FREE BOOKS

Author's List




PREV.   NEXT  
|<   159   160   161   162   163   164   165   166   167   168   169   170   171   172   173   174   175   176   177   178   179   180   181   182   183  
184   185   186   187   188   189   190   191   192   193   194   195   196   197   198   199   200   201   202   203   204   205   206   207   208   >>   >|  
rally supposed that they are formed by the decomposition of proteins. But they are developed in only a few particular species of plants and are always present in these plants in fairly constant quantities. Hence, it appears that, in these species, the production of alkaloids is in some way definitely connected with protein metabolism; but it is certain that this is not a common relationship, as it is manifested by such a limited number of species of plants, and there is absolutely no knowledge as to its character and functions. Some authorities prefer to regard the alkaloids as waste-products of protein metabolism; but here, again, it is difficult to understand why such products should result in certain species of plants and not in others. THE PURINE BASES This is a group of compounds, widely distributed in both plant and animal tissues, all of which are derivatives of the compound known as _purine_, C_{5}H_{4}N_{4}. All of the naturally occurring compounds of this group may be regarded as derived from purine, either by the addition of oxygen atoms, or by the replacing of one or more of its hydrogen atoms with a methyl (CH_{3}) group or an amino (NH_{2}) group. The following structural formula represents the arrangement of the purine nucleus, the numbers being used to designate the nitrogen or carbon atoms to which the additional atoms, or groups, are attached in the more complex compounds of the group. In purine itself, the four hydrogen atoms are attached in the 2, 6, 7, and 8 positions. 6 1N==C-- | | 7 --2C 5C---N-- | | \ | | 8C-- | | // 3N--4C--9N The double bonds, in each case except those between the 4 and 5 carbon atoms, are easily broken apart and readjusted, so that other atoms or groups can be attached to any atom in the nucleus except the 4 and 5 carbon atoms. In all of the statements with reference to the structure of the purine bases, the term "oxy" is used to mean an oxygen atom attached by both its bonds to one of the carbons in the nucleus, instead of its customary use to mean the monovalent OH group replacing a hydrogen, as in the case of all other nomenclature of organic compounds. With this
PREV.   NEXT  
|<   159   160   161   162   163   164   165   166   167   168   169   170   171   172   173   174   175   176   177   178   179   180   181   182   183  
184   185   186   187   188   189   190   191   192   193   194   195   196   197   198   199   200   201   202   203   204   205   206   207   208   >>   >|  



Top keywords:
purine
 

plants

 

species

 

attached

 

compounds

 

hydrogen

 

carbon

 

nucleus

 

groups

 
products

oxygen

 

replacing

 

alkaloids

 

protein

 

metabolism

 

complex

 

additional

 
formula
 
arrangement
 
designate

structural

 

nitrogen

 

numbers

 

represents

 

structure

 

reference

 

statements

 

carbons

 
nomenclature
 

organic


monovalent
 
customary
 

readjusted

 
positions
 
easily
 
broken
 

double

 

naturally

 
manifested
 
limited

number
 

formed

 

relationship

 
connected
 
common
 

absolutely

 

authorities

 

prefer

 

functions

 

character