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吡喃黑菌素生物合成途径的阐明揭示了四胺酸、稠合γ-吡喃酮和亚甲基外桥形成的模式。

Elucidation of Pyranonigrin Biosynthetic Pathway Reveals a Mode of Tetramic Acid, Fused γ-Pyrone, and exo-Methylene Formation.

作者信息

Yamamoto Tsuyoshi, Tsunematsu Yuta, Noguchi Hiroshi, Hotta Kinya, Watanabe Kenji

机构信息

Department of Pharmaceutical Sciences, University of Shizuoka , Shizuoka 422-8526, Japan.

School of Biosciences, The University of Nottingham Malaysia Campus , Semenyih, Selangor Darul Ehsan 43500, Malaysia.

出版信息

Org Lett. 2015 Oct 16;17(20):4992-5. doi: 10.1021/acs.orglett.5b02435. Epub 2015 Sep 28.

Abstract

Successful activation of the pyranonigrin biosynthetic gene cluster and gene knockout in Aspergillus niger plus in vivo and in vitro assays led to isolation of six new products, including a spiro cyclobutane-containing dimeric compound, which served as the basis for the proposed comprehensive pyranonigrin biosynthetic pathway. Two redox enzymes are key to forming the characteristic fused γ-pyrone core, and a protease homologue performs the exo-methylene formation.

摘要

黑曲霉中吡喃尼日林生物合成基因簇的成功激活和基因敲除,以及体内和体外试验,导致分离出六种新产物,包括一种含螺环丁烷的二聚化合物,这为所提出的全面的吡喃尼日林生物合成途径奠定了基础。两种氧化还原酶是形成特征性稠合γ-吡喃核心的关键,一种蛋白酶同源物负责形成亚甲基。

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