Carbohydrates
Biological significance
Role in plant and animal structure
In the early part of the 19th century,
substances such as wood, starch, and linen were found to be composed mainly of
molecules containing atoms of carbon (C), hydrogen (H), and oxygen (O) and to have the general formula C6H12O6
Other organic
molecules with similar formulas were found to have a similar ratio of hydrogen
to oxygen. The general formula Cx(H2O)y is commonly used to represent many carbohydrates, which means
“watered carbon.”
Classification Of
Carbohydrates
Slight changes in
structural arrangements are detectable by living things and influence the
biological significance of isomeric compounds.
It is known, for
example, that the degree of sweetness of various sugars differs according to
the arrangement of the hydroxyl groups (―OH) that
compose part of the molecular structure. A direct correlation that may exist
between taste and any specific structural arrangement, however, has not yet been
established; that is, it is not yet possible to predict the taste of a sugar by
knowing its specific structural arrangement.
Two molecules of a simple sugar that are linked to each other form a disaccharide, or double sugar. The disaccharide sucrose, or table sugar,
consists of one molecule of glucose and one molecule of fructose; the most
familiar sources of sucrose are sugar beets and cane sugar. Milk sugar, or lactose, and maltose are also
disaccharides.
Before the energy in disaccharides can be
utilized by living things, the molecules must be broken down into their
respective monosaccharides.
Oligosaccharides, which consist of
three to six monosaccharide units, are rather infrequently found in natural
sources, although a few plant derivatives have been identified.
Polysaccharides (the term means many sugars) represent most of
the structural and energy-reserve carbohydrates found in nature.
Several hundred
distinct types have thus far been identified. Cellulose, the principal structural component of plants, is a complex polysaccharide comprising many glucose units linked together; it is the most
common polysaccharide.
The starch found in plants and the glycogen found in animals also are complex glucose
polysaccharides.
Starch (from the
Old English word stercan, meaning “to
stiffen”) is found mostly in seeds, roots, and stems, where it is stored as an
available energy source for plants.
Large molecules
that may consist of as many as 10,000 monosaccharide units linked together,
polysaccharides vary considerably in size, in structural complexity, and in
sugar content; several hundred distinct types have thus far been
identified.
Cellulose, the principal structural component of plants, is a complex polysaccharide comprising many glucose units
linked together;
it is the most common polysaccharide.
The starch found
in plants and the glycogen found in animals also are complex glucose
polysaccharides.
Starch (from the
Old English word stercan,
meaning “to stiffen”) is found mostly in seeds, roots, and stems, where it is
stored as an available energy source for plants. Plant starch may be processed
into foods such as bread, or it may be consumed directly—as in potatoes, for instance.
Glycogen, which
consists of branching chains of glucose molecules, is formed in the liver and muscles of higher
animals and is stored as an energy source.
.
The generic nomenclature ending for the monosaccharides is -ose; thus, the term pentose (pent = five) is
used for monosaccharides containing five carbon atoms, and hexose (hex = six) is
used for those containing six.
Biological significance
The importance of carbohydrates to living things can hardly be
overemphasized. The energy stores of most animals and plants
are both carbohydrate and lipid in
nature; carbohydrates are generally available as an immediate energy source,
whereas lipids act as a long-term energy resource and tend to be utilized at a
slower rate.
Glucose, the prevalent
uncombined, or free, sugar circulating in the blood of higher
animals, is essential to cell function.
The proper regulation of glucose metabolism is
of paramount importance to survival.
The ability of ruminants,
such as cattle, sheep, and goats, to convert the polysaccharides present in
grass and similar feeds into protein provides
a major source of protein for humans.
A number of medically
important antibiotics, such as streptomycin, are
carbohydrate derivatives. The cellulose in
plants is used to manufacture paper, wood for construction, and fabrics.
During photosynthesis, an immediate
phosphorous-containing product known as 3-phosphoglyceric acid is formed.
This compound then is transformed into cell wall components such as cellulose,
varying amounts of sucrose, and starch—depending on the plant
type—and a wide variety of polysaccharides, other than cellulose and starch,
that function as essential structural components. For a detailed discussion of
the process of photosynthesis, see photosynthesis.
Role in plant and animal structure
Whereas starches and glycogen represent the major reserve
polysaccharides of living things, most of the carbohydrate found in nature
occurs as structural components in the cell walls of plants.
Carbohydrates in plant cell walls generally consist of several
distinct layers, one of which contains a higher concentration of cellulose than
the others.
The physical and chemical
properties of cellulose are strikingly different from those of the amylose
component of starch.
In most plants, the cell wall is about 0.5 micrometre thick
and contains a mixture of cellulose, pentose-containing polysaccharides
(pentosans), and an inert (chemically unreactive) plastic-like material called lignin.
The amounts of cellulose and pentosan may vary; most plants
contain between 40 and 60 percent cellulose, although higher amounts are
present in the cotton fibre.
Polysaccharides also function as major structural
components in animals. Chitin, which is similar to cellulose, is
found in insects and other arthropods.
Other complex polysaccharides predominate in the structural tissues of higher
animals.
Representative
disaccharides and oligosaccharides
common name
|
component
sugars
|
linkages
|
sources
|
*The linkage joins carbon atom 1 (in the β
configuration) of one glucose molecule and carbon atom 4 of the second
glucose molecule; the linkage may also be abbreviated β-1, 4.
|
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**Note that raffinose and stachyose are
galactosyl sucroses.
|
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cellobiose
|
glucose, glucose
|
β1 → 4*
|
hydrolysis of cellulose
|
gentiobiose
|
glucose, glucose
|
β1 → 6
|
plant glycosides, amygdalin
|
isomaltose
|
glucose, glucose
|
α1 → 6
|
hydrolysis of glycogen, amylopectin
|
raffinose**
|
galactose, glucose, fructose
|
α1 → 6, α1 → 2
|
sugarcane, beets, seeds
|
stachyose**
|
galactose, galactose, glucose, fructose
|
α1 → 6, α1 → 6, α1 → 2
|
soybeans, jasmine, twigs, lentils
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