TY - JOUR
T1 - Enzymatic synthesis of Z-aspartame in liquefied amino acid substrates
AU - Furukawa, Shinya
AU - Hasegawa, Kazuhiro
AU - Fuke, Ichiro
AU - Kittaka, Koji
AU - Nakakoba, Terumitsu
AU - Goto, Masahiro
AU - Kamiya, Noriho
PY - 2013/1/15
Y1 - 2013/1/15
N2 - In this paper, we designed and validated a new media for biotransformation aided by ionic liquefied amino acid substrates. Thermolysin-catalyzed synthesis of Z-aspartame (N-carbobenzoxy-l-aspartame) in which ionic liquids play dual roles as both substrate and reaction medium was conducted. If the protease can retain catalytic activity in this new liquefied amino acid substrate/media, the effective substrate concentration can be maximized, leading to theoretically high yields. In fact, we observed a 34-fold enhancement in the catalytic activity compared with that obtained in a previous report. The yield of Z-aspartame reached at approximately 660mM at 24h with 50mgmL-1 of the enzyme, thus submolar range productivity was achieved. The results suggest the successful construction of a high productivity reaction system for peptide synthesis.
AB - In this paper, we designed and validated a new media for biotransformation aided by ionic liquefied amino acid substrates. Thermolysin-catalyzed synthesis of Z-aspartame (N-carbobenzoxy-l-aspartame) in which ionic liquids play dual roles as both substrate and reaction medium was conducted. If the protease can retain catalytic activity in this new liquefied amino acid substrate/media, the effective substrate concentration can be maximized, leading to theoretically high yields. In fact, we observed a 34-fold enhancement in the catalytic activity compared with that obtained in a previous report. The yield of Z-aspartame reached at approximately 660mM at 24h with 50mgmL-1 of the enzyme, thus submolar range productivity was achieved. The results suggest the successful construction of a high productivity reaction system for peptide synthesis.
UR - http://www.scopus.com/inward/record.url?scp=84868314047&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84868314047&partnerID=8YFLogxK
U2 - 10.1016/j.bej.2012.10.002
DO - 10.1016/j.bej.2012.10.002
M3 - Article
AN - SCOPUS:84868314047
SN - 1369-703X
VL - 70
SP - 84
EP - 87
JO - Biochemical Engineering Journal
JF - Biochemical Engineering Journal
ER -