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The metabolic world of Escherichia coli is not small

机译:大肠杆菌的代谢世界并不小

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摘要

To elucidate the organizational and evolutionary principles of the metabolism of living organisms, recent studies have addressed the graph-theoretic analysis of large biochemical networks responsible for the synthesis and degradation of cellular building blocks [Jeong, H., Tombor, B., Albert, R., Oltvai, Z. N. & Barabási, A. L. (2000) Nature 407, 651-654; Wagner, A. & Fell, D. A. (2001) Proc. R. Soc. London Ser. B 268, 1803-1810; and Ma, H.-W. & Zeng, A.-P. (2003) Bioinformatics 19, 270-277]. In such studies, the global properties of the network are computed by considering enzymatic reactions as links between metabolites. However, the pathways computed in this manner do not conserve their structural moieties and therefore do not correspond to biochemical pathways on the traditional metabolic map. In this work, we reassessed earlier results by digitizing carbon atomic traces in metabolic reactions annotated for Escherichia coli. Our analysis revealed that the average path length of its metabolism is much longer than previously thought and that the metabolic world of this organism is not small in terms of biosynthesis and degradation.
机译:为了阐明生物代谢的组织和进化原理,最近的研究已经对负责细胞构件合成和降解的大型生化网络进行了图论分析[Jeong,H.,Tombor,B.,Albert, R.,Oltvai,ZN&Barabási,AL(2000)Nature 407,651-654; Wagner,A.&Fell,D.A.(2001)Proc。 R. Soc。伦敦系列B 268,1803-1810;和马宏伟&Zeng,A.-P. (2003)Bioinformatics 19,270-277]。在此类研究中,通过将酶促反应视为代谢物之间的联系来计算网络的全局特性。然而,以这种方式计算的途径不保留其结构部分,因此不对应于传统代谢图谱上的生化途径。在这项工作中,我们通过数字化标注在大肠杆菌中的代谢反应中的碳原子痕迹来重新评估早期的结果。我们的分析表明,其代谢的平均路径长度比以前认为的要长得多,并且就生物合成和降解而言,这种生物的代谢世界并不小。

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