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生物化学进化的有序事件。

Ordering events of biochemical evolution.

作者信息

Cunchillos C, Lecointre G

机构信息

Institut Charles Darwin International, Place du Four, 81140 Puycelsi, France.

出版信息

Biochimie. 2007 May;89(5):555-73. doi: 10.1016/j.biochi.2006.12.007. Epub 2007 Jan 4.

Abstract

Metabolic pathways exhibit structures resulting from an evolutionary process. Pathways have been inherited through time with modification, from the earliest periods of life. It is possible to compare the structure of pathways as done in comparative anatomy, i.e. for inferring ancestral pathways or parts of it (ancestral enzymatic functions), using standard phylogenetic reconstruction. Thus a phylogenetic tree of pathways provides a relative ordering of the rise of enzymatic functions. It even becomes possible to order the birth of each complete pathway in time. This particular "DNA-free" conceptual approach to evolutionary biochemistry is reviewed, gathering all the justifications given for it. Then, the method of assigning a given pathway to a time span of biochemical development is revisited. The previous method used an implicit "clock" of metabolic development that is difficult to justify. We develop a new clock-free approach, using functional biochemical arguments. Results of the two methods are not significantly different; our method is just more precise. This suggests that the clock assumed in the first method does not provoke any important artefact in describing the development of biochemical evolution. It is just unnecessary to postulate it. As a result, most of the amino acid metabolic pathways develop forwards, confirming former models of amino acid catabolism evolution, but not those for amino acid anabolism. The order of appearance of sectors of universal cellular metabolism is: (1) amino acid catabolism, (2) amino acid anabolism and closure of the urea cycle, (3) glycolysis and glycogenesis, (4) closure of the pentose-phosphate cycle, (5) closure of the Krebs cycle and fatty acids metabolism, (6) closure of the Calvin cycle.

摘要

代谢途径呈现出由进化过程产生的结构。从生命的最早时期开始,途径就随着时间的推移经过修改而被继承下来。可以像在比较解剖学中那样比较途径的结构,即使用标准的系统发育重建来推断祖先途径或其部分(祖先酶功能)。因此,途径的系统发育树提供了酶功能出现的相对顺序。甚至有可能确定每个完整途径诞生的时间顺序。本文回顾了这种针对进化生物化学的特殊“无DNA”概念方法,并收集了为之提供的所有理由。然后,重新审视了将特定途径分配到生化发展时间跨度的方法。先前的方法使用了一个难以证明其合理性的隐含代谢发展“时钟”。我们开发了一种新的无时钟方法,使用功能性生化论据。两种方法的结果没有显著差异;我们的方法只是更精确。这表明第一种方法中假设的时钟在描述生化进化发展时不会引发任何重要的人为误差。只是没有必要假设它。结果,大多数氨基酸代谢途径是向前发展的,这证实了以前的氨基酸分解代谢进化模型,但不支持氨基酸合成代谢的模型。普遍细胞代谢各部分出现的顺序是:(1)氨基酸分解代谢,(2)氨基酸合成代谢和尿素循环的闭合,(3)糖酵解和糖原生成,(4)戊糖磷酸循环的闭合,(5)三羧酸循环和脂肪酸代谢的闭合,(6)卡尔文循环的闭合。

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