Japan Geoscience Union Meeting 2014

Presentation information

Oral

Symbol M (Multidisciplinary and Interdisciplinary) » M-IS Intersection

[M-IS21_28AM2] Biogeochemistry

Mon. Apr 28, 2014 11:00 AM - 12:45 PM 511 (5F)

Convener:*Muneoki Yoh(Tokyo University of Agriculture and Technology), Hideaki Shibata(Field Science Center fot Northern Biosphere, Hokkaido University), Naohiko Ohkouchi(Japan Agency for Marine-Earth Science and Technology), Youhei Yamashita(Faculty of Environmental Earth Science, Hokkaido University), Chair:Yoshinori Takano(Institute of Biogeosciences, Japan Agency for Marine-Earth Science and Technology (JAMSTEC)), Seiya Nagao(Institute of Nature and Environmental Technology, Kanazawa University), Ichiro Tayasu(Center for Ecological Research, Kyoto University), Tomoya Iwata(Faculty of Life and Environmental Sciences, University of Yamanashi)

11:00 AM - 11:15 AM

[MIS21-08] Enigmas concerning sterols and their surrogates in eukaryotic cell membranes

*Kiyotaka TAKISHITA1, Akinori YABUKI1, Yoshito CHIKARAISHI1, Yoshihiro TAKAKI1, Takao YOSHIDA1, Naohiko OHKOUCHI1 (1.Japan Agency for Marine-Earth Science and Technology)

Keywords:eukaryotes, sterols, tetrahymanol, cell membrane

A large fraction of eukaryotes and bacteria respectively possess sterols and hopanoids, which function as potent stabilizers of cell membranes. Sterols are also associated with fluidity and permeability of eukaryotic cell membranes, and are key to fundamental eukaryotic-specific cellular processes such as phagocytosis. Several steps of de novo sterol biosynthesis require molecular oxygen. For example, the epoxidation of squalene is the first oxygen-dependent step in the sterol pathway; the epoxidized squalene is then cyclized to either lanosterol or cycloartenol by the enzyme oxidosqualene cyclase. In contrast, prokaryotic hopanoid biosynthesis does not require molecular oxygen as a substrate, and the squalene is directly cyclized by the enzyme squalene-hopene cyclase.Until now, it was unclear how bacterivorous unicellular eukaryotes that are abundant in anoxic or low oxygen environments could carry out phagocytosis. These eukaryotes cannot obtain sterols from food bacteria as the latter generally lack them and sterols cannot be synthesized de novo in the absence of molecular oxygen. We have previously provided evidence that the molecule tetrahymanol is synthesized by some anaerobic/microaerophilic eukaryotes and possibly functions as an analogue of sterols in these organisms. Nevertheless, neither sterol, nor tetrahymanol, nor their related molecule has been found in the other anaerobic/microaerophilic eukaryotes, and so it is still enigmatic how these organisms maintain their fluid and permeable membrane system specific to eukaryotes.One more area of confusion is regarding sterols in bivalves with chemosynthetic bacteria inhabiting areas of deep-sea hydrothermal vents and methane seeps, such as Calyptogena spp. and Bathymodiolus spp. In general, bivalves cannot synthesize sterols de novo and it is necessary for them to obtain these molecules from small eukaryotic prey. On the other hand, Calyptogena spp. and Bathymodiolus spp. mainly or exclusively acquire nutrients produced by their bacterial symbionts, rather than from eukaryotes rich in sterols. Nevertheless, these "chemosynthetic bivalves" contain sterols. More curiously, Calyptogena spp. have intermediate metabolites of phytosterols (24-methylenecycloartanal, cycloeucalenol, and obutusifoliol), while Bathymodiolus spp. have high amounts of cholesterol typical of animals. Little attention has been given to how chemosynthetic bivalves produce or acquire these kinds of sterols.In my talk, I will discuss potentially controversial topics regarding sterols and their surrogates in eukaryotic cell membranes, which do not appear in biochemical and geochemical textbooks.