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Fig. 7 | Biotechnology for Biofuels

Fig. 7

From: Increased ethylene production by overexpressing phosphoenolpyruvate carboxylase in the cyanobacterium Synechocystis PCC 6803

Fig. 7

SDS-PAGE/Western immunoblot of the Synechocystis strains created in this study (Table 2) analysed for the presence of phosphoenolpyruvate carboxylase (PEPc). A SDS-PAGE loaded with 31 µg of protein crude extract from Synechocystis strains created in this study under standard treatment (Table 2) and B Western immunoblot using anti-PEPc for the Synechocystis engineered strains (Table 2) in standard treatment. Standard treatment is BG11+ 50 mM Tris pH 8.0, 50 mM NaHCO3, Km (25 µg mL−1), Cm (20 µg mL−1), 5 µM of NiCl2 and 20 µE m−2 s−1. PEPc6803 and PEPc7002 corresponds to purified protein (100 ng loaded) of PEPc from Synechocystis PCC 6803 and Synechococcus PCC 7002, respectively

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