Abstract
Sorbitol (d-glucitol) metabolism in Aerobacter aerogenes PRL-R3 is shown to proceed via the pathway: sorbitol → sorbitol 6-phosphate → d-fructose 6-phosphate. Sorbitol phosphorylation is mediated by a phosphoenolpyruvate (PEP):sorbitol 6-phosphotransferase system, and sorbitol 6-phosphate oxidation by a pyridine-nucleotide-linked dehydrogenase. Mutants deficient in sorbitol 6-phosphate dehydrogenase or a component (enzyme I) of the phosphotransferase system did not grow on sorbitol, whereas revertants which had regained these enzymatic activities grew normally. Extracts of the enzyme I-deficient mutant failed to catalyze the phosphorylation of sorbitol in the presence of PEP, and adenosine 5′-triphosphate could not replace the PEP requirement for sorbitol phosphorylation in extracts of the wild-type strain.
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Selected References
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- Berman M., Zwaig N., Lin E. C. Suppression of a pleiotropic mutant affecting glycerol dissimilation. Biochem Biophys Res Commun. 1970 Jan 23;38(2):272–278. doi: 10.1016/0006-291x(70)90708-4. [DOI] [PubMed] [Google Scholar]
- HORWITZ S. B., KAPLAN N. O. HEXITOL DEHYDROGENASES OF BACILLUS SUBTILIS. J Biol Chem. 1964 Mar;239:830–838. [PubMed] [Google Scholar]
- Hanson T. E., Anderson R. L. Phosphoenolpyruvate-dependent formation of D-fructose 1-phosphate by a four-component phosphotransferase system. Proc Natl Acad Sci U S A. 1968 Sep;61(1):269–276. doi: 10.1073/pnas.61.1.269. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hengstenberg W., Penberthy W. K., Hill K. L., Morse M. L. Phosphotransferase system of Staphylococcus aureus: its requirement for the accumulation and metabolism of galactosides. J Bacteriol. 1969 Aug;99(2):383–388. doi: 10.1128/jb.99.2.383-388.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
- KUNDIG W., GHOSH S., ROSEMAN S. PHOSPHATE BOUND TO HISTIDINE IN A PROTEIN AS AN INTERMEDIATE IN A NOVEL PHOSPHO-TRANSFERASE SYSTEM. Proc Natl Acad Sci U S A. 1964 Oct;52:1067–1074. doi: 10.1073/pnas.52.4.1067. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kaback H. R. The role of the phosphoenolpyruvate-phosphotransferase system in the transport of sugars by isolated membrane preparations of Escherichia coli. J Biol Chem. 1968 Jul 10;243(13):3711–3724. [PubMed] [Google Scholar]
- Kelker N. E., Hanson T. E., Anderson R. L. Alternate pathways of D-fructose metabolism in Aerobacter aerogenes. A specific D-fructokinase and its preferential role in the metabolism of sucrose. J Biol Chem. 1970 Apr 25;245(8):2060–2065. [PubMed] [Google Scholar]
- LISS M., HORWITZ S. B., KAPLAN N. O. D-Mannitol 1-phosphate dehydrogenase and D-sorbitol 6-phosphate dehydrogenase in Aerobacter aerogenes. J Biol Chem. 1962 Apr;237:1342–1350. [PubMed] [Google Scholar]
- LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
- Martinez De Drets G., Arias A. Metabolism of some polyols by Rhizobium meliloti. J Bacteriol. 1970 Jul;103(1):97–103. doi: 10.1128/jb.103.1.97-103.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Neubaur J., Hollmann S. Uber den Abbau von Sorbit durch Bakterien der Rattenfaeces. Hoppe Seylers Z Physiol Chem. 1967 Jul;348(7):871–876. [PubMed] [Google Scholar]
- Pastan I., Perlman R. L. Repression of beta-galactosidase synthesis by glucose in phosphotransferase mutants of Escherichia coli. Repression in the absence of glucose phosphorylation. J Biol Chem. 1969 Nov 10;244(21):5836–5842. [PubMed] [Google Scholar]
- SCOLNICK E. M., LIN E. C. Parallel induction of D-arabitol and D-sorbitol dehydrogenases. J Bacteriol. 1962 Oct;84:631–637. doi: 10.1128/jb.84.4.631-637.1962. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sapico V., Hanson T. E., Walter R. W., Anderson R. L. Metabolism of D-fructose in Aerobacter aerogenes: analysis of mutants lacking D-fructose 6-phosphate kinase and D-fructose 1,6-diphosphatase. J Bacteriol. 1968 Jul;96(1):51–54. doi: 10.1128/jb.96.1.51-54.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Simoni R. D., Levinthal M., Kundig F. D., Kundig W., Anderson B., Hartman P. E., Roseman S. Genetic evidence for the role of a bacterial phosphotransferase system in sugar transport. Proc Natl Acad Sci U S A. 1967 Nov;58(5):1963–1970. doi: 10.1073/pnas.58.5.1963. [DOI] [PMC free article] [PubMed] [Google Scholar]
- TOUSTER O., SHAW D. R. Biochemistry of the acyclic polyols. Physiol Rev. 1962 Apr;42:181–225. doi: 10.1152/physrev.1962.42.2.181. [DOI] [PubMed] [Google Scholar]
- Tanaka S., Fraenkel D. G., Lin E. C. The enzymatic lesion of strain MM-6, a pleiotropic carbohydrate-negative mutant of Escherichia coli. Biochem Biophys Res Commun. 1967 Apr 7;27(1):63–67. doi: 10.1016/s0006-291x(67)80040-8. [DOI] [PubMed] [Google Scholar]
- Tanaka S., Lerner S. A., Lin E. C. Replacement of a phosphoenolpyruvate-dependent phosphotransferase by a nicotinamide adenine dinucleotide-linked dehydrogenase for the utilization of mannitol. J Bacteriol. 1967 Feb;93(2):642–648. doi: 10.1128/jb.93.2.642-648.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tanaka S., Lin E. C. Two classes of pleiotropic mutants of Aerobacter aerogenes lacking components of a phosphoenolpyruvate-dependent phosphotransferase system. Proc Natl Acad Sci U S A. 1967 Apr;57(4):913–919. doi: 10.1073/pnas.57.4.913. [DOI] [PMC free article] [PubMed] [Google Scholar]
- WOLFF J. B., KAPLAN N. O. D-Mannitol 1-phosphate dehydrogenase from Escherichia coli. J Biol Chem. 1956 Feb;218(2):849–869. [PubMed] [Google Scholar]