Researchers working at the SLAC National Accelerator Laboratory have used powerful X-rays to help decipher how certain natural antibiotics defy a longstanding set of chemical reaction rules – a mechanism that has baffled organic chemists for decades. Their result, reported today in Nature, details how five carbon atoms and one oxygen atom in the structure of lasalocid, a natural antibiotic produced by bacteria in soil, can link into a six carbon member ring through an unfavorable chemical reaction pathway that will not occur otherwise. Unlocking this chemical pathway could enable scientists to artificially synthesize many important chemicals currently found only in nature.
Researchers working at the SLAC National Accelerator Laboratory have used powerful X-rays to help decipher how certain natural antibiotics defy a longstanding set of chemical reaction rules – a mechanism that has baffled organic chemists for decades. Their result, reported today in Nature, details how five carbon atoms and one oxygen atom in the structure of lasalocid, a natural antibiotic produced by bacteria in soil, can link into a six carbon member ring through an unfavorable chemical reaction pathway that will not occur otherwise. Unlocking this chemical pathway could enable scientists to artificially synthesize many important chemicals currently found only in nature.
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"Our study has a broad implication because the six-membered ring is a common structural feature found in hundreds of drug molecules produced by nature," said the study's principal investigator, Chu-Young Kim of the National University of Singapore. "We have actually analyzed the genes of six other organisms that produce similar drugs and we are now confident that the chemical mechanism we have uncovered applies to these other organisms as well."
According to "Baldwin's Rules for Ring Closure," this compound should contain a five-membered ring instead of the observed six-membered ring. Baldwin's Rules in organic chemistry are a series of guidelines outlining the relative favorabilities of ring closure reactions in alicyclic compounds
The solution to the molecular mystery depended in large part on a deeper understanding of the unique protein Lsd19, the catalyst that enables the formation of lasalocid's rings. To determine the protein's atomic structure, the researchers hit frozen crystals of Lsd19 with X-rays from SLAC's Stanford Synchrotron Radiation Lightsource and observed how the crystals diffracted the X-rays passing through. "You need atomic-level detail of the crystal's structure to understand what's really happening," said co-author Irimpan Mathews, a staff scientist at SLAC.
"The bugs have taught us a valuable chemistry lesson," Kim said. "With a new understanding of how nature synthesizes the six-membered rings, chemists may be able to develop novel methods that will enable us to produce these drugs with ease in the chemical laboratory. Alternatively, protein engineers may be able to use our results to develop a biofactory where these drugs are mass produced using a fermentation method. Either method will make more effective and more affordable drugs available to the public."
Kim's group has moved on to their next challenge: investigating how nature synthesizes the anti-cancer drug echinomycin. Echinomycin is a peptide antibiotic that help blocks specific bonding sites on a DNA chain.
For further information: http://www.physorg.com/news/2012-03-x-rays-reveal-soil-bacteria-chemistry.html or http://www.nature.com/nature/journal/vaop/ncurrent/full/nature10865.html
Photo: Dr. Kinya Hotta
