Abstract
The transport of D-alanine by Escherichia coli K-12 neither requires nor is stimulated by Na+. The transport of D-alanine by the marine bacterium Alteromonas haloplanktis 214 requires Na+ specifically. Mutants of E. coli which were unable to transport D-alanine were isolated by enrichment for D-cycloserine resistance. One of the mutants was transformed with a gene bank of A. haloplanktis chromosomal DNA. Two transformants, E. coli RM1(pPM1) and E. coli RM1(pPM2) were able to transport D-alanine by a Na+-dependent mechanism. Li+ and K+ were unable to replace Na+. Both transformants contained chimeric plasmids with inserts which hybridized with A. haloplanktis but not E. coli chromosomal DNA or each other. Despite the lack of homology between the inserts, Na+-dependent D-alanine transport in the two transformants could not be distinguished either by kinetic studies or by differences in the capacity of various amino acids to compete for D-alanine uptake.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Reference28 articles.
1. Different mechanisms of energy coupling for the shock-sensitive and shock-resistant amino acid permeases of Escherichia coli;Berger E. A.;J. Biol. Chem.,1974
2. D-Amino acid oxidase from kidney;Burton K.;Methods Enzymol.,1955
3. D-Serine transport system in Escherichia coli K-12;Cosloy S. D.;J. Bacteriol.,1973
4. Kinetic and genetic analyses of D-cycloserine inhibition and resistance in Escherichia coli;Curtiss R.;J. Bacteriol.,1965
5. Davis R. W. D. Botstein and J. R. Roth (ed.). 1980. Advanced bacterial genetics. A manual for genetic engineering p. 203-204. Cold Spring Harbor Laboratory Cold Spring Harbor N.Y.
Cited by
16 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献