Uptake of adenine by purine permeases of Coffea canephora

• Published in: Bioscience, biotechnology, and biochemistry Vol. 83; no. 7; pp. 1300 - 1305
• Main Authors: Kakegawa, Hirofumi, Shitan, Nobukazu, Kusano, Hiroaki, Ogita, Shinjiro, Yazaki, Kazufumi, Sugiyama, Akifumi
• Format: Journal Article
• Language: English
• Published: England Taylor & Francis 03.07.2019; Oxford University Press
• Subjects: Adenine; caffeine; Coffea canephora; purine permease; Adenine; caffeine; Coffea canephora; purine permease
• ISSN: 0916-8451; 1347-6947
• DOI: 10.1080/09168451.2019.1606698

Purine permeases (PUPs) mediate the proton-coupled uptake of nucleotide bases and their derivatives into cytosol. PUPs facilitate uptake of adenine, cytokinins and nicotine. Caffeine, a purine alkaloid derived from xanthosine, occurs in only a few eudicot species, including coffee, cacao, and tea. Although caffeine is not an endogenous metabolite in Arabidopsis and rice, AtPUP1 and OsPUP7 were suggested to transport caffeine. In this study, we identified 15 PUPs in the genome of Coffea canephora. Direct uptake measurements in yeast demonstrated that CcPUP1 and CcPUP5 facilitate adenine - but not caffeine - transport. Adenine uptake was pH-dependent, with increased activity at pH 3 and 4, and inhibited by nigericin, a potassium-proton ionophore, suggesting that CcPUP1 and CcPUP5 function as proton-symporters. Furthermore, adenine uptake was not competitively inhibited by an excess amount of caffeine, which implies that PUPs of C. canephora have evolved to become caffeine-insensitive to promote efficient uptake of adenine into cytosol. CcPUP1 & CcPUP5 distinguish adenine from caffeine. The adenine uptake activity of AtPUP1 is inhibited by caffeine.