Graduate Institute of Pharmaceutical Science, Chia Nan University of Pharmacy and Science, Tainan 71710, Taiwan, Republic of China.
Appl Environ Microbiol. 2010 Apr;76(7):2067-74. doi: 10.1128/AEM.02187-09. Epub 2010 Feb 5.
Deletion of cclA, a component of the COMPASS complex of Aspergillus nidulans, results in the production of monodictyphenone and emodin derivatives. Through a set of targeted deletions in a cclA deletion strain, we have identified the genes required for monodictyphenone and emodin analog biosynthesis. Identification of an intermediate, endocrocin, from an mdpHDelta strain suggests that mdpH might encode a decarboxylase. Furthermore, by replacing the promoter of mdpA (a putative aflJ homolog) and mdpE (a putative aflR homolog) with the inducible alcA promoter, we have confirmed that MdpA functions as a coactivator. We propose a biosynthetic pathway for monodictyphenone and emodin derivatives based on bioinformatic analysis and characterization of biosynthetic intermediates.
缺失 COMPASS 复合物的一个组成部分 cclA,导致产生单二苯甲酮和大黄素衍生物。通过对 cclA 缺失菌株进行一系列靶向缺失,我们已经鉴定出了产生单二苯甲酮和大黄素类似物所需的基因。从 mdpHDelta 菌株中鉴定出中间产物内克罗辛,表明 mdpH 可能编码脱羧酶。此外,通过用诱导型 alcA 启动子替换 mdpA(假定的 aflJ 同源物)和 mdpE(假定的 aflR 同源物)的启动子,我们已经证实 MdpA 作为共激活因子发挥作用。我们基于生物信息学分析和生物合成中间体的特征,提出了单二苯甲酮和大黄素衍生物的生物合成途径。