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Distribution of Fallover in the Carboxylase Reaction and Fallover-Inducible Sites among Ribulose 1,5-Bisphosphate Carboxylase/Oxygenases of Photosynthetic Organisms
Authors:Uemura  Koichi; Tokai  Hiroshi; Higuchi  Takashi; Murayama  Hiroshi; Yamamoto  Hiroshi; Enomoto  Yukito; Fujiwara  Shoko; Hamada  Jin; Yokota  Akiho
Institution:1 Plant Molecular Physiology Laboratory, Research Institute of Innovative Technology for the Earth (RITE) Kizu, Kyoto, 619-02 Japan
2 Department of Agricultural Chemistry, University of Osaka Prefecture Sakai, Osaka, 593 Japan
3 Marine Biology Station, Faculty of Science, Kobe University Tuna, Hyogo, 656-24 Japan
4 National Instutute of Bioscience and Human Technology, Agency of Industrial Science and Technology Tsukuba, 305 Japan
5 Department of Community Medicine, Faculty of Medicine, Toyama Medical and Pharmaceutical University Toyama, 930-01 Japan
6 Graduate School of Biological Sciences, Nara Institute of Science and Technology Takayama, Ikoma, Nara, 630-01 Japan
Abstract:The biphasic reaction course, fallover, of carboxyla-tion catalysedby ribulose 1,5-bisphosphate carboxylase/ox-ygenase (RuBisCO)has been known as a characteristic of the enzyme from higherland plants. Fallover consists of hysteresis in the reactionseen during the initial several minutes and a very slow suicideinhibition by inhibitors formed from the substrate ribulose-l,5-bisphosphate(RuBP). This study examined the relationship between occurrenceof fallover and non-catalytic RuBP-binding sites, and the putativehysteresis-inducible sites (Lys-21 and Lys-30S of the largesubunit in spinach RuBisCO) amongst RuBisCOs of a wide varietyof photosynthetic organisms. Fallover could be detected by followingthe course of the carboxylase reaction at 1 mM RuBP and thenon-catalytic binding sites by alleviation of fallover at 5mM RuBP. RuBisCO from Euglena gracilis showed the same linearreaction course at both RuBP concentrations, indicating an associationbetween an absence of fallover and an absence of the non-catalyticbinding sites. This was supported by the results of an equilibriumbinding assay for this enzyme with a transition state analogue.Green macroalgae and non-green algae contained the plant-type,fallover enzyme. RuBisCOs from Conjugatae, Closterium ehrenbergii,Gona-tozygon monotaenium and Netrium digitus, showed a muchsmaller decrease in activity at 1 mM RuBP than the spinach enzymeand the reaction courses of these enzymes at 5 mM RuBP werealmost linear. RuBisCO of a primitive type Conjugatae, Mesotaeniumcaldariorum, showed the same linear course at both RuBP concentrations.Sequencing of rbcL of these organisms indicated that Lys-305was changed into arginine with Lys-21 conserved. 7 On leave from Research and Development Center, Unitika Ltd.,23 Kozakura, Uji, Kyoto, 611 Japan. 8 Present address: Department of Applied Biological Chemistry,Faculty of Agriculture, Tohoku University, Tsutsumidori-Ama-miyamachi, Sendai, 981 Japan. 9 Present address: National Institute for Basic Biology, Myodaiji,Okazaki, 444 Japan. 10 Present address: Department of Environmental Biology, TokyoPharmaceutical University, Hachioji, Tokyo, 192-03 Japan.
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