Kramer Annemarie, Beck Hans Christian, Kumar Abhishek, Kristensen Lars Peter, Imhoff Johannes F, Labes Antje
Research Unit Marine Ecology, GEOMAR Helmholtz Centre for Ocean Research Kiel, Kiel, Germany.
Centre for Clinical Proteomics, Department for Clinical Biochemistry and Pharmacology, Odense University Hospital, Odense, Denmark.
PLoS One. 2015 Oct 13;10(10):e0140047. doi: 10.1371/journal.pone.0140047. eCollection 2015.
The marine fungus Microascus brevicaulis strain LF580 is a non-model secondary metabolite producer with high yields of the two secondary metabolites scopularides A and B, which exhibit distinct activities against tumour cell lines. A mutant strain was obtained using UV mutagenesis, showing faster growth and differences in pellet formation besides higher production levels. Here, we show the first proteome study of a marine fungus. Comparative proteomics were applied to gain deeper understanding of the regulation of production and of the physiology of the wild type strain and its mutant. For this purpose, an optimised protein extraction protocol was established. In total, 4759 proteins were identified. The central metabolic pathway of strain LF580 was mapped using the KEGG pathway analysis and GO annotation. Employing iTRAQ labelling, 318 proteins were shown to be significantly regulated in the mutant strain: 189 were down- and 129 upregulated. Proteomics are a powerful tool for the understanding of regulatory aspects: The differences on proteome level could be attributed to limited nutrient availability in the wild type strain due to a strong pellet formation. This information can be applied for optimisation on strain and process level. The linkage between nutrient limitation and pellet formation in the non-model fungus M. brevicaulis is in consensus with the knowledge on model organisms like Aspergillus niger and Penicillium chrysogenum.
海洋真菌短柄微囊菌菌株LF580是一种非模式次生代谢产物产生菌,能高产两种次生代谢产物帚曲霉素A和B,这两种产物对肿瘤细胞系具有不同的活性。通过紫外线诱变获得了一个突变菌株,该菌株除了产量更高外,生长更快且在菌球形成方面存在差异。在此,我们展示了对一种海洋真菌的首次蛋白质组学研究。应用比较蛋白质组学来更深入地了解野生型菌株及其突变体的生产调控和生理学。为此,建立了一种优化的蛋白质提取方案。总共鉴定出4759种蛋白质。利用KEGG通路分析和GO注释对菌株LF580的中心代谢途径进行了绘制。采用iTRAQ标记法,结果显示突变菌株中有318种蛋白质受到显著调控:189种下调,129种上调。蛋白质组学是理解调控方面的有力工具:蛋白质组水平上的差异可能归因于野生型菌株中由于强烈的菌球形成导致营养物质供应有限。这些信息可应用于菌株和工艺水平的优化。非模式真菌短柄微囊菌中营养限制与菌球形成之间的联系与黑曲霉和产黄青霉等模式生物的相关知识一致。