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Thermophilic phosphoribosyltransferases Thermus thermophilus HB27 in nucleotide synthesis
Phosphoribosyltransferases are the tools that allow the synthesis of nucleotide analogues using multi-enzymatic cascades. The recombinant adenine phosphoribosyltransferase (TthAPRT) and hypoxanthine phosphoribosyltransferase (TthHPRT) from Thermus thermophilus HB27 were expressed in E.coli strains a...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Beilstein-Institut
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6317416/ https://www.ncbi.nlm.nih.gov/pubmed/30643587 http://dx.doi.org/10.3762/bjoc.14.289 |
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author | Fateev, Ilja V Sinitsina, Ekaterina V Bikanasova, Aiguzel U Kostromina, Maria A Tuzova, Elena S Esipova, Larisa V Muravyova, Tatiana I Kayushin, Alexei L Konstantinova, Irina D Esipov, Roman S |
author_facet | Fateev, Ilja V Sinitsina, Ekaterina V Bikanasova, Aiguzel U Kostromina, Maria A Tuzova, Elena S Esipova, Larisa V Muravyova, Tatiana I Kayushin, Alexei L Konstantinova, Irina D Esipov, Roman S |
author_sort | Fateev, Ilja V |
collection | PubMed |
description | Phosphoribosyltransferases are the tools that allow the synthesis of nucleotide analogues using multi-enzymatic cascades. The recombinant adenine phosphoribosyltransferase (TthAPRT) and hypoxanthine phosphoribosyltransferase (TthHPRT) from Thermus thermophilus HB27 were expressed in E.coli strains and purified by chromatographic methods with yields of 10–13 mg per liter of culture. The activity dependence of TthAPRT and TthHPRT on different factors was investigated along with the substrate specificity towards different heterocyclic bases. The kinetic parameters for TthHPRT with natural substrates were determined. Two nucleotides were synthesized: 9-(β-D-ribofuranosyl)-2-chloroadenine 5'-monophosphate (2-Сl-AMP) using TthAPRT and 1-(β-D-ribofuranosyl)pyrazolo[3,4-d]pyrimidine-4-one 5'-monophosphate (Allop-MP) using TthНPRT. |
format | Online Article Text |
id | pubmed-6317416 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-63174162019-01-14 Thermophilic phosphoribosyltransferases Thermus thermophilus HB27 in nucleotide synthesis Fateev, Ilja V Sinitsina, Ekaterina V Bikanasova, Aiguzel U Kostromina, Maria A Tuzova, Elena S Esipova, Larisa V Muravyova, Tatiana I Kayushin, Alexei L Konstantinova, Irina D Esipov, Roman S Beilstein J Org Chem Full Research Paper Phosphoribosyltransferases are the tools that allow the synthesis of nucleotide analogues using multi-enzymatic cascades. The recombinant adenine phosphoribosyltransferase (TthAPRT) and hypoxanthine phosphoribosyltransferase (TthHPRT) from Thermus thermophilus HB27 were expressed in E.coli strains and purified by chromatographic methods with yields of 10–13 mg per liter of culture. The activity dependence of TthAPRT and TthHPRT on different factors was investigated along with the substrate specificity towards different heterocyclic bases. The kinetic parameters for TthHPRT with natural substrates were determined. Two nucleotides were synthesized: 9-(β-D-ribofuranosyl)-2-chloroadenine 5'-monophosphate (2-Сl-AMP) using TthAPRT and 1-(β-D-ribofuranosyl)pyrazolo[3,4-d]pyrimidine-4-one 5'-monophosphate (Allop-MP) using TthНPRT. Beilstein-Institut 2018-12-21 /pmc/articles/PMC6317416/ /pubmed/30643587 http://dx.doi.org/10.3762/bjoc.14.289 Text en Copyright © 2018, Fateev et al. https://creativecommons.org/licenses/by/4.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0). Please note that the reuse, redistribution and reproduction in particular requires that the authors and source are credited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms) |
spellingShingle | Full Research Paper Fateev, Ilja V Sinitsina, Ekaterina V Bikanasova, Aiguzel U Kostromina, Maria A Tuzova, Elena S Esipova, Larisa V Muravyova, Tatiana I Kayushin, Alexei L Konstantinova, Irina D Esipov, Roman S Thermophilic phosphoribosyltransferases Thermus thermophilus HB27 in nucleotide synthesis |
title | Thermophilic phosphoribosyltransferases Thermus thermophilus HB27 in nucleotide synthesis |
title_full | Thermophilic phosphoribosyltransferases Thermus thermophilus HB27 in nucleotide synthesis |
title_fullStr | Thermophilic phosphoribosyltransferases Thermus thermophilus HB27 in nucleotide synthesis |
title_full_unstemmed | Thermophilic phosphoribosyltransferases Thermus thermophilus HB27 in nucleotide synthesis |
title_short | Thermophilic phosphoribosyltransferases Thermus thermophilus HB27 in nucleotide synthesis |
title_sort | thermophilic phosphoribosyltransferases thermus thermophilus hb27 in nucleotide synthesis |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6317416/ https://www.ncbi.nlm.nih.gov/pubmed/30643587 http://dx.doi.org/10.3762/bjoc.14.289 |
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