Zhang Yongjia, He Penghui, Hu Shiying, Zhang Ruibin, Chen Shouwen
State Key Laboratory of Biocatalysis and Enzyme Engineering, Environmental Microbial Technology Center of Hubei Province, College of Life Sciences, Hubei University, 368 Youyi Avenue, Wuchang District, Wuhan, 430062, China.
Curr Microbiol. 2025 Feb 4;82(3):116. doi: 10.1007/s00284-025-04096-2.
Cell autolysis could lead to a decrease in both cell viability and the production of biochemicals, presenting one of the significant challenges during fermentation. Bacillus licheniformis, a gram-positive bacterium widely used in the production of various biologic products, also confronts the limitation caused by cell autolysis. In this study, we investigated the impact of peptidoglycan hydrolases (LytC, LytD, LytE, CwlC), endopeptidase inhibitor IseA, and prophage gene xpf on cell growth and biochemical synthesis in B. licheniformis DW2. The results showed that the deletion of xpf and overexpression of iseA could significantly increase cell survival. Then, xpf was deleted on iseA overexpressed strain PiseA to construct engineered strain PiseAΔxpf, which further enhanced viable cells. The results of cell autolysis showed that PiseA could reduce cell autolysis significantly compared to the wild-type, but PiseAΔxpf did not further decrease cell autolysis. Furthermore, the production of bacitracin was 792.23 U/mL in the iseA overexpressed strain, which increased by 13.82% compared with the wild-type, but PiseAΔxpf did not further increase bacitracin production. Through detecting intracellular metabolites, we observed that iseA overexpression did not affect intracellular metabolism, but the precursors of bacitracin synthesis in PiseAΔxpf were lower than that of wild-type and PiseA. Finally, we found that the overexpression of iseA could also significantly improve the production of γ-PGA. In general, the overexpression of iseA could enhance the biomass and cell survival by reducing cell lysis without affecting the intracellular metabolites, which provided a potential strategy to improve production of biochemical.
细胞自溶可能导致细胞活力和生化物质产量下降,这是发酵过程中的重大挑战之一。地衣芽孢杆菌是一种广泛用于生产各种生物制品的革兰氏阳性菌,也面临着细胞自溶造成的限制。在本研究中,我们调查了肽聚糖水解酶(LytC、LytD、LytE、CwlC)、内肽酶抑制剂IseA和前噬菌体基因xpf对地衣芽孢杆菌DW2细胞生长和生化合成的影响。结果表明,删除xpf和过表达iseA可显著提高细胞存活率。然后,在过表达iseA的菌株PiseA上删除xpf,构建工程菌株PiseAΔxpf,其活细胞进一步增加。细胞自溶结果表明,与野生型相比,PiseA可显著降低细胞自溶,但PiseAΔxpf并未进一步降低细胞自溶。此外,过表达iseA的菌株中杆菌肽的产量为792.23 U/mL,与野生型相比增加了13.82%,但PiseAΔxpf并未进一步提高杆菌肽产量。通过检测细胞内代谢物,我们观察到过表达iseA不影响细胞内代谢,但PiseAΔxpf中杆菌肽合成的前体低于野生型和PiseA。最后,我们发现过表达iseA也可显著提高γ-PGA的产量。总体而言,过表达iseA可通过减少细胞裂解来提高生物量和细胞存活率,而不影响细胞内代谢物,这为提高生化物质产量提供了一种潜在策略。