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Fig. 2 | Biotechnology for Biofuels

Fig. 2

From: An industrial scale process for the enzymatic removal of steryl glucosides from biodiesel

Fig. 2

A time course of SGase activity (expressed as conversion %) of BGTl and LacS in aqueous buffer. Reactions were performed at 70 °C in phosphate buffer at pH 6.5 for BGTl and citrate buffer at pH 5.5 for LacS. 14 µg of enzyme/mL of buffer spiked with 100 ppm SGs was used. SGase hydrolysis was measured with a coupled enzymatic fluorescence assay. Error bars show the standard deviation of three independent assays

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