Glycosidic Bond

A glycosidic bond is formed between a hemiacetal group of a sugar molecule (such as glucose) and an alcohol functional group to form an acetal. A N-glycosidic bond is formed between the hemiacetal group of a sugar molecule (such as ribose) and a N-H group on an aromatic ring. An example of this is the bond between a nucleobase and the deoxyribose molecule in DNA. A glycosidic bond can also connect two monosaccharides, such as the linkage of glucose and fructose to create sucrose. It is simply the dehydration reaction between the hydroxide on the right edge of one sugar to the hydroxide on the left edge of the other sugar. A water molecule is extracted (causing a dehydration reaction), and a bond is formed, leaving an oxygen atom between the two monosaccharides, and creating a disaccharide.

 

<< PreviousWord BrowserNext >>
interstate 29
theory of multiple intelligences
interstate 83
jarnsaxa
interstate h 2
eva cassidy
chess in early literature
interstate h 3
chteau d'uss
dievturiba
plato's metaphor of the sun
loir et cher
star thistle
flushing meadows
flushing meadows park
candid camera
garret hobart
damage types (starcraft)
university of bonn
peabody award
mylodon
dory
kea
kakapo
ribofuranose
cytidine
dragoon (starcraft)
nucleobase
digital rights management
hemiacetal
body fluids in art
splash damage
acetal
nucleoside
daniel d tompkins
street basketball
uridine
paris brest paris
guggenheim museum bilbao
adenosine
richard mentor johnson
inosine
hypoxanthine
outsider music