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Potent Inhibition of Bacterial DNA Gyrase by Digallic Acid and Other Gallate Derivatives
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Abstract
Bacterial DNA gyrase, an essential enzyme, is a validated target for discovering and developing new antibiotics. Here we screened a pool of polyphenols and discovered that digallic acid is a potent DNA gyrase inhibitor. We also found that several food additives based on gallate, such as dodecyl gallate, potently inhibit bacterial DNA gyrase. Interestingly, the IC
50
of these gallate derivatives against DNA gyrase is correlated with the length of hydrocarbon chain connecting to the gallate. These new bacterial DNA gyrase inhibitors are ATP competitive inhibitors of DNA gyrase. Our results also show that digallic acid and certain gallate derivatives potently inhibit
E. coli
DNA topoisomerase IV. Several gallate derivatives have strong antimicrobial activities against
Staphylococcus aureus
and
methicillin‐resistant Staphylococcus aureus (MRSA)
. This study provides a solid foundation for the design and synthesis of gallate‐based DNA gyrase inhibitors that may be used to combat antibacterial resistance.
Title: Potent Inhibition of Bacterial DNA Gyrase by Digallic Acid and Other Gallate Derivatives
Description:
Abstract
Bacterial DNA gyrase, an essential enzyme, is a validated target for discovering and developing new antibiotics.
Here we screened a pool of polyphenols and discovered that digallic acid is a potent DNA gyrase inhibitor.
We also found that several food additives based on gallate, such as dodecyl gallate, potently inhibit bacterial DNA gyrase.
Interestingly, the IC
50
of these gallate derivatives against DNA gyrase is correlated with the length of hydrocarbon chain connecting to the gallate.
These new bacterial DNA gyrase inhibitors are ATP competitive inhibitors of DNA gyrase.
Our results also show that digallic acid and certain gallate derivatives potently inhibit
E.
coli
DNA topoisomerase IV.
Several gallate derivatives have strong antimicrobial activities against
Staphylococcus aureus
and
methicillin‐resistant Staphylococcus aureus (MRSA)
.
This study provides a solid foundation for the design and synthesis of gallate‐based DNA gyrase inhibitors that may be used to combat antibacterial resistance.
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