Everything Totally Explained


Ask & we'll explain, totally!
Polyphenol
Totally Explained


  NEW! All the latest news in the worlds of computer gaming, entertainment, the environment,  
finance, health, politics, science, stocks & shares, technology and much, much, more.  


View this entry using RSS

Everything about Polyphenol totally explained

Polyphenols are a group of chemical substances found in plants, characterized by the presence of more than one phenol unit or building block per molecule. Polyphenols are generally divided into hydrolyzable tannins (gallic acid esters of glucose and other sugars) and phenylpropanoids, such as lignins, flavonoids, and condensed tannins.

Chemistry

Classification and Nomenclature

The division of polyphenols into tannins, lignins, and flavonoids is derived from the variety of simple polyphenolic units derived from secondary plant metabolism of the shikimate pathway as well as classical divisions based upon the relative importance of each base component to different fields of study. Tannin chemistry originated in the importance of tannic acid to the tanning industry; lignins to the chemistry of soil and plant structure; and flavonoids to the chemistry of plant secondary metabolites for plant defense, and flower color (for example from anthocyanins).
   The largest and best studied polyphenols are the flavonoids, which include several thousand compounds, among them the flavonols, flavones, catechins, flavanones, anthocyanidins, and isoflavonoids.
   The most abundant polyphenols are the condensed tannins, found in virtually all families of plants, and comprising up to 50% of the dry weight of leaves. The convergent evolution of tannin-rich plant communities has occurred on nutrient-poor acidic soils throughout the world. Tannins were once believed to function as anti-herbivore defenses, but more and more ecologists now recognize them as important controllers of decomposition and nitrogen cycling processes. As concern grows about global warming, there's great interest to better understand the role of polyphenols as regulators of carbon cycling, particularly in northern boreal forests.
Base Unit:

Gallic Acid

Flavone

Cinnamic acid
Class/Polymer:
hydrolyzable tannins Flavonoid, condensed tannins
Lignins
Polyphenols are also classified by the type and number of phenolic subcomponents present. More than one subcomponent can be present on a given polyphenol.
Phenol
Pyrocatechol
Pyrogallol
Resorcinol
Phloroglucinol
Hydroquinone
Examples: coumaric acid derived lignins, kaempferol Examples: catechin, quercetin, caffeic and ferulic acid derived lignins, hydroxytyrosol esters Examples: gallocatechins (EGCG), tannins, myricetin, sinapyl alcohol derived lignins Examples: resveratrol Examples: almost all flavonoids Examples: arbutin
The phenolic unit can often be esterified or methylated. It can also be found dimerized or further polymerized, creating a new class of polyphenol. For example, ellagic acid is a dimer of gallic acid and forms the class of ellagitannins, or a catechin and a gallocatechin can combine to form the red compound theaflavin, a process which also results in the large class of brown thearubigins in tea.

In Foods

Notable sources of polyphenols include berries, tea, beer, grapes/wine, olive oil, chocolate/cocoa, walnuts, peanuts, pomegranates, yerba mate, and other fruits and vegetables.
   High levels of polyphenols can generally be found in the fruit skins.

Health benefits

Polyphenols were once briefly known as Vitamin P. However they were quickly found out to be non-essential and reclassified. The health benefits of specific polyphenols such as quercetin are well-established, there are less well-established claims of health benefits from all types of polyphenols.
   Research indicates that polyphenols may have antioxidant characteristics with potential health benefits. They may reduce the risk of cardiovascular disease and cancer.
   Polyphenols have also been investigated as a source of additional health benefit in organic produce, but no conclusion was made.
   Polyphenols bind with nonheme iron (for example from plant sources) in vitro in model systems. This may decrease its absorption by the body.

Further Information

Get more info on 'Polyphenol'.


External Link Exchanges

Do you know how hard it is to get a link from a large encyclopaedia? Well we're different and will prove it. To get a link from us just add the following HTML to your site on a relevant page:

    <a href="http://polyphenol.totallyexplained.com">Polyphenol Totally Explained</a>

Then simply click through this link from your web page. Our crawlers will verify your link, extract the title of your web page and instantly add a link back to it. If you like you can remove the words Totally Explained and embed the link in article text.
   As long as your link remains in place, we'll keep our link to you right here. Please play fair - our crawlers are watching. Your site must be closely related to this one's topic. Any kind of spamming, dubious practises or removing the link will result in your link from us being dropped and, potentially, your whole site being banned.



Copyright © 2007-8 totallyexplained.com | Licensed under the GNU Free Documentation License | Site Map
This article contains text from the Wikipedia article Polyphenol (History) and is released under the GFDL | RSS Version