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Phytic acid



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Phytic acid
Identifiers
CAS number 83-86-3
SMILES C1(OP(=O)(O)(O))C(OP(=O)(O)(O))C(OP(=O)(O)(O))
C(OP(=O)(O)(O))C(OP(=O)(O)(O))C1(OP(=O)(O)(O))
Properties
Molecular formula C6H18O24P6
Molar mass 660.08 g/mol
Except where noted otherwise, data are given for
materials in their standard state
(at 25 °C, 100 kPa)

Infobox disclaimer and references

Phytic acid (known as inositol hexakisphosphate (IP6), or phytate when in salt form) is the principal storage form of phosphorus in many plant tissues, especially bran and seeds.[1]

Additional recommended knowledge

Contents

Significance in Agriculture

Phosphorus in phytate form is, in general, not bioavailable to non-ruminant animals because they lack the digestive enzyme phytase, which is required to separate phosphorus from the phytate molecule. On the other hand, ruminants readily utilize phytate because of the phytase produced by rumen microorganisms.[2]

In most commercial agriculture, non-ruminant livestock such as swine and poultry are fed mainly grains such as soybeans and maize.[citation needed] Because phytate from these grains is unavailable for absorption, the unabsorbed phytate passes through the gastrointestinal tract, elevating the amount of phosphorus in the manure.[2] Excess phosphorus excretion can lead to environmental problems such as eutrophication.[3]

The bioavailability of phytate phosphorus can be increased by supplementation of the diet with phytase enzyme.[citation needed] Also, viable low-phytic acid mutant lines have been developed in several crop species in which the seeds have drastically reduced levels of phytic acid and concomitant increases in inorganic phosphorus.[citation needed] However, reported germination problems have hindered the use of these cultivars thus far.[citation needed]

Food science

Phytic acid is found within the hulls of nuts, seeds, and grains.[1] In-home food preparation techniques can reduce the phytic acid in all of these foods. Simply cooking the food will reduce the phytic acid to some degree. More effective methods are soaking in an acid medium, lactic acid fermentation, and sprouting.[4]

Phytic acid is a strong chelator of important minerals such as calcium, magnesium, iron, and zinc, and can therefore contribute to mineral deficiencies in people whose diets rely on these foods for their mineral intake, such as those in developing countries.[5] In this way, it is an anti-nutrient.[1] For people with a particularly low intake of essential minerals, especially young children and those in developing countries, this effect can be undesirable.

Dietary mineral chelators help, through reducing the available minerals, to prevent over-mineralization of joints, blood vessels, and other parts of the body, which is most common in older persons.[citation needed] They do not correct the disorder that causes this negative distribution of substances, though, and can reduce the availability of these minerals for other essential processes.[citation needed]

Therapeutic Use

Phytic acid may be considered a phytonutrient, providing an antioxidant effect.[6][1] Phytic acid's same mineral binding properties may also prevent colon cancer by reducing oxidative stress in the lumen of the intestinal tract. It may also reduce the risk of colon cancer.[7] Researchers now believe that phytic acid, found in the fiber of legumes and grains, is the major ingredient responsible for preventing colon cancer and other cancers.[1][8]

Phytic acid's chelating effect may serve to prevent, inhibit, or even cure some cancers by depriving those cells of the minerals (especially iron) they need to reproduce.[1] The deprivation of essential minerals like iron would, much like other broad treatments for cancers, also have negative effects on non-cancerous cells. It is unknown whether this would affect other cells in the body that require iron (such as red blood cells) or whether the deprivation of minerals is more localized to the internal colon region.[citation needed]

Phytic acid has no known toxicity and is not known to cause mutagenic activity.[citation needed] It may have more therapeutic value when added to water rather than when naturally absorbed in foods, as it is difficult to free from fiber.[citation needed]

Phytic acid is one of few chelating therapies used for uranium removal.

As a food additive, phytic acid is used as a preservative with E number E391.[citation needed]

Food must be well cooked in order to free IP6 from the fiber and enable it to be absorbed in the gastrointestinal system.[citation needed] IP6 rarely appears in soluble fiber. It is usually attached to the bran, the hard (insoluble) fiber, which is difficult to digest.[citation needed] IP6 is found in legumes, peas, wheat, barley, and oats.[citation needed] Of any studied legumes, whole soybeans have the highest levels of phytic acid.[citation needed]

Those that argue for the beneficial effects of phytic acid, and freeing it up for interaction with the system through cooking, do not argue that cooking destroys the phytic acid.[citation needed]This is a major deviation between those arguing for the merits of processed grain products.[citation needed]

References

  1. ^ a b c d e f http://www.phytochemicals.info/phytochemicals/phytic-acid.php
  2. ^ a b Council for Agricultural Science and Technology (CAST) (2002), , Issue Paper No. 21, Ames, IA, USA: CAST
  3. ^ Mallin, Michael A. & Cahoon, Lawrence B. (2003), " ", Population and Environment 24 (5): 369-385, May 2003, DOI 10.1023/A:1023690824045
  4. ^ http://www.crcpress.com/shopping_cart/products/product_detail.asp?sku=6108&isbn=9780849361081&parent_id=&pc=
  5. ^ http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=12949395&query_hl=16
  6. ^ The Journal of Environmental Nutrition (April 2004 volume 27 issue 4)
  7. ^ http://jn.nutrition.org/cgi/content/full/133/11/3778S
  8. ^ http://carcin.oxfordjournals.org/cgi/content/abstract/21/8/1547
 
This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Phytic_acid". A list of authors is available in Wikipedia.
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