What is life? This question, posed by Erwin Schrödinger in his famous book 'What is Life?' (1944), still remains open. Traditional biology describes life through a set of properties — metabolism, replication, homeostasis — but does not provide a single physical criterion. In recent years, approaches have emerged that define living things through the ability to maintain a coherent state in some asymptotic space, resisting decoherence (the decay of coherence due to interaction with the environment). For multicellular organisms, this coherence is classical in nature, as quantum effects are suppressed at the macroscopic level. However, for a single bacterium, there is a fundamental possibility to rely on a quantum field description of its chromosome as a unified quantum system. Such an approach allows us to rigorously introduce the concept of 'life' at the microscopic level and connect it with the unitary evolution of a quantum state.
The authors construct a Fock space — the mathematical apparatus of quantum field theory, where admissible DNA genetic codes are considered as basis states |γ⟩. For each code and each 'cell' (in an abstract sense — a lattice site), fermionic creation c† and annihilation c operators are introduced, which satisfy anticommutation relations: two bacteria with the same code cannot occupy the same cell. This reflects the idea that each cell can contain at most one bacterium of a given genetic type. Using these operators, effective operators for replication (transfer of the code to another cell), repair (correction of mutations — transition from an erroneous code to the correct one), and death (removal of the bacterium) are constructed. The dynamics of the whole system are described in the Heisenberg picture, where the time evolution of operators is given by some unitary (or generally non-unitary) evolution operator Û(t), obeying the Schrödinger equation with an effective Hamiltonian that includes the energetic 'cost' of various codes. The coherence of identity is quantitatively assessed through the autocorrelation function of the total number of bacteria with a given code: Cγ(t) = ⟨ ˆNγ(t) ˆNγ(0)⟩ / ⟨ ˆNγ(0)²⟩. The lifespan τγ is defined as the integral of this function over time: τγ = ∫₀∞ Cγ(t) dt. This integral measures how long the correlation in time between the presence of the code persists, i.e., how long the system 'remembers' its identity. In the simplest, Markovian approximation (without memory of past events), identity loss occurs with a constant probability λ per unit time, which gives an exponential decay of the correlation: Cγ(t) = $e^{-λ t}$, and then τ = 1/λ.
The central result of the work is a closed formula linking the lifespan of a single-celled organism to a single parameter λ, which describes the rate of identity degradation due to decoherence. In a more general, non-Markovian case, the lifespan captures the entire time profile of the autocorrelation function and can be expressed through the spectrum of the dynamics generator. Numerical values of λ can be obtained from experimental data on mutation rates and repair efficiency. For example, for a typical bacterium with a genome size of about 4.6 million base pairs and an error probability of the order of 10⁻⁹ per base pair per replication, the estimated rate of damage accumulation gives λ ∼ 10⁻⁶–10⁻⁵ per generation. The model predicts that an organism is alive as long as its chromosomal code retains a high degree of state purity, and death is a phase transition of decoherence, after which the identity is irretrievably lost and information about the original code is scattered among many erroneous configurations. Interestingly, repair acts as an active process that counteracts the natural tendency toward an increase in entropy and restores coherence. This agrees with the concept of living systems as dissipative structures that maintain low entropy through an energy flux.
The proposed formalism provides a quantitative, subject-independent measure of biological individuality and death, based on quantum information. This opens the way to a rigorous physical classification of living systems: from viruses (which perhaps do not possess sufficient coherence) to multicellular organisms, where identity is maintained collectively. The model can also be applied to analyze the effectiveness of antibiotics and immune responses, which can be viewed as processes that induce decoherence or block repair. On a fundamental level, the work links biological mortality to the irreversibility of quantum measurement, building bridges between quantum field theory and the theory of complex systems.
In the future, the proposed approach could be extended to multicellular organisms, where identity emerges as a macroscopic coherent state protected by correlations among many cells. A hierarchical model could be built: bacterium → colony → tissue → organism, each level with its own type of coherence. It is also promising to include explicit mechanisms of mutagenesis and selection, which would enable modeling of evolutionary processes. Integration with quantum sensors and genome editing technologies could lead to practical applications in combating pathogens. Moreover, the question remains open about the role of quantum entanglement between different parts of the chromosome, which could further stabilize identity.
The results will impact astrobiology (search for life criteria beyond Earth), quantum biology, and medical physics (quantitative models of aging and carcinogenesis).
The next step will be to estimate the parameter λ for model organisms based on existing data on mutagenesis and repair, as well as experimental verification of predictions about the behavior of autocorrelation functions in bacterial populations, for example, using time-resolved fluorescence microscopy.
The work addresses the fundamental problem of defining life (the phenomenon of 'life' in terms of physics) and connects it with the quantum-classical transition — one of the central problems in the interpretation of quantum mechanics. It also hints at the possibility of a universal criterion for life, analogous to the second law of thermodynamics for entropy, but for biological organization.
This section is addressed to the author of the paper and their colleagues. Neighbouring works were found by meaning-based search across our archive, not by word overlap. We do not review: we show the field around the work.
What the work does
The paper introduces a formal definition of bacterial life through the coherence of its genetic code in Fock space, describing the dynamics with creation/annihilation operators and computing lifespan as the integral of the autocorrelation function of the number of bacteria with a given code. In the Markovian approximation, this yields exponential decay of correlations and a lifetime τ = 1/λ.
Where its strength is
The strong point is the transfer of the concept of quantum coherence to genetic identity and the derivation of a measurable quantity (lifetime) via autocorrelation, which opens a path to predicting cell death before visible signs appear.
Where it could go next
Worth trying
Why this may matter
If the proposed criterion of life proves universal, it could provide a physical foundation for defining life in astrobiology and aid in developing methods for early diagnosis of cell death.
Nearby works in our archive
The closest work in the archive sits at 0.67 by meaning — the usual level for our corpus.
as written by the authors arXiv:2606.31185
What is life? In this work, we take life to mean a dynamical tendency to conserve identity for as long as possible. For a single bacterium, identity is carried by its chromosomal DNA code, so the bacterium is alive precisely insofar as it actively maintains a well-defined chromosomal configuration over time and can, in principle, replicate this configuration into progeny. For a multicellular organism, many cells share essentially the same DNA code and behave as a single coherent entity; in that case, life corresponds to the persistence of a common genetic identity across the cellular ensemble, rather than to the survival of any particular cell. Cell duplication in multicellular organisms likewise serves to maintain this dynamical tendency to conserve identity over time. In previous studies we implemented this idea at the multicellular and colonial scale using a classical notion of coherence, in which an organism is represented by a single nonseparable state over the DNA codes of its constituent cells, while a colony is describable as a separable ensemble. Here we apply the same principle to the simplest possible case, a single bacterium, and show that its biological identity can be identified with the coherence of its chromosomal DNA code within an abstract state space. We then introduce a Fock-space representation in which bacteria carrying given codes occupy fermionic modes, and replication, repair, and death are realized as elementary operators acting on these modes. Within this framework we define the lifetime of a unicellular organism as the integral coherence time of a code-occupation autocorrelation function and, in a minimal Markovian model, obtain a compact expression in which the lifetime coincides with the inverse decay rate of the corresponding identity mode.
Interestingly, the use of fermionic statistics to describe bacteria in an abstract Fock space resembles the Pauli exclusion principle, which forbids two electrons from occupying the same quantum state. Here, the analog is a 'cell' that cannot be occupied by two bacteria with identical codes — this guarantees the uniqueness of the carrier of given genetic information at each point in the model's space-time. This approach echoes Erwin Schrödinger's ideas about an aperiodic crystal as the bearer of life.