A general theory for temperature dependence in biology

Abstract

One of the most fundamental physical constraints on living systems is temperature. Despite its importance, a simple, mechanistic, and general theory that fully predicts the response to temperature across all scales has not yet been derived. Here we develop such a theory based on the fundamental chemical kinetics and statistical physics governing the biochemical reactions that support life. Our mathematical framework includes an explanation for why temperature response curves have a maximum or minimum value and the derivation of a single universal curve onto which data for the temperature dependence of diverse biological quantities covering all levels of organization, collapse. The theory has multiple potential applications including predicting responses to global warming, yields of industrial processes, and epidemic outbreaks. At present, there is no simple, first principles–based, and general model for quantitatively describing the full range of observed biological temperature responses. Here we derive a general theory for temperature dependence in biology based on Eyring–Evans–Polanyi’s theory for chemical reaction rates. Assuming only that the conformational entropy of molecules changes with temperature, we derive a theory for the temperature dependence of enzyme reaction rates which takes the form of an exponential function modified by a power law and that describes the characteristic asymmetric curved temperature response. Based on a few additional principles, our model can be used to predict the temperature response above the enzyme level, thus spanning quantum to classical scales. Our theory provides an analytical description for the shape of temperature response curves and demonstrates its generality by showing the convergence of all temperature dependence responses onto universal relationships—a universal data collapse—under appropriate normalization and by identifying a general optimal temperature, around 25 ∘C, characterizing all temperature response curves. The model provides a good fit to empirical data for a wide variety of biological rates, times, and steady-state quantities, from molecular to ecological scales and across multiple taxonomic groups (from viruses to mammals). This theory provides a simple framework to understand and predict the impact of temperature on biological quantities based on the first principles of thermodynamics, bridging quantum to classical scales.

Publication
Proceedings of the National Academy of Sciences
José Ignacio Arroyo
José Ignacio Arroyo
Scientific Collaborator
Beatriz Díez Moreno
Beatriz Díez Moreno
Associate Professor.
P. Universidad Católica de Chile.
School of Biological Sciences,
Department of Molecular
Genetics and Microbiology,
Santiago, Chile.
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