College of Biological Engineering, Henan University of Technology, Zhengzhou, P. R. China.
J Sci Food Agric. 2021 Jan 30;101(2):486-496. doi: 10.1002/jsfa.10657. Epub 2020 Aug 4.
Aspergillus flavus, a saprophytic fungus, is regularly detected in oil-enriched seeds. During colonization, this organism releases aflatoxins that pose a serious risk to food safety and human health. Therefore, an eco-friendly biological approach to inhibit the pathogen is desirable.
Experimental results indicated that A. flavus spores could not germinate in potato dextrose broth culture medium, when the concentration of Sub3 exceeded 0.15 g L . Morphological evaluation performed by flow cytometry and scanning electron microscopy indicated that spores were shrunken and pitted following Sub3 exposure. Physiological assessment using propidium iodide, 5,5',6,6'-tetrachloro-1,1',3,3'-tetraethylbenzimidazolocarbocyanine iodide, 2,7-dichlorodihydrofluorescein diacetate and 4',6-diamidino-2-phenylindole staining revealed damaged cell membranes, decreased mitochondrial membrane potential, increased intracellular reactive oxygen species levels, and elevated large nuclear condensation and DNA fragmentation. Moreover, mitochondrial dehydrogenase activity was reduced by 29.42% and 45.48% after treatment with 0.1 and 0.15 g L Sub3, respectively. Additionally, colonization capacity in peanut was significantly decreased, and the number of spores on seeds treated with Sub3 was decreased by 26.86% (0.1 g L ) and 77.74% (0.15 g L ) compared with the control group.
Sub3 likely inhibits A. flavus by crossing the cell wall and targeting the cell membrane, disrupting mitochondrial energy metabolism, and inducing DNA damage, leading to spore death. Thus, Sub3 may provide a useful biocontrol strategy to control A. flavus growth in peanuts. © 2020 Society of Chemical Industry.
黄曲霉菌是一种腐生真菌,常存在于富含油脂的种子中。该微生物在定殖过程中会释放黄曲霉毒素,对食品安全和人类健康构成严重威胁。因此,采用环保的生物方法来抑制该病原体是可取的。
实验结果表明,当 Sub3 的浓度超过 0.15g/L 时,黄曲霉菌孢子无法在马铃薯葡萄糖肉汤培养基中发芽。用流式细胞术和扫描电子显微镜进行形态评估表明,Sub3 暴露后孢子会收缩和凹陷。用碘化丙啶、5,5',6,6'-四氯-1,1',3,3'-四乙基苯并咪唑羰花青碘、2,7-二氯二氢荧光素二乙酸酯和 4',6-二脒基-2-苯吲哚染色进行生理评估表明,细胞膜受损,线粒体膜电位降低,细胞内活性氧水平升高,核质浓缩和 DNA 片段化增加。此外,用 0.1 和 0.15g/L Sub3 处理后,线粒体脱氢酶活性分别降低了 29.42%和 45.48%。此外,Sub3 处理后花生的定殖能力显著降低,与对照组相比,Sub3 处理组种子上的孢子数量分别减少了 26.86%(0.1g/L)和 77.74%(0.15g/L)。
Sub3 可能通过穿过细胞壁并靶向细胞膜、破坏线粒体能量代谢以及诱导 DNA 损伤来抑制黄曲霉菌,导致孢子死亡。因此,Sub3 可能为控制花生中黄曲霉菌的生长提供一种有用的生物防治策略。