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解析阿萨希毛霉细胞壁完整性途径。

Analysis of the cell wall integrity pathway of Ashbya gossypii.

机构信息

Carlsberg Laboratory, Yeast Genetics, Gamle Carlsberg Vej 10, DK-1799 Copenhagen V, Denmark.

出版信息

Microbiol Res. 2013 Dec 14;168(10):607-14. doi: 10.1016/j.micres.2013.06.008. Epub 2013 Jul 10.

Abstract

Fungal cells are exposed to rapidly changing environmental conditions, in particular with regard to the osmotic potential. This requires constant remodeling of the cell wall and, therefore, the cell wall integrity (CWI) MAP-kinase pathway plays a major role in shaping the fungal cell wall to protect from adverse external stresses. To provide a comprehensive functional analysis of the Ashbya gossypii CWI pathway we generated a set of ten deletion mutants in conserved components including the cell surface sensors AgWSC1 and AgMID2, a putative Rho1-guanine nucleotide exchange factor, AgTUS1, the protein kinase C, AgPKC1, the MAP-kinases AgBCK1, AgMKK1 and AgMPK1, and transcription factors known to be involved in CWI signaling AgRLM1, AgSWI4 and AgSWI6. Deletion of AgPKC1 shows a severe growth defect with frequent tip cell lysis. Deletion of components of the MAP-kinase module generates a pronounced colony lysis phenotype in older regions of the mycelium. Cytoplasmic leakage was assayed using alkaline phosphatase and β-galactosidase release assays. This indicated that the lysis phenotypes of CWI pathway mutants may be useful to facilitate the isolation of riboflavin from A. gossypii. Remarkably, the Agwsc1 mutant showed a strong (up to 8-fold) increase of riboflavin in the growth medium compared to the parental strain.

摘要

真菌细胞暴露于快速变化的环境条件下,特别是在渗透势方面。这需要不断重塑细胞壁,因此,细胞壁完整性(CWI)MAP 激酶途径在塑造真菌细胞壁以抵御不利外部压力方面起着重要作用。为了对构巢曲霉 CWI 途径进行全面的功能分析,我们生成了一组十个缺失突变体,包括保守成分中的细胞表面传感器 AgWSC1 和 AgMID2、一个假定的 Rho1-鸟苷酸交换因子 AgTUS1、蛋白激酶 C AgPKC1、MAP 激酶 AgBCK1、AgMKK1 和 AgMPK1,以及已知参与 CWI 信号转导的转录因子 AgRLM1、AgSWI4 和 AgSWI6。AgPKC1 的缺失显示出严重的生长缺陷,经常导致尖端细胞裂解。MAP 激酶模块的组件缺失会在菌丝体的较老区域产生明显的菌落裂解表型。使用碱性磷酸酶和β-半乳糖苷酶释放测定法测定细胞质渗漏。这表明 CWI 途径突变体的裂解表型可能有助于从构巢曲霉中分离核黄素。值得注意的是,与亲本菌株相比,Agwsc1 突变体在生长培养基中表现出强烈的(高达 8 倍)核黄素增加。

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