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Ignacio E. Sanchez

Publications and source records attributed to Ignacio E. Sanchez.

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Ecology theory disentangles microbial dichotomies

Microbes are often discussed in terms of dichotomies such as copiotrophic/oligotrophic and fast/slow-growing microbes, defined using the characterisation of microbial growth in isolated cultures. The dichotomies are usually qualitative and/or study-specific, sometimes precluding clear-cut results interpretation. We are able to interpret microbial dichotomies as life history strategies by combining ecology theory with Monod curves, a classical laboratory tool of bacterial physiology. Monod curves relate the specific growth rate of a microbe with the concentration of a limiting nutrient, and provide quantities that directly correspond to key ecological parameters in McArthur and Wilsons r/K selection theory, Tilmans resource competition and community structure theory and Grimes triangle of life strategies. The resulting model allows us to reconcile the copiotrophic/oligotrophic and fast/slow-growing dichotomies as different subsamples of a life history strategy triangle that also includes r/K strategists. We analyzed some ecological context by considering the known viable carbon sources for heterotrophic microbes in the framework of community structure theory. This partly explains the microbial diversity observed using metagenomics. In sum, ecology theory in combination with Monod curves can be a unifying quantitative framework for the study of natural microbial communities, calling for the integration of modern laboratory and field experiments.

q-bio.PE

Amino acid metabolism conflicts with protein diversity

The twenty protein coding amino acids are found in proteomes with different relative abundances. The most abundant amino acid, leucine, is nearly an order of magnitude more prevalent than the least abundant amino acid, cysteine. Amino acid metabolic costs differ similarly, constraining their incorporation into proteins. On the other hand, sequence diversity is necessary for protein folding, function and evolution. Here we present a simple model for a cost-diversity trade-off postulating that natural proteomes minimize amino acid metabolic flux while maximizing sequence entropy. The model explains the relative abundances of amino acids across a diverse set of proteomes. We found that the data is remarkably well explained when the cost function accounts for amino acid chemical decay. More than one hundred proteomes reach comparable solutions to the trade-off by different combinations of cost and diversity. Quantifying the interplay between proteome size and entropy shows that proteomes can get optimally large and diverse.

q-bio.PE