Sequence analysis and complementation studies of the argJ gene encoding ornithine acetyltransferase from Neisseria gonorrhoeae
- PMID: 1339419
- PMCID: PMC205910
- DOI: 10.1128/jb.174.8.2694-2701.1992
Sequence analysis and complementation studies of the argJ gene encoding ornithine acetyltransferase from Neisseria gonorrhoeae
Abstract
Clinical isolates of Neisseria gonorrhoeae frequently are deficient in arginine biosynthesis. These auxotrophs often have defects in the fifth step of the arginine biosynthetic pathway, the conversion of acetylornithine to ornithine. This reaction is catalyzed by the enzyme ornithine acetyltransferase, which is a product of the argJ gene. We have cloned and sequenced the gonococcal argJ gene and found that it contains an open reading frame of 1,218 nucleotides and encodes a peptide with a deduced Mr of 42,879. This predicted size was supported by minicell analysis. This gene was capable of complementing both Escherichia coli argE and argA mutations and of transforming an ArgJ- strain of N. gonorrhoeae to Arg+. Southern blots were able to detect bands that specifically hybridized to the gonococcal argJ gene in genomic DNA from Pseudomonas aeruginosa but not E. coli, a result that reflects the divergent nature of the arginine biosynthetic pathway in these organisms.
Similar articles
-
Cloning and organization of seven arginine biosynthesis genes from Neisseria gonorrhoeae.J Bacteriol. 1989 Mar;171(3):1644-51. doi: 10.1128/jb.171.3.1644-1651.1989. J Bacteriol. 1989. PMID: 2493452 Free PMC article.
-
Genes and enzymes of the acetyl cycle of arginine biosynthesis in the extreme thermophilic bacterium Thermus thermophilus HB27.Microbiology (Reading). 1998 Feb;144 ( Pt 2):479-492. doi: 10.1099/00221287-144-2-479. Microbiology (Reading). 1998. PMID: 9493385
-
Characterization and kinetic mechanism of mono- and bifunctional ornithine acetyltransferases from thermophilic microorganisms.Eur J Biochem. 2000 Aug;267(16):5217-26. doi: 10.1046/j.1432-1327.2000.01593.x. Eur J Biochem. 2000. PMID: 10931207
-
Molecular characterization of the argJ mutation in Neisseria gonorrhoeae strains with requirements for arginine, hypoxanthine, and uracil.Infect Immun. 1992 Mar;60(3):970-5. doi: 10.1128/iai.60.3.970-975.1992. Infect Immun. 1992. PMID: 1339413 Free PMC article.
-
Genetic and biochemical analyses of protein II.Antonie Van Leeuwenhoek. 1987;53(6):421-4. doi: 10.1007/BF00415496. Antonie Van Leeuwenhoek. 1987. PMID: 3130781 Review.
Cited by
-
Metabolic engineering of microorganisms for the production of L-arginine and its derivatives.Microb Cell Fact. 2014 Dec 3;13:166. doi: 10.1186/s12934-014-0166-4. Microb Cell Fact. 2014. PMID: 25467280 Free PMC article.
-
The crystal structure of N-acetyl-L-glutamate synthase from Neisseria gonorrhoeae provides insights into mechanisms of catalysis and regulation.J Biol Chem. 2008 Mar 14;283(11):7176-84. doi: 10.1074/jbc.M707678200. Epub 2008 Jan 9. J Biol Chem. 2008. PMID: 18184660 Free PMC article.
-
Heterologous and homologous expression of the arginine biosynthetic argC~H cluster from Corynebacterium crenatum for improvement of (L) -arginine production.J Ind Microbiol Biotechnol. 2012 Mar;39(3):495-502. doi: 10.1007/s10295-011-1042-4. Epub 2011 Oct 19. J Ind Microbiol Biotechnol. 2012. PMID: 22009057
-
A novel type of N-acetylglutamate synthase is involved in the first step of arginine biosynthesis in Corynebacterium glutamicum.BMC Genomics. 2013 Oct 18;14:713. doi: 10.1186/1471-2164-14-713. BMC Genomics. 2013. PMID: 24138314 Free PMC article.
-
Surprising arginine biosynthesis: a reappraisal of the enzymology and evolution of the pathway in microorganisms.Microbiol Mol Biol Rev. 2007 Mar;71(1):36-47. doi: 10.1128/MMBR.00032-06. Microbiol Mol Biol Rev. 2007. PMID: 17347518 Free PMC article. Review.
References
Publication types
MeSH terms
Substances
Associated data
- Actions
- Actions
- Actions
- Actions
- Actions
- Actions
- Actions
- Actions
- Actions
- Actions
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases