Stereoelectronic Effects in Phosphates

Molecules containing the phosphate (O—PO32-) moiety are ubiquitous in biochemistry. Phosphoryl transfer reactions that break and form the O—P phosphoryl bond are central to biological processes as diverse as energy metabolism and signal transduction. As described by Westheimer, the utility of phosph...

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Other Authors: Ruben, Eliza A. (authoraut)
Format: Others
Language:English
English
Published: Florida State University
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Online Access:http://purl.flvc.org/fsu/fd/FSU_migr_etd-1924
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spelling ndltd-fsu.edu-oai-fsu.digital.flvc.org-fsu_1763912020-06-09T03:08:15Z Stereoelectronic Effects in Phosphates Ruben, Eliza A. (authoraut) Chapman, Michael S. (professor co-directing dissertation) Ellington, W. Ross (professor co-directing dissertation) Fulton, Robert L. (outside committee member) Cross, Timothy A. (committee member) Zhou, Huan-Xiang (committee member) Program in Molecular Biophysics (degree granting department) Florida State University (degree granting institution) Text text Florida State University Florida State University English eng 1 online resource computer application/pdf Molecules containing the phosphate (O—PO32-) moiety are ubiquitous in biochemistry. Phosphoryl transfer reactions that break and form the O—P phosphoryl bond are central to biological processes as diverse as energy metabolism and signal transduction. As described by Westheimer, the utility of phosphates stem from their ability to be kinetically stable while thermodynamically unstable. This dissertation uses electronic structure theory to investigate, at an elementary chemical level, the thermodynamic and kinetic properties of phosphate esters in an attempt to answer the question, "Why nature chose phosphates?". Chapter 1 formulates the question to be answered. Chapter 2 provides the underlying theoretical background to the computational methods employed. In Chapter 3, the anomeric effect, a stereoelectronic effect is first identified as a contributor to the high-energy status of N-phosphoryl-guanidines using electronic structure methods. In Chapter 4 it is further found that the anomeric effect can contribute to the thermodynamic poise of a range of phosphates. Chapter 5 investigates the connection between phosphoryl transfer mechanisms and the anomeric effect. It is found that the anomeric effect promotes O—P bond cleavage and plays a dominant role in the dissociative mechanism of phosphoryl transfer. The impact of other stereoelectronic effects such as hyperconjugation upon the hydrogen bonding properties of phosphates is also examined in Chapter 6. Compelling evidence is obtained suggesting the role of the O—P bond weakening anomeric effect in discriminating phosphoryl transfer potentials and controlling reaction rates in a range of biologically important phosphoryl compounds. Strong correlations between phosphoryl transfer potentials, rates of reaction in solution, O—P bond weakening, and the magnitude of the n(O)→σ*(O—P) anomeric effect is shown. This dissertation articulates a fundamental property of phosphates that may provide an answer to the age old question of "Why nature chose phosphates". A Dissertation Submitted to the Program in Molecular Biophysics in Partial Fulfillment of the Requirements for the Degree of Doctor of Philosophy. Summer Semester, 2007. June 11, 2007. Phosphates, Anomeric Effect Includes bibliographical references. Michael S. Chapman, Professor Co-Directing Dissertation; W. Ross Ellington, Professor Co-Directing Dissertation; Robert L. Fulton, Outside Committee Member; Timothy A. Cross, Committee Member; Huan-Xiang Zhou, Committee Member. Biophysics Molecular biology Microphysics FSU_migr_etd-1924 http://purl.flvc.org/fsu/fd/FSU_migr_etd-1924 This Item is protected by copyright and/or related rights. You are free to use this Item in any way that is permitted by the copyright and related rights legislation that applies to your use. For other uses you need to obtain permission from the rights-holder(s). The copyright in theses and dissertations completed at Florida State University is held by the students who author them. http://diginole.lib.fsu.edu/islandora/object/fsu%3A176391/datastream/TN/view/Stereoelectronic%20Effects%20in%20Phosphates.jpg
collection NDLTD
language English
English
format Others
sources NDLTD
topic Biophysics
Molecular biology
Microphysics
spellingShingle Biophysics
Molecular biology
Microphysics
Stereoelectronic Effects in Phosphates
description Molecules containing the phosphate (O—PO32-) moiety are ubiquitous in biochemistry. Phosphoryl transfer reactions that break and form the O—P phosphoryl bond are central to biological processes as diverse as energy metabolism and signal transduction. As described by Westheimer, the utility of phosphates stem from their ability to be kinetically stable while thermodynamically unstable. This dissertation uses electronic structure theory to investigate, at an elementary chemical level, the thermodynamic and kinetic properties of phosphate esters in an attempt to answer the question, "Why nature chose phosphates?". Chapter 1 formulates the question to be answered. Chapter 2 provides the underlying theoretical background to the computational methods employed. In Chapter 3, the anomeric effect, a stereoelectronic effect is first identified as a contributor to the high-energy status of N-phosphoryl-guanidines using electronic structure methods. In Chapter 4 it is further found that the anomeric effect can contribute to the thermodynamic poise of a range of phosphates. Chapter 5 investigates the connection between phosphoryl transfer mechanisms and the anomeric effect. It is found that the anomeric effect promotes O—P bond cleavage and plays a dominant role in the dissociative mechanism of phosphoryl transfer. The impact of other stereoelectronic effects such as hyperconjugation upon the hydrogen bonding properties of phosphates is also examined in Chapter 6. Compelling evidence is obtained suggesting the role of the O—P bond weakening anomeric effect in discriminating phosphoryl transfer potentials and controlling reaction rates in a range of biologically important phosphoryl compounds. Strong correlations between phosphoryl transfer potentials, rates of reaction in solution, O—P bond weakening, and the magnitude of the n(O)→σ*(O—P) anomeric effect is shown. This dissertation articulates a fundamental property of phosphates that may provide an answer to the age old question of "Why nature chose phosphates". === A Dissertation Submitted to the Program in Molecular Biophysics in Partial Fulfillment of the Requirements for the Degree of Doctor of Philosophy. === Summer Semester, 2007. === June 11, 2007. === Phosphates, Anomeric Effect === Includes bibliographical references. === Michael S. Chapman, Professor Co-Directing Dissertation; W. Ross Ellington, Professor Co-Directing Dissertation; Robert L. Fulton, Outside Committee Member; Timothy A. Cross, Committee Member; Huan-Xiang Zhou, Committee Member.
author2 Ruben, Eliza A. (authoraut)
author_facet Ruben, Eliza A. (authoraut)
title Stereoelectronic Effects in Phosphates
title_short Stereoelectronic Effects in Phosphates
title_full Stereoelectronic Effects in Phosphates
title_fullStr Stereoelectronic Effects in Phosphates
title_full_unstemmed Stereoelectronic Effects in Phosphates
title_sort stereoelectronic effects in phosphates
publisher Florida State University
url http://purl.flvc.org/fsu/fd/FSU_migr_etd-1924
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