Skip to main content
. 2022 Feb 28;12(6):3382–3396. doi: 10.1021/acscatal.1c05856

Table 2. Selected PET Hydrolase Engineering Studies in the Presence of Binding Modules.

binding module enzyme fold improvement reaction condition ref
PcAA14A ThermoPETase 1.3 PET granules (3 g/L) incubated with 8.3 mgEnzyme/gPET in glycine-NaOH buffer (pH 9) for 5 days (137)
RolA IsPETase 1.2 (by weight loss) Preincubation with RolA for 3 h, then degradation of PET fiber waste and high-crystallinity PET powder (15 g/L) at pH 8, 30 °C with 1.3 gEnzyme/gPET for 5 days (136)
1.5 (by HPLC)
HGFI IsPETase 1.3 (by weight loss)
1.6 (by HPLC)
Zwitterionic polypeptide (EK) IsPETase 11 Degradation of amorphous Goodfellow PET film and high-crystallinity (45.2%) beverage bottle with 200 nM enzyme in glycine-NaOH-buffer at pH 9 and 30–40 °C for up to 6 days (138)
CBM A cutinase from T. fusca 1.4–1.5 (only affinity) Incubated with PET fiber and 50 μM enzyme in 50 mM Tris-buffer (pH 8) at 50 °C for 24 h (104)
ChBD LCCICCG 1.2 With 0.6 g/L amorphous Goodfellow PET film, post-consumer waste PET (16% crystallinity), or high crystallinity (40%) PET at 65 °C for 12 h (103)
CBM LCCICCG 1.3
CBM ThC_Cut1 1.4 With amorphous Goodfellow PET film and 25 mM enzyme in 100 mM potassium phosphate buffer (pH 7) at 50 °C (100)
PBM ThC_Cut1 3.8