Scientific American Supplement, No. 275, April 9, 1881. Various
salt be used, it will be seen that the liquid immediately passes through the teguments Nos. 2, 3, 4, and 5, and stops abruptly before the embryo membrane No. 6, which will remain quite dry and brittle for several days, the berry remaining all the time in the water. Should the water penetrate further after several days, it can be ascertained that the entrance was gained through the part No 10 free of this tissue, and this notwithstanding the cells are full of fatty bodies. This membrane alone produces this action, for if the coatings Nos. 2, 3, 4, and 5 be removed, the resistance to the liquid remains the same, while if the whole, or a portion of it, be divided, either by friction between two millstones or by simple incisions, the liquid penetrates the berry within a few hours. This property is analogous to that of the radicules of roots, which take up the bodies most suitable for the nourishment of the plant. It proves, besides, that this membrane, like all those endowed with life, does not obey more the ordinary laws of permeability than those of chemical affinity, and this property can be turned to advantage in the preservation of grain in decortication and grinding.
To determine the action of this tissue through its presence, take 100 grammes of wheat, wash it and remove the first coating by decortication; then immerse it for several hours in lukewarm water, and dry afterwards in an ordinary temperature. It should then be reduced in a small coffee mill, the flour and middlings separated by sifting and the bran repassed through a machine that will crush it without breaking it; then dress it again, and repeat the operation six times at least. The bran now obtained is composed of the embryous membrane, a little flour adhering to it, and some traces of the teguments Nos. 2, 3, 4, and 5. This coarse tissue-weighs about 14 grammes, and to determine its action through its presence, place it in 200 grammes of water at a temperature of 86°; afterwards press it. The liquid that escapes contains chiefly the flour and cerealine. Filter this liquid, and put it in a test glass marked No. 1, which will serve to determine the action of the cerealine.
The bran should now be washed until the water issues pure, and until it shows no bluish color when iodized water and sulphuric acid are added; when the washing is finished the bran swollen by the water is placed under a press, and the liquid extracted is placed, after being filtered, in a test tube. This test tube serves to show that all cerealine has been removed from the blades of the tissue. Finally, these small blades of bran, washed and pressed, are cast, with 50 grammes of lukewarm water, into a test tube, marked No. 3; 100 grammes of diluted starch to one-tenth of dry starch are then added in each test tube, and they are put into a water bath at a temperature of 104° Fahrenheit, being stirred lightly every fifteen minutes. At the expiration of an hour, or at the most an hour and a half, No. 1 glass no longer contains any starch, as it has been converted into dextrine and glucose by the cerealine, and the iodized water only produces a purple color. No. 2 glass, with the same addition, produces a bluish color, and preserves the starch intact, which proves that the bran was well freed from the cerealine contained. No. 3 glass, like No. 1, shows a purple coloring, and the liquid only contains, in place of the starch, dextrine and glucose, i. e, the tissue has had the same action as the cerealine deprived of the tissue, and the cerealine as the tissue freed from cerealine. The same membrane rewashed can again transform the diluted starch several times. This action is due to the presence of the embryous membrane, for after four consecutive operations it still preserves its original weight. As regards the remains of the other segments, they have no influence on this phenomenon, for the coating Nos. 2, 3, 4, and 5, separated by the water and friction, have no action whatever on the diluted starch. Besides its action through its presence, which is immediate, the embryous membrane may also act as a ferment, active only after a development, varying in duration according to the conditions of temperature and the presence or absence of ferments in acting.
I make a distinction here as is seen, between the action through being present, and the action of real ferments, but it is not my intention to approve or disapprove of the different opinions expressed on this subject. I make use of these expressions only to explain more clearly the phenomena I have to speak of, for it is our duty to bear in mind that the real ferments only act after a longer or shorter period of development, while, on the other hand, the effects through presence are immediate.
I now return to the embryous membrane. Various causes increase or decrease the action of this tissue, but it may be said in general that all the agents that kill the embryous membrane will also kill the cerealine. This was the reason why I at first attributed the production of dark bread exclusively to the latter ferment, but it was easy to observe that during the baking, decompositions resulted at over 158° Fah., while the cerealine was still coagulated, and that bread containing bran, submitted to 212° of heat, became liquefied in water at 104°. It was now easy to determine that dark flours, from which the cerealine had been removed by repeated washings, still produced dark bread. It was at this time, in remembering my experiences with organic bodies, I determined the properties of the insoluble tissue, deprived of the soluble cerealine, with analogous properties, but distinguished not alone by its solid organization and state of insolubility, but also by its resistance to heat, which acts as on yeast. There exists, in reality, I repeat, a resemblance between the embryous membrane and the yeast; they have the same immediate composition; they are destroyed by the same poisons, deadened by the same temperatures, annihilated by the same agents, propagated in an analogous manner, and it might be said that the organic tissues endowed with life are only an agglomeration of fixed cells of ferments. At all events, when the blades of the embryous membrane, prepared as already stated, are exposed to a water bath at 212°, this tissue, in contact with the diluted starch, produces the same decomposition; the contact, however, should continue two or three hours in place of one. If, instead of placing these membranes in the water bath, they are enveloped in two pounds of dough, and this dough put in the oven, after the baking the washed membranes produce the same results, which especially proves that this membrane can support a temperature of 212° Fah. without disorganization. We shall refer to this property in speaking of the phenomena of panification.
CEREALINE.–The cells composing the embryous membrane contain, as already stated, the cerealine, but after the germination they contain cerealine and diastase, that is to say, a portion of the cerealine changed into diastase, with which it has the greatest analogy. It is known how difficult it is to isolate and study albuminous substances. The following is the method of obtaining and studying cerealine. Take the raw embryous membrane, prepared as stated, steep it for an hour in spirits of wine diluted with twice its volume of water, and renew this liquid several times until the dextrine, glucose, coloring matters, etc., have been completely removed. The membranes should now be pressed and cast into a quantity of water sufficient to make a fluid paste of them, squeeze out the mixture, filter the liquid obtained, and this liquid will contain the cerealine sufficiently pure to be studied in its effects. Its principal properties are: The liquid evaporated at a low temperature produces an amorphous, rough mass nearly colorless, and almost entirely soluble in distilled water; this solution coagulates between 158° and 167° Fah., and the coagulum is insoluble in acids and weak alkalies; the solution is precipitated by all diluted acids, by phosphoric acid at all the degrees of hydration, and even by a current of carbonic acid. All these precipitates redissolve with an excess of acid, sulphuric acid excepted. Concentrated sulphuric acid forms an insoluble downy white precipitate, and the concentrated vegetable acids, with the exception of tannic acid, do not determine any precipitate. Cerealine coagulated by an acid redissolves in an excess of the same acid, but it has become dead and has no more action on the starch. The alkalies do not form any precipitate, but they kill the cerealine as if it had been precipitated The neutral rennet does not make any precipitate in a solution of cerealine–5 centigrammes of dry cerealine transform in twenty-five minutes 10 grammes of starch, reduced to a paste by 100 grammes of water at 113° Fah. It will be seen that cerealine has a grand analogy with albumen and legumine, but it is distinguished from them by the action of the rennet, of the heat of acids, alcohol, and above all by its property of transforming the starch into glucose and dextrine.
It may be said that some albuminous substances have this property, but it must be borne in mind that these bodies, like gluten, for example, only possess it after the commencement of the decomposition. The albuminous matter approaching nearest to cerealine is the diastase, for it is only a transformation of the cerealine during the germination, the proof of which may be had in analyzing the embryous membrane, which shows more diastase and less cerealine in proportion to the advancement of the germination: it differs, however, from the diastase by