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J Bacteriol. 1970 March; 101(3): 763–769.
PMCID: PMC250388
Comparative Allostery of 3-Deoxy-d-Arabino-Heptulosonate-7-Phosphate Synthetase as a Molecular Basis for Classification
Roy A. Jensen and Sherry L. Stenmark
Department of Microbiology, Baylor College of Medicine, Houston, Texas 77025
Abstract
The allosteric pattern of control for 3-deoxy-d-arabino-heptulosonate 7-phosphate (DAHP) synthetase has previously been shown to be strongly conserved among the member species of a given genus in bacteria. The implications of this finding as a procedural tool of bacterial phylogeny were pursued by a study of two organisms, Sporosarcina ureae and Aeromonas formicans, the taxonomic positions of which have been historically controversial. S. ureae has characteristics of both Bacillaceae and Micrococcaceae, and A. formicans has characteristics of both Enterobacteriaceae and pseudomonads. Since the patterns of control for DAHP synthetase in all four of these microbial groups are different from one another but internally homogeneous within each group, the results obtained from the two test organisms were unambiguous. It was concluded that S. ureae is properly classified within Bacillaceae, probably deserving generic rank, and that A. formicans belongs with the family Enterobacteriaceae.
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Selected References
These references are in PubMed. This may not be the complete list of references from this article.
  • Canale-Parola E, Mandel M, Kupper DG. The classification of sarcinae. Arch Mikrobiol. 1967;58(1):30–34. [PubMed]
  • Cohen GN, Stanier RY, Le Bras G. Regulation of the biosynthesis of amino acids of the aspartate family in Coliform bacteria and Pseudomonads. J Bacteriol. 1969 Sep;99(3):791–801. [PubMed]
  • CRAWFORD IP. A new fermentative pseudomonad, Pseudomonas formicans, n. sp. J Bacteriol. 1954 Dec;68(6):734–738. [PubMed]
  • Crawford IP, Sikes S, Melhorn DK. The natural relationships of Aeromonas formicans. Arch Mikrobiol. 1967;59(1):72–81. [PubMed]
  • DELEY J. PSEUDOMONAS AND RELATED GENERA. Annu Rev Microbiol. 1964;18:17–46. [PubMed]
  • Herndon SE, Bott KF. Genetic relationship between Sarcina ureae and members of the genus Bacillus. J Bacteriol. 1969 Jan;97(1):6–12. [PubMed]
  • Hill LR. An index to deoxyribonucleic acid base compositions of bacterial species. J Gen Microbiol. 1966 Sep;44(3):419–437. [PubMed]
  • IANDOLO JJ, ORDAL ZJ. GERMINATION SYSTEM FOR ENDOSPORES OF SARCINA UREAE. J Bacteriol. 1964 Jan;87:235–236. [PubMed]
  • Jensen RA. A biochemical basis for apparent abortive transformation in Bacillus subtilis. Genetics. 1968 Dec;60(4):707–717. [PubMed]
  • Jensen RA. Metabolic interlock. Regulatory interactions exerted between biochemical pathways. J Biol Chem. 1969 Jun 10;244(11):2816–2823. [PubMed]
  • Jensen RA, Nasser DS. Comparative regulation of isoenzymic 3-deoxy-D-arabino-heptulosonate 7-phosphate synthetases in microorganisms. J Bacteriol. 1968 Jan;95(1):188–196. [PubMed]
  • Jensen RA, Nasser DS, Nester EW. Comparative control of a branch-point enzyme in microorganisms. J Bacteriol. 1967 Nov;94(5):1582–1593. [PubMed]
  • JENSEN RA, NESTER EW. THE REGULATORY SIGNIFICANCE OF INTERMEDIARY METABOLITES: CONTROL OF AROMATIC ACID BIOSYNTHESIS BY FEEDBACK INHIBITION IN BACILLUS SUBTILIS. J Mol Biol. 1965 Jun;12:468–481. [PubMed]
  • Jensen RA, Nester EW. Regulatory enzymes of aromatic amino acid biosynthesis in Bacillus subtilis. I. Purification and properties of 3-deoxy-D-arabino-heptulosonate 7-phosphate synthetase. J Biol Chem. 1966 Jul 25;241(14):3365–3372. [PubMed]
  • Jensen RA, Nester EW. Regulatory enzymes of aromatic amino acid biosynthesis in Bacillus subtilis. II. The enzymology of feedback inhibition of 3-deoxy-D-arabino-heptulosonate 7-phosphate synthetase. J Biol Chem. 1966 Jul 25;241(14):3373–3380. [PubMed]
  • Mandel M. New approaches to bacterial taxonomy: perspective and prospects. Annu Rev Microbiol. 1969;23:239–274. [PubMed]
  • MARMUR J, FALKOW S, MANDEL M. NEW APPROACHES TO BACTERIAL TAXONOMY. Annu Rev Microbiol. 1963;17:329–372. [PubMed]
  • Mazanec K, Kocur M, Martinec T. Electron Microscopy of Ultrathin Sections of Sporosarcina ureae. J Bacteriol. 1965 Sep;90(3):808–816. [PubMed]
  • Nester EW, Jensen RA. Control of aromatic acid biosynthesis in Bacillus subtilis: sequenial feedback inhibition. J Bacteriol. 1966 Apr;91(4):1594–1598. [PubMed]
  • Rosypal S, Rosypalová A, Horejs J. The classification of micrococci and staphylococci based on their DNA base composition and adansonian analysis. J Gen Microbiol. 1966 Aug;44(2):281–292. [PubMed]
  • SMITH LC, RAVEL JM, LAX SR, SHIVE W. The control of 3-deoxy-D-arabino-heptulosonic acid 7-phosphate synthesis by phenylalanine and tyrosine. J Biol Chem. 1962 Nov;237:3566–3570. [PubMed]
  • SRINIVASAN PR, SPRINSON DB. 2-Keto-3-deoxy-D-arabo-heptonic acid 7-phosphate synthetase. J Biol Chem. 1959 Apr;234(4):716–722. [PubMed]
  • Stanier RY, Palleroni NJ, Doudoroff M. The aerobic pseudomonads: a taxonomic study. J Gen Microbiol. 1966 May;43(2):159–271. [PubMed]
  • THOMPSON RS, LEADBETTER ER. On the isolation of dipicolinic acid fromhendospores of Sarcina ureae. Arch Mikrobiol. 1963;45:27–32. [PubMed]