Cross-Catalysis and Weak Interactions: Keys to the Chiral Polarization of the Biosphere

IF 3 4区 化学 Q2 CHEMISTRY, ANALYTICAL
Chirality Pub Date : 2025-10-02 DOI:10.1002/chir.70051
Sergey V. Stovbun, Aleksey A. Skoblin, Dmitry V. Zlenko
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Abstract

Molecular homochirality — the uniformity of chirality in biological molecules — is a fundamental feature of life, yet its origins remain unresolved. The correspondence between the chirality of biological monomers on Earth and that observed in ancient meteorites implies a systematic selection of chirality sign in prebiotic chemistry, rather than a stochastic process. While classical theories attribute symmetry breaking to chiral autocatalysis, such self-amplifying processes are rare and have not been empirically demonstrated in the synthesis of amino acids and carbohydrates. In contrast, chiral cross-catalysis between amino acids and carbohydrates — a mechanism consistent with known chemical behavior — could similarly amplify chiral purity. However, cross-catalysis alone cannot determine the chirality sign due to its inherent symmetry, leaving the origin of the initial bias unexplained. Although weak interactions have been proposed as a potential source of this bias, their effects are theoretically negligible, raising questions about their sufficiency. Our kinetic analysis of cross-catalytic systems reveals that even an infinitesimal preference for left-handed amino acids and right-handed carbohydrates could be sufficient to establish the homochirality observed in life. This mechanism provides a plausible link between prebiotic chemistry and the homochirality of the biosphere, offering a potential resolution to this longstanding enigma.

Abstract Image

交叉催化和弱相互作用:生物圈手性极化的关键。
分子的同手性——生物分子中手性的均匀性——是生命的基本特征,但其起源仍未得到解决。地球上生物单体的手性与在古代陨石中观察到的手性之间的对应关系暗示了在生命前化学中手性标志的系统选择,而不是随机过程。虽然经典理论将对称性破缺归因于手性自催化,但这种自放大过程很少见,而且还没有在氨基酸和碳水化合物的合成中得到实证证明。相比之下,氨基酸和碳水化合物之间的手性交叉催化——一种与已知化学行为一致的机制——同样可以提高手性纯度。然而,由于其固有的对称性,交叉催化本身不能确定手性符号,这使得初始偏倚的起源无法解释。虽然弱相互作用被认为是这种偏差的潜在来源,但它们的影响在理论上是可以忽略不计的,这就提出了它们是否足够的问题。我们对交叉催化系统的动力学分析表明,即使是对左手性氨基酸和右手性碳水化合物的极小偏好,也足以建立在生命中观察到的同手性。这一机制为益生元化学和生物圈的同手性之间提供了一个合理的联系,为这个长期存在的谜团提供了一个潜在的解决方案。
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来源期刊
Chirality
Chirality 医学-分析化学
CiteScore
4.40
自引率
5.00%
发文量
124
审稿时长
1 months
期刊介绍: The main aim of the journal is to publish original contributions of scientific work on the role of chirality in chemistry and biochemistry in respect to biological, chemical, materials, pharmacological, spectroscopic and physical properties. Papers on the chemistry (physiochemical, preparative synthetic, and analytical), physics, pharmacology, clinical pharmacology, toxicology, and other biological aspects of chiral molecules will be published.
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