Guo Demin, Zhao Shengfang, Chen Jie, Han Shuhui, Li Yangtao, Chen Yu, Hu Shengbiao, Hu Yibo
State Key Laboratory of Developmental Biology of Freshwater Fish, Hunan Provincial Key Laboratory for Microbial Molecular Biology, College of Life Science, Hunan Normal University, Changsha, China.
Curr Microbiol. 2025 Jan 9;82(2):75. doi: 10.1007/s00284-024-04058-0.
Remodelling regulatory pathways to directionally increase the efficiency of specific promoters in chassis cells is an effective strategy for the rational construction of expression systems. However, the repeated utilization of one regulator to modify the host cell to improve expression motif efficiency has a limited effect. Therefore, it is preferable to identify new regulatory factors to activate specific pathways and thus further improve the efficiency of target elements. Heterochromatin protein 1 (HP1) is considered a main factor responsible for heterochromatin maintenance; it binds DNA and thus forms a tight structure to repress gene expression in fungi. This study revealed that the overexpression of HepA (a homologue of HP1) increased amylase expression in Penicillium oxalicum. Furthermore, HepA was overexpressed in two engineered strains in which the endoglucanase TaEG and amylase Amy15B were recombinantly expressed under the control of the amylase promoter Pamy15A, resulting in increased production of these two enzymes. Therefore, HepA could be used as a novel facilitator to modify Penicillium chassis cells, in which the efficiency of expression motifs located in the amylase pathway can be further strengthened.
重塑调控途径以定向提高底盘细胞中特定启动子的效率是合理构建表达系统的有效策略。然而,重复利用一种调节因子来修饰宿主细胞以提高表达基序效率的效果有限。因此,最好识别新的调控因子来激活特定途径,从而进一步提高靶元件的效率。异染色质蛋白1(HP1)被认为是负责异染色质维持的主要因子;它与DNA结合,从而形成紧密结构以抑制真菌中的基因表达。本研究表明,HepA(HP1的同源物)的过表达增加了草酸青霉中淀粉酶的表达。此外,在两种工程菌株中过表达HepA,其中内切葡聚糖酶TaEG和淀粉酶Amy15B在淀粉酶启动子Pamy15A的控制下重组表达,导致这两种酶的产量增加。因此,HepA可以用作修饰青霉底盘细胞的新型促进剂,其中位于淀粉酶途径中的表达基序的效率可以进一步提高。