Literature DB >> 19362653

Enzymatic synthesis of TDP-deoxysugars.

Jessica White-Phillip1, Christopher J Thibodeaux, Hung-wen Liu.   

Abstract

Many biologically active bacterial natural products contain highly modified deoxysugar residues that are often critical for the activity of the parent compounds. Most of these deoxysugars are secondary metabolites that are biosynthesized in the form of nucleotide diphosphate (NDP) sugars prior to their transfer to natural product aglycones by glycosyltransferases. Over the past decade, many biosynthetic pathways that lead to the formation of these unusual sugars have been unraveled, and the mechanisms of many key enzymatic transformations involved in these pathways have been elucidated. However, obtaining workable quantities of NDP-deoxysugars for in vitro studies is often a difficult task. This limitation has hindered an in-depth investigation of the substrate specificity of deoxysugar biosynthetic enzymes, many of which are promiscuous with respect to their NDP-sugar substrates and are, thus, potentially useful catalysts for natural product glycoengineering. Presented in this review are procedures for the enzymatic synthesis and purification of a variety of NDP-deoxysugars, including some early intermediates in NDP-deoxysugar biosynthetic pathways, and highly modified NDP-deoxysugars that are late intermediates in their respective biosynthetic pathways. The procedures described herein could be used as general guidelines for the development of specific protocols for the synthesis of other NDP-deoxysugars.

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Year:  2009        PMID: 19362653      PMCID: PMC2776076          DOI: 10.1016/S0076-6879(09)04621-7

Source DB:  PubMed          Journal:  Methods Enzymol        ISSN: 0076-6879            Impact factor:   1.600


  36 in total

1.  Insights into the Branched-Chain Formation of Mycarose: Methylation Catalyzed by an (S)-Adenosylmethionine-Dependent Methyltransferase We are grateful to Dr. Eugene Seno and the Lilly Research Laboratories for their generous gift of the plasmid pHJL311 and to the National Institutes of Health for grants (GM 35 906 and 54 346). H.-w.L. also thanks the National Institute of General Medical Sciences for a MERIT Award. T.M.H. was a trainee of the National Institute of General Medical Sciences (Biotechnology Training Grant: 2 T32 GM08347).

Authors:  Huawei Chen; Zongbao Zhao; Tina M. Hallis; Zhihong Guo
Journal:  Angew Chem Int Ed Engl       Date:  2001-02-02       Impact factor: 15.336

2.  Reversible sugar transfer by glycosyltransferases as a tool for natural product (bio)synthesis.

Authors:  Helge B Bode; Rolf Müller
Journal:  Angew Chem Int Ed Engl       Date:  2007       Impact factor: 15.336

3.  Engineered biosynthesis of macrolide derivatives bearing the non-natural deoxysugars 4-epi-D-mycaminose and 3-n-monomethylamino-3-deoxy-D-fucose.

Authors:  Charles E Melançon; Hung-Wen Liu
Journal:  J Am Chem Soc       Date:  2007-03-28       Impact factor: 15.419

4.  In vitro characterization of the enzymes involved in TDP-D-forosamine biosynthesis in the spinosyn pathway of Saccharopolyspora spinosa.

Authors:  Lin Hong; Zongbao Zhao; Charles E Melançon; Hua Zhang; Hung-wen Liu
Journal:  J Am Chem Soc       Date:  2008-03-18       Impact factor: 15.419

5.  Biosynthesis of desosamine: construction of a new macrolide carrying a genetically designed sugar moiety.

Authors:  S A Borisova; L Zhao; D H Sherman; H W Liu
Journal:  Org Lett       Date:  1999-07-15       Impact factor: 6.005

6.  An enzyme module system for the synthesis of dTDP-activated deoxysugars from dTMP and sucrose.

Authors:  Lothar Elling; Carsten Rupprath; Nicole Günther; Ulrike Römer; Stefan Verseck; Petra Weingarten; Gerald Dräger; Andreas Kirschning; Wolfgang Piepersberg
Journal:  Chembiochem       Date:  2005-08       Impact factor: 3.164

7.  A two-stage one-pot enzymatic synthesis of TDP-L-mycarose from thymidine and glucose-1-phosphate.

Authors:  Haruko Takahashi; Yung-Nan Liu; Hung-Wen Liu
Journal:  J Am Chem Soc       Date:  2006-02-08       Impact factor: 15.419

8.  Deoxysugars in glycopeptide antibiotics: enzymatic synthesis of TDP-L-epivancosamine in chloroeremomycin biosynthesis.

Authors:  H Chen; M G Thomas; B K Hubbard; H C Losey; C T Walsh; M D Burkart
Journal:  Proc Natl Acad Sci U S A       Date:  2000-10-24       Impact factor: 11.205

9.  Deoxysugars in bioactive natural products: development of novel derivatives by altering the sugar pattern.

Authors:  Carmen Méndez; Andriy Luzhetskyy; Andreas Bechthold; José A Salas
Journal:  Curr Top Med Chem       Date:  2008       Impact factor: 3.295

Review 10.  Engineering the glycosylation of natural products in actinomycetes.

Authors:  José A Salas; Carmen Méndez
Journal:  Trends Microbiol       Date:  2007-04-06       Impact factor: 17.079

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  6 in total

1.  Investigating Mithramycin deoxysugar biosynthesis: enzymatic total synthesis of TDP-D-olivose.

Authors:  Guojun Wang; Madan K Kharel; Pallab Pahari; Jürgen Rohr
Journal:  Chembiochem       Date:  2011-09-29       Impact factor: 3.164

2.  Expanding the nucleotide and sugar 1-phosphate promiscuity of nucleotidyltransferase RmlA via directed evolution.

Authors:  Rocco Moretti; Aram Chang; Pauline Peltier-Pain; Craig A Bingman; George N Phillips; Jon S Thorson
Journal:  J Biol Chem       Date:  2011-02-11       Impact factor: 5.157

3.  Structural characterization of AtmS13, a putative sugar aminotransferase involved in indolocarbazole AT2433 aminopentose biosynthesis.

Authors:  Shanteri Singh; Youngchang Kim; Fengbin Wang; Lance Bigelow; Michael Endres; Madan K Kharel; Gyorgy Babnigg; Craig A Bingman; Andrzej Joachimiak; Jon S Thorson; George N Phillips
Journal:  Proteins       Date:  2015-07-01

4.  Pathway Engineering of Anthracyclines: Blazing Trails in Natural Product Glycodiversification.

Authors:  Katelyn V Brown; Benjamin Nji Wandi; Mikko Metsä-Ketelä; S Eric Nybo
Journal:  J Org Chem       Date:  2020-09-22       Impact factor: 4.354

5.  Characterization of Early Enzymes Involved in TDP-Aminodideoxypentose Biosynthesis en Route to Indolocarbazole AT2433.

Authors:  Pauline Peltier-Pain; Shanteri Singh; Jon S Thorson
Journal:  Chembiochem       Date:  2015-09-18       Impact factor: 3.164

6.  A general NMR-based strategy for the in situ characterization of sugar-nucleotide-dependent biosynthetic pathways.

Authors:  Shanteri Singh; Pauline Peltier-Pain; Marco Tonelli; Jon S Thorson
Journal:  Org Lett       Date:  2014-06-09       Impact factor: 6.005

  6 in total

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