Fig. 2From: High-yield production of l-serine through a novel identified exporter combined with synthetic pathway in Corynebacterium glutamicumFluorescence of cytoplasmic proteins and membrane proteins, and the result of amino acid export of SerE by using peptide feeding approach in SSAAI. a Fluorescence of cytoplasmic proteins and membrane proteins of SSAAI-10 (SSAAI harboring plasmid pDXW-10 only, gray bar with slash), SSAAI-egfp (SSAAI overexpressing EGFP protein with pDXW-10, gray bar), and SSAAI-serE-egfp (SSAAI overexpressing SerE-EGFP fusion protein with pDXW-10, white bar). b Extracellular concentration of l-serine in SSAAI (black circles) and serE deletion strain SSAAI ΔserE (gray circles) with 2 mM of the dipeptide Ser–Ser. Extracellular concentration of l-serine in SSAAI (white circles) without the dipeptide Ser–Ser. c Extracellular concentration of l-threonine in SSAAI (black circles) and serE deletion strain SSAAI ΔserE (gray circles) with 2 mM of the dipeptide Thr–Thr. Extracellular concentration of l-threonine in SSAAI (white circles) without the dipeptide Thr–ThrBack to article page