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	<description>All About Sugar</description>
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		<title>Fructose</title>
		<link>http://sugar2sugar.wordpress.com/2008/04/20/fructose/</link>
		<comments>http://sugar2sugar.wordpress.com/2008/04/20/fructose/#comments</comments>
		<pubDate>Sun, 20 Apr 2008 06:15:36 +0000</pubDate>
		<dc:creator>buzzy99</dc:creator>
				<category><![CDATA[Definitions]]></category>
		<category><![CDATA[fructose]]></category>

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		<description><![CDATA[Fructose (also levulose or laevulose) is a simple reducing sugar (monosaccharide) found in many foods and is one of the three most important blood sugars along with glucose and galactose. Honey, tree fruits, berries, melons, and some root vegetables, such as beets, sweet potatoes, parsnips, and onions, contain fructose, usually in combination with sucrose and [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=sugar2sugar.wordpress.com&amp;blog=3527691&amp;post=12&amp;subd=sugar2sugar&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
			<content:encoded><![CDATA[<p align="justify"><b>Fructose</b> (also <b>levulose</b> or <b>laevulose</b>) is a simple <a title="Reducing sugar" href="http://en.wikipedia.org/wiki/Reducing_sugar">reducing</a> <a href="http://en.wikipedia.org/wiki/Sugar" title="Sugar">sugar</a> (<a href="http://en.wikipedia.org/wiki/Monosaccharide" title="Monosaccharide">monosaccharide</a>) found in many foods and is one of the three most important <a title="Blood sugar" href="http://en.wikipedia.org/wiki/Blood_sugar">blood sugars</a> along with <a href="http://en.wikipedia.org/wiki/Glucose" title="Glucose">glucose</a> and <a href="http://en.wikipedia.org/wiki/Galactose" title="Galactose">galactose</a>. Honey, tree fruits, berries, melons, and some root vegetables, such as beets, sweet potatoes, parsnips, and onions, contain fructose, usually in combination with <a href="http://en.wikipedia.org/wiki/Sucrose" title="Sucrose">sucrose</a> and glucose. Fructose is also derived from the digestion of <a href="http://en.wikipedia.org/wiki/Sucrose" title="Sucrose">sucrose</a>, a <a href="http://en.wikipedia.org/wiki/Disaccharide" title="Disaccharide">disaccharide</a> consisting of glucose and fructose that is broken down by <a title="Glycoside hydrolase" href="http://en.wikipedia.org/wiki/Glycoside_hydrolase">glycoside hydrolase</a> <a href="http://en.wikipedia.org/wiki/Enzymes" class="mw-redirect" title="Enzymes">enzymes</a> during digestion. Fructose is the sweetest naturally occurring sugar, estimated to be 20% more sweet than sucrose.</p>
<p align="justify">Fructose is often recommended for, and consumed by, people with diabetes mellitus or hyperglycemia, because it has a very low glycemic index (GI) relative to <a href="http://en.wikipedia.org/wiki/Sugar" title="Sugar">sugar</a> (<a href="http://en.wikipedia.org/wiki/Sucrose" title="Sucrose">sucrose</a>). However, this benefit is tempered by concern that fructose may have an adverse effect on plasma lipid and uric acid levels, and the resulting higher blood levels of fructose can be damaging to proteins. The low GI is due to the unique and lengthy metabolic pathway of fructose, which involves phosphorylation and a multi-step enzymatic process in the liver.<span id="more-12"></span></p>
<p align="justify">Crystalline fructose and high-fructose corn syrup are often mistakenly confused as the same product. The former is simply pure (100%) fructose. The latter is composed of nearly equal amounts of fructose and glucose. Crystalline fructose is held to offer many unique benefits such as improved product texture, taste and stability. Specifically, when combined with other sweeteners and starches, crystalline fructose is said to boost cake height (in baked goods) and mouth-feel of foods and beverages and to produce a pleasing brown surface color and pleasant aroma when baking.</p>
<p align="justify"><img alt="fructose properties" src="http://sugar2sugar.files.wordpress.com/2008/04/fructose-properties.png?w=370&#038;h=590" height="590" hspace="8" width="370" align="top" border="0" /></p>
<p align="justify">
<hr />
<em><strong><font size="1">from: </font></strong></em><a href="http://en.wikipedia.org/wiki/Fructose" target="_blank"><em><strong><font size="1">http://en.wikipedia.org/wiki/Fructose</font></strong></em></a></p>
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			<media:title type="html">fructose properties</media:title>
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		<title>Lactose</title>
		<link>http://sugar2sugar.wordpress.com/2008/04/20/lactose/</link>
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		<pubDate>Sun, 20 Apr 2008 03:22:48 +0000</pubDate>
		<dc:creator>buzzy99</dc:creator>
				<category><![CDATA[Definitions]]></category>
		<category><![CDATA[lactose]]></category>

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		<description><![CDATA[Lactose (also referred to as milk sugar) is a sugar which is found most notably in milk. Lactose makes up around 2-8% of milk (by weight). The name comes from the Latin word for milk, plus the -ose ending used to name sugars. Its systematic name is β-D-galactopyranosyl-(1↔4)β-D-glucopyranose. Lactose is a disaccharide that consists of [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=sugar2sugar.wordpress.com&amp;blog=3527691&amp;post=9&amp;subd=sugar2sugar&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
			<content:encoded><![CDATA[<p align="justify"><strong>Lactose</strong> (also referred to as <em>milk sugar</em>) is a <a title="Sugar" href="http://en.wikipedia.org/wiki/Sugar">sugar</a> which is found most notably in milk. Lactose makes up around 2-8% of milk (by weight). The name comes from the Latin word for milk, plus the -ose ending used to name sugars. Its systematic name is β-D-galactopyranosyl-(1↔4)β-D-glucopyranose.</p>
<p align="justify">Lactose is a <a title="Disaccharide" href="http://en.wikipedia.org/wiki/Disaccharide">disaccharide</a> that consists of β-D-<a title="Galactose" href="http://en.wikipedia.org/wiki/Galactose">galactose</a> and β-D-<a title="Glucose" href="http://en.wikipedia.org/wiki/Glucose">glucose</a> molecules bonded through a β1-4 <a class="mw-redirect" title="Glycosidic" href="http://en.wikipedia.org/wiki/Glycosidic">glycosidic</a> linkage.<span id="more-9"></span></p>
<p align="justify">Lactose has a solubility of 1 in 4.63 measured %w/v. This translates to 0.216 g of lactose dissolving readily in 1 mL of water. The solubility of lactose in water is 18.9049 g at 25°C, 25.1484 g at 40°C and 37.2149 g at 60°C per 100 g solution. Its solubility in ethanol is 0.0111 g at 40°C and 0.0270 g at 60°C per 100 g solution.</p>
<p align="justify"><img src="http://sugar2sugar.files.wordpress.com/2008/04/lactose-properties.png?w=307&#038;h=427" border="0" alt="lactose properties" hspace="8" width="307" height="427" align="top" /></p>
<p align="justify">
<hr /><em><strong><span style="font-size:xx-small;">&gt;&gt;&gt; from: </span></strong></em><a href="http://en.wikipedia.org/wiki/Lactose" target="_blank"><em><strong><span style="font-size:xx-small;">http://en.wikipedia.org/wiki/Lactose</span></strong></em></a></p>
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			<media:title type="html">lactose properties</media:title>
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		<title>Sucrose</title>
		<link>http://sugar2sugar.wordpress.com/2008/04/20/sucrose/</link>
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		<pubDate>Sun, 20 Apr 2008 02:05:29 +0000</pubDate>
		<dc:creator>buzzy99</dc:creator>
				<category><![CDATA[Definitions]]></category>
		<category><![CDATA[sucrose]]></category>

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		<description><![CDATA[Sucrose (common name: table sugar, also called saccharose) is a disaccharide (glucose + fructose) with the molecular formula C12H22O11. Its systematic name is α-D-glucopyranosyl- (1↔2)-β-D-fructofuranoside (ending in &#8220;oside&#8221;, because it’s not a reducing sugar). It is best known for its role in human nutrition and is formed by plants but not by other organisms such [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=sugar2sugar.wordpress.com&amp;blog=3527691&amp;post=7&amp;subd=sugar2sugar&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
			<content:encoded><![CDATA[<p align="justify"><strong>Sucrose</strong> (common name: <strong>table sugar</strong>, also called <strong>saccharose</strong>) is a <a title="Disaccharide" href="http://en.wikipedia.org/wiki/Disaccharide">disaccharide</a> (<a title="Glucose" href="http://en.wikipedia.org/wiki/Glucose">glucose</a> + <a title="Fructose" href="http://en.wikipedia.org/wiki/Fructose">fructose</a>) with the <a class="mw-redirect" title="Molecular formula" href="http://en.wikipedia.org/wiki/Molecular_formula">molecular formula</a> C<sub>12</sub>H<sub>22</sub>O<sub>11</sub>. Its systematic name is α-D-glucopyranosyl- (1↔2)-β-D-fructofuranoside (ending in &#8220;oside&#8221;, because it’s not a <a title="Reducing sugar" href="http://en.wikipedia.org/wiki/Reducing_sugar">reducing sugar</a>). It is best known for its role in human nutrition and is formed by plants but not by other organisms such as animals.</p>
<div class="thumb tleft">Pure sucrose is most often prepared as a fine, white, odorless crystalline powder with a pleasing, sweet taste; the common table sugar. Large crystals are sometimes precipitated from water solutions of sucrose onto a string (or other nucleation surface) to form rock candy, a confection.<span id="more-7"></span></div>
<p align="justify">Like other <a class="mw-redirect" title="Carbohydrates" href="http://en.wikipedia.org/wiki/Carbohydrates">carbohydrates</a>, sucrose has a hydrogen to oxygen ratio of 2:1. It consists of two <a class="mw-redirect" title="Monosaccharides" href="http://en.wikipedia.org/wiki/Monosaccharides">monosaccharides</a>, α-<a title="Glucose" href="http://en.wikipedia.org/wiki/Glucose">glucose</a> and <a title="Fructose" href="http://en.wikipedia.org/wiki/Fructose">fructose</a>, joined by a <a title="Glycosidic bond" href="http://en.wikipedia.org/wiki/Glycosidic_bond">glycosidic </a>bond between carbon atom 1 of the glucose unit and carbon atom 2 of the fructose unit. What is notable about sucrose is that unlike most polysaccharides, the <a title="Glycosidic bond" href="http://en.wikipedia.org/wiki/Glycosidic_bond">glycosidic bond</a> is formed between the reducing ends of both glucose and fructose, and not between the reducing end of one and the nonreducing end of the other. The effect of this inhibits further bonding to other saccharide units. Since it contains no free anomeric carbon atom, it is classified as a nonreducing sugar. Sucrose melts and decomposes at 186 °C to form <a title="Caramel" href="http://en.wikipedia.org/wiki/Caramel">caramel</a>, and when combusted produces carbon, carbon dioxide, and water. Water breaks down sucrose by <a title="Hydrolysis" href="http://en.wikipedia.org/wiki/Hydrolysis">hydrolysis</a>, however the process is so gradual that it could sit in solution for years with negligible change. If the <a title="Enzyme" href="http://en.wikipedia.org/wiki/Enzyme">enzyme</a> <a title="Sucrase" href="http://en.wikipedia.org/wiki/Sucrase">sucrase</a> is added however, the reaction will proceed rapidly.</p>
<p align="justify">Reacting sucrose with <a title="Sulfuric acid" href="http://en.wikipedia.org/wiki/Sulfuric_acid">sulfuric acid</a> dehydrates the sucrose and forms the element <a title="Carbon" href="http://en.wikipedia.org/wiki/Carbon">carbon</a>, as demonstrated in the following equation:</p>
<dl>
<dd>
<div>C<sub>12</sub>H<sub>22</sub>O<sub>11</sub> + H<sub>2</sub>SO<sub>4</sub> <a class="mw-redirect" title="Catalyst" href="http://en.wikipedia.org/wiki/Catalyst">catalyst</a> → 12 C + 11 H<sub>2</sub>O</div>
</dd>
</dl>
<p align="justify"><img src="http://sugar2sugar.files.wordpress.com/2008/04/sucrose-prop.png?w=259&#038;h=798" border="0" alt="sucrose properties" hspace="8" width="259" height="798" align="top" /></p>
<p align="justify"><img style="width:260px;height:276px;" src="http://sugar2sugar.files.wordpress.com/2008/04/sucrose-solubility.png?w=210&#038;h=250" border="0" alt="sucrose solubility" hspace="8" width="210" height="250" align="top" /></p>
<p><strong><em></em></strong></p>
<p align="justify">
<hr />
<p align="justify"><strong><em><span style="font-size:xx-small;">&gt;&gt;&gt; from: </span></em></strong><a href="http://en.wikipedia.org/wiki/Sucrose" target="_blank"><strong><em><span style="font-size:xx-small;">http://en.wikipedia.org/wiki/Sucrose</span></em></strong></a><strong><em></em></strong></p>
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			<media:title type="html">sucrose properties</media:title>
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		<title>Sugar</title>
		<link>http://sugar2sugar.wordpress.com/2008/04/20/sugar/</link>
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		<pubDate>Sun, 20 Apr 2008 00:57:21 +0000</pubDate>
		<dc:creator>buzzy99</dc:creator>
				<category><![CDATA[Definitions]]></category>
		<category><![CDATA[sugar]]></category>

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		<description><![CDATA[Sugar (the word stems from the Sanskrit sharkara) consists of a class of edible crystalline substances including sucrose, lactose, and fructose. Human taste buds interpret its flavor as sweet. Sugar as a basic food carbohydrate primarily comes from sugar cane and from sugar beet, but also appears in fruit, honey, sorghum, sugar maple (in maple [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=sugar2sugar.wordpress.com&amp;blog=3527691&amp;post=3&amp;subd=sugar2sugar&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
			<content:encoded><![CDATA[<p style="text-align:center;"><a href="http://sugar2sugar.files.wordpress.com/2008/04/magnification-of-grains-of-sugar-showing-their-monoclinic-hemihedral-crystalline-structure_800px-sugar_2xmacro.jpg"><img class="aligncenter size-medium wp-image-4" src="http://sugar2sugar.files.wordpress.com/2008/04/magnification-of-grains-of-sugar-showing-their-monoclinic-hemihedral-crystalline-structure_800px-sugar_2xmacro.jpg?w=500&#038;h=333" border="0" alt="" width="500" height="333" /></a></p>
<p style="text-align:justify;"><strong>Sugar</strong> (the word stems from the Sanskrit <em>sharkara</em>) consists of a class of edible crystalline substances including <a title="Sucrose" href="http://en.wikipedia.org/wiki/Sucrose">sucrose</a>, <a title="Lactose" href="http://en.wikipedia.org/wiki/Lactose">lactose</a>, and <a title="Fructose" href="http://en.wikipedia.org/wiki/Fructose">fructose</a>. Human taste buds interpret its flavor as <span class="mw-redirect">sweet</span>. Sugar as a basic food <a title="Carbohydrate" href="http://en.wikipedia.org/wiki/Carbohydrate">carbohydrate</a> primarily comes from <a class="mw-redirect" title="Sugar cane" href="http://en.wikipedia.org/wiki/Sugar_cane">sugar cane</a> and from <a title="Sugar beet" href="http://en.wikipedia.org/wiki/Sugar_beet">sugar beet</a>, but also appears in fruit, honey, sorghum, <span class="mw-redirect">sugar maple</span> (in maple syrup), and in many other sources. It forms the main ingredient in much candy. &#8220;Excessive&#8221; consumption of sugar has been associated<sup> </sup>with increased incidences of type 2 <span class="mw-redirect">diabetes</span>, of obesity and of <span class="mw-redirect">tooth decay</span>.</p>
<p style="text-align:justify;"><strong>In non-scientific use</strong>, the term <em>sugar</em> refers to <a title="Sucrose" href="http://en.wikipedia.org/wiki/Sucrose">sucrose</a> ( also called &#8220;table sugar&#8221; or &#8220;saccharose&#8221; ) &#8211; a white crystalline solid <a title="Disaccharide" href="http://en.wikipedia.org/wiki/Disaccharide">disaccharide</a>. In this informal sense, the word &#8220;sugar&#8221; principally refers to crystalline sugars.<span id="more-3"></span></p>
<p style="text-align:justify;">Humans most commonly use sucrose as their sugar of choice for altering the flavor and properties (such as mouthfeel, preservation, and texture) of <span class="mw-redirect">beverages</span> and food. Commercially produced table sugar comes either from <a class="mw-redirect" title="Sugar cane" href="http://en.wikipedia.org/wiki/Sugar_cane">sugar cane</a> or from <a title="Sugar beet" href="http://en.wikipedia.org/wiki/Sugar_beet">sugar beet</a>. Manufacturing and preparing food may involve other sugars, including <a title="Palm sugar" href="http://en.wikipedia.org/wiki/Palm_sugar">palm sugar</a> and <a title="Fructose" href="http://en.wikipedia.org/wiki/Fructose">fructose</a>, generally obtained from corn (<a title="Maize" href="http://en.wikipedia.org/wiki/Maize">maize</a>) or from fruit.</p>
<p style="text-align:justify;">Sugar may dissolve in water to form a <a title="Syrup" href="http://en.wikipedia.org/wiki/Syrup">syrup</a>. A great many foods exist which principally contain dissolved sugar. Generically known as &#8220;syrups&#8221;, they may also have other more specific names such as &#8220;<a title="Honey" href="http://en.wikipedia.org/wiki/Honey">honey</a>&#8221; or &#8220;<a title="Molasses" href="http://en.wikipedia.org/wiki/Molasses">molasses</a>&#8220;.</p>
<p style="text-align:justify;"><strong>Scientifically</strong>, <em>sugar</em> refers to any <a title="Monosaccharide" href="http://en.wikipedia.org/wiki/Monosaccharide">monosaccharide</a> or <a title="Disaccharide" href="http://en.wikipedia.org/wiki/Disaccharide">disaccharide</a>. Monosaccharides ( also called &#8220;simple sugars&#8221; ), such as <a title="Glucose" href="http://en.wikipedia.org/wiki/Glucose">glucose</a>, store chemical energy which biological cells convert to other types of energy.</p>
<p style="text-align:justify;">In a list of ingredients, any word that ends with &#8220;-ose&#8221; (such as &#8220;glucose&#8221;, &#8220;dextrose&#8221;, &#8220;fructose&#8221;, etc.) will likely denote a sugar. Sometimes such words may also refer to any types of <a class="mw-redirect" title="Carbohydrates" href="http://en.wikipedia.org/wiki/Carbohydrates">carbohydrates</a> soluble in water.</p>
<p style="text-align:justify;"><a title="Glucose" href="http://en.wikipedia.org/wiki/Glucose">Glucose</a> (a type of sugar found in human blood plasma) has the <span class="mw-redirect">molecular formula</span> C<sub>6</sub> H<sub>12</sub> O<sub>6</sub>.</p>
<p style="text-align:justify;"><strong>In culinary terms</strong>, the foodstuff known as <strong>sugar</strong> delivers a <span class="mw-redirect">primary taste</span> sensation of <a title="Sweetness" href="http://en.wikipedia.org/wiki/Sweetness">sweetness</a>. Apart from the many forms of sugar and of sugar-containing foodstuffs, alternative non-sugar-based <a title="Sweetener" href="http://en.wikipedia.org/wiki/Sweetener">sweeteners</a> exist, and these particularly attract interest from people who have problems with their <a title="Blood sugar" href="http://en.wikipedia.org/wiki/Blood_sugar">blood sugar level</a> (such as <a class="mw-redirect" title="Diabetics" href="http://en.wikipedia.org/wiki/Diabetics">diabetics</a>) and people who wish to limit their <a title="Calorie" href="http://en.wikipedia.org/wiki/Calorie">calorie</a>-intake while still enjoying sweet foods. Both natural and synthetic substitutes exist with no significant <a title="Carbohydrate" href="http://en.wikipedia.org/wiki/Carbohydrate">carbohydrate</a> (and thus low-calorie) content: for instance <a title="Stevia" href="http://en.wikipedia.org/wiki/Stevia">stevia</a> (a <a title="Herb" href="http://en.wikipedia.org/wiki/Herb">herb</a>), and <a title="Saccharin" href="http://en.wikipedia.org/wiki/Saccharin">saccharin</a> (produced from naturally occurring but not necessarily naturally <span class="mw-redirect">edible</span> substances by inducing appropriate <a class="mw-redirect" title="Chemical reactions" href="http://en.wikipedia.org/wiki/Chemical_reactions">chemical reactions</a>).</p>
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<h5><em>&gt;&gt;&gt; from: <a href="http://en.wikipedia.org/wiki/Sugar" target="_blank">http://en.wikipedia.org/wiki/Sugar</a></em></h5>
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