Figures & data
Figure 1. The image of GFP-GVs captured through a 40 × objective in a (A) bright field mode and B: Fluorescence mode. C: Enzs-GV upon addition of n-heptanol. D: Image of multilamellar vesicle containing Enzs-GV. In 1C, 1D Scale Bar: 40 μm. Each camera pixel represents 0.2 μm in the images 1A, 1B.
![Figure 1. The image of GFP-GVs captured through a 40 × objective in a (A) bright field mode and B: Fluorescence mode. C: Enzs-GV upon addition of n-heptanol. D: Image of multilamellar vesicle containing Enzs-GV. In 1C, 1D Scale Bar: 40 μm. Each camera pixel represents 0.2 μm in the images 1A, 1B.](/cms/asset/075f1e42-4c04-4eca-9abb-d83e568cfcf0/ianb_a_731413_f0001_b.jpg)
Figure 2. Spectrophotometric monitoring of the Enzs-GV catalyzed oxidation of n-heptanol. The Enzs-GV concentrations used were A = 100 μl, B = 200 μl, C = 400 μl, D = 600 μl, where the count of GV was 5/μl in THB. The concentrations of n-heptanol for the entire sample were fixed (100 μl) and the stock was prepared in DMSO.
![Figure 2. Spectrophotometric monitoring of the Enzs-GV catalyzed oxidation of n-heptanol. The Enzs-GV concentrations used were A = 100 μl, B = 200 μl, C = 400 μl, D = 600 μl, where the count of GV was 5/μl in THB. The concentrations of n-heptanol for the entire sample were fixed (100 μl) and the stock was prepared in DMSO.](/cms/asset/690fe74e-e060-4042-aa05-cf2e5a5043b7/ianb_a_731413_f0002_b.jpg)