Inhibition of synthesis of arabinogalactan by ethambutol in Mycobacterium smegmatis.

Abstract:

:Ethambutol at 3.0 micrograms/ml inhibited the transfer of label from D-[14C]glucose into the D-arabinose residue of arabinogalactan in whole cells of a drug-susceptible strain of Mycobacterium smegmatis. This inhibition began almost immediately after exposure of the cells to the drug. When drug-resistant M. smegmatis was used in a similar experiment, no such drug inhibition was detected. A much higher concentration of ethambutol (greater than 50 micrograms/ml) was required to show this inhibition. The drug also inhibited synthesis of arabinose-containing oligosaccharides when a cell-free enzyme system was used. These results suggest that the site of action of ethambutol is somewhere on the pathway between the conversion of D-glucose to D-arabinose and the transfer of arabinose into arabinogalactan. The primary mode of action of ethambutol appears to be inhibition of arabinogalactan synthesis.

authors

Takayama K,Kilburn JO

doi

10.1128/aac.33.9.1493

subject

Has Abstract

pub_date

1989-09-01 00:00:00

pages

1493-9

issue

9

eissn

0066-4804

issn

1098-6596

journal_volume

33

pub_type

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