Nuevo, M., Meierhenrich, U. J., Muoz-Caro, G. M., Dartois, E., d’Hendecourt, L., Deboffle, D., Auger, G., Blanot, D., Bredehoft, J. H., Nahon, L., (2006) The effects of circularly polarized light on amino acid enantiomers Linsitinib clinical trial produced by the UV irradiation of interstellar ice analogs, Astron. Astrophys., 457:741–751. Nuevo, M., Meierhenrich, U. J., d’Hendecourt, L., Muoz-Caro, G. M., Dartois, E., Deboffle, D., Thiemann, W. H.-P., Bredehoft, J.-H., Nahon, L., (2007) Enantiomeric separation of

complex organic molecules produced from irradiation of interstellar/circumstellar ice analogs, Adv. Space Res., 39, 400–404. Pizzarello, S., Cronin, J. R., (2000) Geochem. Cosmo. Acta, Non-racemic amino acids in the Murray and Murchison meteorites, 64:329–338. Pizzarello, S., Zolensky, M., Turk, K. A., (2003) Geochem. Cosmo. Acta, Nonracemic isovaline in the

Murchison find more meteorite: Chiral distribution and mineral association, 67:1589–1595. Reisse, J., Cronin, J., in: Bordeaux, P. U. d. (Ed.), Les traces du vivant, Presses Universitaires de Bordeaux, Bordeaux 2003, pp. 82–113. E-mail: Louis.​DHendecourt@ias.​u-psud.​fr The Salt-Induced Peptide Formation Reaction as Possible Origin of Biohomochirality Daniel Fitz, Bernd M. Rode Division of Theoretical Chemistry; Institute of General, Inorganic and Theoretical Chemistry; University of Innsbruck The Salt-Induced Peptide Formation PD0332991 datasheet (SIPF) Reaction has been shown to yield considerable amounts of di- and oligopeptides from amino acids in aqueous solution under assumed

prebiotic conditions just with the help of sodium chloride and Cu(II) ions. Strikingly, a few amino acids, especially alanine (Plankensteiner, et al. 2004) and valine (Plankensteiner, et al. 2005), show better reactivity when present in their L-form compared to their D-enantiomers, suggesting that this reaction might have played a keyrole in the origin of biohomochirality. This behaviour may be explained by the geometry of the active, peptide-forming Methocarbamol species. Under the reaction conditions a central copper ion forms a complex containing two amino acids and one choride ligand in a distorted square ‘plane’. This distortion gives rise to central chirality at the copper ion, which, because of its relatively high atomic number, can now provide considerably high parity-violating energy differences (PVEDs, caused by parity violation in weak interactions) between a complex containing L-amino acids and its D-analogue. Ab initio geometry calculations of such active complexes show that the out-of-plane distortion of the ligands is more pronounced for amino acids showing an enantiomeric preference for the L-form than for those which do not (Fitz, et al. 2007).