枯草芽孢杆菌DB104 spo0a突变体转录组谱的时间分辨分析及重组蛋白释放的增强。

IF 2.6 4区 生物学 Q2 MICROBIOLOGY
Journal of Microbiology Pub Date : 2025-05-01 Epub Date: 2025-05-27 DOI:10.71150/jm.2411032
Ji-Su Jun, Soo Ji Kang, Kwang-Won Hong
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引用次数: 0

摘要

Spo0A是枯草芽孢杆菌孢子形成的主要调控因子,在孢子形成早期直接或间接控制500多个基因。尽管Spo0A破坏对孢子形成的影响已经被广泛研究,但对整个生长阶段的基因组反应的全面理解仍然难以捉摸。在这里,我们通过时间过程rna序列检测了Spo0A突变株R211E和野生型的转录组学变化,以确定受影响的生物学过程和途径。利用聚集规律间隔短回文重复序列(CRISPR)-CRISPR相关蛋白(Cas)9系统构建了具有产孢缺陷的R211E菌株,突出了适当的Cas9剂量在基因编辑中的关键作用。3010个差异表达基因(deg)的功能分析显示,在产孢、群体感应、代谢和生物膜形成方面发生了显著变化。R211E破坏Spo0A-AbrB调控通路,减少生物膜形成,增强鞭毛基因表达。上调代谢途径,包括糖酵解、组氨酸和嘌呤生物合成,在营养生长过程中增加细胞数量。此外,突变体显示营养自溶素表达升高,导致细胞活力在固定期降低。我们还介绍了R211E在重组蛋白表达系统中的新潜力,该系统促进了蛋白质释放到上清液中,为枯草芽孢杆菌代谢工程和高效生产系统的未来研究提供了有价值的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Time-resolved analysis of Bacillus subtilis DB104 Spo0A-mutant transcriptome profile and enhancement of recombinant protein release.

Spo0A, the master regulator of sporulation initiation in Bacillus subtilis, controls over 500 genes directly or indirectly in early sporulation stages. Although the effects of Spo0A disruption on sporulation have been extensively studied, a comprehensive understanding of the genomic response throughout growth phases remain elusive. Here, we examined the transcriptomic changes in Spo0A mutant strain, R211E, and wild-type across a time-course RNA-seq to identify impacted biological processes and pathways. The R211E strain, which exhibits sporulation deficiency, was constructed using the clustered regularly interspaced short palindromic repeats (CRISPR)-CRISPR associated protein (Cas)9 system, highlighting the critical role of proper Cas9 dosing in gene editing. Functional analysis of 3,010 differentially expressed genes (DEGs) showed significant alterations in sporulation, quorum sensing, metabolism, and biofilm formation. The R211E disrupted the Spo0A-AbrB regulatory pathway, reducing biofilm formation and enhancing flagellar gene expression. Up-regulated metabolic pathways, including glycolysis, histidine, and purine biosynthesis, increased cell numbers during vegetative growth. Further, the mutant displayed elevated vegetative autolysin expression, resulting in reduced cell viability in the stationary phase. We also introduce the novel potential of R211E in a recombinant protein expression system that facilitated protein release into the supernatant, providing valuable insight for future research in metabolic engineering and efficient production systems in B. subtilis.

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来源期刊
Journal of Microbiology
Journal of Microbiology 生物-微生物学
CiteScore
5.70
自引率
3.30%
发文量
0
审稿时长
3 months
期刊介绍: Publishes papers that deal with research on microorganisms, including archaea, bacteria, yeasts, fungi, microalgae, protozoa, and simple eukaryotic microorganisms. Topics considered for publication include Microbial Systematics, Evolutionary Microbiology, Microbial Ecology, Environmental Microbiology, Microbial Genetics, Genomics, Molecular Biology, Microbial Physiology, Biochemistry, Microbial Pathogenesis, Host-Microbe Interaction, Systems Microbiology, Synthetic Microbiology, Bioinformatics and Virology. Manuscripts dealing with simple identification of microorganism(s), cloning of a known gene and its expression in a microbial host, and clinical statistics will not be considered for publication by JM.
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