Department of Microbial Biotechnology and Cell Biology, Faculty of Science and Technology, University of Debrecen, Debrecen, Hungary.
J Appl Microbiol. 2009 Aug;107(2):514-23. doi: 10.1111/j.1365-2672.2009.04237.x. Epub 2009 May 26.
Elucidation of the regulation of ChiB production in Aspergillus nidulans.
Mutational inactivation of the A. nidulans chiB gene resulted in a nonautolytic phenotype. To better understand the mechanisms controlling both developmental progression and fungal autolysis, we examined a range of autolysis-associated parameters in A. nidulans developmental and/or autolytic mutants. Investigation of disorganization of mycelial pellets, loss of biomass, extra-/intracellular chitinase activities, ChiB production and chiB mRNA levels in various cultures revealed that, in submerged cultures, initialization of autolysis and stationary phase-induced ChiB production are intimately coupled, and that both processes are controlled by the FluG-BrlA asexual sporulation regulatory pathway. ChiB production does not affect the progression of apoptotic cell death in the aging A. nidulans cultures.
The endochitinase ChiB plays an important role in autolysis of A. nidulans, and its production is initiated by FluG-BrlA signalling. Despite the fact that apoptosis is an inseparable part of fungal autolysis, its regulation is independent to FluG-initiated sporulation signalling.
Deletion of chiB and fluG homologues in industrial filamentous fungal strains may stabilize the hyphal structures in the autolytic phase of growth and limit the release of autolytic hydrolases into the culture medium.
阐明 Aspergillus nidulans 中 ChiB 产生的调控机制。
突变失活 A. nidulans chiB 基因导致非自溶表型。为了更好地理解控制发育进程和真菌自溶的机制,我们研究了一系列与自溶相关的参数,包括 A. nidulans 发育和/或自溶突变体。研究发现,在丝状真菌的菌块分散、生物量损失、细胞外/内几丁质酶活性、ChiB 产生和 chiB mRNA 水平等方面,在浸没法培养中,自溶的初始启动和静止期诱导的 ChiB 产生紧密相关,这两个过程都受到 FluG-BrlA 无性孢子形成调控途径的控制。ChiB 产生并不影响老化 A. nidulans 培养物中细胞凋亡的进程。
内切几丁质酶 ChiB 在 A. nidulans 的自溶中起着重要作用,其产生是由 FluG-BrlA 信号启动的。尽管凋亡是真菌自溶不可分割的一部分,但它的调控与 FluG 启动的孢子形成信号是独立的。
在工业丝状真菌菌株中删除 chiB 和 fluG 同源物可能会稳定自溶生长阶段的菌丝结构,并限制自溶水解酶释放到培养基中。