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Derepression of Uridine Diphosphate-Glucose Pyrophosphorylase ( galU ) in capR ( lon ), capS , and capT Mutants and Studies on the
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Mutation of the
capR
(
lon
),
capS
, or
capT
genes in
Escherichia coli
K-12 causes overproduction of capsular polysaccharide leading to a mucoid phenotype. Several of the enzymes involved in capsular polysaccharide synthesis are derepressed in
cap
mutants. Previously it was shown that uridine diphosphate-glucose (UDPG) pyrophosphorylase, an enzyme involved in the synthesis of three of the nucleotide sugar precursors of the capsule, is derepressed in
capR
mutants. The control of
galU
, the gene which codes for UDPG pyrophosphorylase, is described in this study. In addition, it has been found that the enzyme is also derepressed in
capS
and
capT
mutants. The effect of
galU
gene dosage in
cap
mutants and the wild-type strain (all lysogenic for φ80) was studied by infecting them with the purified transducing phage φ80
dgalU
. The level of UDPG pyrophosphorylase increased in proportion to the number of
galU
copies added. The rate of enzyme synthesis in the mutants was about sixfold higher than in the wild type per
galU
gene added for multiplicities of infection from one to twenty. Thus, all the
galU
copies added to the wild-type lysogen were repressed. We obtain greater than 20
galU
copies per cell by infecting the nonlysogenic strain which allows multiplication of φ80
dgalU
. With some number of
galU
copies greater than 20, the rate of UDPG pyrophosphorylase synthesis in the wild type approaches the mutant rate of synthesis. The results suggest that there may indeed be a
galU
repressor pool in the cell which can be completely titrated. This pool must be composed of more than 20
galU
repressor molecules. Since the
capR
,
capS
, and
capT
gene products or combinations thereof are known to control other widely separated operons of the cell besides the
galU
gene, it is postulated that the
galU
repressor may be capable of binding other operators. This would account for the relatively large pool of
galU
repressors per cell.
American Society for Microbiology
Title: Derepression of Uridine Diphosphate-Glucose Pyrophosphorylase (
galU
) in
capR
(
lon
),
capS
, and
capT
Mutants and Studies on the
Description:
Mutation of the
capR
(
lon
),
capS
, or
capT
genes in
Escherichia coli
K-12 causes overproduction of capsular polysaccharide leading to a mucoid phenotype.
Several of the enzymes involved in capsular polysaccharide synthesis are derepressed in
cap
mutants.
Previously it was shown that uridine diphosphate-glucose (UDPG) pyrophosphorylase, an enzyme involved in the synthesis of three of the nucleotide sugar precursors of the capsule, is derepressed in
capR
mutants.
The control of
galU
, the gene which codes for UDPG pyrophosphorylase, is described in this study.
In addition, it has been found that the enzyme is also derepressed in
capS
and
capT
mutants.
The effect of
galU
gene dosage in
cap
mutants and the wild-type strain (all lysogenic for φ80) was studied by infecting them with the purified transducing phage φ80
dgalU
.
The level of UDPG pyrophosphorylase increased in proportion to the number of
galU
copies added.
The rate of enzyme synthesis in the mutants was about sixfold higher than in the wild type per
galU
gene added for multiplicities of infection from one to twenty.
Thus, all the
galU
copies added to the wild-type lysogen were repressed.
We obtain greater than 20
galU
copies per cell by infecting the nonlysogenic strain which allows multiplication of φ80
dgalU
.
With some number of
galU
copies greater than 20, the rate of UDPG pyrophosphorylase synthesis in the wild type approaches the mutant rate of synthesis.
The results suggest that there may indeed be a
galU
repressor pool in the cell which can be completely titrated.
This pool must be composed of more than 20
galU
repressor molecules.
Since the
capR
,
capS
, and
capT
gene products or combinations thereof are known to control other widely separated operons of the cell besides the
galU
gene, it is postulated that the
galU
repressor may be capable of binding other operators.
This would account for the relatively large pool of
galU
repressors per cell.
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