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 HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Marcus, M.
Right arrow Articles by Halpern, Y. S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Marcus, M.
Right arrow Articles by Halpern, Y. S.
J Bacteriol. 1967 April; 93(4): 1409-1415
Copyright © 1967 American Society for Microbiology. All Rights Reserved.

Genetic Analysis of Glutamate Transport and Glutamate Decarboxylase in Escherichia coli1

Menashe Marcus and Yeheskel S. Halpern

a Department of Bacteriology, The Hebrew University-Hadassah Medical School, Jerusalem, Israel

ABSTRACT

The location of the Escherichia coli K-12 genes determining or regulating glutamate transport, and the location of the gene determining glutamate decarboxylase synthesis, were established by conjugation. The ability to grow on glutamate as the sole source of carbon and energy was used to select for glutamate transport recombinants. Two genes determining the ability to grow on glutamate as the sole source of carbon and energy were mapped. One (gltC) is located near mtl (mannitol), and the other (gltH) appears to be located between the gal (galactose) and trp (tryptophan) loci. The glutamate decarboxylase gene (gad) is strongly linked to gltC. The gltC+ recombinants grow on glutamate much faster and accumulate this amino acid to a greater extent than do the gltH+ recombinants. The gltH+ gene functioned only in one female strain (P678), whereas the gltC gene functioned in all the female strains tested (P678, C600, W1).


FOOTNOTES

1 Part of this work was taken from the Ph.D. thesis to be submitted by M. M. to the Senate of the Hebrew University.


J Bacteriol. 1967 April; 93(4): 1409-1415
Copyright © 1967 American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:




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 © 1967 by the American Society for Microbiology. All rights reserved.