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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2016/01/20 02:11:45」(JST)

English Journal

Chloracidobacterium thermophilum gen. nov., sp. nov.: an anoxygenic microaerophilic chlorophotoheterotrophic acidobacterium.

Tank M1, Bryant DA2.
International journal of systematic and evolutionary microbiology.Int J Syst Evol Microbiol.2015 May;65(Pt 5):1426-30. doi: 10.1099/ijs.0.000113. Epub 2015 Feb 9.
A novel anoxygenic photoheterotrophic member of the phylum Acidobacteria , Chloracidobacterium thermophilum strain B sp. nov., was isolated from a cyanobacterial enrichment culture derived from microbial mats associated with Octopus Spring, Yellowstone National Park, WY. C. thermophilum sp. nov. was
PMID 25667398

Stereocontrolled total synthesis of tetrodotoxin from myo-inositol and D-glucose by three routes: aspects for constructing complex multi-functionalized cyclitols with branched-chain structures.

Sato K, Akai S, Yoshimura J.
Natural product communications.Nat Prod Commun.2015 May;10(5):691-702.
This report describes the stereocontrolled total synthesis of the multi-functionalized cyclitol derivative, tetrodotoxin, containing eight asymmetric carbons and different types of branched-chains, from myo-inositol and D-glucose using three different methods. The tetrodotoxin derivatives possess a
PMID 26058138

Elucidation of the Burkholderia cenocepacia hopanoid biosynthesis pathway uncovers functions for conserved proteins in hopanoid-producing bacteria.

Schmerk CL1, Welander PV, Hamad MA, Bain KL, Bernards MA, Summons RE, Valvano MA.
Environmental microbiology.Environ Microbiol.2015 Mar;17(3):735-50. doi: 10.1111/1462-2920.12509. Epub 2014 Jun 24.
Hopanoids are bacterial surrogates of eukaryotic membrane sterols and among earth's most abundant natural products. Their molecular fossils remain in sediments spanning more than a billion years. However, hopanoid metabolism and function are not fully understood. Burkholderia species are environment
PMID 24888970

N-Heterocyclic Carbene-Catalyzed Benzoin Strategy for Divergent Synthesis of Cyclitol Derivatives from Alditols

Total Synthesis of (-)-Tetrodotoxin from D-Glucose : A New Route to Multi-Functionalized Cyclitol Employing the Ferrier(II) Reaction toward (-)-Tetrodotoxin

Total Synthesis of (-)-Tetrodotoxin from D-Glucose: A New Route to Multi-Functionalized Cyclitol Employing the Ferrier(II) Reaction toward (-)-Tetrodotoxin