Bharathi M, Chellapandi P
Molecular Systems Engineering Lab., Department of Bioinformatics, School of Life Sciences, Bharathidasan University, Tiruchirappalli, 620 024, Tamil Nadu, India.
Molecular Systems Engineering Lab., Department of Bioinformatics, School of Life Sciences, Bharathidasan University, Tiruchirappalli, 620 024, Tamil Nadu, India.
Biosystems. 2017 May;155:20-28. doi: 10.1016/j.biosystems.2017.03.002. Epub 2017 Mar 23.
Methanosarcina mazei Go1 is a heterotrophic methanogenic archaean contributing a significant role in global methane cycling and biomethanation process. Phylogenomic relatedness and metabolic discrepancy of this genome were described herein by comparing its whole genome sequence, intergenomic distance, genome function, synteny homologs and origin of replication, and marker genes with very closely related genomes, Methanosarcina acetivorans and Methanosarcina barkeri. Phylogenomic analysis of this study revealed that genome functional feature and metabolic core of M. mazei and M. barkeri could be originated from M. acetivorans. The metabolic core of these genomes shares a common evolutionary origin to perform the metabolic activity at different environmental niches. Genome expansion, dynamics and gene collinearity were constrained and restrained the conservation of the metabolic core genes by duplication events occurring across methanosarcinal genomes. The Darwinian positive selection was an evolutionary constraint to purify the function of core metabolic genes. Using genome-wide metabolic survey, we found the existence of four novel putative metabolic pathways such as complete methanogenesis from acetate, indole-3-acetate biosynthesis V, 4-aminobutyrate degradation III, galactosamine biosynthesis I and siroheme biosynthesis. Overall, the present study would provide a stand point to revisit its phylogenomic status in order to understand the origin and evolution history of this organism.
马氏甲烷八叠球菌Go1是一种异养产甲烷古菌,在全球甲烷循环和生物甲烷化过程中发挥着重要作用。本文通过比较马氏甲烷八叠球菌Go1的全基因组序列、基因组间距离、基因组功能、同线性同源物、复制起点以及与亲缘关系非常近的基因组——嗜乙酸甲烷八叠球菌和巴氏甲烷八叠球菌的标记基因,描述了该基因组的系统发育相关性和代谢差异。本研究的系统发育分析表明,马氏甲烷八叠球菌和巴氏甲烷八叠球菌的基因组功能特征和代谢核心可能起源于嗜乙酸甲烷八叠球菌。这些基因组的代谢核心具有共同的进化起源,以在不同的环境生态位进行代谢活动。基因组扩张、动态变化和基因共线性受到限制,甲烷八叠球菌基因组中的重复事件抑制了代谢核心基因的保守性。达尔文正向选择是一种进化限制,用于纯化核心代谢基因的功能。通过全基因组代谢调查,我们发现了四种新的假定代谢途径,如乙酸完全产甲烷、吲哚 - 3 - 乙酸生物合成途径V、4 - 氨基丁酸降解途径III、半乳糖胺生物合成途径I和西罗血红素生物合成途径。总体而言,本研究将为重新审视其系统发育地位提供一个视角,以便了解该生物体的起源和进化历史。