Pei Di, Liu Zhiming, Hu Biru
College of Sciences, National University of Defense Technology, Changsha, Hunan, China.
China Astronaut Research and Training Center, Beijing, China.
Mol Genet Genomics. 2025 Feb 22;300(1):25. doi: 10.1007/s00438-025-02236-8.
Microbially induced calcium carbonate precipitation (MICP) had emerged as an important biomineralization process with wide-ranging applications in construction, environmental remediation, and space exploration. Sporosarcina pasteurii (S. pasteurii) was a key bacterium in MICP due to its efficient urease activity, yet the regulation of its urease genes remains poorly understood, limiting its practical applications. This study aimed to elucidate the structure and expression regulation mechanism of urease genes in S. pasteurii to enhance its mineralization potential. We compared the growth and urease gene expression of S. pasteurii under three different culture conditions using transcriptome sequencing. Operon, Transcription Start Site (TSS) and Transcription Termination Site (TTS) were predicted based on the distribution of reads on the genome using Rockhopper online analysis software. The 700 bp sequence upstream of the TTS was extracted and promoter prediction was performed by Time-Delay Neural Network (TDNN) method. Finally, we verified the prediction results by RT-PCR. Our results revealed, for the first time, a double operon structure of S. pasteurii urease, with operon 1 containing ureA, ureB, ureC, ureE, and ureF genes, and operon 2 containing ureG and ureD genes. This discovery provides crucial insights into the regulation of urease expression in S. pasteurii, paving the way for more efficient and controllable mineralization applications. The findings of this study not only advanced our understanding of urease gene regulation but also opened new avenues for optimizing S. pasteurii-based biomineralization technologies.
微生物诱导碳酸钙沉淀(MICP)已成为一种重要的生物矿化过程,在建筑、环境修复和太空探索等领域有着广泛应用。巴氏芽孢杆菌(S. pasteurii)因其高效的脲酶活性而成为MICP中的关键细菌,但其脲酶基因的调控机制仍知之甚少,这限制了其实际应用。本研究旨在阐明巴氏芽孢杆菌中脲酶基因的结构和表达调控机制,以增强其矿化潜力。我们使用转录组测序比较了巴氏芽孢杆菌在三种不同培养条件下的生长情况和脲酶基因表达。基于使用Rockhopper在线分析软件在基因组上的reads分布预测操纵子、转录起始位点(TSS)和转录终止位点(TTS)。提取TTS上游700 bp序列,并通过时延神经网络(TDNN)方法进行启动子预测。最后,我们通过RT-PCR验证了预测结果。我们的结果首次揭示了巴氏芽孢杆菌脲酶的双操纵子结构,操纵子1包含ureA、ureB、ureC、ureE和ureF基因,操纵子2包含ureG和ureD基因。这一发现为巴氏芽孢杆菌脲酶表达的调控提供了关键见解,为更高效、可控的矿化应用铺平了道路。本研究结果不仅加深了我们对脲酶基因调控的理解,也为优化基于巴氏芽孢杆菌的生物矿化技术开辟了新途径。