Natural polymers include the RNA and DNA that are so important in genes and life processes. In fact, messenger RNA is what makes possible proteins, peptides, and enzymes. Enzymes help do the chemistry inside living organisms and peptides make up some of the more interesting structural components of skin, hair, and even the horns of rhinos. Other natural polymers include polysaccharides (sugar polymers) and polypeptides like silk, keratin, and hair. Natural rubber is, naturally a natural polymer also, made from just carbon and hydrogen. Let's look at each of the main families of natural polymers closely.
DNA and RNA
RNA and DNA contains polymer backbones which are based on sugar
units. This makes them polysaccharides, although in the case
of RNA and DNA, there are well ordered groups attached to the
sugar units that give these polymers their unique capabilities.
Wood and Potatoes
Another family of polysaccharides includes starch and cellulose.
Starch
is a high molecular weight polysaccharide. Foods like bread, corn, and
potatoes are full of starch. Starch may
have as many as 10,000 sugar units all linked together. The way these
units link up, all in a linear arrangement or with some of them
forming branches, determines what kind of starch or polysaccharide
it is (more about this later). Another very important member
of the polysaccharide family is cellulose.
This is the main polymer that makes up plants and trees. Wood is
primarily cellulose This
polymer is different than starch. (Click here
to find out more.) Starch is soluble n hot water and can easily
be made into useful objects. Cellulose, on the other hand, is
highly crystalline
and almost totally insoluble in anything. Cotton is a form of
cellulose that we use in most of our clothes. The fact that it
is insoluble in hot water is important. Were it otherwise our
clothes would dissolve when we washed them. Cellulose also has
the neat property that when you wet it and run a hot iron over
it, it smoothes out and flattens down. This makes our cotton
clothes look nice (at least for a little while) but still allows
them to clean up easily when we wash them.
Chemically, chitin is poly(N-acetylglucosamine). Here's it's
structure:
As you take a look more closely at each member of these families
of natural polymers, remember this: nature was there first, by
a long shot! One of our jobs as scientists is to figure out
how nature does such a good job so that we can imitate it. For
example, once we figured why silk had such neat properties we
were able to make synthetic silk in the form of nylons.
We still have a long way to go, though, before we can make synthetic
RNA and DNA that will lead to synthetic life. While we may never
get there, trying to figure out how is fun and leads to lots of
important developments in synthetic polymers and other areas including
medicine and biochemistry. This raises the important point that
science is like life. It doesn't deal with just one thing, but
everything mixed together. Polymer science isn't the only science,
and it may not even be the most important science (although we
in the business like to think it is!). It is one of the areas
that can help us understand and use the knowledge we get from
studying nature. In this way, we develop technology.
(Note: Just to clear up this whole science-and-technology question,
science and technology are two different things. Science is the
act of gathering knowledge by observation and experimentation.
Technology is putting this knowledge to use. Example: Using
science we learn that hot gasses expand. Then using technology,
we use the principle hot gasses expanding to make a gasoline engine
that can power a car. See how it works?)
The differences between how nature does nylons and how we do
it is striking. We mostly make nylons from molecules that have
lots of CH2 groups in them. The section on nylons
shows structures for nylon 6 and nylon 6,6, two of the most common
synthetic polyamides. They possess four, five, or six CH2
groups between amide units. Nature, however, is much more economical,
choosing to use only a single carbon between amide groups. What
nature does differently is to substitute this carbon with lots
of different functional segments and groups.
This results in
two key properties. First, the individual segments and the entire
molecule are optically active, or chiral. This means they
are like gloves: there are both right and left and versions.
For some reason, nature chose to use only the left hand version
of the amino acids that are synthesized by plants and animals.
The fact that only one of the two isomers is used leads to some
neat stereochemical consequences. For example, natural polypeptides
can form helical structures while nylons can't. The helical conformations
increase the stability of the natural polypeptides. Did you know
that some bacteria can survive in boiling water? This is because
their natural polymers have been stabilized by such helical
structures. The figure below shows one such helical structure,
called an a-helix.
Small segments of such helical structures are what nature uses
to mold enzymes into certain shapes so that they can do their
catalytic magic. For example, a flexible randomly coiled segment
may be joined by two a-helix segments
so that they can react together on some substrate.
Another key difference between polypeptides and nylons is the
way they are made. We humans make nylons in tons per day in huge
chemical plants where simple molecules are joined together in
large quantities to give products that we need or want. Nature
is much more careful and concise in how she does things. For
a living organism to make an enzyme, another enzyme or active
species must be involved. The synthesis always involves a template,
or recording, of how the individual amino acids are to be joined
together to give the final polymer. This template, or map is
a messenger RNA (mRNA). The message it carries, of course, is
how the peptide-making enzyme involved should make the polypeptide.
Each amino acid is brought to the enzyme by a carrier molecule
and is activated for incorporation by a whole cascade family of
reaction steps. The enzyme adds a single amino acid, one at a
time, as indicated by the mRNA. This is a slow and tedious process
and takes a long time. Sometimes the enzyme gets frustrated,
waiting for the right amino acid to come along, and slaps a wrong
one on instead. To compensate this the enzyme is made to back
up occasionally to check its work. If it has made a mistake,
it has a process for clipping out the wrong amino acid and inserting
the right one. We humans never do this. If we make a mistake,
we simply grind it up and throw it away.
Chitin: The Polymer for the Seafood Lover in You!
Another member of the polysaccharides is chitin. It makes up the shells
of crawfish, shrimp, crabs, lobsters, and other crustaceans. It is hard,
insoluble
and yet
somehow flexible. We haven't figured out how to make synthetic polymers
that have this neat combination of properties. We also haven't
figured out how to do much with chitin, although we do use cellulose
for a lot of chemical applications and to make paper, wooden
houses, wooden shoes, and the like. There's a lot of research
underway to use chitin for different stuff, and maybe someday
we'll make clothes or plastic out of it. This is an area of research
that its important since it uses natural polymers that come from
renewable resources or waste products. (Do you know how many
shrimp lose their shells every year for us?)
We Learn from Nature
Proteins and Polypeptides
Proteins
Proteins were the first examples of polyamides (a
fancy word
for nylon).
Both share many common traits but they are very different in
how they are made and in their physical properties. They are
alike in that the both contain amide linkages in the backbone.
Amides are made from carboxylic acid groups and amine groups
through the loss of water. (For more on this click
here.)
The amide molecular segment is unique in its structure and intermolecular
interactions. Because of the hybridization of the nitrogen, carbon,
and oxygen of the amide group, the segment is basically flat.
More importantly, the hydrogen on the nitrogen and the carbonyl
oxygen are capable of a strong interaction called a hydrogen bond.
Because of this, the amide groups like each other some much that
they for strong associations that give amide-containing polymers
unusual properties. This type of interaction is also discussed
in the section on nylons, and is the key similarity between natural
and synthetic polyamides.
Enzymes
Enzymes are one of the key types of polypeptides and are crucial
to life on earth. All living organisms use enzymes to make, modify,
and chop up the polymers discussed here. Enzymes are the catalysts
that do specific jobs. In fact, oftentimes each enzyme does only
one type of job or makes only one kind of molecule. This means
that there have to be lots of different enzymes, all made of different
combinations of amino acids joined in unique ways in polypeptides,
to do all the jobs that any living organism needs done. We know
that every creature on earth has hundreds or even thousands of
different enzymes to do all the jobs that it requires. What's
really strange is that each one of the enzymes has to be made
by other enzymes. This leads to very complicated control mechanisms:
we don't have the faintest idea (in most cases) how nature decides
what enzymes need to be made and when, or how the enzymes are
turned on and off. We are beginning to figure this out, and the
study of such systems is an important part of biochemistry and
biology.
Riding Down the Silk Road
One of the unique polypeptides that we used very early for its
superb properties was silk. Silk was discovered by the Chinese
long before the birth of Christ. Silk is made by tiny caterpillars
trying to spin cocoons for their transformation into moths. We
steal the silk from the caterpillars which leaves them in limbo,
pretty much. The silk is spun into fibers.
Bundles of very thin individual polymers joined together to be
stronger. This is the way we also make rope, using weak individual
strands bound together in such a way that the total is both flexible
and strong. The structure of silk molecules is unusual for a
polypeptide. It possesses lots of the unsubstituted amino acid,
glycine. Glycine segments are able to form flat extended chains
that can pack together nice and tightly. This gives silk its
unique strength and shiny flexibility. Silk has such unique properties,
especially in hot wet climates, that it dominated trade for centuries
in east Asia. The silk trade between Japan and China controlled
the economics of civilizations in that region for longer than
either country cares to admit. Even in America, silk was important
before World War II for use in silk stockings. When silk was
used for parachute cord, women in America got very upset. This
resulted in chemical companies synthesizing artificial silk, nylon,
to make nylon stockings so that women's feet could stay warm and
the men could go back to fighting their wars.
Return to Level Three Directory |
Return to Macrogalleria Directory |