Literature DB >> 9084174

Molecular genetic analysis of the region containing the essential Pseudomonas aeruginosa asd gene encoding aspartate-beta-semialdehyde dehydrogenase.

Tung T Hoang1,2, Scott Williams1, Herbert P Schweizer3,2, Joseph S Lam4,3.   

Abstract

asd mutants of Gram-negative and some Gram-positive bacteria have an obligate requirement for diaminopimelic acid (DAP), an essential constituent of the cell wall of these organisms. In environments deprived of DAP, for example mammalian tissues, they will undergo lysis. This was previously exploited to develop vaccine strains of Salmonella typhimurium and cloning vectors containing asd as an in vivo selectable marker. As a first step for development of such systems for Pseudomonas aeruginosa, the asd gene from wild-type strain PAO1 was cloned by a combined approach of PCR amplification from chromosomal DNA, construction of mini-libraries and by complementation of an Escherichia coli delta asd mutant. The nucleotide sequence of a 2433 bp Smal-Nsil fragment was determined. This fragment contained the C-terminal 47 nucleotides of leuB, encoding 3-isopropylmalate dehydrogenase; asd, encoding aspartate-beta-semialdehyde dehydrogenase (Asd); and orfA, whose product showed similarity to the Asd proteins from Vibrio spp. By subcloning, asd was localized to a 1.24 kb DNA fragment which in an E. coli T7 expression system strongly expressed a 40,000 Da protein. The amino acid sequence was deduced from the DNA sequence. A comparison of the Asd proteins from P. aeruginosa, E. coli and Haemophilus influenzae revealed greater than 63% identity, demonstrating the conserved nature of Asd in Gram-negative bacteria, and defined the active-site-containing consensus sequence GGNCTVXMLMXXXLGLF as a possible signature motif. Chromosomal delta asd mutants were isolated. They were auxotrophic for DAP, lysine, methionine and threonine, and lysed in the absence of DAP. Genetic analyses indicated that orfA probably is naturally frame-shifted and does not contribute to the Asd phenotype. By PFGE, the asd gene was mapped to between coordinates 1.89 and 2.15 Mbp, or 37-40 min, on the 5.9 Mbp P. aeruginosa chromosome.

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Year:  1997        PMID: 9084174     DOI: 10.1099/00221287-143-3-899

Source DB:  PubMed          Journal:  Microbiology (Reading)        ISSN: 1350-0872            Impact factor:   2.777


  13 in total

1.  Characterization of a Pseudomonas aeruginosa fatty acid biosynthetic gene cluster: purification of acyl carrier protein (ACP) and malonyl-coenzyme A:ACP transacylase (FabD).

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Review 3.  Bacterial type III secretion system as a protein delivery tool for a broad range of biomedical applications.

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4.  Fatty acid biosynthesis in Pseudomonas aeruginosa: cloning and characterization of the fabAB operon encoding beta-hydroxyacyl-acyl carrier protein dehydratase (FabA) and beta-ketoacyl-acyl carrier protein synthase I (FabB).

Authors:  T T Hoang; H P Schweizer
Journal:  J Bacteriol       Date:  1997-09       Impact factor: 3.490

5.  Dual system to reinforce biological containment of recombinant bacteria designed for rhizoremediation.

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6.  The Burkholderia pseudomallei Δasd mutant exhibits attenuated intracellular infectivity and imparts protection against acute inhalation melioidosis in mice.

Authors:  Michael H Norris; Katie L Propst; Yun Kang; Steven W Dow; Herbert P Schweizer; Tung T Hoang
Journal:  Infect Immun       Date:  2011-08-01       Impact factor: 3.441

7.  Functional characterization of an aminotransferase required for pyoverdine siderophore biosynthesis in Pseudomonas aeruginosa PAO1.

Authors:  Chris S Vandenende; Matthew Vlasschaert; Stephen Y K Seah
Journal:  J Bacteriol       Date:  2004-09       Impact factor: 3.490

8.  A bacterial type III secretion-based protein delivery tool for broad applications in cell biology.

Authors:  Simon J Ittig; Christoph Schmutz; Christoph A Kasper; Marlise Amstutz; Alexander Schmidt; Loïc Sauteur; M Alessandra Vigano; Shyan Huey Low; Markus Affolter; Guy R Cornelis; Erich A Nigg; Cécile Arrieumerlou
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9.  Glyphosate resistance as a novel select-agent-compliant, non-antibiotic-selectable marker in chromosomal mutagenesis of the essential genes asd and dapB of Burkholderia pseudomallei.

Authors:  Michael H Norris; Yun Kang; Diana Lu; Bruce A Wilcox; Tung T Hoang
Journal:  Appl Environ Microbiol       Date:  2009-07-31       Impact factor: 4.792

10.  The genome sequence of Geobacter metallireducens: features of metabolism, physiology and regulation common and dissimilar to Geobacter sulfurreducens.

Authors:  Muktak Aklujkar; Julia Krushkal; Genevieve DiBartolo; Alla Lapidus; Miriam L Land; Derek R Lovley
Journal:  BMC Microbiol       Date:  2009-05-27       Impact factor: 3.605

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