Hokkaido University · 생화학·유전·분자생물학
오키노 타츠후미 교수의 연구실은 주로 해양 및 수생 생물에서 유래한 자연물의 분리, 구조 규명 및 생물학적 활성 평가를 중심으로 연구를 진행하고 있습니다. 특히 해양 조류, 조류, 해면 등에서 새로운 항부착 물질, 효소 억제제, 생합성 경로에 관여하는 고유한 화합물을 규명하며 생물학적 기반의 신소재 개발에 기여하고 있습니다. 최근에는 페프티드 유도체의 생합성 메커니즘, 특히 구아니딘 기반 프레닐화 반응의 효소 기반 규명에도 주력하고 있습니다.
표시된 성과는 수집된 데이터 기준으로 산출되며, 일부 차이가 있을 수 있습니다.
Nostopeptins A and B were isolated from the cultured freshwater cyanobacterium Nostoc minutum (NIES-26). Their structures were elucidated on the basis of 2D NMR data and chemical degradation. These cyclic depsipeptides containing Ahp (3-amino-6-hydroxy-2-piperidone) inhibited elastase and chymotrypsin potently.
Two new diterpene formamides were isolated from the marine sponge Acanthella cavernosa collected off Yakushima Island, along with seven known diterpenes. Their structures proved to be kalihipyran derivatives on the basis of spectral data. All nine compounds showed potent antifouling activity against larvae of the barnacle Balanus amphitrite.
Natural antifouling products have been the subject of considerable attention. We screened marine algae for antifouling activity and discovered omaezallenes, the new bromoallene-containing natural products isolated from the red alga Laurencia sp. Described is the isolation, structure elucidation, and total syntheses of omaezallenes. The relative and absolute configurations of natural omaezallenes were unambiguously established through total synthesis. The antifouling activities and ecotoxicity of
Guanidine prenylation is an outstanding modification in alkaloid and peptide biosynthesis, but its enzymatic basis has remained elusive. We report the isolation of argicyclamides, a new class of cyanobactins with unique mono- and bis-prenylations on guanidine moieties, from <i>Microcystis aeruginosa</i> NIES-88. The genetic basis of argicyclamide biosynthesis was established by the heterologous expression and <i>in vitro</i> characterization of biosynthetic enzymes including AgcF, a new guanidin
Six new compounds, omaezol, intricatriol, hachijojimallenes A and B, debromoaplysinal, and 11,12-dihydro-3-hydroxyretinol have been isolated from four collections of <i>Laurencia</i> sp. These structures were determined by MS and NMR analyses. Their antifouling activities were evaluated together with eight previously known compounds isolated from the same samples. In particular, omaezol and hachijojimallene A showed potent activities (EC<sub>50</sub> = 0.15-0.23 µg/mL) against larvae of the barn
Cyanobacteria are reported as rich sources of secondary metabolites that provide biological activities such as enzyme inhibition and cytotoxicity. Ten depsipeptide derivatives (lyngbyabellins) were isolated from a Malaysian <i>Moorea bouillonii</i> and a Red Sea <i>Okeania</i> sp.: lyngbyabellins G (<b>1</b>), O (<b>2</b>), P (<b>3</b>), H (<b>4</b>), A (<b>7</b>), 27-deoxylyngbyabellin A (<b>5</b>), and homohydroxydolabellin (<b>6</b>). This study indicated that lyngbyabellins displayed cytotox
The cyanoremediation technique for heavy metal (HM) removal from wastewater using live cyanobacteria is promising to reduce the pollution risk both for the environment and human health. In this study, two widely recognized freshwater cyanobacteria, <i>Anabaena variabilis</i> and <i>Synechocystis</i> sp., were used to explore their efficacy in HM (As(v), Cd(ii), Cr(vi), Pb(ii)) removal. The different optimum adsorption conditions were pH 8 and 7.5 for <i>A. variabilis</i> and <i>Synechocystis</i>