» Articles » PMID: 26637601

N-Glycosylation Improves the Pepsin Resistance of Histidine Acid Phosphatase Phytases by Enhancing Their Stability at Acidic PHs and Reducing Pepsin's Accessibility to Its Cleavage Sites

Overview
Date 2015 Dec 6
PMID 26637601
Citations 10
Authors
Affiliations
Soon will be listed here.
Abstract

N-Glycosylation can modulate enzyme structure and function. In this study, we identified two pepsin-resistant histidine acid phosphatase (HAP) phytases from Yersinia kristensenii (YkAPPA) and Yersinia rohdei (YrAPPA), each having an N-glycosylation motif, and one pepsin-sensitive HAP phytase from Yersinia enterocolitica (YeAPPA) that lacked an N-glycosylation site. Site-directed mutagenesis was employed to construct mutants by altering the N-glycosylation status of each enzyme, and the mutant and wild-type enzymes were expressed in Pichia pastoris for biochemical characterization. Compared with those of the N-glycosylation site deletion mutants and N-deglycosylated enzymes, all N-glycosylated counterparts exhibited enhanced pepsin resistance. Introduction of the N-glycosylation site into YeAPPA as YkAPPA and YrAPPA conferred pepsin resistance, shifted the pH optimum (0.5 and 1.5 pH units downward, respectively) and improved stability at acidic pH (83.2 and 98.8% residual activities at pH 2.0 for 1 h). Replacing the pepsin cleavage sites L197 and L396 in the immediate vicinity of the N-glycosylation motifs of YkAPPA and YrAPPA with V promoted their resistance to pepsin digestion when produced in Escherichia coli but had no effect on the pepsin resistance of N-glycosylated enzymes produced in P. pastoris. Thus, N-glycosylation may improve pepsin resistance by enhancing the stability at acidic pH and reducing pepsin's accessibility to peptic cleavage sites. This study provides a strategy, namely, the manipulation of N-glycosylation, for improvement of phytase properties for use in animal feed.

Citing Articles

Functional expression, purification, biochemical and biophysical characterizations, and molecular dynamics simulation of a histidine acid phosphatase from Saccharomyces cerevisiae.

Nezhad N, Jamaludin S, Rahman R, Yahaya N, Oslan S, Mohd Shariff F World J Microbiol Biotechnol. 2024; 40(6):171.

PMID: 38630327 DOI: 10.1007/s11274-024-03970-8.


as a Platform for Heterologous Expression of Enzymes Used for Industry.

Khlebodarova T, Bogacheva N, Zadorozhny A, Bryanskaya A, Vasilieva A, Chesnokov D Microorganisms. 2024; 12(2).

PMID: 38399750 PMC: 10892927. DOI: 10.3390/microorganisms12020346.


Glycosylation Contributes to Thermostability and Proteolytic Resistance of rFIP-nha ().

Liu Y, Hoppenbrouwers T, Wang Y, Xie Y, Wei X, Zhang H Molecules. 2023; 28(17).

PMID: 37687215 PMC: 10490071. DOI: 10.3390/molecules28176386.


Acid-resistant enzymes: the acquisition strategies and applications.

Zhang Z, Zhao Z, Huang K, Liang Z Appl Microbiol Biotechnol. 2023; 107(20):6163-6178.

PMID: 37615723 DOI: 10.1007/s00253-023-12702-1.


How Honey Bee Vitellogenin Holds Lipid Cargo: A Role for the C-Terminal.

Leipart V, Halskau O, Amdam G Front Mol Biosci. 2022; 9:865194.

PMID: 35755821 PMC: 9219001. DOI: 10.3389/fmolb.2022.865194.


References
1.
Liu N, Liu G, Li F, Sands J, Zhang S, Zheng A . Efficacy of phytases on egg production and nutrient digestibility in layers fed reduced phosphorus diets. Poult Sci. 2007; 86(11):2337-42. DOI: 10.3382/ps.2007-00079. View

2.
Muller-Steffner H, Kuhn I, Argentini M, Schuber F . Identification of the N-glycosylation sites on recombinant bovine CD38 expressed in Pichia pastoris: their impact on enzyme stability and catalytic activity. Protein Expr Purif. 2009; 70(2):151-7. DOI: 10.1016/j.pep.2009.10.003. View

3.
Shental-Bechor D, Levy Y . Folding of glycoproteins: toward understanding the biophysics of the glycosylation code. Curr Opin Struct Biol. 2009; 19(5):524-33. DOI: 10.1016/j.sbi.2009.07.002. View

4.
Hamuro Y, Coales S, Molnar K, Tuske S, Morrow J . Specificity of immobilized porcine pepsin in H/D exchange compatible conditions. Rapid Commun Mass Spectrom. 2008; 22(7):1041-6. DOI: 10.1002/rcm.3467. View

5.
KORNFELD R, Kornfeld S . Assembly of asparagine-linked oligosaccharides. Annu Rev Biochem. 1985; 54:631-64. DOI: 10.1146/annurev.bi.54.070185.003215. View