Unknown

Dataset Information

0

Effect on catalysis by replacement of catalytic residue from hen egg white lysozyme to Venerupis philippinarum lysozyme.


ABSTRACT: Asn46Asp/Asp52Ser or Asn46Glu/Asp52Ser hen egg white lysozyme (HEL) mutant was designed by introducing the substituted catalytic residue Asp46 or Glu46, respectively, based on Venerupis philippinarum (Vp) lysozyme structure as a representative of invertebrate-type (i-type) lyzozyme. These mutations restored the bell-shaped pH-dependency of the enzyme activity from the sigmoidal pH-dependency observed for the Asp52Ser mutant. Furthermore both lysozyme mutants possessed retaining mechanisms like Vp lysozyme and HEL. The Asn46Glu/Asp52Ser mutant, which has a shorter distance between two catalytic residues, formed a glycosyl adduct in the reaction with the N-acetylglucosamine oligomer. Furthermore, we found the accelerated turnover through its glycosyl adduct formation and decomposition. The turnover rate estimated from the glycosyl formation and decomposition rates was only 20% of the observed hydrolysis rate of the substrate. Based on these results, we discussed the catalytic mechanism of lysozymes.

SUBMITTER: Abe Y 

PROVIDER: S-EPMC5338227 | biostudies-literature | 2016 Sep

REPOSITORIES: biostudies-literature

altmetric image

Publications

Effect on catalysis by replacement of catalytic residue from hen egg white lysozyme to Venerupis philippinarum lysozyme.

Abe Yoshito Y   Kubota Mitsuru M   Takazaki Shinya S   Ito Yuji Y   Yamamoto Hiromi H   Kang Dongchon D   Ueda Tadashi T   Imoto Taiji T  

Protein science : a publication of the Protein Society 20160628 9


Asn46Asp/Asp52Ser or Asn46Glu/Asp52Ser hen egg white lysozyme (HEL) mutant was designed by introducing the substituted catalytic residue Asp46 or Glu46, respectively, based on Venerupis philippinarum (Vp) lysozyme structure as a representative of invertebrate-type (i-type) lyzozyme. These mutations restored the bell-shaped pH-dependency of the enzyme activity from the sigmoidal pH-dependency observed for the Asp52Ser mutant. Furthermore both lysozyme mutants possessed retaining mechanisms like V  ...[more]

Similar Datasets

| S-EPMC4388261 | biostudies-literature
| S-EPMC3537236 | biostudies-literature
| EMPIAR-10542 | biostudies-other
| S-EPMC4500996 | biostudies-literature
| S-EPMC2373952 | biostudies-literature
| S-EPMC3774808 | biostudies-literature
| S-EPMC6648635 | biostudies-literature
| S-EPMC3975892 | biostudies-literature
| S-EPMC3318136 | biostudies-literature
| S-EPMC15451 | biostudies-literature