Bharathi M, Senthil Kumar N, Chellapandi P
Molecular Systems Engineering Lab, Department of Bioinformatics, School of Life Sciences, Bharathidasan University, Tiruchirappalli, India.
Human Genetics Lab, Department of Biotechnology, School of Life Sciences, Mizoram University (Central University), Aizawl, India.
Front Genet. 2020 Dec 16;11:593990. doi: 10.3389/fgene.2020.593990. eCollection 2020.
M1 (MRU) is a rod-shaped rumen methanogen with the ability to use H and CO, and formate as substrates for methane formation in the ruminants. Enteric methane emitted from this organism can also be influential to the loss of dietary energy in ruminants and humans. To date, there is no successful technology to reduce methane due to a lack of knowledge on its molecular machinery and 73% conserved hypothetical proteins (HPs; operome) whose functions are still not ascertained perceptively. To address this issue, we have predicted and assigned a precise function to HPs and categorize them as metabolic enzymes, binding proteins, and transport proteins using a combined bioinformatics approach. The results of our study show that 257 (34%) HPs have well-defined functions and contributed essential roles in its growth physiology and host adaptation. The genome-neighborhood analysis identified 6 operon-like clusters such as , TRAM, , and , which are responsible for protein folding, sudden heat-shock, host defense, and protection against the toxicities in the rumen. The functions predicted from MRU operome comprised of 96 metabolic enzymes with 17 metabolic subsystems, 31 transcriptional regulators, 23 transport, and 11 binding proteins. Functional annotation of its operome is thus more imperative to unravel the molecular and cellular machinery at the systems-level. The functional assignment of its operome would advance strategies to develop new anti-methanogenic targets to mitigate methane production. Hence, our approach provides new insight into the understanding of its growth physiology and lifestyle in the ruminants and also to reduce anthropogenic greenhouse gas emissions worldwide.
M1(MRU)是一种杆状瘤胃产甲烷菌,能够利用氢气、一氧化碳和甲酸作为反刍动物甲烷生成的底物。这种生物体排放的肠道甲烷也会影响反刍动物和人类饮食能量的损失。迄今为止,由于缺乏对其分子机制的了解以及73%的保守假设蛋白(HPs;操纵子组)功能仍未明确,尚无成功的减少甲烷排放的技术。为了解决这个问题,我们使用综合生物信息学方法对HPs进行了精确的功能预测和分配,并将它们分类为代谢酶、结合蛋白和转运蛋白。我们的研究结果表明,257个(34%)HPs具有明确的功能,并在其生长生理和宿主适应中发挥了重要作用。基因组邻域分析确定了6个操纵子样簇,如TRAM等,它们负责蛋白质折叠、热休克、宿主防御以及抵抗瘤胃中的毒性。从MRU操纵子组预测的功能包括96种具有17个代谢子系统的代谢酶、31个转录调节因子、23个转运蛋白和11个结合蛋白。因此,对其操纵子组进行功能注释对于在系统水平上揭示分子和细胞机制更为迫切。其操纵子组的功能分配将推进开发新的抗产甲烷靶点以减少甲烷生成的策略。因此,我们的方法为理解其在反刍动物中的生长生理和生活方式以及减少全球人为温室气体排放提供了新的见解。