Literature DB >> 35796896

On the Origin of Sugar Handedness: Facts, Hypotheses and Missing Links-A Review.

R Fernando Martínez1, Louis A Cuccia2, Cristóbal Viedma3, Pedro Cintas4.   

Abstract

By paraphrasing one of Kipling's most amazing short stories (How the Leopard Got His Spots), this article could be entitled "How Sugars Became Homochiral". Obviously, we have no answer to this still unsolved mystery, and this perspective simply brings recent models, experiments and hypotheses into the homochiral homogeneity of sugars on earth. We shall revisit the past and current understanding of sugar chirality in the context of prebiotic chemistry, with attention to recent developments and insights. Different scenarios and pathways will be discussed, from the widely known formose-type processes to less familiar ones, often viewed as unorthodox chemical routes. In particular, problems associated with the spontaneous generation of enantiomeric imbalances and the transfer of chirality will be tackled. As carbohydrates are essential components of all cellular systems, astrochemical and terrestrial observations suggest that saccharides originated from environmentally available feedstocks. Such substances would have been capable of sustaining autotrophic and heterotrophic mechanisms integrating nutrients, metabolism and the genome after compartmentalization. Recent findings likewise indicate that sugars' enantiomeric bias may have emerged by a transfer of chirality mechanisms, rather than by deracemization of sugar backbones, yet providing an evolutionary advantage that fueled the cellular machinery.
© 2022. The Author(s), under exclusive licence to Springer Nature B.V.

Entities:  

Keywords:  Amino acid interactions; Carbohydrates; Homochirality; Prebiotic chemistry; Ribonucleosides

Mesh:

Substances:

Year:  2022        PMID: 35796896     DOI: 10.1007/s11084-022-09624-9

Source DB:  PubMed          Journal:  Orig Life Evol Biosph        ISSN: 0169-6149            Impact factor:   1.120


  103 in total

1.  Symmetry breaking by spontaneous crystallization--is it the most plausible source of terrestrial handedness we have long been looking for?--A reappraisal.

Authors:  Martin Avalos; Reyes Babiano; Pedro Cintas; Jose L Jimenez; Juan C Palacios
Journal:  Orig Life Evol Biosph       Date:  2004-08       Impact factor: 1.950

2.  Diastereoselective cycloadditions of 1,3-thiazolium-4-olates with chiral 1,2-diaza-1,3-butadienes

Authors: 
Journal:  J Org Chem       Date:  2000-08-25       Impact factor: 4.354

Review 3.  Mirror symmetry breaking at the molecular level.

Authors:  V Avetisov; V Goldanskii
Journal:  Proc Natl Acad Sci U S A       Date:  1996-10-15       Impact factor: 11.205

4.  Deuterium studies reveal a new mechanism for the formose reaction involving hydride shifts.

Authors:  Chandrakumar Appayee; Ronald Breslow
Journal:  J Am Chem Soc       Date:  2014-03-04       Impact factor: 15.419

5.  Synergic effect of vicinal stereocenters in [3 + 2] cycloadditions of carbohydrate azadipolarophiles and mesoionic dipoles: origin of diastereofacial selectivity.

Authors:  M Avalos; R Babiano; P Cintas; F R Clemente; R Gordillo; J L Jiménez; J C Palacios
Journal:  J Org Chem       Date:  2001-07-27       Impact factor: 4.354

6.  Why ribose was selected as the sugar component of nucleic acids.

Authors:  Gaspar Banfalvi
Journal:  DNA Cell Biol       Date:  2006-03       Impact factor: 3.311

7.  Analyses of Aliphatic Aldehydes and Ketones in Carbonaceous Chondrites.

Authors:  José C Aponte; Daniel Whitaker; Matthew W Powner; Jamie E Elsila; Jason P Dworkin
Journal:  ACS Earth Space Chem       Date:  2019-02-20       Impact factor: 3.475

8.  Cross-Chiral, RNA-Catalyzed Exponential Amplification of RNA.

Authors:  Grant A L Bare; Gerald F Joyce
Journal:  J Am Chem Soc       Date:  2021-11-03       Impact factor: 15.419

9.  Magneto-chiral anisotropy: From fundamentals to perspectives.

Authors:  Matteo Atzori; Cyrille Train; Elizabeth A Hillard; Narcis Avarvari; Geert L J A Rikken
Journal:  Chirality       Date:  2021-09-19       Impact factor: 2.437

10.  Chiral recognition in gas-phase cyclodextrin: amino acid complexes--is the three point interaction still valid in the gas phase?

Authors:  S Ahn; J Ramirez; G Grigorean; C B Lebrilla
Journal:  J Am Soc Mass Spectrom       Date:  2001-03       Impact factor: 3.262

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