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Fig. 1 | Microbial Cell Factories

Fig. 1

From: Deciphering how LIP2 and POX2 promoters can optimally regulate recombinant protein production in the yeast Yarrowia lipolytica

Fig. 1

Comparison of pLIP2 and pPOX2 induction using DsRed fluorescence as a proxy. Strains JMY2656 (pPOX2-RedStar2; in dark gray) and JMY3742 (pLIP2-RedStar2; in light gray) were grown in culture media until carbon source depletion (i.e., 48 h). Complex and defined media (CM and DM, respectively) were used, to which the following carbon sources were added: D glucose; G glycerol; OA oleic acid; DOA glucose and oleic acid (ratio of 1 to 1 C-mol); and GOA glycerol and oleic acid (ratio of 1 to 1 C-mol). The values depicted are the mean raw fluorescence and specific fluorescence calculated from three independent replicates; the bars represent the standard deviation. FU fluorescence unit; SFU specific fluorescence unit

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Microbial Cell Factories

ISSN: 1475-2859

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