract, 0.4 mg/L biotin, and 100 mM potassium phosphate [pH 6.0]) containing 1% (w/v) glycerol (Buffered Glycerol-complex Medium). The inocula were placed in an incubator shaker at 29°C/250 rpm for 36–38 h until a wet cell weight of 30 g/L was achieved."
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