a Department of Biochemistry and Biophysics, University of California, Davis, California 95616
ABSTRACT
Cycloheximide (actidione) has an immediate inhibitory effect on amino acid transport by nitrogen-starved or carbon-starved mycelium suspended in phosphate buffer. High concentrations of phosphate alone are slightly inhibitory; cycloheximide appears to potentiate the effect of phosphate. Ca2+ reverses the inhibition of transport caused by phosphate plus cycloheximide. Ca2+ did not relieve the inhibition of protein synthesis. Cycloheximide promotes a continual uptake of 45Ca2+ by the mycelium. The cumulative results suggest that (i) membrane-bound Ca2+ is involved in amino acid transport, (ii) cycloheximide labilizes the membrane-bound Ca2+, and (iii) phosphate forms a complex with Ca2+ making it unavailable for its role in transport. The effect of cycloheximide described above is observed within 1 to 2 min after addition of the antibiotic. This initial inhibition occurs more rapidly with 103 M cycloheximide than with 105 M cycloheximide. However, after a longer preincubation time, a curious inverse relationship between cycloheximide concentration and amino acid transport is observed. The mycelium incubated with 105 M cycloheximide remains strongly inhibited (unless the antibiotic is washed away). The mycelium incubated with 103 M cycloheximide recovers about 40% of the transport activity lost during the rapid initial phase. We have no obvious explanation for the inverse effect.
1 Present address: Institute for Enzyme Research, University of Wisconsin, Madison, Wis. 53706.
| Appl. Environ. Microbiol. | Infect. Immun. | Eukaryot. Cell |
|---|---|---|
| Mol. Cell. Biol. | J. Virol. | Microbiol. Mol. Biol. Rev. |
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