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Molecular cloning and characterization of the aroD gene encoding 3-dehydroquinase from Salmonella typhi

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The aroD gene from Salmonella typhi, encoding 5-dehydroquinate hydrolyase (3-dehydroquinase), has been cloned into Escherichia coli and the DNA sequence determined. The aroD gene was isolated from a cosmid gene bank by complementation of an S. typhimurium aroD mutant. Analysis of the DNA sequence revealed the presence of an open reading frame capable of encoding a protein of 252 amino acids with a calculated M r of 27706. Comparison of the deduced S. typhi 3-dehydroquinase protein sequence with that elucidated for E. coli revealed 69 % homology. Alignment of the S. typhi sequence and equivalent Aspergillus nidulans and Saccharomyces cerevisiae sequences showed that homology was lower, at 24%, but still significant. Use of a minicell expression system demonstrated that a polyclonal antibody raised against E. coli 3-dehydroquinase cross-reacted with its S. typhi counterpart.
Title: Molecular cloning and characterization of the aroD gene encoding 3-dehydroquinase from Salmonella typhi
Description:
The aroD gene from Salmonella typhi, encoding 5-dehydroquinate hydrolyase (3-dehydroquinase), has been cloned into Escherichia coli and the DNA sequence determined.
The aroD gene was isolated from a cosmid gene bank by complementation of an S.
typhimurium aroD mutant.
Analysis of the DNA sequence revealed the presence of an open reading frame capable of encoding a protein of 252 amino acids with a calculated M r of 27706.
Comparison of the deduced S.
typhi 3-dehydroquinase protein sequence with that elucidated for E.
coli revealed 69 % homology.
Alignment of the S.
typhi sequence and equivalent Aspergillus nidulans and Saccharomyces cerevisiae sequences showed that homology was lower, at 24%, but still significant.
Use of a minicell expression system demonstrated that a polyclonal antibody raised against E.
coli 3-dehydroquinase cross-reacted with its S.
typhi counterpart.

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