首页> 外文期刊>International Journal of Food Microbiology >Development of a green fluorescent tagged strain of Aspergillus carbonarius to monitor fungal colonization in grapes.
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Development of a green fluorescent tagged strain of Aspergillus carbonarius to monitor fungal colonization in grapes.

机译:开发了绿色荧光标记的碳曲霉菌株,以监测葡萄中的真菌定植。

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An enhanced green fluorescent protein has been used to tag an OTA-producing strain of Aspergillus carbonarius (W04-40) isolated from naturally infected grape berries. Transformation of the fungus was mediated by Agrobacterium tumefaciens. The most efficient transformation occurred when the co-cultivation was done with 104 conidia due to higher frequency of resistance colonies (894 per 104 conidia) and lower background obtained. To confirm the presence of the hph gene in hygromycin resistant colonies, 20 putative transformants were screened by PCR analysis. The hph gene was identified in all the transformants. Variation on the expression levels of the eGFP was detected among the transformants and 50% of them appeared bright green fluorescent under the microscope. Microscopic analysis of all the bright fluorescent transformants revealed homogeneity of the fluorescent signal, which was clearly visible in the hyphae as well as in the conidia. eGFP expression in A. carbonarius was shown to be stable in all transformants. Confocal Laser scanning microscopy images of grape berries infected with the eGFP transformant demonstrated fungal penetration into the berry tissues. OTA production was importantly increased in the eGFP transformant in comparison with the wild type strain and pathogenicity on grape berries was slightly decreased after four days of inoculation. However, no differences in virulence were found after seven days of inoculation, thus allowing utilization of this eGFP mutant for in situ analysis of A. carbonarius infection of grape berries. To our knowledge, this is the first report describing the construction of a GFP-tagged strain belonging to Aspergillus section Nigri for monitoring Aspergillus rot on grape berries.
机译:一种增强的绿色荧光蛋白已用于标记从自然感染的葡萄浆果中分离出的生产OTA的碳曲霉(ii。carbonarius)(W04-40)菌株。真菌的转化是由根癌农杆菌介导的。当与10 4 分生孢子共培养时,由于抗性菌落的频率较高(每10 4 分生孢子894个)和获得的背景较低,因此最有效的转化发生。为了确认潮霉素抗性菌落中 hph 基因的存在,通过PCR分析筛选了20个推定的转化体。在所有转化子中都鉴定出了 hph 基因。在转化体中检测到eGFP表达水平的变化,并且在显微镜下,其中50%呈现亮绿色荧光。显微镜分析所有明亮的荧光转化子,发现荧光信号的同质性,在菌丝和分生孢子中均清晰可见。 eGFP在 A中的表达。在所有转化子中,Carbonarius 被证明是稳定的。共聚焦激光扫描显微镜观察到的葡萄浆果被eGFP转化子感染后,表明真菌渗透到了浆果组织中。与野生型菌株相比,eGFP转化株中OTA的产量显着增加,接种4天后葡萄浆果的致病性略有降低。然而,接种7天后没有发现毒力的差异,因此允许将该eGFP突变体用于i A的原位分析。葡萄浆果的无花果感染。据我们所知,这是第一份报告,描述了属于曲霉 Nigri部分的GFP标记菌株的构建,该菌株用于监测葡萄浆果上的<曲>曲霉腐烂。

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