You are here

قراءة كتاب Animal Proteins

تنويه: تعرض هنا نبذة من اول ١٠ صفحات فقط من الكتاب الالكتروني، لقراءة الكتاب كاملا اضغط على الزر “اشتر الآن"

‏اللغة: English
Animal Proteins

Animal Proteins

تقييمك:
0
No votes yet
المؤلف:
دار النشر: Project Gutenberg
الصفحة رقم: 3

colspan="2">GELATINE AND GLUE.

1. PROPERTIES OF GELATINE AND GLUE. 200 2. RAW MATERIALS AND PRELIMINARY TREATMENT. 220 3. EXTRACTION. 230 4. CLARIFICATION AND DECOLORIZATION. 234 5. BLEACHING. 241 6. EVAPORATION. 248 7. COOLING AND DRYING. 255 8. USES OF GELATINE AND GLUE. 260 9. THE EVOLUTION OF THE GELATINE AND GLUE INDUSTRY. 265
PART VI. MISCELLANEOUS PROTEINS AND BYE-PRODUCTS. 1. BYE-PRODUCTS OF THE LEATHER TRADES. 268 2. BYE-PRODUCTS OF THE GELATINE AND GLUE TRADES. 272 3. FOOD PROTEINS. 274 4. MISCELLANEOUS ANIMAL PROTEINS. 279     INDEX. 283

ANIMAL PROTEINS


INTRODUCTION

Proteins are organic compounds of natural origin, being found in plants and in animals, though much more plentifully in the latter. They are compounds of great complexity of composition, and of very high molecular weight. The constitution of none of them is fully understood, but although there are a great number of different individual proteids, they present typical resemblances and divergences which serve to differentiate them from other groups of organic bodies, and also from one another.

Proteins resemble one another in both proximate and ultimate analysis. They contain the usual elements in organic compounds, but in proportions which do not vary over very wide limits. This range of variation is given approximately below:—

Element. Per cent.
Carbon 49 to 55
Hydrogen 6.4 to 7.3
Oxygen 17 to 26
Nitrogen 13 to 19
Sulphur 0.3 to 3.0


The most characteristic feature of the protein group is the amount of nitrogen usually present. This is generally nearer the higher limit, seldom falling below 15 per cent. This range for the nitrogen content is determined largely by the nature of constituent groups which go to form the proteid molecule. Roughly speaking, proteins consist of chains of amido-acids and acid amides with smaller proportions of aromatic groups, carbohydrate groups and thio compounds attached. In these chains an acid radical may combine with the amido group of another amido acid, the acid group of the latter combining with an amido group of another amido acid, and so on. Hydrogen may be substituted in these chains by alkyl or aromatic groups. There is obviously infinite possibility of variation in constitution for compounds of this character, the general nature of which varies very little. Practically all of the proteins are found in the colloid state, and this makes them very difficult to purify and renders the ultimate analysis in many cases doubtful. It is, for example, often difficult to ascertain their moisture content, for many are easily hydrolyzed with water only, and many part easily with the elements of water, whilst on the other hand many are lyophile colloids and practically cannot be dehydrated or dried. A few, such as gelatin and some albumins, have been crystallized.

The constituent groups have been investigated chiefly by hydrolytic methods. The chains of amido acids are split up during hydrolysis, and individual amido acids may thus be separated. The hydrolysis may be assisted either by acids, alkalies or ferments, but follows a different course according to the nature of the assistant. Under approximately constant conditions of hydrolysis, the products obtained are in approximately constant proportions, and this fact has been utilized by Van Slyke in devising a method of proximate analysis. It is not possible in this volume to enter deeply into the constitution of the different proteids. Reference must be made to works on pure chemistry, especially to those on advanced organic chemistry. It will be interesting, however, to mention some of the amido acids and groups commonly occurring in proteids. These comprise ornithine (1:4 diamido valeric acid), lysine (1:5 diamido-caproic acid), arginine (1 amido, 4 guanidine valeric acid), histidine, glycine (amidoacetic acid), alanine (amido propionic acid), amido-valeric acid (amido-iso-caproic acid), liacine, pyrollidine carboxylic acid, aspartic acid, glutamic acid (amido-glutaric acid), phenyl-alanine, serine (hydroxy-amido propionic acid), purine derivatives (e.g. guanine), indol derivatives (e.g. tryptophane and skatol

Pages