首页> 外文期刊>Microbiological Research >StPBS2, a MAPK kinase gene, is involved in determining hyphal morphology, cell wall development, hypertonic stress reaction as well as the production of secondary metabolites in Northern Corn Leaf Blight pathogen Setosphaeria turcica
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StPBS2, a MAPK kinase gene, is involved in determining hyphal morphology, cell wall development, hypertonic stress reaction as well as the production of secondary metabolites in Northern Corn Leaf Blight pathogen Setosphaeria turcica

机译:STPBS2,MAPK激酶基因,参与确定亚酚形态,细胞壁发育,高渗应力反应以及北玉米叶枯燥病原体塞洛尼亚植物孢子植物的二次代谢物

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摘要

Mitogen activated protein kinase kinase (MAPKK) is a crucial component in the MAPK signaling pathway. However, the functions of MAPKKs in foliar pathogens remain poorly understood. In the current study, a MAPKK gene designated as StPBS2 was cloned from Setosphaeria turcica and the functions of this gene were investigated by RNAi technology. Four independent StPBS2 gene silence transformants with different efficiencies were confirmed by real time PCR. Compared to the wild type strain (WT), these transformants showed decreased colony growth, shortened hyphae cell length, broadened cell width and an obvious reduction in conidium yield. Moreover, the cell wall of the transformants was thicker and they were also more sensitive to substances that interfere with cell wall biosynthesis than WT. Additionally, the transformants displayed higher sensitivity to hypertonic stress than WT and the sensitivity was associated with the level of silencing of StPBS2. They were also resistant to the fungicides iprodione, procymidone and fludioxonil, to which WT almost completely sensitive. The transformants produced more red secondary metabolites than WT and the production was enhanced with increasing silencing level and increased glucose content in PDA medium. Our results suggest that StPBS2 is involved in morphogenesis, condiogenesis, cell wall development, hypertonic stress reaction and resistance to fungicides, as well as in the biosynthesis of secondary metabolites in S. turcica.
机译:促丝糖型活化蛋白激酶激酶(MAPKK)是MAPK信号通路中的关键组分。然而,Mapkks在叶酸病原体中的功能仍然明白很差。在目前的研究中,将指定为STPBS2的MAPKK基因由SetOphaeria Turcica克隆,并通过RNAi技术研究了该基因的功能。通过实时PCR确认具有不同效率的四种独立的STPBS2基因沉默转化体。与野生型菌株(WT)相比,这些转化体表现出降低的菌落生长,缩短菌丝细胞长度,扩大细胞宽度和胞子产量明显降低。此外,转化体的细胞壁较厚,并且它们对干扰细胞壁生物合成的物质也比wt更敏感。另外,转化体对高渗应力的敏感性高于WT,并且灵敏度与STPBS2的沉默水平相关。它们也抵抗杀真菌剂Iprodione,procymidone和Fludioxonil,几乎完全敏感。转化体产生比wt更多的红色次级代谢产物,并且通过增加沉默水平和PDA培养基中的葡萄糖含量增加了生产。我们的研究结果表明,STPBS2涉及形态发生,髁突,细胞壁发育,高渗应力反应和对杀菌剂的抗性,以及在Turcica中的次生代谢物的生物合成中。

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