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Appl Environ Microbiol. 1970 June; 19(6): 883-889
Copyright © 1970 American Society for Microbiology. All Rights Reserved.

Enzymatic Removal of Diacetyl from Beer ¹

III. Enzyme Protection and Regeneration of Cofactor

Department of Microbiology, Oregon State University, Corvallis, Oregon 97331

ABSTRACT

Use of diacetyl reductase, a reduced nicotinamide adenine dinucleotide (NADH)-requiring enzyme, to eliminate diacetyl off-flavor in beer was studied. The crude enzyme was extracted from Aerobacter aerogenes and partially purified by ammonium sulfate precipitation or Sephadex chromatography. In the semipure state, the enzyme was inactivated by lyophilization; in a crude state, the lyophilized extract remained stable for at least 4 months at — 20 C. A 50% reduction in specific activity within 5 min was observed when crude diacetyl reductase was suspended (5 mg of protein/ml) in phosphate buffer at pH 5.5 or below; a similar inactivation rate was observed when the crude enzyme was dissolved in a 5% aqueous ethyl alcohol solution. Effective crude enzyme activity in beer at a natural pH of 4.1 required protection of the enzyme in 10% gelatin. Incorporation of yeast cells with the gel-protected enzyme provided regeneration of NADH. Combinations of yeast, enzyme, and gelatin were tested to obtain data analyzed by regression analysis to determine the optimal concentration of each component of the system required to reduce the level of diacetyl in spiked (0.5 ppm) beer to less than 0.12 ppm within 48 hr at 5 C. The protected enzyme system was also effective in removing diacetyl from orange juice (pH 3.8) and some distilled liquors.

² Department of Chemical Engineering, Case Western Reserve University, Cleveland, Ohio.

³ Charles Pfizer and Sons, Inc., Milwaukee, Wis.

¹ Technical Paper no. 2825 from the Oregon Agricultural Experiment Station.