With many bioactive non-ribosomal peptides and polyketides produced in fungi, studies of their biosyntheses are an active area of research. Practical limitations of working with mega-dalton synthetases including cell lysis and protein extraction to recombinant gene and pathway expression has slowed understanding of many secondary metabolic processes relative to bacterial counterparts. Recent advances in accessing fungal biosynthetic machinery are beginning to change this. Here we describe the successes of some studies of thiotemplate biosynthesis in fungal systems, along with very recent advances in chemical tagging and mass spectrometric strategies to selectively study biosynthetic conveyer belts in isolation, and within a few years, in endogenous fungal proteomes.

译文

由于真菌中产生了许多具有生物活性的非核糖体肽和聚酮化合物,因此对其生物合成的研究是一个活跃的研究领域。使用mega-dalton合成酶 (包括细胞裂解和蛋白质提取到重组基因和途径表达) 的实际局限性,相对于细菌对应物,减慢了对许多次级代谢过程的理解。获取真菌生物合成机械的最新进展已开始改变这一点。在这里,我们描述了真菌系统中硫模板生物合成的一些研究的成功,以及化学标签和质谱策略的最新进展,以选择性隔离的生物合成传送带,并在几年内,内源性真菌蛋白质组。

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