Literature DB >> 3495900

Vitamin K-dependent carboxylase: increased efficiency of the carboxylation reaction.

B A Soute, M M Ulrich, C Vermeer.   

Abstract

The in vitro vitamin K-dependent carboxylation of peptide- or protein-bound glutamate residues is generally studied in detergent-solubilized microsomes from rat or cow liver. Under the conditions usually employed, the efficiency of the carboxylation reaction is low (less than 1% of the carboxylatable residues is converted into gammacarboxyglutamate). Here we describe that this efficiency may be raised to 30% by carrying out the following adaptations: 1) carboxylase was purified about 100-fold from the solubilized microsomes, so that the enzyme was obtained in a highly concentrated form and could be added in excess: 2) the HCO-3 concentration in the reaction mixtures was raised to 50 mM and 3) a substrate was selected (decarboxylated osteocalcin from bovine bone) the Km of which had been shown to be low (10 microM) and it was added in rate-limiting amounts. Besides the fact that under these conditions the carboxylation reaction occurred with a higher efficiency than before, the adaptations also enabled us to express the carboxylation activity in terms of moles CO2 incorporated per mole of substrate.

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Year:  1987        PMID: 3495900

Source DB:  PubMed          Journal:  Thromb Haemost        ISSN: 0340-6245            Impact factor:   5.249


  5 in total

Review 1.  Gamma-carboxyglutamate-containing proteins and the vitamin K-dependent carboxylase.

Authors:  C Vermeer
Journal:  Biochem J       Date:  1990-03-15       Impact factor: 3.857

2.  Functional Study of the Vitamin K Cycle Enzymes in Live Cells.

Authors:  J-K Tie; D W Stafford
Journal:  Methods Enzymol       Date:  2016-11-22       Impact factor: 1.600

3.  Vitamin K-dependent carboxylase: affinity purification from bovine liver by using a synthetic propeptide containing the gamma-carboxylation recognition site.

Authors:  B R Hubbard; M M Ulrich; M Jacobs; C Vermeer; C Walsh; B Furie; B C Furie
Journal:  Proc Natl Acad Sci U S A       Date:  1989-09       Impact factor: 11.205

4.  A mutation in the propeptide of Factor IX leads to warfarin sensitivity by a novel mechanism.

Authors:  K Chu; S M Wu; T Stanley; D W Stafford; K A High
Journal:  J Clin Invest       Date:  1996-10-01       Impact factor: 14.808

5.  Stimulation of the dithiol-dependent reductases in the vitamin K cycle by the thioredoxin system. Strong synergistic effects with protein disulphide-isomerase.

Authors:  B A Soute; M M Groenen-van Dooren; A Holmgren; J Lundström; C Vermeer
Journal:  Biochem J       Date:  1992-01-01       Impact factor: 3.857

  5 in total

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