Some structural aspects of vanadium bromoperoxidase from Ascophyllum nodosum.

The stability of the vanadium containing bromoperoxidase from Ascophyllum nodosum was studied. The enzyme was very resistant against chemical denaturation. Denaturation did not occur upon incubation in 4 M guanidine hydrochloride. Circular dichroism measurements showed that the secondary structure was not affected upon incubation in 4% sodium dodecyl sulphate. The sedimentation coefficient and the molecular mass, determined by ultracentrifugation were 6.96 S and 97 kDa, respectively, indicating a very compact molecule. The protein molecule contained 16 cysteine residues, all of which participated in the formation of disulfide bridges. Circular dichroism-measurements in the far ultraviolet region revealed that the protein consisted of a large amount of alpha-helix (74%), and no beta-pleated sheet. The dissociation constant of the apoprotein vanadium-complex was 55 nM (at pH 8.5), and rapidly increased at lower pH. The data suggest that the protonation of a group with a pKa higher than 8.5 prevents the binding of vanadate. Structural analogues of vanadate (phosphate and arsenate) were competitive inhibitors with respect to the reconstitution of the bromoperoxidase. The inhibition constants were 60 and 120 microM for phosphate and arsenate, respectively. The binding of hydrogen peroxide to the enzyme was visualized by optical spectroscopy. Upon addition of H2O2 the optical absorption spectrum showed a small, but significant, decrease in absorption in the 315 nm region, which was restored upon addition of bromide, or by allowing the solution to stand for several hours. These changes are ascribed to the formation of a stable enzyme-peroxo-intermediate, in line with a previous analysis of the steady-state kinetics.

The brown alga Ascophyllum nodosum contains two different vanadium bromoperoxidases.

Haloperoxidases have been detected in a variety of organisms, including bacteria, fungi, algae, and mammals. Mammalian haloperoxidases are known to be directly involved in the oxidative destruction of microorganisms. The algal bromoperoxidases are probably involved in the biosynthesis of bromometabolites, most of which show considerable bactericidal activity. From the brown seaweed Ascophyllum nodosum (order, Fucales) two different bromoperoxidases have been isolated, which both contain vanadium as an essential element for enzymic activity. The location of these two enzymes, determined by activity staining of cross-sections of algal parts, was different. Bromoperoxidase I (which has been described before) was located inside the thallus, particularly around the conceptacles, whereas bromoperoxidase II was present at the thallus surface of the alga. The molecular masses of these bromoperoxidases as judged from sodium dodecyl sulfate-gel electrophoresis were 97 and 106 kDa, respectively. Some of the enzymatic properties (pH optimum and Km for bromide) of the two enzymes were slightly different, whereas the amino acid compositions were more or less equal. The isoelectric point of the two proteins was the same, namely 5.0. On sodium dodecyl sulfate-polyacrylamide gels both enzymes could be stained with periodic acid Schiff's reagent, so both are glycoproteins. Since only bromoperoxidase II could be bound to a concanavalin A-Sepharose column, these enzymes contain different carbohydrates. Both enzymes display a considerable thermostability. However, the chemical stability of the two bromoperoxidases differed. Bromoperoxidase II could also be inactivated by dialysis at low pH and reactivation was only possible with the transition metal vanadium and not with other metal ions. The presence of vanadium in this enzyme could be established with atomic absorption spectrophotometry and electron paramagnetic resonance. The EPR signals of both bromoperoxidases, which were observed after reduction with sodium dithionite, were similar: only minor differences were observed in the hyperfine coupling. In immunoblotting experiments these two bromoperoxidases were found to cross-react, so they have common antigenic determinants.

Vanadium containing bromoperoxidase: An example of an oxidoreductase with high operational stability in aqueous and organic media.

The conversion is described of phenolsulphonephtalein (phenol red) to 3,3',5,5'-tetrabromophenolsulphonephthalein (bromophenol blue) by bromoper-oxidase from the brown alga Ascophyllum nodosum. This reaction provides a convenient assay for the detection of bromoperoxidase activity in vitro. Bromoperoxidase was shown to be stable under turnover conditions for three weeks at room temperature, catalyzing the bromination of phenol red into bromophenol blue. When stored at room temperature in organic sol vents such as acetone, methanol, ethanol [present up to 60% (v/v)], and 1-propanol [40% (v/v)], bromoperoxidase was stable for more than one month. As far as we know this is the first example of an oxidoreductase which displays such great stability. This enhances the applicability of the enzyme in organic synthesis.