Lecithin

Lecithin is a generic term to designate any group of yellow-brownish fatty substances occurring in animal and plant tissues, and in egg yolk, composed of phosphoric acid, choline, fatty acids, glycerol, glycolipids, triglycerides, and phospholipids (e.g., phosphatidylcholine, phosphatidylethanolamine, and phosphatidylinositol).

Lecithin was first isolated in 1846 by the French chemist and pharmacist Theodore Gobley;[1] in 1850 he named the phosphatidylcholine "Léchithine".[2] Gobley originally isolated lecithin from egg yolk—λέκιθος (lekithos) is 'egg yolk' in ancient Greek—and established the complete chemical formula of phosphatidylcholine in 1874;[3] in-between he had demonstrated the presence of lecithin in a variety of biological matters including venous blood, bile, human brain tissue, fish eggs, fish roe, chicken and sheep brain.

Lecithin can easily be extracted chemically (using hexane) or mechanically from readily available sources such as soy beans. It has low solubility in water. In aqueous solution its phospholipids can form either liposomes, bilayer sheets, micelles, or lamellar structures, depending on hydration and temperature. This results in a type of surfactant that is usually classified as amphipathic. Lecithin is sold as a food supplement and for medical uses. In cooking, it is sometimes used as an emulsifier and to prevent sticking, for example in non-stick cooking spray.

Contents

Biology

Phosphatidylcholine occurs in all cellular organisms, being one of the major components of the phospholipid portion of the cell membrane.

Production

Commercial lecithin, as used by food manufacturers, is a mixture of phospholipids in oil. The lecithin is obtained by degumming the extracted oil of the seeds. The lecithin is a mixture of various phospholipids, and the composition depends on the origin of the lecithin. A major source of lecithin is soybean oil. Because of the EU-requirement to declare additions of allergens in foods, in addition to regulations regarding genetically modified crops, a gradual shift to other sources of lecithin (e.g., sunflower oil) is taking place. The main phospholipids in lecithin from soya and sunflower are phosphatidyl choline, phosphatidyl inositol, phosphatidyl ethanolamine, and phosphatidic acid. They are often abbreviated to PC, PI, PE, and PA, respectively.

Hydrolysed lecithin

To modify the performance of lecithin to make it suitable for the product to which it is added, it may be hydrolysed enzymatically. In hydrolysed lecithins, a portion of the phospholipids have one fatty acid removed by phospholipase. Such phospholipids are called lyso-phospholipids. The most commonly used phospholipase is phospholipase A2, which removes the fatty acid at the C2 position of glycerol. Lecithins may also be modified by a process called fractionation. During this process, lecithin is mixed with an alcohol, usually ethanol. Some phospholipids, such as phosphatidylcholine, have good solubility in ethanol, whereas most other phospholipids do not dissolve well in ethanol. The ethanol is separated from the lecithin sludge, after which the ethanol is removed by evaporation to obtain a phosphatidylcholine-enriched lecithin fraction.

Properties and applications

Lecithin has emulsification and lubricant properties, and is a surfactant. Lecithin can be totally metabolized (see Inositol) by humans, so is well tolerated by humans and non-toxic when ingested; some emulsifiers can only be excreted via the kidneys.

Lecithin is used for applications in human food, animal feed, pharmaceutical, paint, and other industrial applications.

Applications listed by one manufacturer in addition to food applications include:[4]

Use with food, and health effects

The non-toxicity of lecithin leads to its use with food, as an additive or in food preparation. It is used commercially in foods requiring a natural emulsifier or lubricant. In the food industry it has multiple uses: In confectionery it reduces viscosity, replaces more expensive ingredients, controls sugar crystallization and the flow properties of chocolate, helps in the homogeneous mixing of ingredients, improves shelf life for some products, and can be used as a coating. In emulsions and fat spreads it stabilizes emulsions, reduces spattering during frying, improves texture of spreads and flavour release. In doughs and bakery it reduces fat and egg requirements, helps even distribution of ingredients in dough, stabilizes fermentation, increases volume, protects yeast cells in dough when frozen, and acts as a releasing agent to prevent sticking and simplify cleaning. It improves wetting properties of hydrophilic powders (e.g., low-fat proteins) and lipophilic powders (e.g., cocoa powder), controls dust, and helps complete dispersion in water.[4] It can be used as a component of cooking sprays to prevent sticking and as a releasing agent.

For example, lecithin is the emulsifier that keeps cocoa and cocoa butter in a candy bar from separating. In margarines, especially those containing high levels of fat (>75%), lecithin is added as an 'anti-spattering' agent for shallow frying.

It is approved by the United States Food and Drug Administration for human consumption with the status "Generally Recognized As Safe." Lecithin is admitted by the EU as a food additive, designated by E number E322. There are studies that show soy-derived lecithin has significant effects on lowering cholesterol and triglycerides, while increasing HDL ("good cholesterol") levels in the blood.[5][6] However, studies on egg lecithin have been inconsistent and contradictory since the 1920s.[7]

New studies suggest gut bacteria metabolites of choline promote atherosclerosis in mice through TMAO production and "augmented macrophage cholesterol accumulation and foam cell formation". [8] Mice fed with egg-yolk derived lecithin, developed arterial plaque in spite of no increase in cholesterol or triglyceride levels.[9]

Compatibility with special diets

A proven benefit and suggested use for lecithin is for those taking niacin to treat high cholesterol. Niacin treatment can deplete choline, necessitating an increased amount of lecithin or choline in the diet.[10][11] [12] [13] [14] Egg-derived lecithin may be a concern for those following some specialized diets. Egg lecithin is not a concern for those on low-cholesterol diets, because the lecithin found in eggs markedly inhibits the absorption of the cholesterol contained in eggs.[15] There is no general agreement among vegetarians concerning egg-derived lecithin; vegans and lacto-vegetarians would likely abstain from it.

Religious restrictions

Soy-derived lecithin is considered by some to be kitniyot and prohibited on Passover for Ashkenazi Jews when many grain-based foods are forbidden, but not at other times. This does not necessarily affect Sephardi Jews who do not have the same restrictions on rice and kitniyot during Pesach/Passover. (Reb Yehonatan Levy, Shomer Kashrut Mashgiach - based upon halachic rulings of CRC - Chicago Rabbinic Council, and from shiurim/lessons by Rabbi D. Raccah on "Pesach Preparations" following commentary from former Rishon-LeTzion Rav Ovadia Yosef).[16]

Muslims are not forbidden to eat lecithin per se; however, since it may be derived from animal as well as plant sources care needs to be taken to ensure this source is halal. The lecithin that is derived from plants and egg yolks is permissible, as is that derived from animals slaughtered according to the rules of dhabihah.[17]

References

  1. ^ Gobley (1846) "Recherches chimiques sur le jaune d'œuf" (Chemical researches on egg yolk), Journal de Pharmacie et de Chemie, series 3, vol. 9, pages 81-91; on page 84, Gobley gives the proceedure by which he extracted and characterized lecithin.
  2. ^ Gobley (1850) "Recherches chemiques sur les œufs de carpe" (Chemical researches on carp eggs), Journal de Pharmacie et de Chemie, series 3, vol. 17, pages 401-430; see especially page 411: "Je propose de donner au premier le nom de Léchithine (de λεχιθος, jaune d'œuf), parce qu'on le rencontre en grande quantité dans le jaune d'œuf,..." (I propose to give the first [substance] the name "Lecithin" (from λεχιθος, egg yolk), because one finds it in large quantities in egg yolk,....)
  3. ^ Theodore Gobley "Sur la lécithine et la cérébrine"; Journal de Pharmacie et de Chimie 1874,t20, 98-103, 161-166". 
  4. ^ a b Supplier's website with lecithin applications
  5. ^ Iwata T, Kimura Y, Tsutsumi K, Furukawa Y, Kimura S (February 1993). "The effect of various phospholipids on plasma lipoproteins and liver lipids in hypercholesterolemic rats". J. Nutr. Sci. Vitaminol. 39 (1): 63–71. doi:10.3177/jnsv.39.63. PMID 8509902. 
  6. ^ Jimenez MA, Scarino ML, Vignolini F, Mengheri E (July 1990). "Evidence that polyunsaturated lecithin induces a reduction in plasma cholesterol level and favorable changes in lipoprotein composition in hypercholesterolemic rats". J. Nutr. 120 (7): 659–67. PMID 2366101. http://jn.nutrition.org/cgi/pmidlookup?view=long&pmid=2366101. 
  7. ^ Kaayla T. Daniel, PhD, CCN (Winter 2003). "Soy Lecithin: From Sludge to Profit". Wise Traditions in Food, Farming, and the Healing Arts 4 (4). http://www.westonaprice.org/soy-alert/694-soy-lecithin-from-sludge-to-profit.html. 
  8. ^ Hazen, Stanley L.; et al (7 April 2011). "Gut flora metabolism of phosphatidylcholine promotes cardiovascular disease". Nature 472 (7341): 57–63. doi:10.1038/nature09922. PMC 3086762. PMID 21475195. http://www.nature.com/nature/journal/v472/n7341/full/nature09922.html. Retrieved 9 April 2011. 
  9. ^ Zeneng Wang et al., (2011 April 7) "Gut flora metabolism of phosphatidylcholine promotes cardiovascular disease", Nature, Vol. 472(7341): 57–63 [1]
  10. ^ J Nutr. 1965 Jan;85:107-12., FATTY LIVERS PRODUCED IN ALBINO RATS BY EXCESS NIACIN IN HIGH FAT DIETS. II. EFFECT OF CHOLINE SUPPLEMENTS.
  11. ^ British Journal of Nutrition (1996), 75:471-481 Cambridge University Press, Cholesterol-lowering effect of soyabean lecithin in normolipidaemic rats by stimulation of biliary lipid secretion
  12. ^ Iowa State University Animal Industry Report 2006, Soy Lecithin but Not Egg Lecithin Decreased the Plasma Cholesterol Concentration in Golden Syrian Hamsters
  13. ^ Life Sciences, Volume 67, Issue 21, 13 October 2000, Pages 2563-2576, Dietary polyenylphosphatidylcholine decreases cholesterolemia in hypercholesterolemic rabbits: Role of the hepato-biliary axis.
  14. ^ J Pharm Pharmacol. 2005 Jul;57(7):889-96, Phytostanol tablets reduce human LDL-cholesterol.
  15. ^ Kansas State University, 29-Oct-2001, Why Eggs Don't Contribute Much Cholesterol To Diet.
  16. ^ OK Kosher Certification, Keeping Kosher for Pesach. Retrieved on Sept 10, 2008.
  17. ^ Islamic Food and Nutrition Council of America FAQ, IFANCA: Consumer FAQ. Retrieved on July 7, 2010.

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