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Novel Key Metabolites Reveal Further Branching of the Roquefortine/Meleagrin Biosynthetic Pathway

机译:新的关键代谢物揭示了罗福福汀/美乐格林生物合成途径的进一步分支

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摘要

Metabolic profiling and structural elucidation of novel secondary metabolites obtained from derived deletion strains of the filamentous fungus Penicillium chrysogenum were used to reassign various previously ascribed synthetase genes of the roquefortine/meleagrin pathway to their corresponding products. Next to the structural characterization of roquefortine F and neoxaline,which are for the first time reported for P. chrysogenum, we identified the novel metabolite roquefortine L, including its degradation products, harboring remarkable chemical structures. Their biosynthesis is discussed, questioning the exclusive role of glandicoline A as key intermediate in the pathway. The results reveal that further enzymes of this pathway are rather unspecific and catalyze more than one reaction, leading to excessive branching in the pathway with meleagrin and neoxaline as end products of two branches.
机译:从丝状真菌青霉青霉的衍生缺失菌株获得的新的次生代谢产物的代谢谱和结构解析被用于将roquefortine / meleagrin途径的各种先前归类的合成酶基因重新分配给它们的相应产物。继首次报道了有关菊苣青霉的roquefortine F和neoxaline的结构表征之后,我们鉴定了新型代谢产物roquefortine L,包括其降解产物,具有明显的化学结构。讨论了它们的生物合成,质疑了腺嘌呤林A作为途径中关键中间体的排他性作用。结果表明,该途径的其他酶相当不特异性,并且催化一个以上的反应,从而导致该途径中过多的分支,其中麦来精和新沙星作为两个分支的最终产物。

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