Transport of L-glutamic acid in the fission yeast Schizosaccharomyces pombe
Language English Country Netherlands Media print
Document type Journal Article
PubMed
1347456
DOI
10.1016/0005-2736(92)90088-4
PII: 0005-2736(92)90088-4
Knihovny.cz E-resources
- MeSH
- Biological Transport drug effects MeSH
- Cycloheximide pharmacology MeSH
- Fungal Proteins chemistry metabolism MeSH
- Glutamates chemistry metabolism MeSH
- Kinetics MeSH
- Hydrogen-Ion Concentration MeSH
- Glutamic Acid MeSH
- Schizosaccharomyces drug effects metabolism MeSH
- Substrate Specificity MeSH
- Carrier Proteins chemistry metabolism MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Cycloheximide MeSH
- Fungal Proteins MeSH
- Glutamates MeSH
- Glutamic Acid MeSH
- Carrier Proteins MeSH
Transport of L-glutamic acid into the fission yeast Schizosaccharomyces pombe grown to the early stationary phase and preincubated for 60 min with 1% D-glucose is practically unidirectional and is mediated by a single uphill transport system with a KT of 170 microM and Jmax of 4.8 nmol min-1 (mg dry wt.)-1. The system proved to be rather non-specific since all the amino acids transported into the cells acted as potent competitive inhibitors. It has a pH optimum at 3.0-4.0, the accumulation ratio of L-glutamic acid is highest at a suspension density of 0.6-1.0 mg dry wt. per ml and decreases with increasing L-glutamic acid concentrations in the external medium. The system present in the cells after preincubation with D-glucose is unstable and its activity decays after washing the cells with water or after stopping the cytosolic proteinsynthesis with cycloheximide, with a half-time of 24 min in a reaction significantly retarded by phenylmethylsulfonyl fluoride, a serine proteinase inhibitor. The synthesis of the transport protein appears to be repressible by ammonium ions.
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