Affiliation:
1. Division of Research and Laboratories, National Jewish Hospital, Denver, Colorado
2. Department of Microbiology, University of Colorado School of Medicine, Denver, Colorado
Abstract
Harold
, F. M. (National Jewish Hospital, Denver, Colo.),
and J. R. Baarda
. Interaction of arsenate with phosphate-transport systems in wild-type and mutant
Streptococcus faecalis
. J. Bacteriol.
91:
2257–2262. 1966.—Arsenate competitively inhibits the growth of
Streptococcus faecalis
, primarily by competition with phosphate for a common transport system. Arsenate is itself accumulated by the cells; the uptake requires metabolic energy, and the intracellular arsenate level may reach 0.01
m
. Cells loaded with arsenate have lost the capacity to take up radioactive glutamate, rubidium, phosphate, or arsenate itself, apparently by the uncoupling of adenosine triphosphate generation. The
p
H dependence of arsenate uptake is complex. At low concentrations of extracellular arsenate, uptake by the wild-type strain 9790 exhibits a single maximum about
p
H 8; mutant PT-1, previously shown to be defective in phosphate uptake, takes up essentially no arsenate. At high concentrations of arsenate, uptake by the wild type is bimodal with maxima at
p
H 5.5 and 9; the uptake curve for mutant PT-1 corresponds to the shoulder in the curve for the wild type. The apparent dissociation constant for arsenate uptake by the wild type is approximately 10
−5
m
from
p
H 5 to 9, whereas that for mutant PT-1 is about 5 × 10
−5
M at
p
H 5 and rises rapidly with increasing
p
H. The results confirm the earlier conclusion that the lesion in mutant PT-1 resides in the transport of phosphate and arsenate. It is proposed that the wild type has two distinct transport systems, whereas the mutant has lost the one with alkaline
p
H optimum.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Reference13 articles.
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5. Arsenate uptake and release in relation to the inhibition of transport and glycolysis in yeast;JUNG C.;Biochem. Pharmacol.,1965
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