TY - JOUR
T1 - Casein-based scaffold for artificial cellulosome design
AU - Budinova, Geisa A.L.G.
AU - Mori, Yutaro
AU - Tanaka, Tsutomu
AU - Kamiya, Noriho
N1 - Funding Information:
This research was supported by the Advanced Low Carbon Technology Research and Development Program (ALCA) from the Japan Science and Technology Agency (JST). We thank Dr. Yoshiro Tahara, Dr. Kosuke Minamihata and Mr. Takashi Matsuzaki for their help in statistical analysis and additional experiments.
Publisher Copyright:
© 2017 Elsevier Ltd
PY - 2018/3
Y1 - 2018/3
N2 - Cellulosomal systems are known as highly efficient biocatalysts in the degradation of lignocellulosic biomass in nature, but they remain unsuitable for industrial applications. In seeking alternatives to natural cellulosomes, casein was chosen as a scaffold for cellulase clustering. Casein is recognized as an excellent substrate for microbial transglutaminase (MTG) because it contains naturally reactive glutamine and lysine residues. A substrate peptide containing an MTG-reactive lysine residue was inserted into the C-terminus of the endoglucanase Cel5A and Cel6A from Thermobifida fusca using genetic engineering. The engineered cellulases, EG(Cel5A) and EG(Cel6A), were conjugated onto casein in different ratios by an MTG-mediated site-specific protein crosslinking reaction. Overall, a more than two-fold increase was observed when EG(Cel5A) was conjugated onto N,N-dimethylcasein, but a small or no change was observed for EG(Cel6A).
AB - Cellulosomal systems are known as highly efficient biocatalysts in the degradation of lignocellulosic biomass in nature, but they remain unsuitable for industrial applications. In seeking alternatives to natural cellulosomes, casein was chosen as a scaffold for cellulase clustering. Casein is recognized as an excellent substrate for microbial transglutaminase (MTG) because it contains naturally reactive glutamine and lysine residues. A substrate peptide containing an MTG-reactive lysine residue was inserted into the C-terminus of the endoglucanase Cel5A and Cel6A from Thermobifida fusca using genetic engineering. The engineered cellulases, EG(Cel5A) and EG(Cel6A), were conjugated onto casein in different ratios by an MTG-mediated site-specific protein crosslinking reaction. Overall, a more than two-fold increase was observed when EG(Cel5A) was conjugated onto N,N-dimethylcasein, but a small or no change was observed for EG(Cel6A).
UR - http://www.scopus.com/inward/record.url?scp=85042087173&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85042087173&partnerID=8YFLogxK
U2 - 10.1016/j.procbio.2017.12.013
DO - 10.1016/j.procbio.2017.12.013
M3 - Article
AN - SCOPUS:85042087173
SN - 1359-5113
VL - 66
SP - 140
EP - 145
JO - Process Biochemistry
JF - Process Biochemistry
ER -