Journal of Dairy Science
Volume 92, Issue 7 , Pages 3057-3068, July 2009

Glycation and phosphorylation of α-lactalbumin by dry heating: Effect on protein structure and physiological functions

  • H. Enomoto

      Affiliations

    • United Chair of Applied Resource Chemistry, Course of Bioresource Science for Processing, United Graduate School of Agricultural Sciences, Kagoshima University, Kagoshima 890-0065, Japan
  • ,
  • Y. Hayashi

      Affiliations

    • United Chair of Applied Resource Chemistry, Course of Bioresource Science for Processing, United Graduate School of Agricultural Sciences, Kagoshima University, Kagoshima 890-0065, Japan
  • ,
  • C.P. Li

      Affiliations

    • Department of Food and Pharmacy Engineering, School of Chemistry Science and Technology, Yunnan University, Kunming 650091, China
  • ,
  • S. Ohki

      Affiliations

    • Food Technology Research Institute, Division of Research and Development, Meiji Dairies Corporation, 540 Naruda, Odawara, Kanagawa 250-0862, Japan
  • ,
  • H. Ohtomo

      Affiliations

    • Food Technology Research Institute, Division of Research and Development, Meiji Dairies Corporation, 540 Naruda, Odawara, Kanagawa 250-0862, Japan
  • ,
  • M. Shiokawa

      Affiliations

    • Food Technology Research Institute, Division of Research and Development, Meiji Dairies Corporation, 540 Naruda, Odawara, Kanagawa 250-0862, Japan
  • ,
  • T. Aoki

      Affiliations

    • Department of Biochemical Science and Technology, Faculty of Agriculture, Kagoshima University, Kagoshima 890-0065, Japan
    • Corresponding Author InformationCorresponding author.

Received 5 January 2009; accepted 27 February 2009.

Abstract 

α-Lactalbumin (α-LA) was glycated with maltopentaose (MP) through the Maillard reaction (MP-α-LA) and subsequently phosphorylated by dry heating in the presence of pyrophosphate to investigate its structure and physiological functions. Glycation occurred effectively, and the sugar content of α-LA increased by approximately 22.3% through the Maillard reaction. The phosphorylation of MP-α-LA was enhanced with an increase in the dry-heating time from 1 to 5 d, and the phosphorous content of MP-α-LA increased by approximately 1.01% by dry heating at pH 4.0 and 85°C for 5 d in the presence of pyrophosphate. The electrophoretic mobility of α-LA increased with an increase in the phosphorylation level. The circular dichroism spectra showed that the change in the secondary structure of the α-LA molecule by glycation and subsequent phosphorylation was slight. However, the Trp fluorescence intensity was increased by phosphorylation after glycation. In addition, the differential scanning calorimetry thermograms of α-LA showed that the denaturation temperature of MP-α-LA was decreased by phosphorylation. These results indicated that molten (partially unfolded) conformations of α-LA were formed by dry heating in the presence of pyrophosphate after glycation. The anti-α-LA antibody response was significantly reduced by glycation and subsequent phosphorylation. The suppressive effect of α-LA on the production of proinflammatory cytokines such as IL-6 and tumor necrosis factor-α from THP-1 cells after stimulation with lipopolysaccharide was significantly enhanced by glycation with MP and was further enhanced by phosphorylation after glycation. The Ca phosphate-solubilizing ability of α-LA was enhanced by phosphorylation. The apoptotic activity of α-LA was reduced by glycation and subsequent phosphorylation. These results suggest that phosphorylation by dry heating in the presence of pyrophosphate after glycation with MP through the Maillard reaction is a useful method for improvement of the physiological functions of α-LA.

Key words: α-lactalbumin, glycation, phosphorylation, physiological function

 

PII: S0022-0302(09)70622-8

doi:10.3168/jds.2009-2014

Journal of Dairy Science
Volume 92, Issue 7 , Pages 3057-3068, July 2009