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Characterization of the biotin uptake system encoded by the biotin-inducible bioYMN operon of Corynebacterium glutamicum
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Abstract
Background
The amino acid-producing Gram-positive
Corynebacterium glutamicum
is auxotrophic for biotin although biotin ring assembly starting from the precursor pimeloyl-CoA is still functional. It possesses AccBC, the α-subunit of the acyl-carboxylases involved in fatty acid and mycolic acid synthesis, and pyruvate carboxylase as the only biotin-containing proteins. Comparative genome analyses suggested that the putative transport system BioYMN encoded by
cg2147, cg2148
and
cg2149
might be involved in biotin uptake by
C. glutamicum
.
Results
By comparison of global gene expression patterns of cells grown with limiting or excess supply of biotin or with dethiobiotin as supplement replacing biotin revealed that expression of genes coding for enzymes of biotin ring assembly and for the putative uptake system was regulated according to biotin availability. RT-PCR and 5'-RACE experiments demonstrated that the genes
bioY, bioM
, and
bioN
are transcribed from one promoter as a single transcript. Biochemical analyses revealed that BioYMN catalyzes the effective uptake of biotin with a concentration of 60 nM biotin supporting a half-maximal transport rate. Maximal biotin uptake rates were at least five fold higher in biotin-limited cells as compared to cells grown with excess biotin. Overexpression of
bioYMN
led to an at least 50 fold higher biotin uptake rate as compared to the empty vector control. Overproduction of BioYMN alleviated biotin limitation and interfered with triggering L-glutamate production by biotin limitation.
Conclusions
The operon
bioYMN
from
C. glutamicum
was shown to be induced by biotin limitation. Transport assays with radio-labeled biotin revealed that BioYMN functions as a biotin uptake system. Overexpression of
bioYMN
affected L-glutamate production triggered by biotin limitation.
Springer Science and Business Media LLC
Title: Characterization of the biotin uptake system encoded by the biotin-inducible bioYMN operon of Corynebacterium glutamicum
Description:
Abstract
Background
The amino acid-producing Gram-positive
Corynebacterium glutamicum
is auxotrophic for biotin although biotin ring assembly starting from the precursor pimeloyl-CoA is still functional.
It possesses AccBC, the α-subunit of the acyl-carboxylases involved in fatty acid and mycolic acid synthesis, and pyruvate carboxylase as the only biotin-containing proteins.
Comparative genome analyses suggested that the putative transport system BioYMN encoded by
cg2147, cg2148
and
cg2149
might be involved in biotin uptake by
C.
glutamicum
.
Results
By comparison of global gene expression patterns of cells grown with limiting or excess supply of biotin or with dethiobiotin as supplement replacing biotin revealed that expression of genes coding for enzymes of biotin ring assembly and for the putative uptake system was regulated according to biotin availability.
RT-PCR and 5'-RACE experiments demonstrated that the genes
bioY, bioM
, and
bioN
are transcribed from one promoter as a single transcript.
Biochemical analyses revealed that BioYMN catalyzes the effective uptake of biotin with a concentration of 60 nM biotin supporting a half-maximal transport rate.
Maximal biotin uptake rates were at least five fold higher in biotin-limited cells as compared to cells grown with excess biotin.
Overexpression of
bioYMN
led to an at least 50 fold higher biotin uptake rate as compared to the empty vector control.
Overproduction of BioYMN alleviated biotin limitation and interfered with triggering L-glutamate production by biotin limitation.
Conclusions
The operon
bioYMN
from
C.
glutamicum
was shown to be induced by biotin limitation.
Transport assays with radio-labeled biotin revealed that BioYMN functions as a biotin uptake system.
Overexpression of
bioYMN
affected L-glutamate production triggered by biotin limitation.
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