1984FEMS Microbiology LettersRequires access

Alanyl turnover from lipoteichoic acid to teichoic acid inStaphylococcus aureus

R. Haas, Hans-Georg Koch, Werner Fischer

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Abstract

The metabolism of d-alanyl substituents of lipoteichoic acid (LTA) and teichoic acid was studied in Staphylococcus aureus. Double labelling with [3H]glycerol and d-[14C]alanine revealed that during the chase LTA was stable whereas its 14C label rapidly decreased. Half-time comparison indicated an enzyme- rather than a base-catalyzed process. Correlated with the loss of [14C]alanine from LTA was an increase of the radioactivity in wall-linked alanine ester which, after hydrolysis with HF, proved to be linked to teichoic acid. These results suggest that LTA-alanine is the donor for alanine esterification of teichoic acid. In connection with previous data we hypothesize that the loss of alanine from LTA is compensated by de novo incorporation.

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The metabolism of d-alanyl substituents of lipoteichoic acid (LTA) and teichoic acid was studied in Staphylococcus aureus. Double labelling with [3H]glycerol and d-[14C]alanine revealed that during the chase LTA was stable whereas its 14C label rapidly decreased. Half-time comparison indicated an enzyme- rather than a base-catalyzed process. Correlated with the loss of [14C]alanine from LTA was an increase of the radioactivity in wall-linked alanine ester which, after hydrolysis with HF, proved to be linked to teichoic acid. These results suggest that LTA-alanine is the donor for alanine esterification of teichoic acid. In connection with previous data we hypothesize that the loss of alanine from LTA is compensated by de novo incorporation.

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Available abstract

The metabolism of d-alanyl substituents of lipoteichoic acid (LTA) and teichoic acid was studied in Staphylococcus aureus. Double labelling with [3H]glycerol and d-[14C]alanine revealed that during the chase LTA was stable whereas its 14C label rapidly decreased. Half-time comparison indicated an enzyme- rather than a base-catalyzed process. Correlated with the loss of [14C]alanine from LTA was an increase of the radioactivity in wall-linked alanine ester which, after hydrolysis with HF, proved to be linked to teichoic acid. These results suggest that LTA-alanine is the donor for alanine esterification of teichoic acid. In connection with previous data we hypothesize that the loss of alanine from LTA is compensated by de novo incorporation.

Key concepts: Teichoic acid, Lipoteichoic acid, Alanine, Staphylococcus aureus, Biochemistry, Chemistry, Hydrolysis, Enzyme

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