» Articles » PMID: 17408843

Ordering Events of Biochemical Evolution

Overview
Journal Biochimie
Specialty Biochemistry
Date 2007 Apr 6
PMID 17408843
Citations 7
Authors
Affiliations
Soon will be listed here.
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.

Citing Articles

Molecular Evolution of Lysine Biosynthesis in Agaricomycetes.

Song Z, He M, Zhao R, Qi L, Chen G, Yin W J Fungi (Basel). 2022; 8(1).

PMID: 35049977 PMC: 8779187. DOI: 10.3390/jof8010037.


Semi-Quantitative Targeted Gas Chromatography-Mass Spectrometry Profiling Supports a Late Side-Chain Reductase Cycloartenol-to-Cholesterol Biosynthesis Pathway in Brown Algae.

Girard J, Lanneau G, Delage L, Leroux C, Belcour A, Got J Front Plant Sci. 2021; 12:648426.

PMID: 33986764 PMC: 8112355. DOI: 10.3389/fpls.2021.648426.


Origin of an ancient hormone/receptor couple revealed by resurrection of an ancestral estrogen.

Markov G, Gutierrez-Mazariegos J, Pitrat D, Billas I, Bonneton F, Moras D Sci Adv. 2017; 3(3):e1601778.

PMID: 28435861 PMC: 5375646. DOI: 10.1126/sciadv.1601778.


Categorizing ideas about trees: a tree of trees.

Fisler M, Lecointre G PLoS One. 2013; 8(8):e68814.

PMID: 23950877 PMC: 3737276. DOI: 10.1371/journal.pone.0068814.


The independent prokaryotic origins of eukaryotic fructose-1, 6-bisphosphatase and sedoheptulose-1, 7-bisphosphatase and the implications of their origins for the evolution of eukaryotic Calvin cycle.

Jiang Y, Wang D, Wen J BMC Evol Biol. 2012; 12:208.

PMID: 23083334 PMC: 3503850. DOI: 10.1186/1471-2148-12-208.