Chemoenzymatic synthesis of CMP-N-acetyl-7-fluoro-7-deoxy-neuraminic acid

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  • Medizinische Hochschule Hannover (MHH)
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OriginalspracheEnglisch
Seiten (von - bis)2075-2082
Seitenumfang8
FachzeitschriftCarbohydrate Research
Jahrgang343
Ausgabenummer12
PublikationsstatusVeröffentlicht - 10 Feb. 2008

Abstract

7-Fluoro sialic acid was prepared and activated as cytidine monophosphate (CMP) ester. The synthesis started with d-glucose, which was efficiently converted into N-acetyl-4-fluoro-4-deoxy-d-mannosamine. Aldolase catalyzed transformation yielded the corresponding fluorinated sialic acid which was activated as CMP ester using three different synthetases in the presence as well as in the absence of pyrophosphatase which possesses inhibitory properties. Finally, conditions were optimized to perform a one-pot reaction starting from fluorinated mannosamine, which yielded the 7-fluoro-7-deoxy-CMP-sialic acid by incubation with three enzymes.

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Chemoenzymatic synthesis of CMP-N-acetyl-7-fluoro-7-deoxy-neuraminic acid. / Hartlieb, Sina; Günzel, Almut; Gerardy-Schahn, Rita et al.
in: Carbohydrate Research, Jahrgang 343, Nr. 12, 10.02.2008, S. 2075-2082.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Hartlieb S, Günzel A, Gerardy-Schahn R, Münster-Kühnel AK, Kirschning A, Dräger G. Chemoenzymatic synthesis of CMP-N-acetyl-7-fluoro-7-deoxy-neuraminic acid. Carbohydrate Research. 2008 Feb 10;343(12):2075-2082. doi: 10.1016/j.carres.2008.02.003
Hartlieb, Sina ; Günzel, Almut ; Gerardy-Schahn, Rita et al. / Chemoenzymatic synthesis of CMP-N-acetyl-7-fluoro-7-deoxy-neuraminic acid. in: Carbohydrate Research. 2008 ; Jahrgang 343, Nr. 12. S. 2075-2082.
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title = "Chemoenzymatic synthesis of CMP-N-acetyl-7-fluoro-7-deoxy-neuraminic acid",
abstract = "7-Fluoro sialic acid was prepared and activated as cytidine monophosphate (CMP) ester. The synthesis started with d-glucose, which was efficiently converted into N-acetyl-4-fluoro-4-deoxy-d-mannosamine. Aldolase catalyzed transformation yielded the corresponding fluorinated sialic acid which was activated as CMP ester using three different synthetases in the presence as well as in the absence of pyrophosphatase which possesses inhibitory properties. Finally, conditions were optimized to perform a one-pot reaction starting from fluorinated mannosamine, which yielded the 7-fluoro-7-deoxy-CMP-sialic acid by incubation with three enzymes.",
keywords = "Chemoenzymatic synthesis, CMP-7-F-sialic acid, Sugar nucleotide",
author = "Sina Hartlieb and Almut G{\"u}nzel and Rita Gerardy-Schahn and M{\"u}nster-K{\"u}hnel, {Anja K.} and Andreas Kirschning and Gerald Dr{\"a}ger",
note = "Funding information: We thank Dipl.-Biochem. Melanie Oschlies for her expertise and for supplying samples of the CMP-sialic acid synthetases from mouse and rainbow trout. This work was supported by the Deutsche Forschungsgemeinschaft (Grants Ki 397/8-1 and Ki 397/9-1; GE 801/6-1) and the Fonds der Chemischen Industrie.",
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Download

TY - JOUR

T1 - Chemoenzymatic synthesis of CMP-N-acetyl-7-fluoro-7-deoxy-neuraminic acid

AU - Hartlieb, Sina

AU - Günzel, Almut

AU - Gerardy-Schahn, Rita

AU - Münster-Kühnel, Anja K.

AU - Kirschning, Andreas

AU - Dräger, Gerald

N1 - Funding information: We thank Dipl.-Biochem. Melanie Oschlies for her expertise and for supplying samples of the CMP-sialic acid synthetases from mouse and rainbow trout. This work was supported by the Deutsche Forschungsgemeinschaft (Grants Ki 397/8-1 and Ki 397/9-1; GE 801/6-1) and the Fonds der Chemischen Industrie.

PY - 2008/2/10

Y1 - 2008/2/10

N2 - 7-Fluoro sialic acid was prepared and activated as cytidine monophosphate (CMP) ester. The synthesis started with d-glucose, which was efficiently converted into N-acetyl-4-fluoro-4-deoxy-d-mannosamine. Aldolase catalyzed transformation yielded the corresponding fluorinated sialic acid which was activated as CMP ester using three different synthetases in the presence as well as in the absence of pyrophosphatase which possesses inhibitory properties. Finally, conditions were optimized to perform a one-pot reaction starting from fluorinated mannosamine, which yielded the 7-fluoro-7-deoxy-CMP-sialic acid by incubation with three enzymes.

AB - 7-Fluoro sialic acid was prepared and activated as cytidine monophosphate (CMP) ester. The synthesis started with d-glucose, which was efficiently converted into N-acetyl-4-fluoro-4-deoxy-d-mannosamine. Aldolase catalyzed transformation yielded the corresponding fluorinated sialic acid which was activated as CMP ester using three different synthetases in the presence as well as in the absence of pyrophosphatase which possesses inhibitory properties. Finally, conditions were optimized to perform a one-pot reaction starting from fluorinated mannosamine, which yielded the 7-fluoro-7-deoxy-CMP-sialic acid by incubation with three enzymes.

KW - Chemoenzymatic synthesis

KW - CMP-7-F-sialic acid

KW - Sugar nucleotide

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U2 - 10.1016/j.carres.2008.02.003

DO - 10.1016/j.carres.2008.02.003

M3 - Article

C2 - 18353292

AN - SCOPUS:45049086802

VL - 343

SP - 2075

EP - 2082

JO - Carbohydrate Research

JF - Carbohydrate Research

SN - 0008-6215

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