日本地球惑星科学連合2014年大会

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セッション記号 M (領域外・複数領域) » M-IS ジョイント

[M-IS21_28AM2] 生物地球化学

2014年4月28日(月) 11:00 〜 12:45 511 (5F)

コンビーナ:*楊 宗興(東京農工大学)、柴田 英昭(北海道大学北方生物圏フィールド科学センター)、大河内 直彦(海洋研究開発機構)、山下 洋平(北海道大学 大学院地球環境科学研究院)、座長:高野 淑識(海洋研究開発機構)、長尾 誠也(金沢大学環日本海域環境研究センター)、陀安 一郎(京都大学生態学研究センター)、岩田 智也(山梨大学生命環境学部)

11:00 〜 11:15

[MIS21-08] 真核生物の細胞膜に存在するステロールおよびその代替物質に関する謎

*瀧下 清貴1矢吹 彬憲1力石 嘉人1高木 善弘1吉田 尊雄1大河内 直彦1 (1.海洋研究開発機構)

キーワード:真核生物, ステロール, テトラヒマノール, 細胞膜

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.