Alcoholic Fermentation: Second Edition, 1914Harden, Arthur
Science
Alcoholic Fermentation: Second Edition, 1914
Harden, Arthur
Fermentation
The reaction is produced by all races of brewer's yeast which have
been tried, as well as by active yeast preparations and extracts and
by wine yeasts [Neuberg and Karczag, 1911, 4; Neuberg and Kerb, 1912,
2]. The phenomenon can readily be exhibited as a lecture experiment by
shaking up 2 g. of pressed yeast with 12 c.c. of 1 per cent. pyruvic
acid, placing the mixture in a Schrötter's fermentation tube, closing
the open limb by means of a rubber stopper carrying a long glass
tube and plunging the whole in water of 38-40°. Comparison tubes of
yeast and water and yeast and 1 per cent. glucose may be started at
the same time, and it is then seen that glucose and pyruvic acid are
fermented at approximately the same rate [Neuberg and Karczag, 1911,
1]. If English top yeast be used it is well to take 0·5 per cent.
pyruvic acid solution and to saturate the liquids with carbon dioxide
before commencing the experiment. The production of acetaldehyde can
be readily demonstrated by distilling the mixture at the close of
fermentation and testing for the aldehyde either by Rimini's reaction
(a blue coloration with diethylamine and sodium nitroprusside) or by
means of p-nitrophenylhydrazine which precipitates the hydrazone,
melting at 128·5° [Neuberg and Karczag, 1911, 2, 3]. [p082]
As the result of quantitative experiments it has been shown that 80
per cent. of the theoretical amount of acetaldehyde can be recovered.
The salts of the acids are also attacked, the carbonate of the metal,
which may be strongly alkaline, being formed. Thus taking the case
of pyruvic acid, the salts are decomposed according to the following
equation:--
2CH{3}·CO·COOK + H{2}O = 2CH{3}·CHO + K{2}CO{3} + CO{2}.
Under these conditions a considerable portion of the aldehyde
undergoes condensation to aldol [Neuberg, 1912]:--
2CH{3}·CHO = CH{3}·CH(OH)·CH{2}·CHO.
This change appears to be due entirely to the alkali and not to an
enzyme since the aldol obtained yields inactive β-hydroxybutyric
acid on oxidation [Neuberg and Karczag, 1911, 3; Neuberg, 1912]. The
various preparations derived from yeast which are capable of producing
alcoholic fermentation also effect the decomposition of pyruvic acid
in the same manner as living yeast. They are, however, more sensitive
to the acidity of the pyruvic acid, and it is therefore advisable to
employ a salt of the acid in presence of excess of a weak acid, such
as boric or arsenious acid, which decomposes the carbonate formed but
has no inhibiting action on the enzyme [Harden, 1913; Neuberg and
Rosenthal, 1913].
Public-domain text, read in full here on John Shaqi.
Reviews
Reviews
No reviews yet
Be the first to share your thoughts on this work.
Elsewhere in the archive
Join the Discussion
Join the discussion
Sign in to leave a comment or review.
Sign InorCreate an account