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Molecular cloning and analysis of the argC gene from Corynebacterium glutamicum

Authors
Chun J.-Y.Lee E.-J.Lee H.-S.Cheon C.-I.Min K.-H.Lee M.-S.
Issue Date
Oct-1998
Publisher
Academic Press
Keywords
Arginine biosynthetic gene; Corynebacterium glutamicum; N-acetylglutamate 5-semialdehyde dehydrogenase
Citation
Biochemistry and Molecular Biology International, v.46, no.3, pp 437 - 447
Pages
11
Journal Title
Biochemistry and Molecular Biology International
Volume
46
Number
3
Start Page
437
End Page
447
URI
https://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/150383
DOI
10.1080/15216549800203962
ISSN
1039-9712
Abstract
The argC gene encoding N-acetylglutamate 5-semialdehyde dehydrogenase has been cloned from Corynebacterium glutamicum by transforming Escherichia coli arginine auxotroph with the genomic DNA library. Based on the restriction map of the cloned DNA, we have subcloned and sequenced the minimal DNA fragment complementing the E. coli argC mutant. The coding region of the cloned gene is 1041 nucleotides long with a predicted molecular mass of about 38 kDa polypeptide. Enzyme activity and size of the expressed protein in the E. coli auxotroph carrying the recombinant argC gene revealed that the cloned gene indeed codes for N-acetylglutamate 5-semialdehyde dehydrogenase. Computer analysis of the amino acid sequences of the predicted protein revealed a strong similarity to the corresponding protein of other bacteria.
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