Qazi Sohail S, Khachatourians George G
Microbial Biotechnology/Molecular Microbiology Labs, Department of Applied Microbiology and Food Science, College of Agriculture, University of Saskatchewan, Saskatoon, Canada.
Arch Microbiol. 2008 Jun;189(6):589-96. doi: 10.1007/s00203-008-0355-9. Epub 2008 Feb 20.
Secretion of catabolic extracellular enzymes (ECE) is the hallmark of the infection of insects through the cuticle by entomopathogenic fungi (EPF). In this paper, we show that germinating conidia of Beauveria bassiana (Bb) regulate the synthesis of ECE through a multiple control mode during the initial stages of germination. We tested Bb conidial growth on aphid exuviae with or without supplementation of additional carbon and/or nitrogen (C/N) compounds. To understand the interrelation between conidial germination during growth, the synthesis of ECE activity, free amino nitrogen (FAN), glucose and fungal dry weight biomass were measured. Immediately (0.25 h) upon incubation of conidia, activity of subtilisin-like Pr1 and trypsin-like Pr2 enzymes and chitinase (NAGase) was observed in the culture filtrates. At 0.25 h, addition of exogenous C-source resulted in higher activities of Pr1 and Pr2, respectively. Conversely at 0.25 h, addition of N-sources repressed the synthesis of Pr2, but that of Pr1. C/N repression was observed only for exponentially growing mycelia. NAGase activity remained at basal level and unaffected by added C/N. We conclude that C/N repression occurs only when it is necessary for the Bb infective structures to establish a nutritional relationship with the host structures.
分泌分解代谢性胞外酶(ECE)是昆虫病原真菌(EPF)通过表皮感染昆虫的标志。在本文中,我们表明球孢白僵菌(Bb)的萌发分生孢子在萌发初期通过多种控制模式调节ECE的合成。我们测试了在添加或不添加额外碳和/或氮(C/N)化合物的情况下,Bb分生孢子在蚜虫蜕上的生长情况。为了解生长过程中分生孢子萌发、ECE活性合成、游离氨基氮(FAN)、葡萄糖和真菌干重生物量之间的相互关系,我们进行了相关测量。分生孢子接种后立即(0.25小时),在培养滤液中观察到类枯草杆菌蛋白酶Pr1、类胰蛋白酶Pr2酶和几丁质酶(NAGase)的活性。在0.25小时时,添加外源碳源分别导致Pr1和Pr2的活性更高。相反,在0.25小时时,添加氮源抑制了Pr2的合成,但对Pr1没有影响。仅在指数生长的菌丝体中观察到C/N抑制。NAGase活性保持在基础水平,不受添加的C/N影响。我们得出结论,只有当Bb感染结构需要与宿主结构建立营养关系时,才会发生C/N抑制。