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黑曲霉微菌落在液体摇瓶培养中的异质性。

Heterogeneity of Aspergillus niger microcolonies in liquid shaken cultures.

机构信息

Microbiology and Kluyver Centre for Genomics of Industrial Fermentation, Institute of Biomembranes, Utrecht University, Padualaan 8, 3584 CH Utrecht, The Netherlands.

出版信息

Appl Environ Microbiol. 2011 Feb;77(4):1263-7. doi: 10.1128/AEM.02134-10. Epub 2010 Dec 17.

Abstract

The fungus Aspergillus niger forms (sub)millimeter microcolonies within a liquid shaken culture. Here, we show that such microcolonies are heterogeneous with respect to size and gene expression. Microcolonies of strains expressing green fluorescent protein (GFP) from the promoter of the glucoamlyase gene glaA or the ferulic acid esterase gene faeA were sorted on the basis of diameter and fluorescence using the Complex Object Parametric Analyzer and Sorter (COPAS) technology. Statistical analysis revealed that the liquid shaken culture consisted of two populations of microcolonies that differ by 90 μm in diameter. The population of small microcolonies of strains expressing GFP from the glaA or faeA promoter comprised 39% and 25% of the culture, respectively. Two populations of microcolonies could also be distinguished when the expression of GFP in these strains was analyzed. The population expressing a low level of GFP consisted of 68% and 44% of the culture, respectively. We also show that mRNA accumulation is heterogeneous within microcolonies of A. niger. Central and peripheral parts of the mycelium were isolated with laser microdissection and pressure catapulting (LMPC), and RNA from these samples was used for quantitative PCR analysis. This analysis showed that the RNA content per hypha was about 45 times higher at the periphery than in the center of the microcolony. Our data imply that the protein production of A. niger can be improved in industrial fermentations by reducing the heterogeneity within the culture.

摘要

黑曲霉在液体摇瓶培养中形成(亚)毫米级的微菌落。在这里,我们表明,这些微菌落在大小和基因表达方面存在异质性。通过使用复杂物体参数分析器和分选器(COPAS)技术,基于直径和荧光,从表达来自葡糖淀粉酶基因 glaA 或阿魏酸酯酶基因 faeA 启动子的绿色荧光蛋白(GFP)的菌株的微菌落中进行分选。统计分析表明,液体摇瓶培养物由两种直径相差 90μm 的微菌落群体组成。表达 GFP 来自 glaA 或 faeA 启动子的菌株的小微菌落群体分别占培养物的 39%和 25%。当分析这些菌株中 GFP 的表达时,也可以区分两种微菌落群体。表达低水平 GFP 的群体分别占培养物的 68%和 44%。我们还表明,黑曲霉微菌落中的 mRNA 积累存在异质性。使用激光微切割和压力弹射(LMPC)分离微菌落的中心和外周部分,并使用这些样品的 RNA 进行定量 PCR 分析。该分析表明,微菌落中心和外周的每条菌丝的 RNA 含量相差约 45 倍。我们的数据表明,通过减少培养物内的异质性,可以提高工业发酵中黑曲霉的蛋白质生产。

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