JB
Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Shieh, K. Z.
Right arrow Articles by Hedrick, L. R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Shieh, K. Z.
Right arrow Articles by Hedrick, L. R.

 Previous Article  |  Next Article 

J Bacteriol. 1966 December; 92(6): 1638-1644
Copyright © 1966 American Society for Microbiology. All Rights Reserved.

Energy Requirement for L-Glutamate Uptake and Utilization by Hansenula subpelliculosa Cells

K. Z. Shieh and L. R. Hedrick

Department of Biology, Illinois Institute of Technology, Chicago, Illinois

ABSTRACT

SHIEH, K. Z. (Illinois Institute of Technology, Chicago), AND L. R. HEDRICK. Energy requirement for L-glutamate uptake and utilization by Hansenula subpelliculosa cells. J. Bacteriol. 92:1638–1644. 1966.—Cells of the yeast Hansenula subpelliculosa require an energy source for the uptake of glutamate. A lag period of 20 to 40 min was required after the addition of glucose to the cells before glutamate uptake was initiated. When cells were preincubated in glucose, and washed with distilled water prior to the addition of glutamate, there was no lag period. Preincubation in glucose and glutamate lowered both the rate and the total uptake of glutamate as compared with cells preincubated in glucose alone. This is attributed to the partial utilization of the glucose-metabolite by glutamate or to the partial saturation of binding sites by glutamate during the preincubation period. Transport of glutamate by these yeast cells appears to be via a carrier, where energy is required for the binding of the amino acid to nonspecific binding sites. In addition to total uptake, some aspects of the C14-glutamate utilization were measured. Of the total uptake, 58% was metabolized and converted to CO2, 25.2% remained in the soluble pool, and 16.8% was incorporated into trichloroacetic acid-insoluble products. When the available energy source was depleted, the processes of uptake, metabolism, and incorporation ceased, even though there was an ample supply of glutamate present within the cells. Removal of cells from glutamate and addition of glucose reinitiated the incorporation of glutamate into proteins and other trichloroacetic acid-insoluble compounds. Therefore, an additional energy source is required with this species of yeast for glutamate uptake, for the priming of mechanisms required for its metabolism, and for its incorporation.


J Bacteriol. 1966 December; 92(6): 1638-1644
Copyright © 1966 American Society for Microbiology. All Rights Reserved.







Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
Appl. Environ. Microbiol. Infect. Immun. Eukaryot. Cell
Mol. Cell. Biol. J. Virol. Microbiol. Mol. Biol. Rev.
ALL ASM JOURNALS

Copyright © 1966 by the American Society for Microbiology. All rights reserved.