Literature DB >> 3994659

On the nature of L-xylulose reductase deficiency in essential pentosuria.

A B Lane.   

Abstract

Essential pentosuria is the result of a partial deficiency of L-xylulose reductase. Red blood cells of normal individuals have been found to contain two L-xylulose reductases: a major and a minor isozyme. Red cells from pentosurics contain only one isozyme. The residual enzyme of pentosurics and the normal minor isozyme have similar Michaelis constants for L-xylulose and xylitol, similar activity responses to pH, and similar rates of migration when electrophoresed or subjected to ion-exchange chromatography. It is suggested that homozygosity for the pentosuria allele results in the absence of the major isozyme and that the residual isozyme of pentosurics is identical to the minor isozyme of normal individuals.

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Year:  1985        PMID: 3994659     DOI: 10.1007/bf00499113

Source DB:  PubMed          Journal:  Biochem Genet        ISSN: 0006-2928            Impact factor:   1.890


  9 in total

1.  Pentose metabolism and pentosuria.

Authors:  O TOUSTER
Journal:  Am J Med       Date:  1959-05       Impact factor: 4.965

2.  A sensitive and stereospecific enzymatic assay for xylulose.

Authors:  J HICKMAN; G ASHWELL
Journal:  J Biol Chem       Date:  1959-04       Impact factor: 5.157

3.  Studies of pentose metabolism in normal subjects and in patients with pentosuria and pentosuria trait.

Authors:  Y KUMAHARA; D S FEINGOLD; I M FREEDBERG; H H HIATT
Journal:  J Clin Endocrinol Metab       Date:  1961-08       Impact factor: 5.958

4.  Studies on the glucuronic acid pathway of glucose metabolism.

Authors:  F EISENBERG; P G DAYTON; J J BURNS
Journal:  J Biol Chem       Date:  1959-02       Impact factor: 5.157

5.  Essential pentosuria.

Authors:  A K KHACHADURIAN
Journal:  Am J Hum Genet       Date:  1962-09       Impact factor: 11.025

6.  Paper chromatography of the urinary sugar in essential pentosuria.

Authors:  H D BARNES; B M BLOOMBERG
Journal:  S Afr J Med Sci       Date:  1953-12

7.  L-xylulosuria in a Lebanese family.

Authors:  W M POLITZER; H FLEISCHMANN
Journal:  Am J Hum Genet       Date:  1962-09       Impact factor: 11.025

8.  The enzymatic defect in essential pentosuria.

Authors:  Y M Wang; J Van Eys
Journal:  N Engl J Med       Date:  1970-04-16       Impact factor: 91.245

9.  Genetics of glutamic-pyruvic transaminase: its inheritance, common and rare variants, population distribution, and differences in catalytic activity.

Authors:  S H Chen; E R Giblett; J E Anderson; B L Fossum
Journal:  Ann Hum Genet       Date:  1972-04       Impact factor: 1.670

  9 in total
  3 in total

1.  Analysis of polyols in urine by liquid chromatography-tandem mass spectrometry: a useful tool for recognition of inborn errors affecting polyol metabolism.

Authors:  M M C Wamelink; D E C Smith; C Jakobs; N M Verhoeven
Journal:  J Inherit Metab Dis       Date:  2005       Impact factor: 4.982

2.  Garrod's fourth inborn error of metabolism solved by the identification of mutations causing pentosuria.

Authors:  Sarah B Pierce; Cailyn H Spurrell; Jessica B Mandell; Ming K Lee; Sharon Zeligson; Michael S Bereman; Sunday M Stray; Siv Fokstuen; Michael J MacCoss; Ephrat Levy-Lahad; Mary-Claire King; Arno G Motulsky
Journal:  Proc Natl Acad Sci U S A       Date:  2011-10-31       Impact factor: 11.205

Review 3.  Garrod's Croonian Lectures (1908) and the charter 'Inborn Errors of Metabolism': albinism, alkaptonuria, cystinuria, and pentosuria at age 100 in 2008.

Authors:  Charles R Scriver
Journal:  J Inherit Metab Dis       Date:  2008-10-12       Impact factor: 4.982

  3 in total

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