An unusual case of 'uncompetitive activation' by ascorbic acid: Purification and kinetic properties of a myrosinase from Raphanus sativus seedlings

Mikio Shikita, Jed W Fahey, Tamara R. Golden, W. David Holtzclaw, Paul Talalay

Research output: Contribution to journalArticle

Abstract

Myrosinase (thioglucoside glucohydrolase; EC 3.2.3.1) is a plant enzyme that hydrolyses glucosinolates, principally to isothiocyanates. Myrosinase was purified to homogeneity in good yield from 8-day-old seedlings of Raphanus sativus (daikon) using a four-step procedure involving chromatographies on anion exchange, hydrophobic Phenyl-Sepharose, gel filtration and concanavalin A-Sepharose. In order to stabilize the enzyme and to avoid excessive peak broadening during chromatography, 30% (v/v) glycerol was added to dialysis and chromatography buffers. The purified enzyme was eluted as a single peak from a gel-filtration sizing column with an apparent molecular mass of 120 kDa. The enzyme was resolved into two subunits with molecular masses of 61 and 62 kDa by SDS/PAGE. Ascorbic acid activated the purified enzyme more than 100-fold. The V(max) and K(m) values for the hydrolysis of allyl glucosinolate (sinigrin) were 2.06 μmol/min per mg of protein and 23 μM in the absence of ascorbate and 280 μmol/min per mg of protein and 250 μM in the presence of 500 μM ascorbate, respectively. As the ascorbate concentration was increased from 50 to 500 μM, the V(max) and K(m) values increased in parallel, and thus the V(max)/K(m) ratio remained constant. Similarly, raising the concentrations of sinigrin increased the concentration of ascorbic acid required for half-maximal activation (K2). At a sinigrin concentration of 250 μM, the K8 for ascorbic acid was 55 μM. Sulphate, a reaction product, was a competitive inhibitor of activity, having a K(i) of 60 mM with respect to sinigrin and of 27 mM with respect to ascorbate. Thus activation of myrosinase from R. sativus by ascorbic acid exemplifies an unusual and possibly unique example of linear 'uncompetitive activation' (i.e. a proportionate increase in V(max) and K(m)) of an enzyme. The enzyme also had β-glucosidase activity and hydrolysed p-nitrophenyl-β-D-glucopyranoside.

Original languageEnglish (US)
Pages (from-to)725-732
Number of pages8
JournalBiochemical Journal
Volume341
Issue number3
DOIs
StatePublished - Aug 1 1999

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Raphanus
Seedlings
Ascorbic Acid
Purification
Chemical activation
Kinetics
Enzymes
Chromatography
Glucosinolates
Molecular mass
Gel Chromatography
Hydrolysis
Thioglucosides
Gels
Isothiocyanates
Glucosidases
Dialysis
thioglucosidase
Reaction products
Glycerol

Keywords

  • β-thioglucoside
  • Glucohydrolase
  • Glucosinolate
  • Isothiocyanate
  • Sinigrin

ASJC Scopus subject areas

  • Biochemistry

Cite this

An unusual case of 'uncompetitive activation' by ascorbic acid : Purification and kinetic properties of a myrosinase from Raphanus sativus seedlings. / Shikita, Mikio; Fahey, Jed W; Golden, Tamara R.; Holtzclaw, W. David; Talalay, Paul.

In: Biochemical Journal, Vol. 341, No. 3, 01.08.1999, p. 725-732.

Research output: Contribution to journalArticle

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KW - β-thioglucoside

KW - Glucohydrolase

KW - Glucosinolate

KW - Isothiocyanate

KW - Sinigrin

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