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	<title>Khymos &#187; milk</title>
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	<link>http://blog.khymos.org</link>
	<description>- dedicated to molecular gastronomy</description>
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		<title>Speeding up the Maillard reaction</title>
		<link>http://blog.khymos.org/2008/09/26/speeding-up-the-maillard-reaction/</link>
		<comments>http://blog.khymos.org/2008/09/26/speeding-up-the-maillard-reaction/#comments</comments>
		<pubDate>Fri, 26 Sep 2008 16:59:04 +0000</pubDate>
		<dc:creator>Martin Lersch</dc:creator>
				<category><![CDATA[experiments]]></category>
		<category><![CDATA[molecular gastronomy]]></category>
		<category><![CDATA[acid]]></category>
		<category><![CDATA[amino acid]]></category>
		<category><![CDATA[baking soda]]></category>
		<category><![CDATA[base]]></category>
		<category><![CDATA[egg]]></category>
		<category><![CDATA[eggs]]></category>
		<category><![CDATA[everyday science]]></category>
		<category><![CDATA[fructose]]></category>
		<category><![CDATA[glucose]]></category>
		<category><![CDATA[lactose]]></category>
		<category><![CDATA[lye]]></category>
		<category><![CDATA[maillard]]></category>
		<category><![CDATA[Maillard reaction]]></category>
		<category><![CDATA[milk]]></category>
		<category><![CDATA[pH]]></category>
		<category><![CDATA[protein]]></category>
		<category><![CDATA[reducing sugar]]></category>
		<category><![CDATA[temperature]]></category>
		<category><![CDATA[video]]></category>

		<guid isPermaLink="false">http://blog.khymos.org/?p=399</guid>
		<description><![CDATA[Ever thought about how pretzels and salt sticks get their nice brown color? The products of the Maillard reaction provide tastes, smells and colors that are much desired and lend their charachteristics to a variety of foods. In this post I will focus on the factors that influence how fast the Maillard reaction proceeds. And [...]]]></description>
			<content:encoded><![CDATA[<p><img src="http://blog.khymos.org/wp-content/2008/09/saltstenger.jpg" alt="" title="saltstenger" width="450" height="450" class="alignnone size-full wp-image-465" /><br />
<em>Ever thought about how pretzels and salt sticks get their nice brown color?</em></p>
<p>The products of the <a href="http://en.wikipedia.org/wiki/Maillard_reaction">Maillard reaction</a> provide tastes, smells and colors that are much desired and lend their charachteristics to a variety of foods. In this post I will focus on the factors that influence how fast the Maillard reaction proceeds. And more specifically I&#8217;ll give examples on how the Maillard reaction can be speeded up. This is not about <em>fast food</em>, nor is it about saving time. It&#8217;s more about controlling the browning reaction by speeding it up or slowing it down in order to get a desired end result.</p>
<p>The Maillard reaction is, to put it simple, a reaction between an amino acid and a sugar (there&#8217;s more on the chemistry at the end of the post). To speed it up you can do one or more of the following:<br />
<span id="more-399"></span></p>
<table border="1" width="450">
<tbody>
<tr>
<td>add</td>
<td>protein (egg, milk)<br />reducing sugar (glucose, fructose or lactose)</td>
</tr>
<tr>
<td>remove</td>
<td>water</td>
</tr>
<tr>
<td>increase</td>
<td>temperature<br />pH</td>
</tr>
</tbody>
</table>
<p>Chances are you have already utilized this in the kitchen without knowing. When eggs or milk are used for glazing, they act as a protein source for the Maillard reaction, giving a nice brown color. Milk also provides lactose which is a reducing sugar. You&#8217;ve probably also observed that temperature does influence browning. Water content is indirectly related to temperature &#8211; as long as there is water present, temperature will stay below 100 °C. But once the bread crust dries out the conditions are just right to get the Maillard reaction running.</p>
<p>The same principles are applied to microwaveable pies. The microwaves primarily interact with water and hence only bring the temperature up to the boiling point of water. In order to get sufficient Maillard productcs at these temperatures reducing sugars and amino acids are added to the crust (as exemplified in this <a href="http://www.google.com/patents?id=T_EaAAAAEBAJ">patent</a> where dextrose and whey solids are used). Not so surprisingly there is also a <a href="http://www.google.com/patents?id=PUc7AAAAEBAJ">patent</a> on how to avoid excessive browning in cookies which calls for addition of a polycarboxylic acid ester to lower pH and hence slow down the Maillard reaction.</p>
<p>Pretzels are an extreme example of how the Maillard reaction can be tweaked. Before baking the pretzels are brushed with <a href="http://en.wikipedia.org/wiki/Lye">lye</a>, a dilute solution of sodium hydroxide, which is very basic. The high pH speeds up the bottleneck of the Maillard reaction (see end of post for details).</p>
<p><img src="http://blog.khymos.org/wp-content/2008/09/onions_baking_soda.jpg" alt="" title="onions_baking_soda" width="450" height="450" class="alignnone size-full wp-image-466" /><br />
<em>A pinch of baking soda can bring out a new taste dimension when browning onions</em></p>
<p>Another basic ingredient found in most kitchens is <a href="http://en.wikipedia.org/wiki/Baking_soda">baking soda</a> (sodium bicarbonate, NaHCO<sub>3</sub>). It&#8217;s used as a leavning agent which requires addition of an acid to function. Since it is a weak base, it can be used to increase the pH and hence the speed of the Maillard reaction, for instance when browning onions. This basic task, <a href="http://www.washingtonpost.com/wp-dyn/content/article/2008/04/15/AR2008041500751.html">which isn&#8217;t always so easy after all</a>, benefits greatly from a pinch of baking soda (and surprisingly it seems that this hasn&#8217;t  been done before!). To illustrate this I&#8217;ve made a time lapse video of chopped onions being fried with and without baking soda. The frying took 11 min, but things are speeded up about 10x.</p>
<p><object width="425" height="344"><param name="movie" value="http://www.youtube.com/v/t3IFLtZZipk&#038;hl=en&#038;fs=1"></param><param name="allowFullScreen" value="true"></param><embed src="http://www.youtube.com/v/t3IFLtZZipk&#038;hl=en&#038;fs=1" type="application/x-shockwave-flash" allowfullscreen="true" width="425" height="344"></embed></object></p>
<p>Samples taken throughout the experiment are shown in the picture below. Even after 4 min there is a visible difference. After 11 min, the small addition of baking soda has yielded onions which taste remarkably sweet with strong caramel notes, compared to the control which tastes like fried onions.</p>
<p><img src="http://blog.khymos.org/wp-content/2008/09/onions_browning_time.jpg" alt="" title="onions_browning_time" width="450" height="450" class="alignnone size-full wp-image-468" /></p>
<p>Another example of how baking soda is used to speed up the Maillard reaction is <a href="http://en.wikipedia.org/wiki/Dulce_de_leche">dulce de leche</a>, a popular sauce/caramel candy in Latin America. It&#8217;s made by slowly boiling sweetened milk. Baking soda is not a <a href="http://www.wikihow.com/Make-Dulce-De-Leche">required</a> ingredient, but is <a href="http://www.wikihow.com/Make-Dulce-De-Leche">often</a> <a href="http://www.foodnetwork.com/recipes/alton-brown/dulce-de-leche-recipe/">included</a>. The baking soda gives dulce de leche a darker color and also contributes to the flavor.</p>
<p><img src="http://farm1.static.flickr.com/31/59763358_fb789efd23.jpg?v=0" alt="" /><br />
<em><a href="http://flickr.com/photos/audinou/59763358/">Photo</a> by <a href="http://flickr.com/photos/audinou/">audinou</a> from flickr.com.</em></p>
<p>It should perhaps be added that baking soda is frequently used in Chinese cooking, for instance in tempura batters and marinades. Once there, the baking soda will certainly speed up the Maillard reaction, but it also affects the texture of meat &#8211; I&#8217;ll have to return to that topic later.</p>
<p>To round of this post I will briefly touch upon one of the reasons why pH influences the Maillard reaction. The first step involves a reaction between a reducing sugar (depicted as R(C=O)H) and an amino acid (depicted as R&#8217;NH2) followed by loss of water to yield a Schiff base. The Schiff base rearranges to the Amadori product (not shown). Of these first steps the formation of the Schiff base is the bottleneck (rate limiting step). The reactivity of the amino acid is influenced by the pH. A <em>simplified</em> reasoning goes like this: At low pH the amino group is protonated, yielding it less nucleophilic. At higher pH, the nitrogen becomes more nucleophilic and at very high pH the amino group can even be deprotonated. It should be noted that the fate of the Amadori product is also in large determined by pH and hence pH will affect more than just the rate, but this is far beyond the scope of this blog post.</p>
<p><img src="http://blog.khymos.org/wp-content/2008/09/maillard-first-step.png" alt="" title="maillard-first-step" width="450" height="214" class="alignnone size-full wp-image-467" /></p>
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		</item>
		<item>
		<title>Lightstruck flavor in beer</title>
		<link>http://blog.khymos.org/2007/02/16/lightstruck-flavor-in-beer/</link>
		<comments>http://blog.khymos.org/2007/02/16/lightstruck-flavor-in-beer/#comments</comments>
		<pubDate>Fri, 16 Feb 2007 20:14:59 +0000</pubDate>
		<dc:creator>Martin Lersch</dc:creator>
				<category><![CDATA[academic articles]]></category>
		<category><![CDATA[molecular gastronomy]]></category>
		<category><![CDATA[science]]></category>
		<category><![CDATA[tips & tricks]]></category>
		<category><![CDATA[3-methylbut-2-ene-1-thiol]]></category>
		<category><![CDATA[beer]]></category>
		<category><![CDATA[brown glass]]></category>
		<category><![CDATA[butter]]></category>
		<category><![CDATA[clear glass]]></category>
		<category><![CDATA[corona]]></category>
		<category><![CDATA[degradation]]></category>
		<category><![CDATA[flavor]]></category>
		<category><![CDATA[light]]></category>
		<category><![CDATA[lightstruck]]></category>
		<category><![CDATA[lime]]></category>
		<category><![CDATA[marketing]]></category>
		<category><![CDATA[MBT]]></category>
		<category><![CDATA[milk]]></category>
		<category><![CDATA[off flavour]]></category>
		<category><![CDATA[olive oil]]></category>
		<category><![CDATA[oxidation]]></category>
		<category><![CDATA[radical]]></category>
		<category><![CDATA[riboflavin]]></category>
		<category><![CDATA[skunk]]></category>
		<category><![CDATA[skunky]]></category>
		<category><![CDATA[sun glass]]></category>
		<category><![CDATA[sun light]]></category>
		<category><![CDATA[thiol]]></category>
		<category><![CDATA[UV]]></category>

		<guid isPermaLink="false">http://blog.khymos.org/2007/02/16/lightstruck-flavor-in-beer/</guid>
		<description><![CDATA[Some years ago, a group of researches studied the formation of lightstruck flavor in beer (Chem. Eur. J. 2001, 4554). They found that isohumulones, compounds contributing to the bitter taste of beer, decomposed when exposed to ultraviolet light. In a recent blogpost, Harold McGee elaborates on this and it turns out that the way this [...]]]></description>
			<content:encoded><![CDATA[<p>Some years ago, a group of researches studied the formation of lightstruck flavor in beer (<a href="http://www3.interscience.wiley.com/cgi-bin/abstract/85514669/ABSTRACT"><em>Chem. Eur. J</em>. <strong>2001</strong>, 4554</a>). They found that isohumulones, compounds contributing to the bitter taste of beer, decomposed when exposed to ultraviolet light. In a recent blogpost, <a href="http://curiouscook.blogspot.com/2006/11/in-dark-olive-oil-milk-butter-and-beer.html">Harold McGee elaborates on this</a> and it turns out that the way this happens is even more complex than first anticipated. The researchers (<a href="http://pubs.acs.org/cgi-bin/abstract.cgi/jafcau/2006/54/i17/abs/jf060515v.html"><em>J. Agric. Food Chem</em>, <strong>2006</strong>, 6123</a>) found that <a href="http://en.wikipedia.org/wiki/Riboflavin">riboflavin</a> (vitamin B2) acts as a photosensitizer in beer (and in olive oil, milk and butter) which catalyzes the conversion of oxgyen to a more reactive type of oxygen (<a href="http://en.wikipedia.org/wiki/Singlet_oxygen">singlet oxygen</a>). This oxygen then &#8220;destroys&#8221; isohumulone and in the process radicals are formed.</p>
<p><img id="image118" src="http://blog.khymos.org/wp-content/2007/02/isohumulone1.jpg" alt="isohumulone1.jpg" /></p>
<p>As shown in the figure, the radical reacts with sulfur containing proteins, thereby forming a <a href="http://en.wikipedia.org/wiki/Thiol">thiol</a> called 3-methylbut-2-ene-1-thiol or just MBT for short. The amazing thing about this compound is that <strong>we can smell it at concentrations as low as a few parts per billion</strong> (ppb). The perhaps not-so-amazing thing is that this compound gives beer a <a href="http://en.wikipedia.org/wiki/Skunked_beer">&#8220;skunky&#8221; aroma</a>. Obviously one would want to avoid this, and that&#8217;s why beer is sold in dark brown glass bottles that act as the beer&#8217;s own sunglasses. Canned beer of course will not go skunky (well not until it&#8217;s poured into a glass and served outside in bright sunlight &#8211; that will turn any beer skunky within minutes). </p>
<p>Unfortunately however, not all beer is sold in dark bottles! One well known brand is shown in the picture below&#8230;</p>
<p><img id="image107" src="http://blog.khymos.org/wp-content/2007/02/mex_beer.jpg" alt="corona.jpg" /></p>
<p>And yes &#8211; as you might have figured out, 3-methylbut-2-ene-1-thiol is present in Corona beer (and other brands sold in clear bottles, to a lesser extent MBT is also found in green bottled beer). For some references to &#8220;skunky&#8221; off flavours in beer check out these links: <a href="http://www.tastebeer.com.au/beer/43">here</a>, <a href="http://www.evansale.com/skunked_beer.html">here</a> and <a href="http://www.beerinfo.com/rfdb/#link3-2">here</a>. The ubiquitious slice of lime served with Corona beer is nothing but clever marketing since it helps camouflage the smelly thiol formed! (but how well does lime actually camouflage the thiol aroma?)</p>
<p>The take home message is: keep your olive oil, milk, butter and beer away from sunlight! </p>
<img src="http://blog.khymos.org/?ak_action=api_record_view&id=97&type=feed" alt="" />]]></content:encoded>
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		<item>
		<title>Drink your tea without milk!</title>
		<link>http://blog.khymos.org/2007/01/10/drink-your-tea-without-milk/</link>
		<comments>http://blog.khymos.org/2007/01/10/drink-your-tea-without-milk/#comments</comments>
		<pubDate>Tue, 09 Jan 2007 23:44:23 +0000</pubDate>
		<dc:creator>Martin Lersch</dc:creator>
				<category><![CDATA[academic articles]]></category>
		<category><![CDATA[molecular gastronomy]]></category>
		<category><![CDATA[catechins]]></category>
		<category><![CDATA[flavonoid]]></category>
		<category><![CDATA[milk]]></category>
		<category><![CDATA[polyphenol]]></category>
		<category><![CDATA[tea]]></category>

		<guid isPermaLink="false">http://blog.khymos.org/2007/01/10/drink-your-tea-without-milk/</guid>
		<description><![CDATA[Experimental and clinical studies indicate that tea exerts protection against cardiovascular diseases. However, a group of German researchers (abstract, European Heart Journal 2007, ASAP contents) have found that the beneficial effects of drinking tea may be reduced if milk is added to the tea. (Picture by IreneM entiteld &#8220;coffee with a &#8220;drop&#8221; of milk&#8221; from [...]]]></description>
			<content:encoded><![CDATA[<p>Experimental and clinical studies indicate that tea exerts protection against cardiovascular diseases. However, a group of German researchers (<a href="http://eurheartj.oxfordjournals.org/cgi/content/abstract/ehl442v1">abstract</a>, <em>European Heart Journal</em> <strong>2007</strong>, ASAP contents) have found that the beneficial effects of drinking tea may be reduced if milk is added to the tea.</p>
<p><img width="400" src="http://images.dpchallenge.com/images_challenge/602/440344.jpg" alt="milk drop hits coffee" /><br />
(Picture by <a href="http://www.dpchallenge.com/image.php?IMAGE_ID=440344">IreneM</a> entiteld <em>&#8220;coffee with a &#8220;drop&#8221; of milk&#8221;</em> from <a href="http://www.dpchallenge.com">DPchallenge</a> &#8211; OK, it&#8217;s not tea, but I just love this picture!)</p>
<p>By measuring the blood vessel&#8217;s ability to expand (and thereby reduce the blood pressure) the researchers found that this ability was improved by tea, but the effect was completely blunted if milk was added to the tea. It was found that the caseins were responsible for the observed inhibition, probably by formation of complexes with catechins. It is believed that catechins (<a href="http://en.wikipedia.org/wiki/Polyphenol">polyphenolic</a> compounds, belong to the group of <a href="http://en.wikipedia.org/wiki/Flavonoids">flavonoids</a>, structure of <a href="http://en.wikipedia.org/wiki/Epicatechin">epicatechin</a> shown below) trigger the release of other active substances that are responsible for the expansion of blood vessels (also known as <a href="http://en.wikipedia.org/wiki/Vasodilation">vasodilation</a>).</p>
<p><img width="300" id="image75" src="http://blog.khymos.org/wp-content/2007/01/epicatechin.png" alt="epicatechin"/></p>
<p>The results of this study are not limited to tea, because catechins are found in many other foods, including citrus fruits, wine and <a href="http://www.chocolate.org/flavonoids.html">chocolate</a>.</p>
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