TY - JOUR
T1 - Preparation of porous chitin beads from waste crayfish shell and application in the co-immobilization of PLP and its dependent enzyme
AU - Wei, Guoguang
AU - Zhang, Chi
AU - Zhou, Ning
AU - Wu, Bin
AU - Li, Hui
AU - Zhang, Alei
AU - Ouyang, Pingkai
AU - Chen, Kequan
N1 - Publisher Copyright:
© 2023
PY - 2023/12/1
Y1 - 2023/12/1
N2 - In this study, co-immobilization of PLP and its dependent enzyme were investigated using a novel type of porous chitin bead (PCB). Crayfish shell was used to prepare PCB via dissolution of it to form beads, followed by the removal of CaCO3 and protein in-situ. Scanning electron microscopy, Fourier transform infrared spectroscopy, and Brunauer-Emmett-Teller method showed that the PCB had abundant porous structures with deacetylation degree of 33 % and the specific surface area of 35.87 m2/g. Then, the beads are used to co-immobilize pyridoxal 5-phosphate (PLP) and L-lysine decarboxylase fused with chitin-binding protein (SpLDC-ChBD). Laser scanning confocal microscopy revealed that the beads could co-immobilize PLP and SpLDC-ChBD successfully. In addition, a packed bed was also constructed using the PCB containing co-immobilized SpLDC-ChBD and PLP. The substrate conversion remained at 91.09 % after 48 h with 50 g/L L-lysine, which showed good continuous catalysis ability. This study provides a novel method for co-immobilization of enzyme and PLP, as well as develops a new application of waste crustacean shells.
AB - In this study, co-immobilization of PLP and its dependent enzyme were investigated using a novel type of porous chitin bead (PCB). Crayfish shell was used to prepare PCB via dissolution of it to form beads, followed by the removal of CaCO3 and protein in-situ. Scanning electron microscopy, Fourier transform infrared spectroscopy, and Brunauer-Emmett-Teller method showed that the PCB had abundant porous structures with deacetylation degree of 33 % and the specific surface area of 35.87 m2/g. Then, the beads are used to co-immobilize pyridoxal 5-phosphate (PLP) and L-lysine decarboxylase fused with chitin-binding protein (SpLDC-ChBD). Laser scanning confocal microscopy revealed that the beads could co-immobilize PLP and SpLDC-ChBD successfully. In addition, a packed bed was also constructed using the PCB containing co-immobilized SpLDC-ChBD and PLP. The substrate conversion remained at 91.09 % after 48 h with 50 g/L L-lysine, which showed good continuous catalysis ability. This study provides a novel method for co-immobilization of enzyme and PLP, as well as develops a new application of waste crustacean shells.
KW - Co-immobilization
KW - Continuous catalysis
KW - Crayfish shell
KW - L-Lysine decarboxylase
KW - Porous chitin bead
KW - Pyridoxal 5-phosphate
UR - http://www.scopus.com/inward/record.url?scp=85168994047&partnerID=8YFLogxK
U2 - 10.1016/j.carbpol.2023.121322
DO - 10.1016/j.carbpol.2023.121322
M3 - 文章
C2 - 37739544
AN - SCOPUS:85168994047
SN - 0144-8617
VL - 321
JO - Carbohydrate Polymers
JF - Carbohydrate Polymers
M1 - 121322
ER -