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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2017/01/12 14:22:49」(JST)

Microbial transformation of hederagenin by Cunninghamella echinulate, Mucor subtilissimus, and Pseudomonas oleovorans.

Liu Z1, Lu YH2, Feng X2,3, Zou YX3, Diao Z4, Chu ZY3.
Journal of Asian natural products research.J Asian Nat Prod Res.2016 Sep 26:1-7. [Epub ahead of print]
The pentacyclic triterpenoid hederagenin (1) was subjected to biotransformation by Cunninghamella echinulate CGMCC 3.2000, Mucor subtilissimus CGMCC 3.2454 and Pseudomonas oleovorans CGMCC 1.1641. Three metabolites were obtained. On the basis of nuclear magnetic resonance and high-resolution mass sp
PMID 27666872

Nenoff P1, Overbeck C2, Uhrlaß S3, Krüger C3, Gräser Y4.
Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete.Hautarzt.2016 Sep 1. [Epub ahead of print]
A 10-year-old girl suffered from tinea corporis with erythematosquamous and centrifugal growing, sparse itching lesions of her right lower arm. Fluorescence optical Blankophor® preparation from skin scrapings revealed fungal hyphae. On Sabouraud's dextrose agar, the fast growing dermatophyte forme
PMID 27586990

Talaromyces neofusisporus and T. qii, two new species of section Talaromyces isolated from plant leaves in Tibet, China.

Wang QM1, Zhang YH2, Wang B3, Wang L1.
Scientific reports.Sci Rep.2016 Jan 4;6:18622. doi: 10.1038/srep18622.
Two new species isolated from plant leaves belonging to Talaromyces section Talaromyces are reported, namely T. neofusisporus (ex-type AS3.15415 (T) = CBS 139516 (T)) and T. qii (ex-type AS3.15414 (T) = CBS 139515 (T)). Morphologically, T. neofusisporus is featured by forming synnemata on CY
PMID 26725318

Ushijima Shuji,Nagasawa Eiji,Kigawa Shiro [他]
Mycoscience : official journal of the Mycological Society of Japan 56(1), 10-13, 2015-01
NAID 40020325336

岡崎亮,折谷隆之,原義博
植物化学調節学会研究発表記録集 (34), 161-162, 1999-10-01
… As a result, we revealed that Cercospora cruenta metabolized the substrate to the mixture of four diastereomer, and Cunninghamella echinulate metabolized the substrate to the mixture of two enantiomer, we decided the stereochemistry of the metabolites by a comparison with the synthesized chiral specimen, and we examined their biological activity on stomatal openings of commelina communis. …
NAID 110001853494