ReviewDietary roles of phytate and phytase in human nutrition: A review
Introduction
Plant-based food products are the main staple food for human beings in many parts of the world. They constitute an important source of carbohydrates, protein, dietary fibre, vitamins and non-nutrients (Katina et al., 2005). Among all the antinutritional components, phytic acid is of prime concern for human nutrition and health management. The chemical description for phytic acid is myoinositol (1,2,3,4,5,6) hexakisphosphoric acid. The unique structure of phytic acid offers it the ability to strongly chelate with cations such as calcium, magnesium, zinc, copper, iron and potassium to form insoluble salts. It therefore adversely affects the absorption and digestion of these minerals by animals (Raboy, 2001). Salts of phytic acid are designated as phytates (myo-inositol-1,2,3,4,5,6-hexakisphosphates) which are mostly present as salts of the mono- and divalent cations K+, Mg2+ and Ca2+. Phytate accumulates in the seeds during the ripening period and is the main storage form of both phosphate and inositol in plant seeds and grains (Loewus, 2002). Phosphorus, in this form, is not utilised by human beings, dogs, pigs, birds or agastric animals because they lack the intestinal digestive enzyme phytase (Holm, Kristiansen, & Pedersen, 2002). Phytate works in a broad pH-region as a highly negatively charged ion and therefore its presence in the diet has a negative impact on the bioavailability of divalent and trivalent mineral ions such as Zn2+, Fe2+/3+, Ca2+, Mg2+, Mn2+ and Cu2+ (Fredlund et al., 2006, Lopez et al., 2002, Lönnerdal, 2002). Besides, phytate has also been reported to form complexes with proteins at both low and high pH values. These complex formations alter the protein structure, which may result in decreased protein solubility, enzymatic activity and proteolytic digestibility. Hitherto, massive investigations have been carried out on the negative aspects of phytate that have offered overwhelming evidence that dietary phytate is an antinutrient component. As a solution, the phytate-degrading enzyme, phytase, is in vogue for degradating phytate during food processing and in the gastrointestinal tract. Major efforts have been made to reduce the amount of phytate in foods by different processes and/or the addition of exogenous enzymes. In spite of many negative aspects on human health, the consumption of phytate, however, has been reported to have some favourable effects. The outcome of surveillance of populations consuming vegetarian-type diets has shown lower incidence of cancer, which suggests that phytate has an anticarcinogen effect (Shamsuddin, 2002, Vucenik and Shamsuddin, 2003). The metal binding characteristics of phytate endow it an anti-oxidant function, inhibiting the production of hydroxyl radicals that normalise cell homeostasis (Minihane & Rimbach, 2002) and it also acts as a natural food anti-oxidant (Raboy, 2003). Dietary phytate may have health benefits for diabetes patients because it lowers the blood glucose response by reducing the rate of starch digestion and slowing gastric emptying (Thompson, 1993). Likewise, phytate has also been shown to regulate insulin secretion (Barker & Berggren, 1999). It is believed that phytate reduces blood clots, cholesterol and triglycerides and thus prevents heart diseases (Jariwalla et al., 1990, Onomi et al., 2004). It is also suggested that it prevents renal stone development (Grases et al., 2000a, Grases et al., 2000b, Selvam, 2002). It is used as a complexing agent for removal of traces of heavy metal ions (Wise, 1982). In vitro studies have indicated that phytic acid incubated with HIV-1 infected T cells inhibits the replication of HIV-1 (Otake et al., 1999, Otake et al., 1989). Hitherto, many literature reviews, primarily focussing on the antinutritional aspects of phytate, have been published but information on the beneficial effect of phytate is still very scarce and scattered. The purpose of this review is to discuss both negative and prophylactic and therapeutic effects of phytate and the mechanisms responsible for these effects.
Section snippets
Phytate
Phytic acid is the hexaphosphoric ester of the hexahydric cyclic alcohol meso-inositol (Fig. 1). Phytic acid (known as inositol hexakisphosphate (IP6), or phytate when in salt form) is the principal storage form of phosphorus in many plant tissues. Inositol penta- (IP5), tetra- (IP4) and triphosphate (IP3) are also called phytates. Molecular formula: C6H18O24P6 and molecular mass: 660.04 g mol−1.
Phytate is formed during maturation of the plant seed and in dormant seeds it represents 60–90% of the
Negative aspects of phytate
Table 2 presents an overview of the negative interactions of phytate with nutrients and the mode of actions for the negative effects of phytate.
Chemical interaction of phytate in gastrointestinal (GI) tract
The interaction of phytate with minerals and other dietary nutrients is pH-dependent (Reddy, 2002). In the human body, food digesta pass from low pH in the stomach to neutral pH, prevailing in the upper small intestine. During digesta movement, dietary phytate-mineral complexes may dissociate and may form other complexes through the gastrointestinal tract. In the upper part of the small intestine, which is characterised by maximum mineral absorption, the insoluble complexes are highly unlikely
Degradation of phytate
The dephosphorylation of phytate is a prerequisite for improving nutritional value because removal of phosphate groups from the inositol ring decreases the mineral binding strength of phytate. This results in increased bioavailability of essential dietary minerals (Sandberg et al., 1999). Various food processing and preparation techniques, along with the addition of exogenous enzymes, are the major efforts made to reduce the amount of phytate in foods. Hydrolysis of phytate during food
Phytate as anti-oxidant in food products
Oxidation of food is a destructive process, causing substantial loss of nutritional value. Foods with high contents of unsaturated fatty acid and iron are more prone to undergo oxidation in the presence of oxygen. Even at very low percentages of oxygen (as low as 1%), the oxidation reaction can proceed and produce undesirable flavour changes, discoloration, nutritional losses and microbiological spoilage. The oxidation reaction can be minimised through the addition of anti-oxidant. In this
Therapeutic uses of phytate
Table 3 presents various therapeutic effects of phytate.
Conclusion
In the past few decades, scientists and entrepreneurs working in the field of human nutrition, human health and environmental protection have been focusing their attention on phytate and phytase. Dietary phytate has received much investigative attention as an antinutrient. We chose not to review this area of research extensively. The interactions of phytate and dietary minerals and beneficial health effects of phytate have been the subject of this review. The interactions of phytate and
References (198)
- et al.
Comparative toxicities of selected minor dietary non-nutrients with chemopreventive properties
Cancer Letter
(1993) - et al.
Effects of various phytase sources on phytic acid content, mineral extractability and protein digestibility of Tarhana
Food Chemistry
(2006) - et al.
Iron absorption from bread in humans: Inhibiting effects of cereal fibre, phytate and inositol phosphates with different numbers of phosphate groups
Journal of Nutrition
(1992) - et al.
Phytase activity in sourdough lactic acid bacteria: Purification and characterisation of a phytase from Lactobacillus sanfranciscensis CB1
International Journal of Food Microbiology
(2003) - et al.
Absorption of zinc and retention of calcium: Dose-dependent inhibition by phytate
Journal of Trace elements in Medicine and Biology
(2006) - et al.
Production of two types of phytase from Aspergillus oryzae during industrial koji making
Journal of Bioscience and Bioengineering
(2003) - et al.
MGN-3/biobran, modified arabinoxylan from rice bran, sensitizes human breast cancer cells to chemotherapeutic agent, daunorubicin
Cancer Detection and Prevention
(2008) - et al.
Antioxidant functions of phytic acid
Free Radical Biology and Medicine
(1990) - et al.
Phytic acid: A natural antioxidant
Journal of Biological Chemistry
(1987) - et al.
Iron-catalysed hydroxyl radical formation. Stringent requirement for free iron coordination site
Journal of Biological Chemistry
(1984)