Mirror Life: Bridging Chirality, Ethics, and the Foundations of Life Creation

Abstract

Abstract Biological homochirality, defined by the exclusive use of L‐amino acids and D‐sugars in terrestrial life, is essential for molecular recognition, enzymatic specificity, and cellular function. Recent advances in synthetic chemistry and molecular engineering have enabled the creation of mirror‐image biomolecules such as D‐peptides, L‐DNA, and L‐RNA, laying the foundation for orthogonal biological systems. These systems encompass engineered bacteria, viruses, and protocells composed entirely of D‐amino acids and L‐nucleotides. Mirror organisms represent a novel class of synthetic life with transformative potential in biomedicine. They may be used to develop protease‐resistant drugs, nuclease‐stable genetic elements, biosensors, and tissue engineering scaffolds, applications where biological durability and immune invisibility are advantageous. However, their unnatural chirality raises significant biosafety concerns. These organisms may escape immune detection, resist host antimicrobial defenses, and evade ecological regulators such as predation and microbial competition. This introduces the risk of uncontrolled proliferation in clinical or environmental settings. This review examines stereoselective synthesis of mirror biomolecules, construction of functional mirror subsystems, and engineering of mirror‐life architectures. It also discusses recent progress in chiral biomaterials, including L‐DNA hydrogels, nanostructures, and metamaterials, with potential applications in drug delivery, sensing, and regenerative medicine.