Literature DB >> 11029436

Positive selection for mutations affecting bioconversion of aromatic compounds in Agrobacterium tumefaciens: analysis of spontaneous mutations in the protocatechuate 3,4-dioxygenase gene.

D Parke1.   

Abstract

A positive selection method for mutations affecting bioconversion of aromatic compounds was applied to a mutant strain of Agrobacterium tumefaciens A348. The nucleotide sequence of the A348 pcaHGB genes, which encode protocatechuate 3,4-dioxygenase (PcaHG) and beta-carboxy-cis,cis-muconate cycloisomerase (PcaB) for the first two steps in catabolism of the diphenolic protocatechuate, was determined. An omega element was introduced into the pcaB gene of A348, creating strain ADO2077. In the presence of phenolic compounds that can serve as carbon sources, growth of ADO2077 is inhibited due to accumulation of the tricarboxylate intermediate. The toxic effect, previously described for Acinetobacter sp., affords a powerful selection for suppressor mutations in genes required for upstream catabolic steps. By monitoring loss of the marker in pcaB, it was possible to determine that the formation of deletions was minimal compared to results obtained with Acinetobacter sp. Thus, the tricarboxylic acid trick in and of itself does not appear to select for large deletion mutations. The power of the selection was demonstrated by targeting the pcaHG genes of A. tumefaciens for spontaneous mutation. Sixteen strains carrying putative second-site mutations in pcaH or -G were subjected to sequence analysis. All single-site events, their mutations revealed no particular bias toward multibase deletions or unusual patterns: five (-1) frameshifts, one (+1) frameshift, one tandem duplication of 88 bp, one deletion of 92 bp, one nonsense mutation, and seven missense mutations. PcaHG is considered to be the prototypical ferric intradiol dioxygenase. The missense mutations served to corroborate the significance of active site amino acid residues deduced from crystal structures of PcaHG from Pseudomonas putida and Acinetobacter sp. as well as of residues in other parts of the enzyme.

Entities:  

Mesh:

Substances:

Year:  2000        PMID: 11029436      PMCID: PMC94750          DOI: 10.1128/JB.182.21.6145-6153.2000

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  39 in total

1.  Substitution, insertion, deletion, suppression, and altered substrate specificity in functional protocatechuate 3,4-dioxygenases.

Authors:  D A D'Argenio; M W Vetting; D H Ohlendorf; L N Ornston
Journal:  J Bacteriol       Date:  1999-10       Impact factor: 3.490

2.  Organization and sequences of p-hydroxybenzaldehyde dehydrogenase and other plasmid-encoded genes for early enzymes of the p-cresol degradative pathway in Pseudomonas putida NCIMB 9866 and 9869.

Authors:  C N Cronin; J Kim; J H Fuller; X Zhang; W S McIntire
Journal:  DNA Seq       Date:  1999

3.  Combined genetic and physical map of the complex genome of Agrobacterium tumefaciens.

Authors:  B W Goodner; B P Markelz; M C Flanagan; C B Crowell; J L Racette; B A Schilling; L M Halfon; J S Mellors; G Grabowski
Journal:  J Bacteriol       Date:  1999-09       Impact factor: 3.490

4.  Analysis of a 1600-kilobase Rhizobium meliloti megaplasmid using defined deletions generated in vivo.

Authors:  T C Charles; T M Finan
Journal:  Genetics       Date:  1991-01       Impact factor: 4.562

5.  Characterization of Bradyrhizobium japonicum pcaBDC genes involved in 4-hydroxybenzoate degradation.

Authors:  M J Lorite; J Sanjuan; L Velasco; J Olivares; E J Bedmar
Journal:  Biochim Biophys Acta       Date:  1998-05-11

6.  Construction of mobilizable vectors derived from plasmids RP4, pUC18 and pUC19.

Authors:  D Parke
Journal:  Gene       Date:  1990-09-01       Impact factor: 3.688

7.  Structure of Acinetobacter strain ADP1 protocatechuate 3, 4-dioxygenase at 2.2 A resolution: implications for the mechanism of an intradiol dioxygenase.

Authors:  M W Vetting; D A D'Argenio; L N Ornston; D H Ohlendorf
Journal:  Biochemistry       Date:  2000-07-11       Impact factor: 3.162

8.  Cloning, sequencing, and expression of the Pseudomonas putida protocatechuate 3,4-dioxygenase genes.

Authors:  R W Frazee; D M Livingston; D C LaPorte; J D Lipscomb
Journal:  J Bacteriol       Date:  1993-10       Impact factor: 3.490

9.  Characterization of PcaQ, a LysR-type transcriptional activator required for catabolism of phenolic compounds, from Agrobacterium tumefaciens.

Authors:  D Parke
Journal:  J Bacteriol       Date:  1996-01       Impact factor: 3.490

10.  Efflux pumps involved in toluene tolerance in Pseudomonas putida DOT-T1E.

Authors:  J L Ramos; E Duque; P Godoy; A Segura
Journal:  J Bacteriol       Date:  1998-07       Impact factor: 3.490

View more
  4 in total

1.  Analysis of hydroxycinnamic acid degradation in Agrobacterium fabrum reveals a coenzyme A-dependent, beta-oxidative deacetylation pathway.

Authors:  Tony Campillo; Sébastien Renoud; Isabelle Kerzaon; Ludovic Vial; Jessica Baude; Vincent Gaillard; Floriant Bellvert; Cécile Chamignon; Gilles Comte; Xavier Nesme; Céline Lavire; Florence Hommais
Journal:  Appl Environ Microbiol       Date:  2014-03-21       Impact factor: 4.792

2.  Coordinated Regulation of Species-Specific Hydroxycinnamic Acid Degradation and Siderophore Biosynthesis Pathways in Agrobacterium fabrum.

Authors:  Jessica Baude; Ludovic Vial; Camille Villard; Tony Campillo; Céline Lavire; Xavier Nesme; Florence Hommais
Journal:  Appl Environ Microbiol       Date:  2016-05-31       Impact factor: 4.792

3.  Toxicity caused by hydroxycinnamoyl-coenzyme A thioester accumulation in mutants of Acinetobacter sp. strain ADP1.

Authors:  Donna Parke; L Nicholas Ornston
Journal:  Appl Environ Microbiol       Date:  2004-05       Impact factor: 4.792

4.  Reconstruction and analysis of a genome-scale metabolic model for Agrobacterium tumefaciens.

Authors:  Nan Xu; Qiyuan Yang; Xiaojing Yang; Mingqi Wang; Minliang Guo
Journal:  Mol Plant Pathol       Date:  2021-01-12       Impact factor: 5.663

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.