TY - JOUR
T1 - Peptide Epimerase Responsible for d-Amino Acid Introduction in Poly-γ-glutamic Acid Biosynthesis
AU - Kato, Hinata
AU - Sakuta, Moeka
AU - Tsunoda, Takeshi
AU - Nakashima, Yu
AU - Morita, Hiroyuki
AU - Ogasawara, Yasushi
AU - Dairi, Tohru
N1 - Publisher Copyright:
© 2023 American Chemical Society.
PY - 2024/1/8
Y1 - 2024/1/8
N2 - Poly-γ-glutamic acid (PGA) is a natural polymer of d- and/or l-glutamic acid (Glu) linked by isopeptide bonds. We recently showed that PGA synthetase, an enzyme complex composed of PgsB, PgsC, and PgsA, uses only l-Glu for polymerization, and d-Glu residues are introduced by peptide epimerization. However, it remains unclear which of the three enzymes is responsible for epimerization because in vitro functional characterization of the membrane-associated PgsBCA complex has never been successful. Here, we performed gene exchange experiments and showed that PgsA is responsible for the epimerization. Additionally, we identified a region in PgsA that modulates epimerization activity based on homology modeling from the recently solved structure of MslH, which showed 53% identity to PgsA. Our results suggested that d/l-ratios of the PGA product can be altered by introducing amino acid substitutions in this region, which will be useful for the production of PGA with controlled d/l-ratios.
AB - Poly-γ-glutamic acid (PGA) is a natural polymer of d- and/or l-glutamic acid (Glu) linked by isopeptide bonds. We recently showed that PGA synthetase, an enzyme complex composed of PgsB, PgsC, and PgsA, uses only l-Glu for polymerization, and d-Glu residues are introduced by peptide epimerization. However, it remains unclear which of the three enzymes is responsible for epimerization because in vitro functional characterization of the membrane-associated PgsBCA complex has never been successful. Here, we performed gene exchange experiments and showed that PgsA is responsible for the epimerization. Additionally, we identified a region in PgsA that modulates epimerization activity based on homology modeling from the recently solved structure of MslH, which showed 53% identity to PgsA. Our results suggested that d/l-ratios of the PGA product can be altered by introducing amino acid substitutions in this region, which will be useful for the production of PGA with controlled d/l-ratios.
UR - http://www.scopus.com/inward/record.url?scp=85180932425&partnerID=8YFLogxK
U2 - 10.1021/acs.biomac.3c01000
DO - 10.1021/acs.biomac.3c01000
M3 - 学術論文
C2 - 38095677
AN - SCOPUS:85180932425
SN - 1525-7797
VL - 25
SP - 349
EP - 354
JO - Biomacromolecules
JF - Biomacromolecules
IS - 1
ER -