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. Author manuscript; available in PMC: 2018 Oct 1.
Published in final edited form as: Biotechnol J. 2017 Sep 4;12(10):10.1002/biot.201700239. doi: 10.1002/biot.201700239

Figure 2.

Figure 2

The activity assays for tA16ACII and CS ABC. CS-A and CS-B (DS) were used as substrates for the same protein concentration of tA16ACII and CS ABC expressed in E. coli. Assay were carried out in a quartz crystal cuvette at 37 °C and each consisted of 50 μL of 20 mg/mL CS-A or CS-B, 640 μL of digestion buffer (50 mM ammonium acetate, pH 7.4), and 10 μL of the same concentration of tA16ACII or CS ABC. Absorbance was measured at 232 nm.