Molecular and biochemical characterization of rice pectin methylesterase inhibitors (OsPMEIs)

• Published in: Plant physiology and biochemistry Vol. 101; pp. 105 - 112
• Main Authors: Nguyen, Hong Phuong, Jeong, Ho Young, Kim, Hun, Kim, Young Chang, Lee, Chanhui
• Format: Journal Article
• Language: English
• Published: France Elsevier Masson SAS 01.04.2016
• Subjects: Cell Membrane - genetics; Cell Membrane - metabolism; Cell wall modifications; Cloning, Molecular; Enzyme Inhibitors - metabolism; Gene Expression Regulation, Plant - physiology; Oryza - genetics; Oryza - metabolism; Pectin; Pectin methylesterase inhibitors; Pectin methylesterases; Plant cell walls; Plant Proteins - biosynthesis; Plant Proteins - genetics; Rice; Pectin methylesterases; Pectin methylesterase inhibitors; Pectin; Plant cell walls; Cell wall modifications; Rice
• ISSN: 0981-9428; 1873-2690
• DOI: 10.1016/j.plaphy.2016.01.021

Cell wall modifications such as partial degradation and depolymerization by cell wall hydrolases are normal cellular processes and are required for the functionalities of different cell types. Pectin, one of the major cell wall polysaccharides, is predominantly found in primary cell walls and middle lamellae and is subjected to in muro modification, primarily by cell wall-localized pectin methylesterases (PMEs). Molecular biochemical studies have demonstrated that enzymatic activities of PMEs are governed by multiple pectin methylesterase inhibitors (PMEIs), which consequently control the pectin methylesterification status. Although a few studies in Arabidopsis have shown the importance of this PMEI-mediated regulation in the biophysical properties of cell walls, little is known about the molecular physiological functions of rice PMEIs. We found 49 members of the PMEI family in the rice genome. Analysis of their transcript levels by quantitative real-time PCR and meta expression analysis showed that they are regulated spatially and temporally, as well as in response to diverse stresses. Quantification of cell wall-bound methylesters indicated that the degree of pectin methylesterification is developmentally regulated; in particular, higher PMEI activities were detected in cell wall proteins prepared from young leaves. Furthermore, an activity assay demonstrated that two recombinant OsPMEI proteins (OsPMEI8 and 12) were able to inhibit the enzymatic activity of a commercial PME protein. Subcellular localization indicated that OsPMEI8 is targeted to the middle lamella and OsPMEI12 is localized in the plasma membrane and nucleus. Taken together, our findings provide the first molecular and biochemical evidence for functional characterization of PMEIs in rice growth and development. •Forty-nine members of OsPMEI genes showed spatial/temporal expression.•The degree of pectin methylesterification status is developmentally regulated.•Two OsPMEI proteins were biochemically characterized.