Key Laboratory of Pathogenic Fungi and Mycotoxins of Fujian Province, Key Laboratory of Biopesticide and Chemical Biology of the Ministry of Education and School of Life Sciences, Fujian Agriculture and Forestry University, Fuzhou 350002, China.
Toxins (Basel). 2019 Jan 14;11(1):41. doi: 10.3390/toxins11010041.
s is one of the fungi from the big family of genus and it is capable of colonizing a large number of seed/crops and living organisms such as animals and human beings. (also called ) is an integral part of the mitogen activated protein kinase signal of the high osmolarity glycerol pathway. In this study, the gene was deleted () then complemented (∆) using homologous recombination and the osmotic stress was induced by 1.2 mol/L D-sorbital and 1.2 mol/L sodium chloride. The result showed that ∆ mutant caused a significant influence on conidial formation compared to wild-type and ∆ strains It was also found that responds to both the osmotic stress and the cell wall stress. In the absence of osmotic stress, ∆ mutant produced more sclerotia in contrast to other strains, whereas all strains failed to generate sclerotia under osmotic stress. Furthermore, the deletion of resulted in the increase of Aflatoxin B₁ production compared to other strains. The virulence assay on both maize kernel and peanut seeds showed that ∆ strain drastically produced more conidia and Aflatoxin B₁ than wild-type and complementary strains. AfSakA-mCherry was located to the cytoplasm in the absence of osmotic stress, while it translocated to the nucleus upon exposure to the osmotic stimuli. This study provides new insights on the development and evaluation of aflatoxin biosynthesis and also provides better understanding on how to prevent infections which would be considered the first step towards the prevention of the seeds damages caused by .
s 是 属真菌大家族中的一员,能够定植于大量的种子/作物以及动物和人类等生物体。 (也称为 ) 是高渗透压甘油途径中丝裂原活化蛋白激酶信号的一个组成部分。在这项研究中,使用同源重组技术删除了 基因(∆),然后进行了互补(∆),并通过 1.2 mol/L D-山梨醇和 1.2 mol/L 氯化钠诱导渗透胁迫。结果表明,与野生型和 ∆ 菌株相比,∆ 突变体对分生孢子形成有显著影响。还发现 对渗透胁迫和细胞壁应激都有反应。在没有渗透胁迫的情况下,∆ 突变体产生的菌核比其他菌株多,而所有菌株在渗透胁迫下都无法产生菌核。此外,与其他菌株相比,删除 导致黄曲霉毒素 B₁产量增加。在玉米籽粒和花生种子上的毒力测定表明,与野生型和互补菌株相比,∆ 菌株产生的分生孢子和黄曲霉毒素 B₁明显更多。在没有渗透胁迫的情况下,AfSakA-mCherry 位于细胞质中,而在受到渗透刺激时则转移到细胞核中。这项研究为黄曲霉生物合成的发展和评估提供了新的见解,并更好地了解了如何预防 感染,这将被认为是预防由 引起的种子损伤的第一步。