Cyanogenic glycosides are chemical compounds that occur
naturally in many plants, including species of Prunus (wild cherry), Sambucus
(elderberry), Manihot (cassava), and Linum (flax), Bambusa (bamboo), and Sorghum
(sorghum). Chemically, they are defined as glycosides of the a-hydroxynitriles.
These compounds are potentially toxic as they are readily broken down by
enzymic hydrolysis to liberate hydrogen cyanide when the plant suffers physical
damage. Occurrence in Foods There are approximately 25 known cyanogenic
glycosides, and a number of these can be found in the edible parts of some
important food plants.
These include amygdalin (almonds), dhurrin (sorghum),
lotaustralin (cassava), linamarin (cassava, lima beans), prunasin (stone fruit), and taxiphyllin (bamboo shoots). Some of the main food sources of cyanogenic
glycosides and their estimated potential yield of hydrogen cyanide are released on
hydrolysis. Bitter apricot kernels have been marketed as a health food in the
UK and elsewhere. They can contain high levels of the cyanogenic glycoside
amygdalin.
Effects on Health
The toxicity of a cyanogenic plant depends
largely on the amount of hydrogen cyanide that could be released on consumption
of the plant. Adequate processing or preparation is required to ensure that
detoxification of the food is complete before consumption. However, if the
processing or preparation is insufficient to ensure detoxification, the
potential hydrogen cyanide concentration released during consumption can be
high.
Upon consumption of the food, the enzyme b-glycosidase will be released
and hydrolysis of the cyanogenic glycoside will commence, resulting in hydrogen
cyanide formation. Certain gut microflora also produces b-glycosidases, which
can contribute to the breakdown of cyanogenic glycosides into hydrogen cyanide.
Hydrogen cyanide is cytotoxic and blocks the activity of cytochrome oxidase –
an enzyme critical for cellular respiration.
When cytochrome oxidase is
blocked, ATP production stops, and cellular organelles cease to function.
However, cyanide is readily detoxified in animals as all animal tissues contain
the enzyme rhodanese – a thiosulfate sulfurtransferase enzyme that converts
cyanide to thiocyanate, which is then excreted in the urine. Acute poisoning only
occurs when this detoxification mechanism is overwhelmed.
The symptoms of acute
cyanide poisoning include rapid breathing, drop in blood pressure, raised pulse
rate, dizziness, headache, stomach pains, vomiting, diarrhea, confusion,
twitching, and convulsions. In extreme cases, death may occur. The minimum
lethal dose of hydrogen cyanide taken orally is approximately 0.5–3.5 mg/kg body weight or 35–245mg for a person weighing 75 kg. The chronic effects of
cyanide consumption are associated with regular long-term consumption of foods
containing cyanogenic glycosides in individuals with poor nutrition.
These
effects are most notable in the tropics, where cassava, and to a lesser extent,
sorghum, bamboo shoots, and lima beans are staple components of human diets.
Malnutrition, growth retardation, diabetes, congenital malformations,
neurological disorders, and myelopathy are all associated with cassava-eating
populations subject to chronic cyanide intake. There are a number of documented
cases of poisoning caused by the consumption of apricot kernels. One report
concerned a 41-year-old female found comatose after eating approximately 30
bitter apricot kernels, who eventually recovered after treatment.
There are
also case reports of children being poisoned after consumption of wild apricot
kernels and where the kernels were made into sweets without proper processing.
The UK Committee on Toxicity recommended in March 2006 that a tolerable daily
intake (TDI) of 20 mg cyanide/kg BW/day be applied, which is the equivalent of
1–2 bitter apricot kernels per day. There are over 2500 known species of plants
that produce cyanogenic glycosides, usually in combination with a corresponding
hydrolytic enzyme – a beta-glycosidase.
When the cell structure of the plant is
disrupted in some way, for example by predation, the beta-glycosidase is
brought into contact with its substrate – the cyanogenic glycoside. This leads
to the breakdown of the glycoside into sugar and a cyanohydrin, which rapidly
decomposes to release hydrogen cyanide. The purpose of the reaction is to
protect the plant from predation. Stability in Foods Cyanogenic glycosides
break down when the cells of the plant are damaged, for example during
preparation and processing, and release hydrogen cyanide. Hydrogen cyanide
itself is not heated and stable and does not survive boiling and cooking processes.
It can also be eliminated by fermentation. Processing Adequate processing of
cyanogenic glycoside-containing plants should be sufficient to significantly reduce
or remove the toxic agents prior to consumption. Processing procedures, such as
peeling and slicing disrupt the cell structure of the plant so that
b-glycosidases are released and the cyanogenic glycosides are hydrolyzed.
Hydrogen cyanide is thus released and can be removed by cooking processes such
as baking, boiling, or roasting. Fermentation is also used to remove hydrogen
cyanide. These methods are particularly suitable for products such as cassava
and bamboo shoots. There are two main types of cassava – bitter cassava and
sweet cassava. The sweet variety contains a significantly lower concentration
of cyanogenic glycosides than the bitter variety, and it is the sweet variety
that is used commercially.
Cassava is consumed largely as cassava flour, cassava
chips, and tapioca pearls, all of which are processed products with a long
history of safe consumption. Treatments for removing cyanogenic compounds from
flaxseed include boiling in water, dry and wet autoclaving, and acid treatment
followed by autoclaving. Solvent extraction has also been used to remove
cyanogenic glycosides from flaxseed and oil.
Legislation
A safe level of
cyanide in cassava flour for human consumption has been set by the WHO at 10
ppm. Low levels of cyanide are also present in almonds, sweet apricot kernels
and in the stones of other fruit such as cherries, as well as in bitter apricot
kernels. In the UK, the maximum level of cyanide that can be present as a
result of using such materials as flavourings is regulated under the terms of
the Flavourings in Food Regulations 1992 (as amended).
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