Department of Microbiology and Microbial Engineering and State Key Laboratory of Genetic Engineering, School of Life Sciences, Fudan University, Shanghai, 200438, China.
Institute for Preservation and Conservation of Chinese Ancient Books, Fudan University, Shanghai, 200433, China.
BMC Microbiol. 2020 Nov 16;20(1):351. doi: 10.1186/s12866-020-02039-4.
For microorganisms on a paper surface, the lack of water is one of the most important stress factors. A strain of Bacillus megaterium FDU301 was isolated from plaques on a paper surface using culture medium with polyethylene glycol 200 (PEG200) to simulate an arid condition. Global transcriptomic analysis of B. megaterium FDU301 grown under normal and simulated arid conditions was performed via RNA-seq technology to identify genes involved in arid stress adaptation.
The transcriptome of B. megaterium FDU301 grown in LB medium under arid (15% PEG200 (w/w)) and normal conditions were compared. A total of 2941 genes were differentially expressed, including 1422 genes upregulated and 1519 genes downregulated under arid conditions. Oxidative stress-responsive regulatory genes perR, fur, and tipA were significantly upregulated, along with DNA protecting protein (dps), and catalase (katE). Genes related to Fe uptake (feoB), sporulation stage II (spoIIB, spoIIE, spoIIGA), small acid-soluble spore protein (sspD), and biosynthesis of compatible solute ectoine (ectB, ectA) were also highly expressed to various degrees. Oxidative phosphorylation-related genes (atpB, atpE, atpF, atpH, atpA, atpG, atpD, atpC) and glycolysis-related genes (pgk, tpiA, frmA) were significantly downregulated.
This is the first report about transcriptomic analysis of a B. megaterium to explore the mechanism of arid resistance. Major changes in transcription were seen in the arid condition simulated by PEG200 (15%), with the most important one being genes related to oxidative stress. The results showed a complex mechanism for the bacteria to adapt to arid stress.
对于纸张表面的微生物来说,缺水是最重要的压力因素之一。使用含有聚乙二醇 200(PEG200)的培养基从纸张表面的斑块中分离到一株巨大芽孢杆菌 FDU301,以模拟干旱条件。通过 RNA-seq 技术对在正常和模拟干旱条件下生长的巨大芽孢杆菌 FDU301 进行全基因组转录组分析,以鉴定参与干旱适应的相关基因。
比较了在 LB 培养基中生长的巨大芽孢杆菌 FDU301 在干旱(15%PEG200(w/w))和正常条件下的转录组。共有 2941 个基因差异表达,其中干旱条件下有 1422 个基因上调,1519 个基因下调。氧化应激反应调节基因 perR、fur 和 tipA 显著上调,同时 DNA 保护蛋白(dps)和过氧化氢酶(katE)也上调。与 Fe 摄取(feoB)、孢子形成阶段 II(spoIIB、spoIIE、spoIIGA)、小酸溶性孢子蛋白(sspD)和相容性溶质 ectoine 的生物合成(ectB、ectA)相关的基因也以不同程度高度表达。氧化磷酸化相关基因(atpB、atpE、atpF、atpH、atpA、atpG、atpD、atpC)和糖酵解相关基因(pgk、tpiA、frmA)显著下调。
这是首次关于巨大芽孢杆菌转录组分析以探索其干旱抗性机制的报道。在 PEG200(15%)模拟的干旱条件下,转录发生了重大变化,最重要的是与氧化应激相关的基因。结果表明,细菌适应干旱胁迫的机制复杂。