Noise-induced symmetry breaking far from equilibrium and the emergence of biological homochirality

被引:27
作者
Jafarpour, Farshid [1 ]
Biancalani, Tommaso [2 ]
Goldenfeld, Nigel [3 ,4 ]
机构
[1] Purdue Univ, Dept Phys & Astron, 525 Northwestern Ave, W Lafayette, IN 47907 USA
[2] MIT, Dept Phys, Phys Living Syst, Cambridge, MA 02139 USA
[3] Univ Illinois, Loomis Lab Phys, Dept Phys, 1110 West Green St, Urbana, IL 61801 USA
[4] Univ Illinois, Carl R Woese Inst Genom Biol, 1206 West Gregory Dr, Urbana, IL 61801 USA
基金
美国国家航空航天局;
关键词
PARITY CONSERVATION; AMINO-ACIDS; EVOLUTION; ORIGIN; AUTOCATALYSIS; MODELS; RNA; BIOMOLECULES; RACEMIZATION;
D O I
10.1103/PhysRevE.95.032407
中图分类号
O35 [流体力学]; O53 [等离子体物理学];
学科分类号
070204 ; 080103 ; 080704 ;
摘要
The origin of homochirality, the observed single-handedness of biological amino acids and sugars, has long been attributed to autocatalysis, a frequently assumed precursor for early life self-replication. However, the stability of homochiral states in deterministic autocatalytic systems relies on cross-inhibition of the two chiral states, an unlikely scenario for early life self-replicators. Here we present a theory for a stochastic individual-level model of autocatalytic prebiotic self-replicators that are maintained out of thermal equilibrium. Without chiral inhibition, the racemic state is the global attractor of the deterministic dynamics, but intrinsic multiplicative noise stabilizes the homochiral states. Moreover, we show that this noise-induced bistability is robust with respect to diffusion of molecules of opposite chirality, and systems of diffusively coupled autocatalytic chemical reactions synchronize their final homochiral states when the self-replication is the dominant production mechanism for the chiral molecules. We conclude that nonequilibrium autocatalysis is a viable mechanism for homochirality, without imposing additional nonlinearities such as chiral inhibition.
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页码:15 / 32
页数:18
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