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Biology subjects

Dourado, H.

Publications and source records attributed to Dourado, H..

8 recordsLinked to original sources

Growth costs of suboptimal protein allocation in nonlinear models of growing cells

Microbial growth depends on how cells allocate their limited proteome among competing functions. Although many proteins are expressed near levels that maximize growth, deviations from these optima are common and can impose substantial fitness costs. Modeling the growth costs of suboptimal protein allocation remains challenging because protein expression influences growth through multiple interacting mechanisms, including biosynthetic demands, enzyme kinetics, and limits on cellular density. Here we analyze these effects using growth balance analysis (GBA), a nonlinear framework that predicts steady-state growth and biomass composition of coarse-grained microbial models from basic cellular constraints. The optimal biomass compositions predicted for these models include not only protein concentrations but also the reactant concentrations required to saturate enzymes through nonlinear rate laws, thereby capturing more complex resource trade-offs than in conventional linear resource allocation models. Using these GBA models, we compute optimal biomass compositions with individual proteins fixed at suboptimal levels. The resulting relationships between suboptimal protein allocation and growth rate are consistent with qualitative experimental patterns in bacteria, with growth effects depending on protein function (including idle proteins), environmental conditions, toxic byproducts, and alternative reactions. These results indicate a practical and tractable approach for modeling growth costs arising from suboptimal protein allocation, and suggest a basis for predictive modeling in metabolic engineering and synthetic biology.

systems biology↗

Growth Mechanics and the emergence of metabolic oscillations in growing cells

Unicellular organisms exhibit oscillations in metabolic activity and gene expression, even when growing in static media with no external dynamic stimuli. The cause and possible function of these endogenous oscillations are still not fully understood, with different hypotheses including its origin as a byproduct of misguided regulatory processes. To investigate whether such oscillations could be functional rather than incidental, we introduce Growth Mechanics (GM) as a general mathematical framework to study the dynamic resource allocation in models of whole self-replicating cells, built exclusively on the first principles of fitness maximization, mass conservation, nonlinear reaction kinetics, and constant cell density. Inspired by the physical theory of classical mechanics, we first find the simplest mathematical description the problem in terms of generalized coordinates, and then solve the optimal dynamical resource allocation for cells growing in any given medium using the Euler-Lagrange equation, resulting in analytical "equations of optimal motion" (EOM) that apply for growing cells in general. We then solve these equations numerically for simple growing cell models and show that, in general, oscillations are necessary to maximize cell fitness by getting more saturated reactions at the time they are most needed. We also show how the EOM predict the emergence of quasi-linear dependencies of the metabolic oscillation frequency and the ribosome protein allocation with the cell growth rate at different growth media, in line with the "growth laws" observed experimentally in microbes. This work contributes to the foundations of theoretical cell biology with general quantitative principles and a bridge to theoretical tools of physics.

biophysics↗

Cell Growth Simulator: a user-friendly web server for growth balance analysis

GBA Solver is a web-based application that enables efficient construction and numerical solution of coarse-grained growth balance analysis (GBA) models containing up to 20 reactions. The platform features an intuitive spreadsheet-based interface that eliminates the need for programming, integrates kinetic parameters from the BRENDA enzyme database, and provides interactive visualizations for model exploration. By lowering technical barriers, GBA Solver makes GBA modeling accessible to a wider scientific community, expanding the computational toolkit for investigating cell metabolism and growth. GBA Solver is freely available at: https://cellgrowthsim.com/. The source code is available at: https://gitlab.cs.uni-duesseldorf.de/general/ccb/GBASolver.

cell biology↗

Growth balance analysis models of cyanobacteria for understanding resource allocation strategies

Cyanobacteria have emerged as attractive microbial cell factories, as they can convert atmospheric CO2 and sunlight into valuable chemicals. To increase their growth and productivity, one should aim to optimize the allocation of limited cellular resources across different metabolic processes. Here, we developed two growth balance analysis (GBA) models for the cyanobacterium Synechocystis sp. PCC 6803. In its biological assumptions, the models closely related to an existing coarse-grained model, while its mathematical formulation is heavily streamlined. We show that the GBA models provide virtually identical predictions about cellular resource allocation among photosynthesis, carbon metabolism, and the protein translation machinery under different environmental conditions as the previous, mathematically more involved model. Our model also captures the effects of photodamage on proteome allocation and the resulting growth rates. We further show how the GBA model can be easily extended to include more reactions, leading to a second GBA model capable of new predictions about the cellular resource allocation. Balanced growth models of the type presented here can easily expanded to include more biological details, providing a useful toolbox for the understanding of the physiological capabilities of cyanobacteria, their allocation of cellular resources, and the potential of their bioengineering for optimized biomass production.

systems biology↗

Growth Mechanics: General principles of optimal cellular resource allocation in balanced growth

The physiology of biological cells evolved under physical and chemical constraints such as mass conservation, nonlinear reaction kinetics, and limits on cell density. For unicellular organisms, the fitness that governs this evolution is mainly determined by the balanced cellular growth rate. We previously introduced Growth Balance Analysis (GBA) as a general framework to model such nonlinear systems, and we presented analytical conditions for optimal balanced growth in the special case that the active reactions are known. Here, we develop Growth Mechanics (GM) as a more general, succinct, and powerful analytical description of the growth optimization of GBA models, which we formulate in terms of a minimal number of dimensionless variables. GM uses Karush-Kuhn-Tucker (KKT) conditions in a Lagrangian formalism. It identifies fundamental principles of optimal resource allocation in GBA models of any size and complexity, including the analytical conditions that determine the set of active reactions at optimal growth. We identify from first principles the economic values of biochemical reactions, expressed as marginal changes in cellular growth rate; these economic values can be related to the costs and benefits of proteome allocation into the reactions catalysts. Our formulation also generalizes the concepts of Metabolic Control Analysis to models of growing cells. GM unifies and extends previous approaches of cellular modeling and analysis, putting forward a program to analyze cellular growth through the stationarity conditions of a Lagrangian function. GM thereby provides a general theoretical toolbox for the study of fundamental mathematical properties of balanced cellular growth.

biophysics↗

The protein translation machinery is expressed for maximal efficiency in Escherichia coli

Protein synthesis is the most expensive process in fast-growing bacteria1,2. The economic aspects of protein synthesis at the cellular level have been investigated by estimating ribosome activity3-5 and the expression of ribosomes3,6, tRNA7-9, mRNA2, and elongation factors10,11. The observed growth-rate dependencies form the basis of powerful phenomenological bacterial growth laws5,12-16; however, a quantitative theory allowing us to understand these phenomena on the basis of fundamental biophysical and biochemical principles is currently lacking. Here, we show that the observed growth-rate dependence of the concentrations of ribosomes, tRNAs, mRNA, and elongation factors in Escherichia coli can be predicted accurately by minimizing cellular costs in a detailed mathematical model of protein translation; the mechanistic model is only constrained by the physicochemical properties of the molecules and requires no parameter fitting. We approximate the costs of molecule species through their masses, justified by the observation that cellular dry mass per volume is roughly constant across growth rates17 and hence represents a limited resource. Our results also account quantitatively for observed RNA/protein ratios and ribosome activities in E. coli across diverse growth conditions, including antibiotic stresses. Our prediction of active and free ribosome abundance facilitates an estimate of the deactivated ribosome reserve14,18,19, which reaches almost 50% at the lowest growth rates. We conclude that the growth rate dependent composition of E colis protein synthesis machinery is a consequence of natural selection for minimal total cost under physicochemical constraints, a paradigm that might generally be applied to the analysis of resource allocation in complex biological systems.

biophysics↗

An Analytical Theory of Cellular Growth

The biological fitness of unicellular organisms is largely determined by their balanced growth rate, i.e., by the rate with which they replicate their biomass composition. Natural selection on this growth rate occurred under a set of physicochemical constraints, including mass conservation, reaction kinetics, and limits on dry mass per volume; mathematical models that maximize the balanced growth rate while accounting explicitly for these constraints are inevitably nonlinear and have been restricted to small, non-realistic systems. Here, we lay down a general theory of balanced growth states, providing explicit expressions for protein concentrations, fluxes, and the growth rate. These variables are functions of the concentrations of cellular components, for which we calculate marginal fitness costs and benefits that can be related to metabolic control coefficients. At maximal growth rate, the net benefits of all concentrations are equal. Based solely on physicochemical constraints, the growth balance analysis (GBA) framework introduced here unveils fundamental quantitative principles of cellular growth and leads to experimentally testable predictions.

biophysics↗

Enzymes And Substrates Are Balanced At Minimal Combined Mass Concentration In Vivo

A fundamental problem in biology is how cells organize their resource investment. Cellular metabolism, for example, typically involves hundreds of enzymes and metabolites, but it is unclear according to which principles their concentrations are set. Reasoning that natural selection will drive cells towards achieving a given physiological state at minimal cost, we derive a general equation that predicts the concentration of a metabolite from the concentration of the most abundant and costly enzyme consuming it. Simulations of cellular growth as well as experimental data demonstrate that costs are approximately proportional to molecular masses. For effectively irreversible reactions, the cell maximizes its metabolic efficiency by investing equally into substrate and unbound enzyme molecules. Without fitting any free parameters, the resulting model predicts in vivo substrate concentrations from enzyme concentrations and substrate affinities with high accuracy across data from E. coli and diverse eukaryotes (R2=0.79, geometric mean fold-error 1.74). The corresponding organizing principle - the minimization of the summed mass concentrations of solutes - may facilitate reducing the complexity of kinetic models and will contribute to the design of more efficient synthetic cellular systems.

systems biology↗