マンガン酸化を操る天然物 ――深海細菌が作るロイヒケリン C と金属との関わり――

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2026-03-04 東京大学

東京大学大学院薬学系研究科の研究グループは、深海火山由来細菌 Halomonas LOB-5 が産生する天然物「ロイヒケリンC」の全合成に成功し、その金属との関係を解明した。改良型無痕跡型Staudingerライゲーションと固相合成法を組み合わせ、天然物および構造類縁体の合成を実現。解析の結果、ロイヒケリンCは鉄Fe(III)と強く結合するだけでなく、自然界ではほとんど進行しないマンガンMn(II)のMn(III)への酸化を促進し、通常不安定なMn(III)を安定化することが判明した。人工類縁体ではこの作用が見られず、天然構造が重要であることが示された。本成果は、深海など極限環境での微生物と金属循環の関係理解を深めるとともに、天然物の未知機能解明における全合成と分子編集の有効性を示す研究である。

<関連情報>

ロイヒケリンCの全合成と機能解析:Mn(III)安定化とMn(II)酸化の構造基盤 Total Synthesis and Functional Analysis of Loihichelin C: Structural Basis for Mn(III) Stabilization and Mn(II) Oxidation

Mizuki Sawada,Hiromu Kakizawa,Aoi Takeuchi,Hiroaki Itoh,Masayuki Inoue
JACS Au  Published: February 27, 2026
DOI:https://doi.org/10.1021/jacsau.5c01730

Abstract

Loihichelin C (1a) is a peptidic siderophore isolated from cultures of the bacterium Halomonas LOB-5 collected from deep-sea vent environments. Compound 1a is believed to promote microbial growth by coordinating to an Fe(III) ion via one hydroxycarboxylate and two hydroxamates and facilitating the uptake of Fe(III). In addition, 1a is implicated in Mn(II)-oxidation by the producing bacterium. To obtain insights into the Fe(III)-chelating and Mn(II)-oxidizing functions of 1a, we chemically synthesized and functionally assessed 1a, and two analogs 1b and 1c, in which the hydroxy group of hydroxycarboxylate was stereochemically inverted and deleted, respectively. We devised an efficient solid-phase synthetic strategy to assemble the unusual sequences of 1a1c. The strong binding affinity of 1a toward Fe(III) surpassed the affinities of 1b and 1c. Furthermore, 1a facilitated Mn(II) oxidation under aerobic conditions and stabilized metastable Mn(III), whereas 1b and 1c underwent oxidative degradation by Mn(III). These data indicated that the properly oriented hydroxy group of 1a not only promotes single electron transfer from Mn(II) to electron-deficient O2 by forming a negatively charged Mn(II) complex but also protects further oxidation of the resultant Mn(III) to Mn(IV) by preventing the coordination of O2. Overall, this molecular editing approach revealed the structural requirements for stabilizing the Mn(III) oxidation state and identified the mechanism of Mn(II) oxidation in the presence of 1a for the first time.

有機化学・薬学
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