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Role of Glutamine Synthetase in Nitrogen Metabolite Repression in Aspergillus nidulans
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ABSTRACT
Glutamine synthetase (GS), EC
6.3.1.2
, is a central enzyme in the assimilation of nitrogen and the biosynthesis of glutamine. We have isolated the
Aspergillus nidulans glnA
gene encoding GS and have shown that
glnA
encodes a highly expressed but not highly regulated mRNA. Inactivation of
glnA
results in an absolute glutamine requirement, indicating that GS is responsible for the synthesis of this essential amino acid. Even when supplemented with high levels of glutamine, strains lacking a functional
glnA
gene have an inhibited morphology, and a wide range of compounds have been shown to interfere with repair of the glutamine auxotrophy. Heterologous expression of the prokaryotic
Anabaena glnA
gene from the
A. nidulans alcA
promoter allowed full complementation of the
A. nidulans glnA
Δ mutation. However, the
A. nidulans fluG
gene, which encodes a protein with similarity to prokaryotic GS, did not replace
A. nidulans glnA
function when similarly expressed. Our studies with the
glnA
Δ mutant confirm that glutamine, and not GS, is the key effector of nitrogen metabolite repression. Additionally, ammonium and its immediate product glutamate may also act directly to signal nitrogen sufficiency.
American Society for Microbiology
Title: Role of Glutamine Synthetase in Nitrogen Metabolite Repression in
Aspergillus nidulans
Description:
ABSTRACT
Glutamine synthetase (GS), EC
6.
3.
1.
2
, is a central enzyme in the assimilation of nitrogen and the biosynthesis of glutamine.
We have isolated the
Aspergillus nidulans glnA
gene encoding GS and have shown that
glnA
encodes a highly expressed but not highly regulated mRNA.
Inactivation of
glnA
results in an absolute glutamine requirement, indicating that GS is responsible for the synthesis of this essential amino acid.
Even when supplemented with high levels of glutamine, strains lacking a functional
glnA
gene have an inhibited morphology, and a wide range of compounds have been shown to interfere with repair of the glutamine auxotrophy.
Heterologous expression of the prokaryotic
Anabaena glnA
gene from the
A.
nidulans alcA
promoter allowed full complementation of the
A.
nidulans glnA
Δ mutation.
However, the
A.
nidulans fluG
gene, which encodes a protein with similarity to prokaryotic GS, did not replace
A.
nidulans glnA
function when similarly expressed.
Our studies with the
glnA
Δ mutant confirm that glutamine, and not GS, is the key effector of nitrogen metabolite repression.
Additionally, ammonium and its immediate product glutamate may also act directly to signal nitrogen sufficiency.
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<p><strong><span dir="ltr" role="presentation">1. Introduction</span></strong&...

