Fig. 4From: Development of a silicon limitation inducible expression system for recombinant protein production in the centric diatoms Thalassiosira pseudonana and Cyclotella cryptica Comparison of eGFP expression driven by Si inducible and non Si inducible promoters in Si-replete media and after 24 h of Si starvation. The net eGFP fluorescence was calculated as product of eGFP intensity/cell and no. of cells expressing eGFP derived from imaging flow cytometry. To compensate for different levels of expression, eGFP was measured with a 488-nm laser with 100 mW power output without filter (TpNRp, TprpL41p, TpFcpp) and 30 mW power output after blocking saturation with neutral density filter 1.0 (TpSIT1p, TPSIT2p, Thaps3_9619p, and CcSITp). Error bars represent standard errors of mean (SEM), n = 20,000. NR nitrate reductase promoter, rpL41p ribosomal protein L41 promoter, Fcpp fucoxanthin chlorophyll a/c binding protein promoterBack to article page