Department of Biotechnology (with Jointly Merged Institute of Bioinformatics and Biotechnology), Savitribai Phule Pune University, Pune, India.
Department of Botany, Savitribai Phule Pune University, Pune, India.
Gene. 2024 Dec 20;930:148860. doi: 10.1016/j.gene.2024.148860. Epub 2024 Aug 14.
Since ectoine is a high-value product, overviewing strategies for identifying novel microbial sources becomes relevant. In the current study, by following a genome mining approach, the ectoine biosynthetic cluster in a tropical marine strain of Nocardiopsis dassonvillei (NCIM 5124) was located and compared with related organisms. Transcriptome analysis of Control and Test samples (with 0 and 5% NaCl, respectively) was carried out to understand salt induced stress response at the molecular level. There were 4950 differentially expressed genes with 25 transcripts being significantly upregulated in Test samples. NaCl induced upregulation of the ectoine biosynthesis cluster and some other genes (stress response, chaperone/Clp protease, cytoplasm, ribonucleoprotein and protein biosynthesis). The production of ectoine as a stress response molecule was experimentally validated via LCMS analysis. The investigation sheds light on the responses exhibited by this actinomycete in coping up with salt stress and provides a foundation for understanding salt induced molecular interactions.
由于海藻糖是一种高价值产品,因此寻找新的微生物来源的策略变得尤为重要。在本研究中,通过采用基因组挖掘方法,我们定位了热带海洋放线菌诺卡氏菌(NCIM 5124)中海藻糖生物合成簇,并与相关生物进行了比较。对对照和测试样品(分别含 0%和 5%NaCl)进行转录组分析,以在分子水平上了解盐诱导的应激反应。有 4950 个差异表达基因,其中 25 个转录本在测试样品中显著上调。NaCl 诱导海藻糖生物合成簇和其他一些基因(应激反应、伴侣/Clp 蛋白酶、细胞质、核糖核蛋白和蛋白质生物合成)的上调。通过 LCMS 分析实验验证了海藻糖作为应激反应分子的产生。该研究揭示了这种放线菌在应对盐胁迫时表现出的反应,为理解盐诱导的分子相互作用提供了基础。