Search for Extraterrestrial Life using Chiral Molecules: Mandelate Racemase as a Test Case

The possible existence of extraterrestrial life forms has been of interest to humans for many millennia. In the past few decades space travel has provided an opportunity to search life outside of Earth. Chiral molecules are critical molecules in Earth-based life and are among the first chemical mo...

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Main Author: Thaler, Tracey Lyn
Published: Georgia Institute of Technology 2007
Subjects:
Online Access:http://hdl.handle.net/1853/14527
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spelling ndltd-GATECH-oai-smartech.gatech.edu-1853-145272013-01-07T20:16:42ZSearch for Extraterrestrial Life using Chiral Molecules: Mandelate Racemase as a Test CaseThaler, Tracey LynIrreversible protein denaturationEnzymatic reactivity at subzero temperaturesEnolase superfamilyPolarimetric assayThe possible existence of extraterrestrial life forms has been of interest to humans for many millennia. In the past few decades space travel has provided an opportunity to search life outside of Earth. Chiral molecules are critical molecules in Earth-based life and are among the first chemical molecules sought after as proof of potential extraterrestrial life; however, identification of these chiral molecules is difficult due the lack of sensitive instruments. The objective of this work is to develop a benchmark reaction to be used as a guide in the development of instrumentation, such as a polarimeter, to be used in the search for extraterrestrial life. To achieve this objective, to investigate the enzyme mandelate racemase (MR), which catalyzes the racemization between the enantiomers of mandelate. MR is a member of the enolase superfamily, which contains a (alpha/beta)7-b barrel domain, the fold most frequently found among all known protein structures. Activity of the enzyme was measured at low temperatures and in non-aqueous media, as these are the conditions that represent extraterrestrial terrain. We find that mandelate racemase (MR) is active in concentrated ammonium salt solutions and water-in-oil microemulsions in a temperature range between 30C to 70C; however, the enzyme is not active in several organic cryosolvents. The stability of the structure of MR was also explored. Using differential scanning calorimetry (DSC) we observe the unfolding of the enzyme was irreversible and therefore kinetically controlled. We also found proof for divergent evolution of the enolase superfamily, providing evidence for divergent evolution across the MR and muconate lactonizing enzyme (MLE) subfamilies has been demonstrated. However, we also conclude that reactions yielding a polarimetric signal, such as racemizations employed in this work, are suitable as a tool to find signs of life.Georgia Institute of Technology2007-05-25T17:24:37Z2007-05-25T17:24:37Z2007-04-06Dissertationhttp://hdl.handle.net/1853/14527
collection NDLTD
sources NDLTD
topic Irreversible protein denaturation
Enzymatic reactivity at subzero temperatures
Enolase superfamily
Polarimetric assay
spellingShingle Irreversible protein denaturation
Enzymatic reactivity at subzero temperatures
Enolase superfamily
Polarimetric assay
Thaler, Tracey Lyn
Search for Extraterrestrial Life using Chiral Molecules: Mandelate Racemase as a Test Case
description The possible existence of extraterrestrial life forms has been of interest to humans for many millennia. In the past few decades space travel has provided an opportunity to search life outside of Earth. Chiral molecules are critical molecules in Earth-based life and are among the first chemical molecules sought after as proof of potential extraterrestrial life; however, identification of these chiral molecules is difficult due the lack of sensitive instruments. The objective of this work is to develop a benchmark reaction to be used as a guide in the development of instrumentation, such as a polarimeter, to be used in the search for extraterrestrial life. To achieve this objective, to investigate the enzyme mandelate racemase (MR), which catalyzes the racemization between the enantiomers of mandelate. MR is a member of the enolase superfamily, which contains a (alpha/beta)7-b barrel domain, the fold most frequently found among all known protein structures. Activity of the enzyme was measured at low temperatures and in non-aqueous media, as these are the conditions that represent extraterrestrial terrain. We find that mandelate racemase (MR) is active in concentrated ammonium salt solutions and water-in-oil microemulsions in a temperature range between 30C to 70C; however, the enzyme is not active in several organic cryosolvents. The stability of the structure of MR was also explored. Using differential scanning calorimetry (DSC) we observe the unfolding of the enzyme was irreversible and therefore kinetically controlled. We also found proof for divergent evolution of the enolase superfamily, providing evidence for divergent evolution across the MR and muconate lactonizing enzyme (MLE) subfamilies has been demonstrated. However, we also conclude that reactions yielding a polarimetric signal, such as racemizations employed in this work, are suitable as a tool to find signs of life.
author Thaler, Tracey Lyn
author_facet Thaler, Tracey Lyn
author_sort Thaler, Tracey Lyn
title Search for Extraterrestrial Life using Chiral Molecules: Mandelate Racemase as a Test Case
title_short Search for Extraterrestrial Life using Chiral Molecules: Mandelate Racemase as a Test Case
title_full Search for Extraterrestrial Life using Chiral Molecules: Mandelate Racemase as a Test Case
title_fullStr Search for Extraterrestrial Life using Chiral Molecules: Mandelate Racemase as a Test Case
title_full_unstemmed Search for Extraterrestrial Life using Chiral Molecules: Mandelate Racemase as a Test Case
title_sort search for extraterrestrial life using chiral molecules: mandelate racemase as a test case
publisher Georgia Institute of Technology
publishDate 2007
url http://hdl.handle.net/1853/14527
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