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Better Living Through Chiral Chemistry

Atario writes "A long time ago, I remember reading in some science magazine that someone had the bright idea of using enantiomers (the two forms of asymmetrical molecules, like left- and right-handed versions of the same one) to make zero-calorie sugar -- turns out, in general, that sugars are all asymmetrical, and everything generates and uses only one of the two chiralities (handednesses) for each one. If we consume a mirrored version of, say, sucrose, we might get all of the sweet but none of the calories. Sweet-tooths rejoice! But nothing ever came of it. Now, however, Wired has an interesting article that explains what the holdup has been and indicates the logjam may break soon, but, as it turns out, in a non-synthetic, albeit nonzero-calorie, way."

18 of 68 comments (clear)

  1. Why don't you drink Aquafina instead of Mt. Dew??? by Anonymous Coward · · Score: 2, Funny

    you Gnu hippies

  2. Sure there are no side effects by cybermancer · · Score: 2, Interesting

    Seems like every time they come out with a new 0-cal sweetener, that is safer then the last, it turns out to have some unforseen side effect that makes it worse then the last.

    --
    "Anything is possible with enough programmers, time and pizza." (Substitute caffeine for time as needed.)
    1. Re: Sure there are no side effects by Black+Parrot · · Score: 3, Funny


      > Seems like every time they come out with a new 0-cal sweetener, that is safer then the last, it turns out to have some unforseen side effect that makes it worse then the last.

      Fortunately, this one merely makes the water in your toilet spiral down the wrong way when you flush it.

      --
      Sheesh, evil *and* a jerk. -- Jade
  3. The one time patents would be a Good Thing... by RobertB-DC · · Score: 2, Insightful

    For once, a patent would appear to be supporting innovation. An individual with an idea sees the potential, files a patent, and goes on a quest to commercialize the product. There could be no better case study of how patent law is supposed to encourage innovation.

    But alas, it's not to be. From the article:
    The patent on tagatose as an additive expires in 2006, the two patents on production methods a few years later. [Inventor Gilbert] Levin hopes to see his sugar substitute flood the market before then.

    Meanwhile, the current silliness at the patent office will help ensure that Levin will join the legions of brilliant inventors with "died nearly destitute" included somewhere in their epitaphs. Instead of an individual getting his due from an actual original thought, big corporations are set to reap millions from ridiculous "business method" patents. Again, from the article:
    Kellogg's obtained a patent in 2002 to use tagatose in "improved sucrose-free, noncarcinogenic, reduced-calorie, insulin-independent" sweet cereals. Wrigley and Kraft have patents of their own.

    It's situations like this that make me glad to be a wage slave, with all my original ideas signed over to my own^h^h^hemployer.

    --
    Stressed? Me? Of course not. Stress is what a rubber band feels before it breaks, silly.
    1. Re:The one time patents would be a Good Thing... by Alsee · · Score: 3, Funny

      Kraft have patents of their own

      Patent sprinkling Viagra on cheese as a drug delivery system.

      BEHOLD, THE POWER OF CHEESE!

      -

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      - - You can't take something off the Internet! That's like trying to take pee out of a swimming pool.
  4. Whoa by xenocide2 · · Score: 3, Funny

    For Levin, it was a third tour at Hopkins; he received a bachelor's in 1947 and a master's in sanitary engineering a year later.

    And I always thought that a janitor was an entry level position.

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  5. Serendipity and poor laboratory technique by drox · · Score: 2, Interesting

    I was impressed by the role serendipity has played in the discovery of sweeteners. But

    In 1937, a University of Illinois grad student discovered another sweetener when he set his cigarette on a lab bench during an experiment - testing a would-be antifever drug - and then took a drag off the cyclamate-coated end.

    might be taking things a bit too far. Smoking in the laboratory? My how times have changed!

    Still, the cyclamates are now banned (in the US anyway), while you can still buy cigarettes in any quik-E-mart. You just can't smoke them in the laboratory! Or in most public buildings.

  6. non-nutritive "food" by dpilot · · Score: 4, Funny

    Two years of Newtrition investment and research had produced CHOW(TM). CHOW(TM) contained spun, plaited, and woven protein molecules, capped and coded, carefully designed to be ignored by even the most ravenous digestive tract enzymes; no-cal sweeteners; mineral oils replacing vegetable oils; fibrous materials, colorings, and flavorings. The end result was a foodstuff almost indistinguishable from any other except for two things. Firstly, the price, which was slightly hgher, and secondly the nutritional content, which was roughly equivalent to that of a Sony Walkman. It didn't matter how much you ate, you lost weight.*

    * And hair. And skin tone. And, if you ate enought of it long enough, vital signs.

    From Good Omens, by Terry Pratchett and Neil Gaiman. (pg 110 in my copy)

    --
    The living have better things to do than to continue hating the dead.
  7. Stereochemistry - handedness overly simplistic by Zeio · · Score: 4, Insightful

    Some compounds are listed as d- and l- refer to the highest-numbered asymmetric stereogenic centers. They also do not indicate the sign of rotation of plane-polarized light.

    Most interesting organic compounds have multiple stereogenic centers. One of the main reasons plants are used to obtain starting materials for various modern drugs, ergot infested rye (indole substrate), poppies, indica sativa all provide starting points that make it so that creating synthetic materials based on these plant extracts as starting reagents is far easier due to the fact plant enzymes can place each stereogenic center in the right conformation and in wet chemistry this is exceedingly difficult. Mentioning some of the starting plants for illicit drugs is no mistake; they are notoriously sensitive to chiral conformation, and provide some of the most interesting sterochemical research subject matter. Also, due to the draconian laws surrounding federally controlled substances and their precursors, it isn't easy to study these things, despite being hugely important.

    To say that stereochemistry is limited to 2-handedness is a ridiculous oversimplification of reality. If I'm not mistaken, C6-H12-O6 "glucose"; has D-glucose has 4 chiral carbon atoms (2^4 = 16 possible stereoisomers) - I believe only one of which is able to provide calories.

    Various notations for stereochemistry exist, and one must factor out canonical conformations and take into account the bending of the various stereogenic centers in 3d-space, leading to notations that include "boat" and "chair."

    Now, as to the practicality of stereogenics and its use in zero calorie metabolism: this is probably less difficult than separating U238 and U235, but one could probably get an enzyme of modify bacteria to plunk out zero-cal conformations, but in large scale synthetic operations, getting picky with chirality could be problematic / costly. Things are ridiculously hard to separate, and you need to use special techniques such as using tartrate salts and other expensive and slow ways of picking out the various conformations of chiral compounds.

    --
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    1. Re:Stereochemistry - handedness overly simplistic by mike3411 · · Score: 2, Informative

      This is a pretty good comment, but I'd like to add that the reason why a certain enantiomer of a sugar would not convey calories is because it would fail to react with digestive enzymes. However, any chemical that is altered to remove specificity for these enzymes is also likely to cease its specificity for the taste receptors that register "sweet". While I believe that taste receptors might be a little bit more lenient, I would bet that this would be one of the problems. The extreme difficulty/cost of seperating enantiomers being another, as noted in the parent. which is why other approaches are yielding results more quickly, such as the undigestible "fat" of Olestra.

      and btw IAABOC (i am a bioorganic chemist)

      well, in training. give me a few years ; )

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    2. Re:Stereochemistry - handedness overly simplistic by MillionthMonkey · · Score: 3, Informative

      To say that stereochemistry is limited to 2-handedness is a ridiculous oversimplification of reality. If I'm not mistaken, C6-H12-O6 "glucose"; has D-glucose has 4 chiral carbon atoms (2^4 = 16 possible stereoisomers) - I believe only one of which is able to provide calories.

      It isn't as neat as that.

      In general N chiral carbons means 2^N possible configurations. Half of these are mirror images (enantiomers) of each other. That means there are 2^(N-1) distinct epimers. These are distinct chemicals in their own right. They don't just taste different and rotate light backwards. They have different melting points, solubilities, IR spectra, etc.

      So glucose, with its 4 chiral carbons, is a member of a family of eight related epimers. Any two of the 8 will differ from each other in that between 1 to 3 (1 to N-1) carbons have flipped chirality, making them diastereomers of each other- some carbons are flipped, some aren't. And each has a D and an L form.

      The 8 epimers of glucose (including glucose itself) have names: allose, altrose, glucose, mannose, gulose, idose, galactose, and talose. Collectively they are referred to as aldohexoses. As far as I know, most are digestible and taste more or less sweet. Gulose is nonfermentable. Galactose is less sweet than glucose but certainly has calories since it's a component of lactose. Finding information on what the rare ones taste like is difficult. They don't appear in many cookbooks and the people who work with them don't seem to be terribly interested in telling us what they taste like.

    3. Re:Stereochemistry - handedness overly simplistic by Tower · · Score: 2, Funny

      >Galactose is less sweet than glucose

      I for one welcome our new sugar epimer overlords.

      --
      "It's tough to be bilingual when you get hit in the head."
    4. Re:Stereochemistry - handedness overly simplistic by Sgt+York · · Score: 2, Informative
      Taste and scent receptors are more lenient. They are not the typical "one receptor, one ligand" forms that you see everywhere else. They are designed to react to a wide array of similar molecules as opposed to having a high affinity for one molecule, and virtually none for anything else. "Sweet" receptors can react to any sugar, even disaccharides. For example, two enantiomers of glucose are much more similar chemically and biochemically than are glucose and fructose. Both fructose and glucose have the same apparent effect (they both taste similarly sweet).

      As far as separation goes, try this:

      Take a small peptide analogous to the binding sequence of a glucose transporter, high affinity metabolic enzyme, etc. There are quite a few you can chose from. Select for enantiomer specificity. Synthesize a large quantity. Mass production of a small peptide isn't terribly expensive, e.g. aspartame. Bind it to your matrix of choice and pack a column. Run your mix through it and now, the biologically active form is gone, leaving you with the inactive forms coming out of the column. When it gets "full", wash it all out and reuse.

      and btw IAABOC (i am a bioorganic chemist)

      Me too. In fact, the reason I came up with this is because I'm collecting fractions of an enzyme by an affinity column right now.

      --

      There is a reason for everything. Sometimes that reason just sucks.

  8. Re:You can't patent sugar! by CaptKilljoy · · Score: 2, Funny

    You mean "You can't patent sugar that's just fucked up!", right?

  9. Re:Composition doesn't determine taste by Bowling+Moses · · Score: 2, Informative

    Most of this is correct, except that cellulose is actually a polymer made up of glucose. More specifically, cellulose is beta(1,4)-linked glucose. This online lecture has a picture of cellulose both as a linear chain and as how linear chains can form a more complex sheets (not pictured: the sheets can then stack). We can't use cellulose because we don't have cellulase, a series of enzymes that can hydrolyze the chain. It's been a while, but I think it pops off glucose pairs, not monomers but I could be mistaken.

  10. Celebrity deathmatch: Murphy vs Darwin by Alsee · · Score: 3, Funny

    In 1879, chemists Ira Remsen and Constantine Fahlberg synthesized a derivative of coal tar called orthobenzoyl sulfimide. One day, Fahlberg spilled the substance on his hand, which later that evening he touched to his mouth. It tasted sweet. He filed for a patent and called the substance saccharin. In 1937, a University of Illinois grad student discovered another sweetener when he set his cigarette on a lab bench during an experiment - testing a would-be antifever drug - and then took a drag off the cyclamate-coated end. In 1965, a chemist named Jim Schlatter was working on a compound to treat gastric ulcers. He licked his finger to grab a sheet of paper and tasted aspartame for the first time. Then there was the 1976 discovery of sucralose by a King's College student working with chemically altered sugars. The student - not a native English speaker - mistook his professor's instruction to "test" the material and tasted a mouthful.

    Thus conclusively proving that Murphy's law defeats Darwin's law.

    -

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  11. Sweeteners are safer than sugar. by Benm78 · · Score: 2, Interesting
    You should consider the way these substances are tested. If you would test a artificial sweetener in an animal experiment, you would probably use a dose larger than the dose you expect in humans.

    This is very common practice, since it would take too many animals to do a proper test at the expected dose. To determine a 1/million fatality, you would need millions of lab rats if you'd test at the human dose.

    So, if you would test at 100 times the expected dose in humans, this would be a proper experiment for an artificial sweetener.

    However, if we would do the same experiment with ordinary sugar, you would get very strange results. If you would look at the risks of consuming 100 grams of sugar a day in a human, the experiment would involve daily consumption of 10 kilograms of sugar a day. Needless to say, the mortality in the subjects of such experiment would be 100% within a week or so (probably sooner).

    But when testing at the normal dose, I would not be surprised if you'd find that a group on sweetener would have a better life expectancy than a group on 'real' sugar.

    A one-in-a-million chance on cancer would, in my opinion, be better than a one-in-ten chance of contracting obesitas, diabetes and/or cardiovascular problems.

    When looking at the total risk, it would be wise to ban sugar and favour sweeters right here, right now. Luckily, people can choose for themselves, but I think they should be informed better.

  12. Ah, yes, the puritan brigade by Atario · · Score: 2, Insightful

    ..."Lightly Sarcastic" division.

    No one is saying they can't not eat something. They just want to. Anything wrong with that? If science can provide a way to do so with no (or less) negative side-effects, where's the harm?

    Saying "never mind technological advances, concentrate on getting along with the way things are" results in stagnation. If it weren't for human vices such as laziness and gluttony, we'd still be walking from cave to cave every morning to assemble our spear-hunting parties for the day.

    Why do you drive a car, or ride a bike, or take a train, or use a computer or a telephone? To avoid all the tedium of the alternatives -- a.k.a. laziness.

    Why do you buy food at the grocery store instead of growing and/or hunting your own? To avoid all the hard labor and time consumption of farming and ranching -- a.k.a. laziness -- and because you'd never be able to make enough of the foods you like -- a.k.a. gluttony -- and because hunting can be dangerous -- a.k.a. cowardice.

    Why do you seek a better job or business than the one you have? Because you want more money -- a.k.a. greed.

    The list goes on. Human weaknesses drive human progress.

    --
    "A great democracy must be progressive or it will soon cease to be a great democracy." --Theodore Roosevelt