Literature DB >> 4723773

Synthesis, characterization and properties of uridine 5'-( -D-apio-D-furanosyl pyrophosphate).

P K Kindel, R R Watson.   

Abstract

1. A method was developed for synthesizing UDP-apiose [uridine 5'-(alpha-d-apio-d-furanosyl pyrophosphate)] from UDP-glucuronic acid [uridine 5'-(alpha-d-glucopyranosyluronic acid pyrophosphate)] in 62% yield with the enzyme UDP-glucuronic acid cyclase. 2. UDP-apiose had the same mobility as uridine 5'-(alpha-d-xylopyranosyl pyrophosphate) when chromatographed on paper and when subjected to paper electrophoresis at pH5.8. When [(3)H]UDP-[U-(14)C]glucuronic acid was used as the substrate for UDP-glucuronic acid cyclase, the (3)H/(14)C ratio in the reaction product was that expected if d-apiose remained attached to the uridine. In separate experiments doubly labelled reaction product was: (a) hydrolysed at pH2 and 100 degrees C for 15min; (b) degraded at pH8.0 and 100 degrees C for 3min; (c) used as a substrate in the enzymic synthesis of [(14)C]apiin. In each type of experiment the reaction products were isolated and identified and were found to be those expected if [(3)H]UDP-[U-(14)C]apiose was the starting compound. 3. Chemical characterization established that the product containing d-[U-(14)C]apiose and phosphate formed on alkaline degradation of UDP-[U-(14)C]apiose was alpha-d-[U-(14)C]apio-d-furanosyl 1:2-cyclic phosphate. 4. Chemical characterization also established that the product containing d-[U-(14)C]apiose and phosphate formed on acid hydrolysis of alpha-d-[U-(14)C]apio-d-furanosyl 1:2-cyclic phosphate was d-[U-(14)C]apiose 2-phosphate. 5. The half-life periods for the degradation of UDP-[U-(14)C]apiose to alpha-d-[U-(14)C]apio-d-furanosyl 1:2-cyclic phosphate and UMP at pH8.0 and 80 degrees C, at pH8.0 and 25 degrees C and at pH8.0 and 4 degrees C were 31.6s, 97.2min and 16.5h respectively. The half-life period for the hydrolysis of UDP-[U-(14)C]-apiose to d-[U-(14)C]apiose and UDP at pH3.0 and 40 degrees C was 4.67min. After 20 days at pH6.2-6.6 and 4 degrees C, 17% of the starting UDP-[U-(14)C]apiose was degraded to alpha-d-[U-(14)C]apio-d-furanosyl 1:2-cyclic phosphate and UMP and 23% was hydrolysed to d-[U-(14)C]apiose and UDP. After 120 days at pH6.4 and -20 degrees C 2% of the starting UDP-[U-(14)C]apiose was degraded and 4% was hydrolysed.

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Year:  1973        PMID: 4723773      PMCID: PMC1177691          DOI: 10.1042/bj1330227

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  18 in total

1.  Structural investigations on T1 lipopolysaccharides.

Authors:  M Berst; C G Hellerqvist; B Lindberg; O Lüderitz; S Svensson; O Westphal
Journal:  Eur J Biochem       Date:  1969-12

2.  Biosynthesis of D-apiose. V. NAD+-dependent biosynthesis of UDP-apiose and UDP-xylose from UDP-D-glucuronic acid with an enzyme preparation from Lemna minor L.

Authors:  H Sandermann; H Grisebach
Journal:  Biochim Biophys Acta       Date:  1970-05-12

3.  Crystallization and properties of uridine diphosphate glucose pyrophosphorylase from liver.

Authors:  G J Albrecht; S T Bass; L L Seifert; R G Hansen
Journal:  J Biol Chem       Date:  1966-06-25       Impact factor: 5.157

4.  An artefact in the chromatography of sugar nucleotides using solvents containing ammonium acetate.

Authors:  K C Tovey; R M Roberts
Journal:  J Chromatogr       Date:  1970-03-04

5.  The synthesis of isomers of D-apiofuranosyl 1-phosphate.

Authors:  J Mendicino; R Hanna
Journal:  J Biol Chem       Date:  1970-11-25       Impact factor: 5.157

6.  Biosynthesis of D-apiose. IV. Formation of UDP-apiose from UDP-D-glucuronic acid in cell-free extracts of parsley (Apium petroselinum L.) and Lemna minor.

Authors:  H Sandermann; G T Tisue; H Grisebach
Journal:  Biochim Biophys Acta       Date:  1968-10-15

7.  Enzymic synthesis of uridine diphosphoglucose-14-C.

Authors:  D K Fitzgerald; K E Ebner
Journal:  Anal Biochem       Date:  1966-04       Impact factor: 3.365

8.  Uridine diphosphate alpha-D-galactofuranose, an intermediate in the biosynthesis of galactofuranosyl residues.

Authors:  A G Trejo; G J Chittenden; J G Buchanan; J Baddiley
Journal:  Biochem J       Date:  1970-04       Impact factor: 3.857

9.  D-apiose reductase from Aerobacter aerogenes.

Authors:  D L Neal; P K Kindel
Journal:  J Bacteriol       Date:  1970-03       Impact factor: 3.490

10.  The biosynthesis of galactofuranosyl residues in galactocarolose.

Authors:  A G Trejo; J W Haddock; G J Chittenden; J Baddiley
Journal:  Biochem J       Date:  1971-03       Impact factor: 3.857

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  4 in total

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Authors:  W D Reiter; G F Vanzin
Journal:  Plant Mol Biol       Date:  2001-09       Impact factor: 4.076

2.  Developmental Control of Apiogalacturonan Biosynthesis and UDP-Apiose Production in a Duckweed.

Authors:  J M Longland; S C Fry; A J Trewavas
Journal:  Plant Physiol       Date:  1989-07       Impact factor: 8.340

3.  Biosynthetic origin of mycobacterial cell wall arabinosyl residues.

Authors:  M Scherman; A Weston; K Duncan; A Whittington; R Upton; L Deng; R Comber; J D Friedrich; M McNeil
Journal:  J Bacteriol       Date:  1995-12       Impact factor: 3.490

4.  Analysis of UDP-D-apiose/UDP-D-xylose synthase-catalyzed conversion of UDP-D-apiose phosphonate to UDP-D-xylose phosphonate: implications for a retroaldol-aldol mechanism.

Authors:  Sei-hyun Choi; Steven O Mansoorabadi; Yung-nan Liu; Tun-Cheng Chien; Hung-wen Liu
Journal:  J Am Chem Soc       Date:  2012-08-15       Impact factor: 15.419

  4 in total

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