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

References

• Cronin C. N. cDNA cloning, recombinant expression and site-directed mutagenesis of bovine liver carnitine octanoyltransferase. Arg505 binds the carboxylate group of carnitine. European Journal of Biochemistry 1997; 247: 1029–1037
   PubMedGoogle Scholar
• Chalmers R. M., Fewson C. A. Purification and characterization of benzaldehyde dehydrogenase I from Acinetobacter calcoaceticus. Biochemical Journal 1989; 263: 913–919
   PubMed Web of Science ®Google Scholar
• Frazee R. W., Livingston D. ML, LaPorte D. C., Lipscomb J. D. Cloning, sequencing, and expression of the Pseudomonas putida protocatechuate 3,4-dioxygenase genes. Journal of Bacteriology 1993; 175: 6194–6202
   PubMed Web of Science ®Google Scholar
• Gibson D. T., Zylstra G. L., Chauhan S. Biotransformations catalyzed by toluene dioxygenase from Pseudomanas putida F1. Pseudomonas: Biotransformation, Pathogenesis, and Evolving Biotechnology, S. Silver, A.M. Chakrabarty, B. Iglewski, S. Kaplan. American Society for Microbiology, Washington, D.C. 1990; 121–132
   Google Scholar
• Harayama S., Timmis K. N. Aerobic biodegradation of aromatic hydrocarbons by bacteria. Degradation of Environmental Pollutants by Microorganisms and Their Metalloenzymes. Metal Ions in Biological Systems, H. Sigel, A. Sigel. Marcel Dekker, Inc., New York 1992; Vol. 28: 99–156
   Google Scholar
• Higgins D. G., Bleasby A. J., Fuchs R. Improved software for multiple sequence alignment. Computer Applications in the Biosciences 1992; 8: 189–91
   PubMedGoogle Scholar
• Hofmann K., Stoffel W. TMbase - A database of membrane spanning proteins segments. Biological Chemistry Hoppe-Seyler 1993; 347: 66–70
   Google Scholar
• Hopper D. J. Thehydroxylation of p-cresol and its conversion to p-hydroxybenzaldehyde in Pseudomonas putida. Biochemical and Biophysical Research Communications 1976; 69: 462–468
   PubMed Web of Science ®Google Scholar
• Hsu L. C., Tani K., Fujiyoshi T., Kurachi K., Yoshida A. Cloning of cDNAs for human aldehyde dehydrogenases 1 and 2. Proceedings of the National Academy of Science U.S.A. 1985; 82: 3771–3775
   PubMed Web of Science ®Google Scholar
• Inoue J., Shaw J. P., Rekik M., Harayama S. Overlapping substrate specificities of benzaldehyde dehydrogenase (the xylC gene product) and 2-hydroxymuconic semialdehyde dehydrogenase (the xylG gene product) encoded by TOL plasmid pWW0 of Pseudomonas putida. Journal of Bacteriology 1995; 177: 1196–1201
   PubMed Web of Science ®Google Scholar
• Jain R. K., Bayly R. C., Skurray R. A. Characterization and physical analysis of a 3,5-xylenol degradative plasmid in Pseudomonas putida. Journal of General Microbiology 1984; 130: 3019–3028
   Google Scholar
• Jones D. E., Brennan M. D., Hempel J., Lindahl R. Cloning and complete nucleotide sequence of a full-length cDNA encoding a catalytically functional tumor-associated aldehyde dehydrogenase. Proceedings of the National Academy of Science U.S.A. 1988; 85: 1782–1786
   PubMed Web of Science ®Google Scholar
• Keat M. J., Hopper D. J. Aromatic-aldehyde dehydrogenases from Pseudomonas putida N.C.I.B. 9869. Biochemical Society Transactions 1975; 3: 385–386
   PubMed Web of Science ®Google Scholar
• Kim J., Fuller J. H., Cecchini G., McIntire W. S. Cloning, sequencing and expression of the structural genes for the cytochrome and flavoprotein subunits of p-cresol methylhydroxylase from two strains of Pseudomonas putida. Journal of Bacteriology 1994; 176: 6349–6361
   PubMed Web of Science ®Google Scholar
• Liu 2-J., Sun Y-J., Rose J., Chung Y-J., Hsiao C-D., Chang W-R., Kuo I., Perozich J., Lindahl R., Hempel J., Wang B-C. The first strucure of an aldehyde dehydrogenase reveals novel interactions between NAD and the Rossman fold. Nature Structural Biology 1997; 4: 317–326
   PubMedGoogle Scholar
• MacKintosh R. W., Fewson C. A. Benzyl alcohol dehydrogenase and benzaldehyde dehydrogenase II from Acinetobacter calcoaceticus. Biochemical Journal 1988; 250: 743–751
   PubMed Web of Science ®Google Scholar
• Marck C. DNA Strider: a “C” program for the fast analysis of DNA and protein sequences on the Apple Macintosh family of computers. Nucleic Acids Research 1988; 16: 1829–1836
   PubMed Web of Science ®Google Scholar
• Nakai K., Kanehisa M. Expert system for predicting protein localization sites in Gram-negative bacteria. Proteins 1991; 11: 95–110
   PubMed Web of Science ®Google Scholar
• Olsen R. H., Kukor J. J., Kaphammer B. A novel toluene-3-monooxygenase pathway cloned from Pseudomonas pickettii PKO1. Journal of Bacteriology 1994; 176: 3749–3756
   PubMed Web of Science ®Google Scholar
• Platt T. Transcription termination and the regulation of gene expression. Annual Review of Biochemistry 1986; 55: 339–372
   PubMed Web of Science ®Google Scholar
• Ronald S., Farinha M. A., Allan B. J., Kropinski A. M. Cloning and physical mapping of transcriptional regulatory (Sigma) factors from Pseudomonas aeruginosa. Pseudomonas Molecular Biology and Biotechnology, E. Galli, S. Silver, B. Witholt. American Society for Microbiology, Washington, D. C. 1992; 249–257
   Google Scholar
• Shields M. S., Montgomery S. O., Chapman P. J., Cuskey S. M., Pritchard P. H. Novel pathway of toluene catabolism in the trichloroethylene-degrading bacterium G4. Applied and Environmental Microbiology 1989; 55: 1624–1629
   PubMed Web of Science ®Google Scholar
• Wang X. P., Weiner H. Involvement of glutamate 268 in the active site of human liver mitochondrial (class 2) aldehyde dehydrogenase as probed by site-directed mutagenesis. Biochemistry 1995; 34: 237–243
   PubMed Web of Science ®Google Scholar
• Whited G. M., Gibson D. T. (a) Toluene-4-monooxygenase, a three-component enzyme system that catalyzes the oxidation of toluene to p-cresol in Pseudomonas mendocina KR1. Journal of Bacteriology 1991; 173: 3010–3016
   PubMed Web of Science ®Google Scholar
• Whited G. M., Gibson D. T. (b) Separation and partial characterization of the enzymes of the toluene-4-monooxygenase catabolic pathway in Pseudomonas mendocina KR1. Journal of Bacteriology 1991; 173: 3017–3020
   PubMed Web of Science ®Google Scholar
• Wright A., Olsen R. H. Self-mobilization and organization of the genes encoding the toluene metabolic pathway of Pseudomonas mendocina KR1. Applied and Environmental Microbiology 1994; 60: 235–242
   PubMed Web of Science ®Google Scholar