A colony of Streptomyces coelicolor bacteria secretes an antibiotic compound (red) into the surrounding medium.Credit: Dr Jeremy Burgess/Science Photo Library
By studying the process through which a soil bacterium naturally produces a well-known drug, scientists have discovered a powerful antibiotic that could help to fight drug-resistant infections.
In experiments described in the Journal of the American Chemical Society on Monday1, the team studied the multi-step pathway that the bacterium Streptomyces coelicolor uses to make the antibiotic methylenomycin A, which was first identified in 19652,3. They discovered an intermediate compound — called premethylenomycin C lactone — whose antimicrobial activity was 100 times stronger than that of the final product. Tiny doses of it killed strains of bacteria known to cause hard-to-treat infections.
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The discovery was a ‘surprise’, says study co-author Gregory Challis, a chemical biologist at the University of Warwick in Coventry, UK. “As humans, we anticipate that evolution perfects the end product, and so you’d expect the final molecule to be the best antibiotic, and the intermediates to be less potent,” he says. But the finding “is a great example of what a ‘blind watchmaker’ evolution is. And it’s a good way of exemplifying it in a very molecular way,” adds Challis.
Antimicrobial resistance is a growing threat, projected to cause 39 million deaths worldwide over the next 25 years. Researchers say that the discovery of a potent antimicrobial compound might lead to fresh drugs to tackle resistance.
The work underscores “the potential of such studies to identify new bioactive chemical scaffolds from ‘old’ pathways”, says Gerard Wright, a biochemist at McMaster University in Hamilton, Canada.
Accidental discovery
In 2006, Challis and his colleagues began studying the molecular pathway through which Streptomyces coelicolor produces methylenomycin A. To do this, they deleted the genes encoding enzymes involved in each step, one by one. Their work built on earlier efforts in 2002 to sequence the bacterium’s genome4.
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