Investigating the interaction between the violaxanthin cycle enzyme zeaxanthin epoxidase and the thylakoid membrane

• Published in: Journal of photochemistry and photobiology. B, Biology Biology, 2012-09, Vol.114, p.119-125
• Main Authors: Schaller, Susann, Wilhelm, Christian, Strzałka, Kazimierz, Goss, Reimund
• Format: Article
• Language: English
• Subjects: amino acid sequences; detergents; Detergents - chemistry; Hydrogen-Ion Concentration; Hydrophobic and Hydrophilic Interactions; hydrophobicity; Membrane protein; membrane proteins; Oxidoreductases - metabolism; photobiology; photochemistry; photosystem II; Photosystem II Protein Complex - metabolism; Protein Binding; Salts - chemistry; sodium carbonate; spinach; Spinacia oleracea; Spinacia oleracea - enzymology; Thylakoid membrane; thylakoids; Thylakoids - enzymology; Thylakoids - metabolism; violaxanthin; Violaxanthin cycle; Xanthophylls - chemistry; Xanthophylls - metabolism; Zeaxanthin epoxidase
• ISSN: 1011-1344; 1873-2682
• DOI: 10.1016/j.jphotobiol.2012.05.019

► Zeaxanthin epoxidase (ZEP) is a peripheral membrane protein. ► ZEP is located at the stromal side of the thylakoid membrane. ► ZEP is constitutively but rather weakly bound. ► Binding is probably realized by a helix-like protein domain. In the present study the interaction between the violaxanthin cycle enzyme zeaxanthin epoxidase (ZEP) and the thylakoid membrane was investigated. Isolated, active thylakoid membranes of spinach (Spinacia oleracea L.) were subjected to different salt and detergent treatments that are generally used to isolate peripheral and integral membrane proteins. These salt and detergent treatments included the use of the salts NaBr, Na2CO3 and Tris and the detergents octylglucoside (OG) and dodecylmaltoside (DM). After the treatments the activity of the ZEP was determined in washed thylakoid membranes. To obtain additional information about the mode of ZEP binding to the membrane a hydrophobicity plot based on the amino acid sequence of the protein was constructed. The plot was then compared to a diagram obtained for the photosystem II antenna Lhcb1 protein whose integration into the thylakoid membrane is known. The results of the salt and detergent treatments of the thylakoid membrane suggest that the ZEP is a peripheral, rather weakly bound membrane protein. Results from the hydrophobicity plots indicate the existence of specialized protein domains which may realize the partial integration and binding of the ZEP to the thylakoid membrane.