Enzymatic synthesis of [7-14C, 7-3H]- and [1-13C]sedoheptulose 7- phosphate and [1-13C]ido-heptulose 7-phosphate

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Original languageEnglish
Pages (from-to)369-377
Number of pages9
JournalJournal of Molecular Catalysis B: Enzymatic
Volume6
Issue number3
Publication statusPublished - 11 Mar 1999
Externally publishedYes

Abstract

The enzymatic synthesis of isotopically labeled D-sedoheptulose 7- phosphate from either labeled D-glucose or labeled L-serine is described. [7- 14C, 7-3H]Sedoheptulose 7-phosphate is prepared with transketolase from xylulose 5-phosphate, as C2 donor, and D-[5-14C, 5-3H]ribose 5-phosphate, which in turn is generated from D-[6-14C, 6-3H]glucose with the glycolytic enzymes. [1-13C]Sedoheptulose 7-phosphate is obtained in a one-pot reaction in 69% yield from unlabeled ribose 5-phosphate and L-[3-13C]serine via hydroxypyruvate as the C2 donor using the enzymes alanine racemase, D-amino acid oxidase, catalase and transketolase. By the latter route labeled 1- 13C]ido-heptulose 7-phosphate was also prepared when xylose 5-phosphate was substituted for the ribose 5-phosphate.

Keywords

    Enzymatic synthesis, Hydroxypyruvate, ido- Heptulose 7-phosphate, Labeled compounds, Sedoheptulose 7-phosphate, Transketolase

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Enzymatic synthesis of [7-14C, 7-3H]- and [1-13C]sedoheptulose 7- phosphate and [1-13C]ido-heptulose 7-phosphate. / Lee, Sungsook; Kirschning, Andreas; Müller, Michael et al.
In: Journal of Molecular Catalysis B: Enzymatic, Vol. 6, No. 3, 11.03.1999, p. 369-377.

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title = "Enzymatic synthesis of [7-14C, 7-3H]- and [1-13C]sedoheptulose 7- phosphate and [1-13C]ido-heptulose 7-phosphate",
abstract = "The enzymatic synthesis of isotopically labeled D-sedoheptulose 7- phosphate from either labeled D-glucose or labeled L-serine is described. [7- 14C, 7-3H]Sedoheptulose 7-phosphate is prepared with transketolase from xylulose 5-phosphate, as C2 donor, and D-[5-14C, 5-3H]ribose 5-phosphate, which in turn is generated from D-[6-14C, 6-3H]glucose with the glycolytic enzymes. [1-13C]Sedoheptulose 7-phosphate is obtained in a one-pot reaction in 69% yield from unlabeled ribose 5-phosphate and L-[3-13C]serine via hydroxypyruvate as the C2 donor using the enzymes alanine racemase, D-amino acid oxidase, catalase and transketolase. By the latter route labeled 1- 13C]ido-heptulose 7-phosphate was also prepared when xylose 5-phosphate was substituted for the ribose 5-phosphate.",
keywords = "Enzymatic synthesis, Hydroxypyruvate, ido- Heptulose 7-phosphate, Labeled compounds, Sedoheptulose 7-phosphate, Transketolase",
author = "Sungsook Lee and Andreas Kirschning and Michael M{\"u}ller and Chris Way and Floss, {Heinz G.}",
note = "Funding information: We are greatly indebted to Professor Kenji Soda, Kansai University, and Professor Nobuyoshi Esaki, Kyoto University, for their generous gifts of alanine dehydrogenase and alanine racemase and to Dr. Michael Breuer, BASF Ludwigshafen, for kindly providing several transaminases. Financial support of this work by Bayer and by the US Public Health Service through NIH grant AI20264 is gratefully acknowledged. A.K. thanks the Alexander v. Humboldt Foundation for a Lynen fellowship and M.M. thanks the Deutsche Forschungsgemeinschaft for postdoctoral fellowship support.",
year = "1999",
month = mar,
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doi = "10.1016/S1381-1177(98)00131-3",
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volume = "6",
pages = "369--377",
journal = "Journal of Molecular Catalysis B: Enzymatic",
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Download

TY - JOUR

T1 - Enzymatic synthesis of [7-14C, 7-3H]- and [1-13C]sedoheptulose 7- phosphate and [1-13C]ido-heptulose 7-phosphate

AU - Lee, Sungsook

AU - Kirschning, Andreas

AU - Müller, Michael

AU - Way, Chris

AU - Floss, Heinz G.

N1 - Funding information: We are greatly indebted to Professor Kenji Soda, Kansai University, and Professor Nobuyoshi Esaki, Kyoto University, for their generous gifts of alanine dehydrogenase and alanine racemase and to Dr. Michael Breuer, BASF Ludwigshafen, for kindly providing several transaminases. Financial support of this work by Bayer and by the US Public Health Service through NIH grant AI20264 is gratefully acknowledged. A.K. thanks the Alexander v. Humboldt Foundation for a Lynen fellowship and M.M. thanks the Deutsche Forschungsgemeinschaft for postdoctoral fellowship support.

PY - 1999/3/11

Y1 - 1999/3/11

N2 - The enzymatic synthesis of isotopically labeled D-sedoheptulose 7- phosphate from either labeled D-glucose or labeled L-serine is described. [7- 14C, 7-3H]Sedoheptulose 7-phosphate is prepared with transketolase from xylulose 5-phosphate, as C2 donor, and D-[5-14C, 5-3H]ribose 5-phosphate, which in turn is generated from D-[6-14C, 6-3H]glucose with the glycolytic enzymes. [1-13C]Sedoheptulose 7-phosphate is obtained in a one-pot reaction in 69% yield from unlabeled ribose 5-phosphate and L-[3-13C]serine via hydroxypyruvate as the C2 donor using the enzymes alanine racemase, D-amino acid oxidase, catalase and transketolase. By the latter route labeled 1- 13C]ido-heptulose 7-phosphate was also prepared when xylose 5-phosphate was substituted for the ribose 5-phosphate.

AB - The enzymatic synthesis of isotopically labeled D-sedoheptulose 7- phosphate from either labeled D-glucose or labeled L-serine is described. [7- 14C, 7-3H]Sedoheptulose 7-phosphate is prepared with transketolase from xylulose 5-phosphate, as C2 donor, and D-[5-14C, 5-3H]ribose 5-phosphate, which in turn is generated from D-[6-14C, 6-3H]glucose with the glycolytic enzymes. [1-13C]Sedoheptulose 7-phosphate is obtained in a one-pot reaction in 69% yield from unlabeled ribose 5-phosphate and L-[3-13C]serine via hydroxypyruvate as the C2 donor using the enzymes alanine racemase, D-amino acid oxidase, catalase and transketolase. By the latter route labeled 1- 13C]ido-heptulose 7-phosphate was also prepared when xylose 5-phosphate was substituted for the ribose 5-phosphate.

KW - Enzymatic synthesis

KW - Hydroxypyruvate

KW - ido- Heptulose 7-phosphate

KW - Labeled compounds

KW - Sedoheptulose 7-phosphate

KW - Transketolase

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U2 - 10.1016/S1381-1177(98)00131-3

DO - 10.1016/S1381-1177(98)00131-3

M3 - Article

AN - SCOPUS:0033545532

VL - 6

SP - 369

EP - 377

JO - Journal of Molecular Catalysis B: Enzymatic

JF - Journal of Molecular Catalysis B: Enzymatic

SN - 1381-1177

IS - 3

ER -

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