physical shape of starch granules. If wheat starch is compared with maize at low
moisture and low screw speed the energy inputs are fairly similar, but at high
screw speed the maize creates almost twice as much specific mechanical energy
(SME) as the wheat starch. This is probably because of the polygonal shape of
almost half of the starch granules found in normal samples of maize compared
with the smooth globular or lenticular granules of wheat.
Composition of granules
The major constituents of starch granules, representing 97–98% of the dry
matter, are the two physical forms of starch, amylose (AM) and amylopectin
(AP). In addition there are trace amounts of lipid (0.5–1%), mainly in the form
of lysolecithin, dispersed throughout the starch rings and 0.1 to 0.2% of proteins
adhering to the surface layers.
5
The two starch polymers each represent a
polydisperse fam ily in terms of the molecular size range.
Amylose (AM) polymers range in size from 100 to 200 kD and are linear
polymers with one or two branches at C-6 of a glucose residue. They complex
with lysolecithin and similar monoacyl lipids of saturated fatty acids > 6 carbon
atoms. There are variations in AM levels in starches from different cereals and
tubers and within varieties from the same types. In wheat, rye and oats the levels
of AM are normally within 20–27% of the total starch but in maize, barley and
rice it can vary from 5 to 30% and for maize it can be as high as 70%. The
highest levels are found in the amylomaize and the lowest forms in the waxy
barley, maize or rice.
Starch polymers are formed in nature from glucose units, during the
development of the seeds on the plants. A linear polymer of 100 to 200 glucose
units is formed which has been called amylose (AM). Some of the linear chains
are built up into larger branched chain molecules called amylopectin (AP).
These are very large polydisperse molecules up to 10
8
D in molecular weight
containing 500,000 glucose units. The structure of AP is dendritic with a main
chain resembling the tru nk of a tree and secondary chains as the larger branches
and many smaller chains as the fine twig-like branches. These outer chains are
20 glucose units in length and can link the AP trees together in intermolecular
double helices to form a rigid struct ure.
Amylopectin (AP) polymers are much larger than AM and their molecular
ranges are difficult to measure because the procedures used to isolate these giant
molecules can easily lead to degradation. The ranges reported are from 2 to
10
8
D but there are n o accurate comparisons of AP from different cereal or tubers
types. The interactions between the chains are difficult to release without
breaking the main chains and reducing the polymer size. It is easier to measure
the lengths of the side chains by hydrolysing the whole molecule with a
debranching enzyme such as pullulanase. This enzyme releases all the starch
chains from the main tree-like structure as small molecules of 16–20 glucose
units or 3 to 4 kD. These relatively short outer chains serve to form the
intermolecular bonds between individual AP molecules and are used to explain
the differences in stability to retrogradation of different forms of cereal starch.
14 Extrusion cooking