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Reprinted from New Beer in an Old Bottle: E duard Buchner and the Growth of
Biochemical Knowledge, pp. 25–31, ed. A . Cornish-Bowden, Universitat de
València, Spain, 1997
ALCOHOLIC FERMENTATION
WITHOUT YEAST CELLS*
Eduard Buchner
Until now it has not been possible to separate fermenting activity from
living yeast cells; the following describes a procedure that solves this
problem.
One thousand grams of brewer’s yeast1 that had been cleaned as
a prerequisite for the preparation of compressed yeast, but to which no
potato starch had been added, is carefully mixed with the same
weight of quartz sand2 and 250 g Kieselguhr. It is then triturated until
the mass has become moist and pliable. Now 100 g of water are added
to the paste, it is wrapped in filter cloth and gradually subj ected to a
pressure of 400–500 atmospheres: 350 cc press j uice are obtained. The
residual cake is again triturated, sieved, and 100 g water are added. A
further 150 cc of press j uice result when the cake is again subj ected to
the same pressure in the hydraulic press. One kg of yeast hence
yields 500 cc press j uice, containing about 300 cc cell substances.
Traces of turbidity are now removed by shaking the press j uice with
4 g of Kieselguhr and filtering through paper with repeated refiltration
of the first portions.
The resulting press j uice is a clear, slightly opalescent yellow
liquid with a pleasant yeast odour. A single determination of the spe-
cific gravity gave a value of 1.0416 (17°C). A large amount of coagu-
lum separates upon boiling, so that the liquid almost completely
*Preliminary Note, receiv ed 11 J anuary . Translated from Ber. D t. Chem.
Ges. 30, 117– 124 (1897) by H. C. Friedmann, taking ac
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