What
is a hormone?
As plants grow their genotype is expressed in the phenotype which is modified
by the environmental conditions that they experience. Somehow the rates of
growth and differentiation of cells in different parts of the plant are
coordinated in response to these inputs.
There
has to be communication between these levels: how does the plant receive and
respond to environmental inputs or "signals"? What comunication is
there inside the plant to adjust growth and development to the environment?
When
growing plants commercially we can ask similar questions:
- what environmental input will produce the kind of growth that we want?
- or can we modify the growth by applying a chemical regulator?
- can change the genotype to achieve the kind of growth we want (by traditional breeding or by genetic manipulation)?
The
answers to each of these questions depends on an understanding of how plant
growth is regulated. Hormones in animals cooordinate body functions by being
produced in one place and acting in another. Plants do not have a circulatory
system and "action at a distance" may not be a feature of plant
hormones. They are molecules that are not directly involved in metabolic or
developmental processes but they act at low concentrations to modify those
processes.
There
are five generally recognized classes of plant hormone, some of the classes are
represented by only one compound, others by several different compounds. They
are all organic compounds, they may resemble molecules which turn up elsewhere
in plant structure or function, but they are not directly involved as nutrients
or metabolites.
There
is only one naturally occurring auxin: indole-3-acetic acid (IAA) and this is
chemically related to the amino acid tryptophan.
There
are many synthetic auxins - aromatic compounds with carboxylic sidechains often
affect plant growth in the same way that IAA does. These are used commercially
rather than IAA because they are cheaper and more stable. For example
naphthalene acetic acid (NAA) is used to control fruit set and sucker growth on
trees after pruning. Indole butyric acid is used to promote rooting in
cuttings. Far and away the biggest use of auxin-like compounds is as herbicides
(2,4-D and MCPA). Applied at high concentration they promote uncoordinated
growth and finally death, particularly in broad-leaved weeds.
There
are a number of naturally occuring cytokinins all related to the nucleotide adenine. They can occur as the free base or as a
riboside. Synthetic cytokinins include benzyladenine and kinetin. Cytokinins
are used in tissue culture media, and for growth control in fruit.
Ethylene
Ethylene is the only gaseous hormone in
the plant world; it is a simple hydrocarbon gas that is derived from the amino acid, methionine, via an unusual cyclic
compound which is also an amino acid, ACC (1-aminocyclopropane-1-carboxylic
acid).
The
gas is used commercially for ripening fruit, particularly bananas. There are
also synthetic compounds, such as ethephon (chloro-ethanephosphonic acid) that
can be sprayed onto plants in solution; once inside the tissues ethephon breaks
down to liberate ethylene. Ethephon is used to promote ripening on the tree,
leaf abscision in ornamentals, growth control in seedlings and flowering in
pineapples.
Abscisic
acid (ABA) is one of two related compounds (the other is xanthoxin) that are in
the isoprenoid group and related to carotenoids ABA is a very expensive material and
so far there are no synthetic analogs or practical uses
The
gibberellins (GAs) are the largest group with over 70 compounds although not
all are biologically active. Like ABA they are derived from the isoprenoid pathway. Gibberellins are used
commercially to break dormancy of "difficult" seeds, and to promote
set of grapes and other fruits.
Many
growth retardants used on flowering pot plants, woody plants and turf are
"anti- gibberellins". Compounds such as ancymidol and uniconazole
block GA synthesis and produce dwarf plants. Genetic dwarfs are often deficient
in gibberellin.
Hormone
action
At the cell level hormones attach to a protein receptor which sends a signal down a transduction pathway to switch on particular genes. Through transcription and translation this leads to production of an enzyme protein which actually causes the change in plant growth. A good example from the early stages of plant development is the role of GA in cereal seed germination. As the seed imbibes water the embryo produces GA. This induces synthesis of amylase in the aleurone layer which secretes the enzyme to the endosperm. Amylase breaks down starch to glucose which diffuses to the embryo and is used for the early stages of plant growth.
At the cell level hormones attach to a protein receptor which sends a signal down a transduction pathway to switch on particular genes. Through transcription and translation this leads to production of an enzyme protein which actually causes the change in plant growth. A good example from the early stages of plant development is the role of GA in cereal seed germination. As the seed imbibes water the embryo produces GA. This induces synthesis of amylase in the aleurone layer which secretes the enzyme to the endosperm. Amylase breaks down starch to glucose which diffuses to the embryo and is used for the early stages of plant growth.
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